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Sex differences in human physiology

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For general sex differences in humans, see Sex differences in humans.

Example of male and female anatomy from front and back.
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Sex differences in human physiology are distinctions of physiological characteristics associated with either male or female humans. These differences are caused by the effects of the different sex chromosome complement in males and females, and differential exposure to gonadal sex hormones during development. Sexual dimorphism is a term for the phenotypic difference between males and females of the same species.

The process of meiosis and fertilization (with rare exceptions) results in a zygote with either two X chromosomes (an XX female) or one X and one Y chromosome (an XY male) which then develops the typical female or male phenotype. Physiological sex differences include discrete features such as the respective male and female reproductive systems, as well as average differences between males and females including size and strength, bodily proportions, hair distribution, breast differentiation, voice pitch, and brain size and structure.

Sex determination and differentiation

The human Y chromosome showing the SRY gene. SRY is a gene which regulates sexual differentiation.
See also: Sexual differentiation in humans

The human genome consists of two copies of each of 23 chromosomes (a total of 46).[1] One set of 23 comes from the mother and one set comes from the father.[1] Of these 23 pairs of chromosomes, 22 are autosomes, and one is a sex chromosome.[1] There are two kinds of sex chromosomes–X and Y. In humans and in almost all other mammals, females carry two X chromosomes, designated XX, and males carry one X and one Y, designated XY.[1]

A human egg contains only one set of chromosomes (23) and is a haploid. Sperm also have only one set of 23 chromosomes and are therefore haploid. When an egg and sperm fuse at fertilization, the two sets of chromosomes come together to form a unique diploid individual with 46 chromosomes.[2]

The sex chromosome in a human egg is always an X chromosome since a female only has X sex chromosomes. In sperm, about half the sperm have an X chromosome and half have a Y chromosome.[2] If an egg fuses with sperm with a Y chromosome, the resulting individual is male. If an egg fuses with sperm with an X chromosome, the resulting individual is female.[2] There are rare exceptions to this rule in which, for example, XX individuals develop as males or XY individuals develop as females.[3] Chromosomes are not the final determinant of sex. In some cases, for example, chromosomally female babies that have been exposed to high levels of androgens before birth can develop masculinized genitals by the time they are born.[4] There are other variations of sex chromosomes that lead to a variety of different physical expressions.[5]

The X-chromosome carries a larger number of genes in comparison to the Y-chromosome. In humans, X-chromosome inactivation enables males and females to have an equal expression of the genes on the X-chromosome since females have two X-chromosomes while males have a single X and a Y chromosome. X-chromosome inactivation is random in the somatic cells of the body as either the maternal or paternal X-chromosome can become inactivated in each cell. Thus, females are genetic mosaics.[6]

Size and body shape

See also: Secondary sex characteristics, Human body shape, and Female body shape
  • Externally, the most sexually dimorphic portions of the human body are the chest, the lower half of the face, and the area between the waist and the knees.[7]
  • Males weigh more than females on average.[8]
  • On average, males are taller than females by about 10%.[8]
  • On average, males have a larger waist in comparison to their hips (see waist–hip ratio) than females.[9][10]
  • In females, the index and ring fingers tend to be either more similar in size or their index finger is slightly longer than their ring finger, whereas male's ring finger tends to be longer.[11]

Skeleton and muscular system

Skeleton

Comparison between a male (left) and a female pelvis (right).

The female skeleton is generally less massive, smoother, and thinner than the male;[12] its rib cage is more rounded and smaller, its lumbar curve greater, and a generally longer and smaller female waist results from the chest being more narrow at the base, and the pelvis generally not as high.[12]

The pelvis is, in general, different between the human female and male skeleton.[12][13] Although variations exist and there may be a degree of overlap between typically male or female traits,[12][13] the pelvis is the most dimorphic bone of the human skeleton and is therefore likely to be accurate when using it to ascertain a person's sex.[13] It differs both in overall shape and structure. The female pelvis, which is adapted for gestation and childbirth, is less high, but proportionately wider and more circular than in the male; its sacrum—the triangular bone at the upper posterior of the pelvic cavity, serving as the base of the spine—is also wider.[12] The female pelvis is tilted anteriorly, often resulting in the more sway-backed appearance.

In females, the acetabula, the concave surfaces to which the balls of the femurs attach via ligaments, are located farther apart,[14][15] which increases the distance between the most outer points of the femurs (their greater trochanters) and thus the width of the hips.[15] Female femurs are therefore more generally angled (laterally, further away from vertical).[15] This greater angle applies a larger portion of the gravitational or vertical load as valgus torque (rotational force against the knee).[15] This, combined with the female's weaker tendons and ligaments and a narrower intercondylar notch, causes increased susceptibility to injury of the ACL in female athletes.[16][17]

The pelvis of the human male is slightly narrower.[12] One hypothesis is that this makes it more optimized for walking and that the wider female pelvis is an evolutionary compromise between efficient walking and the need for successful childbirth.[18] This is termed the obstetrical dilemma.[19][20] Disagreement exists as to the strength of the hypothesis.[19][20]

Males and females do not differ in their number of ribs; both normally have twelve pairs.[21]

The following further generalizations have been made regarding male-female skeletal differences:

  • Males in general have denser, stronger bones, tendons, and ligaments.[12]
  • Female skulls and head bones differ in size and shape from the male skull, with the male mandible generally wider, larger, and squarer than the female.[12][22] In addition, males generally have a more prominent brow, an orbital with rounded border, and more greatly projecting mastoid processes.[12]
  • Males have a more pronounced Adam's apple or thyroid cartilage and deeper voices due to larger vocal cords.[23]
  • Males have larger teeth than females and a greater proportion of the tooth in males is made up of dentine, whereas females have proportionately more enamel.[24]

Muscle mass and strength

Pubertal changes in males lead to a ten times increase in testosterone. Because of this and because males go through puberty for longer, females typically have lower total muscle mass than males, and also have lower muscle mass in comparison to total body mass.[8] Males convert more of their caloric intake into muscle and expendable circulating energy reserves, while females tend to convert more into fat deposits.[25] As a consequence, males are generally physically stronger than females.[8] Research suggests that, while males have greater total muscle areas than females, the number of muscle fibers in males and females are alike. Instead of muscle fiber composition as the main reason for male's greater absolute strength, the data indicates that it is total muscle area that is responsible for this difference.[26] Males' individual muscle fibers are larger than women's, which results in their more muscular appearance. Their larger muscle fibers appear responsible for their more considerable absolute force production.[26]

The sex difference in muscle mass remains after adjusting for body weight and height.[26] Males are usually stronger than females when adjusting for differences in total body mass, due to the higher male muscle-mass to body-mass ratio.[8][27] The greater muscle mass is reported to be due to a greater capacity for muscular hypertrophy as a result of higher levels of circulating testosterone in males.[28]

The studies often show different results about the body strength difference between the both sexes. Two studies, conducted in the four European Union countries, involving 2,000 participants (1,000 men and 1 000 women) concluded that females are 74 - 92% as strong as males, as many women (211 of 1,000) are still physically stronger than average men.[29][30] The differences is smaller in lower body strength and higher in upper body strength.[27] Some researches shows gross measures of body strength suggest that females are approximately 50-60% as strong as males in the upper body, and 60-70% as strong in the lower body.[31] One study of muscle strength in the elbows and knees—in 45 and older males and females—found the strength of females to range from 42 to 63% of male strength.[32] Males have greater hand grip strength than females.[33][34] Differences in width of arm, thighs and calves appear during puberty.

Respiratory system

Males typically have larger tracheae and main bronchi and greater lung volume per body mass.[35] They also have larger hearts,[36] 10% higher red blood cell count, and higher haemoglobin hence greater oxygen-carrying capacity.[37][38] They have higher circulating clotting factors (vitamin K, prothrombin and platelets). These differences lead to faster clotting of blood and higher peripheral pain tolerance.[39]

Sex differences in the trachea and main bronchi are not apparent until at least age 14.[35] On average, females have smaller lungs than males at birth.[35]

Skin and hair

See also: Androgenic hair and Human skin

Skin

Males' skin is thicker and oilier than females' skin.[40] Females have more subcutaneous fat than males. This helps keep them warmer and enables them to survive lower temperatures than males during the cold.[41] As a result of greater vasoconstriction, while the surface of female skin is colder than male skin, the deep-skin temperature in females is higher than in males.[42]

Males generally have darker skin than females.[43][44] The lighter skin in females helps their bodies synthesize more Vitamin D from sunlight and absorb more calcium, which is needed during pregnancy and lactation.[44]

Hair

On average, males have more body hair than females. Males have relatively more of a type of hair called terminal hair, especially on the face, chest, abdomen and back. Females have more vellus hair, which is thinner, shorter, and lighter, and therefore less visible.[45]

Although males grow hair faster than females, baldness is more prevalent in males than in females. The main cause for this is male pattern baldness. Male pattern baldness is a condition where hair loss occurs in a typical pattern of a receding hairline and hair thinning on the crown. It is caused by hormones and genetic predisposition.[46]

Color

Some studies suggest that red and blond hair are more common in females than in males (red more so than blond).

In lighter-complected humans, male skin is visibly redder; this is due to greater blood volume rather than melanin.[47][48] Conversely, females are lighter-skinned than males in some studied human populations.[49][50] The differences in color are mainly caused by higher levels of melanin in the skin, hair and eyes in males.[51][52]

In one study, almost twice as many females as males had red or auburn hair. A higher proportion of females were also found to have blond hair, whereas males were more likely to have black or dark brown hair.[53] Another study found green eyes, which are a result of lower melanin levels, to be much more common in females than in males, at least by a factor of two.[54][55]

A different study found that while females tend to have a lower frequency of black hair, males have a higher frequency of platinum blond hair, blue eyes and lighter skin. According to this one theory the cause for this is a higher frequency of genetic recombination in females than in males, possibly due to sex-linked genes, and as a result females tend to show less phenotypical variation in any given population.[56][57][58]

The human sexual dimorphism in color seems to be greater in populations that are medium in skin color than in very light or very dark-colored populations.[54]

Sexual organs and reproductive systems

See also: Human male reproductive system and Human female reproductive system
The human male reproductive system.
The human female reproductive system.
The male and female perineum

Males and females have different sex organs. Females have two ovaries that store the eggs, and a uterus which is connected to a vagina. The external genitals are called the vulva. Males have testicles that produce sperm. The testicles are placed in the scrotum behind the penis, which are external extremities.[59] It is worth noting that between 1.7% and 4% of humans may be classified as intersex, which can mean (among other forms of variation) that one or more of the internal or external genitalia associated with their sex assignment is absent, different from the typical presentation, etc.[60]

Male orgasm (and the corresponding release of ejaculate containing sperm from the testes) is essential for reproduction, whereas female orgasm is not. The female orgasm was originally believed to have no function other than pleasure. Later evidence suggests that it evolved as a discriminatory advantage in regards to mate selection.[61]

Female ejaculation has been observed for 2,000 years. It refers to the release of fluid experienced by some females during orgasm. The components of the ejaculate are comparable to that of the male ejaculate. The release of this fluid is a product of the Skene's gland (female prostate), located within the walls of the urethra. The female prostate is much smaller than the male prostate but seems to behave in a similar fashion. Female ejaculate, though, does not contain sperm.[62] The female prostate is visible through MRI and ultrasound.[62]

Reproductive capacity and cost

Males typically produce billions of sperm each month,[63] many of which are capable of fertilization. Females typically produce one ovum a month that can be fertilized into an embryo. Thus during a lifetime males are able to father a significantly greater number of children than females can give birth to. The most fertile female, according to the Guinness Book of World Records, was the wife of Feodor Vassilyev of Russia (1707–1782) who had 69 surviving children. The most prolific father of all time is believed to be the last Sharifian Emperor of Morocco, Mulai Ismail (1646–1727) who reportedly fathered more than 800 children from a harem of 500 women.

Mutation rate

Males undergo a greater number of germline cell divisions than females, and as a consequence the male germline accumulates more DNA replication errors that result in a higher mutation rate in males than in females.[64]

Fertility

Female fertility declines after age 30 and ends with the menopause.[65][66] Female physical experiences vary depending on external forces such as diet, marriage patterns, culture, and other aspects. In Western nations menstruation begins to affect females at 13 and menopause starts around 51. In non-industrialized countries, on the other hand, most females begin menstruation at a later age.[67] More lactation in the lifetime of non-western females inhibits ovulation and extends the number of fertile years.[68] Pregnancy in the 40s or later has been correlated with increased risk of Down syndrome in children.[69] Males are capable of fathering children into old age. Paternal age effects in children include multiple sclerosis,[70] autism,[71] breast cancer[72] and schizophrenia,[73] as well as reduced intelligence.[74]

Adriana Iliescu was reported as the world's oldest woman to give birth, at age 66. Her record stood until Maria del Carmen Bousada de Lara gave birth to twin sons at Sant Pau Hospital in Barcelona, Spain on December 29, 2006, at the age of 67. In both cases IVF was used. The oldest known father was former Australian miner Les Colley, who fathered a child at age 93.[75]

Brain and nervous system

Main article: Neuroscience of sex differences

Brain

The brains of humans were long believed to be different for males and females.[76] However, this has been called into question by recent developments in neuroscience. For example, studies published in 2018,[77] 2019,[78] and 2021,[79] among others, have challenged the idea of sexual dimorphism regarding the brain, with one study concluding firmly that "brains are not meaningfully aligned along a male-female continuum."[80] When the size of one's head is accounted for, brain differences between sexes are no longer clear, and they are not generalizable across geographic regions (i.e., what is considered a brain sex distinction in Europeans may not correlate to sex distinctions between Asian populations).[79][77][81]

Brain size

The human brain. Differences in male and female brain size are relative to body size.[82]

Early research into the differences between male and female brains showed that male brains are, on average, larger than female brains. This research was frequently cited to support the assertion that women are less intelligent than men.[82][83] One of the most influential early researchers on this topic was Paul Broca. In 1861, he examined 432 human brains from cadavers and found that the brains of males had an average weight of 1325 grams, while the brains of females had an average weight of 1144 grams. This study, however, did not control for differences in body size or age.[83][84] Later studies have shown that while male's brains are an average of 10-15% larger and heavier than female's brains, there is relatively no difference when controlling for body weight. This means the brain-to-body mass ratio is, on average, approximately the same for both sexes.[82][83] Comparing a male and a female of the same body size, an average difference of 100 grams in brain-mass is present, the male having the bigger and heavier brain. This difference of 100 grams applies over the whole range of human sizes.[85][86]

Brain structure

The male and female brains show some differences in internal structure. One difference is the proportions of white matter relative to grey matter.

Structural brain differences usually correspond to sexually dimorphic attributes that bring about functional brain differences.

On average, female brains have a larger ratio of grey matter to the white matter than males (particularly in the dorsolateral prefrontal cortex and superior temporal gyrus), even when sex-differences in the total intracranial volume are taken into consideration. Most notably, males have a larger amount of white matter in the frontal and temporal perisylvian region, and in the temporal stem and optic radiation, of the left hemisphere, whereas females have a larger amount of gray matter in the superior temporal gyrus, planum temporale, Heschl gyrus, cingulate gyrus, inferior frontal, and central sulci margins, of the left hemisphere.

The degree of hemispheric asymmetry in males corresponds to the relative size of corpus callosum; however, this is not true in females. An increase in hemispheric asymmetry in male brains causes a male sex-dependent decrease in inter-hemispheric connectivity. Many studies suggest that, on average, female brains have more commissural tracts involved in inter-hemispheric connectivity than males. Specifically, studies suggests that:

  • The anterior commissure is larger in females than males.
  • The massa intermedia is more abundant in females than males.
  • Females have a larger ratio of the cross-sectional area of the corpus callosum to cerebral volume and to forebrain size than males.

Several studies have reached contrary conclusions.

There are also differences in the structure of specific areas of the brain. On average, the SDN has been repeatedly found to be considerably larger in males than in females. The volume of the SDN was 2.2 times as large in males as in females. On average, the BSTc is twice as large in males as in females. On average, the INAH-3 is significantly larger in males than in females regardless of age. Two studies found that men have larger parietal lobes, an area responsible for sensory input including spatial sense and navigation; though, another study failed to find any statistically significant difference.[87][88] At the same time, females have larger Wernicke's and Broca's areas, areas responsible for language processing.[89] Studies using MRI scanning have shown that the auditory and language-related regions in the left hemisphere are proportionally expanded in females versus in males. Conversely, the primary visual, and visuo-spatial association areas of the parietal lobes are proportionally larger in males.[90] The corpus callous is located at the sagittal divide and is the primary commissure in the human brain. It connects the left and right hemispheres of the cerebral cortex, which allows them to communicate with each other. With respect to language, males predominantly use their left hemisphere but females use both their right and left hemispheres. The right hemisphere controls emotion, so using the right hemisphere adds more prosody to speech.[91] In males, the corpus callosum is larger than females.[92] However, the splenium and the isthmus subregions of the corpus callosum are larger in females. The genu subregion is larger in males. These subregions may serve as the basis for sex differences in language.[93] However, a 1997 meta-study concluded that there is no relative size difference, and that the larger corpus callosum in males is due to generally larger brains in males on average; a small man and a large man would therefore have the same distinctions as the average man and the average woman.[94][95]

In total and on average, females have a higher percentage of grey matter in comparison to males, and males a higher percentage of white matter.[96][97] However, some researchers maintain that as males have larger brains on average than females, when adjusted for total brain volume, the grey matter differences between sexes is small or nonexistent. Thus, the percentage of grey matter appears to be more related to brain size than it is to sex.[98][99]

In 2005, Haier et al. reported that, compared with males, females show fewer grey matter areas associated with intelligence, but more white matter areas associated with intelligence. He concluded that "men and women apparently achieve similar IQ results with different brain regions, suggesting that there is no singular underlying neuroanatomical structure to general intelligence and that different types of brain designs may manifest equivalent intellectual performance."[100] Using brain mapping, it was shown that males have more than six times the amount of gray matter related to general intelligence than females, and females have nearly ten times the amount of white matter related to intelligence than males.[101] They also report that the brain areas correlated with IQ differ between the sexes. In short, males and females apparently achieve similar IQ results with different brain regions.[100] However, a 2019 article called the base assertions of articles such as Haier, et al., finding there is no significant, consistent difference in grey and white matter between males and females.[102]

The amygdala is the structure that responds to emotionally arousing information, respond to the environment, and reacts with stress. The male amygdala was believed to be proportionally larger than that in females, causing sex to be a determining factor in reactions to stress. However, this is not the case.[103] The hippocampus, crucial for memory storage and spatial mapping of the physical environment, was likewise thought to be larger in females than in males.[104]

A brain study done by the NIH showed that the females had greater volume in the prefrontal cortex, orbitofrontal cortex, superior temporal cortex, lateral parietal cortex, and insula, whereas males had greater volume in the ventral temporal and occipital regions.[105]

Other than external genitals, there are few physical differences before puberty. Small differences in height and start of physical maturity are seen. In the first decade of human life, there is a significant amount of overlap between children of both sexes. The gradual growth in sex difference throughout a person's life is a product of various hormones. Testosterone is the major active hormone in male development while estrogen is the dominant female hormone. These hormones are not, however, limited to each sex. Both males and females have both testosterone and estrogen.[106]

Sensory systems

See also: Sex differences in sensory systems
  • Some studies have shown that females have a more sensitive sense of smell than males, both in the differentiation of odors and in the detection of slight or faint odors.
  • Females have more pain receptors in the skin. That may contribute to the lower pain tolerance of females.[107] While most females expect to be less tolerant to pain, males expect to be more tolerant and therefore report agitation later. Due to variation across societies of gender roles, results of pain studies also vary depending on gender expectations.[108]
  • Females also report a higher prevalence of many pain-related diseases and syndromes, particularly auto-immune diseases. In a 2005 study, Holdcroft and Beckley show a higher female prevalence of many conditions of the head and neck (e.g., migraine), limbs (e.g., carpal tunnel syndrome), internal organs (IBS), and more general conditions (multiple sclerosis).[109] Fewer conditions show a male prevalence: e.g., cluster headache, gout.
  • In addition to defined diseases and syndromes, many common "everyday" pains appear to overburden females rather than males. Therefore, studies consistently find that females report more severe pain, more frequent pain, longer-lasting pain, and wider-ranging pain than males.[110] For example, common painful conditions such as dysmenorrhea may predispose females to more widespread musculoskeletal pains.
  • Females show higher performance levels on tests of verbal fluency. This may be because the female auditory cortex is denser than that of the male. This difference and other sensory differences like it could be because of the sex hormones that impact the fetal brain during development.[111]

Immune system

Strength and type of immune response differ in males and females. Generally speaking, females have a stronger immune response than males.[112][113] This results in males having a higher morbidity and mortality from infectious diseases than females do, and lower rates of auto-immune diseases.[114]

Tissues and hormones

  • Females generally have a higher body fat percentage than males,[1] whereas males generally have more muscle tissue mass.
  • Females usually have lower blood pressure than males, and female's hearts beat faster, even when they are asleep.[115]
  • Males and females have different levels of certain hormones. Males have a higher concentration of androgens while females have a higher concentration of estrogens.
  • To date, wound healing studies have chiefly reported a female advantage in healing of dermal wounds.[116][117][118][119][120] On the other hand, studies have found a male advantage in healing rates of mucosal wounds.[121][122] Thus, sex advantages in wound healing appear to be tissue specific.
  • Adult males have approximately 5.2 million red blood cells per cubic millimeter of blood, whereas females have approximately 4.6 million.[123]
  • Females typically have more white blood cells (stored and circulating), more granulocytes, and B and T lymphocytes. Additionally, they produce more antibodies at a faster rate than males. Hence they develop fewer infectious diseases and succumb for shorter periods.[39]
  • Findings from a 2018 study revealed that there are several differences in cellular characteristics (e.g., cytoskeleton) of female and male cells.[124]

Health

Life span

Females live longer than males in most countries around the world. In Russia, however, the sex-associated gap has been increasing as male life expectancy declines.[125]

The longer average life span of females can lead to skewed statistical results in regard to sex differences. For example, females are often seen to be at a higher risk of bone fracture due to osteoporosis. Although females do lose bone density faster than males after menopause, the data shows a larger disparity because there are more older females in the population.[126]

DNA damage during aging

The gender gap in life expectancy suggests differences in the aging process between males and females. A key factor underlying aging is considered to be DNA damage, particularly DNA double-strand breaks, and the capability to repair these damages declines with age.[127] Repair of DNA double-strand breaks is catalyzed by multiple pathways and expression of these repair pathways was found to be subject to changes upon aging.[127] These age-related changes in the expression of double-strand break repair pathways were observed to be distinctly different in men and women.[127]

Illness and injury

Sex chromosome disorders

Certain diseases and conditions are clearly sex-related in that they are caused by the same chromosomes that regulate sex differentiation. Some conditions are X-linked recessive, in that the gene is carried on the X chromosome. Genetic females (XX) will show symptoms of the disease only if both their X chromosomes are defective with a similar deficiency, whereas genetic males (XY) will show symptoms of the disease if their only X chromosome is defective. (A female may carry such a disease on one X chromosome but not show symptoms if the other X chromosome works sufficiently.) For this reason, such conditions are far more common in males than in females.

X-linked recessive disorders include:[128]

  • Red-green colour blindness
  • Haemophilia A (factor VIII)
  • Haemophilia B (factor IX)
  • Duchenne Muscular Dystrophy
  • X-linked agammaglobulinaemia
  • X-linked ichythyosis
  • Becker muscular dystrophy
  • Non-specific X-linked mental retardation

X-linked dominant disorders include:[129]

There are diseases that are caused by a defective Y chromosome or a defective number of them.

Differences not linked to sex chromosomes

The World Health Organization (WHO) has produced a number of reports on gender and health.[130] The following trends are shown:

  • Overall rates of mental illness are similar for males and females. There is no significant sex difference in rates of schizophrenia and bipolar depression. Females are more likely to suffer from unipolar depression, anxiety, eating disorders, and post-traumatic stress disorder. Males are more likely to suffer from alcoholism and antisocial personality disorder, as well as developmental psychiatric disorders such as autism spectrum disorders and Tourette syndrome.
  • Females are more likely to suffer from depression, due in part to their generally lower social status (e.g., higher rates of poverty), which is a powerful predictor for depression.[131]
  • While males are more likely to suffer from alcoholism, females are more prone to addiction. This is because estrogen boosts the release of dopamine in brain regions important for regulating drug-seeking behavior, making women more vulnerable to dependence.[132]
  • Schizophrenia does not show prevalence differences of significance among sexes, but there is a difference in the brain structures related. Females naturally have a higher orbitofrontal-to-amygdala ratio (OAR) than males, but not schizophrenic females (lower OAR). Males with schizophrenia however, have a higher orbitofrontal-to-amygdala ratio than that of healthy males.[111]
  • Before menopause, females are less likely to suffer from cardiovascular disease. However, for older men and postmenopausal women, this gap is much narrower as postmenopausal women are at higher risk of cardiovascular disease than premenopausal women.[133][134]
  • Overall, males are more likely to suffer from cancer, with much of this driven by lung cancer. In most countries, more men than women smoke, although this gap is narrowing especially among young women.[135]
  • Females are more likely to be blind than males. The American Academy of Ophthalmology and The International Agency for the Prevention of Blindness note that this may be linked to higher life expectancy and age-related conditions, and that females are less likely to get timely treatments for conditions that lead to blindness, such as cataracts and trachoma.[136][137]
  • Females are more likely to suffer from osteoarthritis and osteoporosis. The density of bones depends upon the stresses that are put on them through exercise. Exercise and activity in childhood help to build up higher density bones. Although in Britain female's bones are less dense even before menopause, in some African societies, males and females are equally susceptible to osteoporosis.[138]

Infectious disease prevalence varies - this is largely due to cultural and exposure factors. In particular the WHO notes that:[130]

  • Worldwide, more males than females are infected with HIV. The exception is sub-Saharan Africa, where more females than males are infected.
  • Adult males are more likely to be diagnosed with tuberculosis.

Some other sex-related health differences include:

See also

Notes

  1. ^ a b c d Mills, Melinda C.; Barban, Nicola; Tropf, Felix C. (2020). An Introduction to Statistical Genetic Data Analysis. MIT Press. p. 9. ISBN 978-0262357449.
  2. ^ a b c Solomon, Eldra; Martin, Charles; Martin, Diana W.; Berg, Linda R. (2014). Biology. Cengage Learning. pp. 218, 240. ISBN 978-1305179899.
  3. ^ Snustad, D. Peter; Simmons, Michael J. (2015). Principles of Genetics. John Wiley & Sons. p. 100. ISBN 978-1119142287.
  4. ^ Birke 2001, pp. 310–311.
  5. ^ Rieger, Rigomar; Michaelis, Arnd; Green, Melvin M. (2012). Glossary of Genetics: Classical and Molecular. Springer Science & Business Media. p. 449. ISBN 978-3642753336.
  6. ^ Carrel L, Willard HF (March 2005). "X-inactivation profile reveals extensive variability in X-linked gene expression in females". Nature. 434 (7031): 400–404. Bibcode:2005Natur.434..400C. doi:10.1038/nature03479. PMID 15772666. S2CID 4358447.
  7. ^ Gray, Henry (1918). Gray's Anatomy of the Human Body (20th ed.). Lea & Febiger. ASIN B000TW11G6.
  8. ^ a b c d e Robert-McComb, Jacalyn; Norman, Reid L.; Zumwalt, Mimi (2014). The Active Female: Health Issues Throughout the Lifespan. Springer Science+Business Media. pp. 223–238. ISBN 978-1461488842.
  9. ^ Kościński, Krzysztof (2014). "Assessment of Waist-to-Hip Ratio Attractiveness in Women: An Anthropometric Analysis of Digital Silhouettes". Archives of Sexual Behavior. 43 (5): 989–997. doi:10.1007/s10508-013-0166-1. ISSN 0004-0002. PMC 4050298. PMID 23975738.
  10. ^ Stevens, J; Katz, EG; Huxley, RR (2010). "Associations between gender, age and waist circumference". European Journal of Clinical Nutrition. 64 (1): 6–15. doi:10.1038/ejcn.2009.101. ISSN 0954-3007. PMC 5909719. PMID 19738633.
  11. ^ Halpern, Diane F. (2013). Sex Differences in Cognitive Abilities: 4th Edition. Psychology Press. p. 188. ISBN 978-1136722837.
  12. ^ a b c d e f g h i Patton, Kevin T.; Thibodeau, Gary A. (2018). Anthony's Textbook of Anatomy & Physiology - E-Book. Elsevier Health Sciences. p. 276. ISBN 9780323709309.
  13. ^ a b c Iscan, Mehmet Yasar; Steyn, Maryan (2013). The Human Skeleton in Forensic Medicine: (3rd Ed.). Charles C Thomas Publisher. pp. 146–147. ISBN 9780398088798.
  14. ^ Amerman, Erin C. (2021). Exploring Anatomy in the Laboratory, Second Edition. Morton Publishing Company. p. 163. ISBN 9781640431836.
  15. ^ a b c d Delavier, Frédéric (2003). Women's Strength Training Anatomy. Human Kinetics. pp. 44–45. ISBN 9780736048132.
  16. ^ Magee, David J.; Zachazewski, James E.; Quillen, William S.; Manske, Robert C. (2010). Athletic and Sport Issues in Musculoskeletal Rehabilitation. Elsevier Health Sciences. p. 261. ISBN 9781437715729.
  17. ^ Fernandez de las Penas, Cesar; Cleland, Joshua; Dommerholt, Jan (2015). Manual Therapy for Musculoskeletal Pain Syndromes: an evidence- and clinical-informed approach. Elsevier Health Sciences. p. 468. ISBN 9780702055775.
  18. ^ Thompson, Tim; Black, Sue (2006). Forensic Human Identification: An Introduction. CRC Press. p. 203. ISBN 9781420005714.
  19. ^ a b Geller, Pamela L.; Stockett, Miranda K. (2007). Feminist Anthropology: Past, Present, and Future. University of Pennsylvania Press. pp. 58–64. ISBN 9780812220056.
  20. ^ a b Warrener, Anna G.; Lewton, Kristi L.; Pontzer, Herman; Lieberman, Daniel E. (11 March 2015). "A Wider Pelvis Does Not Increase Locomotor Cost in Humans, with Implications for the Evolution of Childbirth". PLOS ONE. 10 (3): e0118903. Bibcode:2015PLoSO..1018903W. doi:10.1371/journal.pone.0118903. PMC 4356512. PMID 25760381.
  21. ^ Lawrence E., Wineski (2018). Snell's Clinical Anatomy Rehabilitation. Lippincott Williams & Wilkins. p. 451. ISBN 978-1975107024.
  22. ^ Burns, Karen Ramey (2015). Forensic Anthropology Training Manual. Routledge. p. 198. ISBN 9781317348290.
  23. ^ Standring, Susan (2015). Gray's Anatomy E-Book: The Anatomical Basis of Clinical Practice. Elsevier Health Sciences. p. 588. ISBN 9780702068515.
  24. ^ Klales, Alexandra R. (2020). Sex Estimation of the Human Skeleton: History, Methods, and Emerging Techniques. Academic Press. p. 150. ISBN 978-0128157688.
  25. ^ Vella, Chantal; Kravitz, Len. "Gender Differences in Fat Metabolism". The University of New Mexico. Retrieved 22 August 2014.
  26. ^ a b c Legato, Marianne J. (2017). Principles of Gender-Specific Medicine: Gender in the Genomic Era. Academic Press. pp. 526, 528. ISBN 978-0128035429.
  27. ^ a b Ben Mansour, Ghassen; Kacem, Asma; Ishak, Mohamed; Grélot, Laurent; Ftaiti, Foued (2021-11-28). "The effect of body composition on strength and power in male and female students". BMC Sports Science, Medicine and Rehabilitation. 13 (1): 150. doi:10.1186/s13102-021-00376-z. ISSN 2052-1847. PMC 8628437. PMID 34839825.
  28. ^ Hoeger, Wener W.K.; Hoeger, Sharon A. (2016). Fitness and Wellness. Cengage Learning. p. 250. ISBN 978-1305887282.
  29. ^ Petrov, Georgi (2012). The Human nature and The Society. Bulgarressurs. p. 55. ISBN 9789548885119. One of the most controversial topics is the difference in physical strength and weather it exist. In 2008 two independent studies, made from 6 universities in Netherlands, Sweden, France and Denmark, involving 2,000 participants, of which 1,000 men and 1,000 women proves that adult female participants are 74 - 92 % as strong as males on average. But many women still physically stronger than average men, after 211 of females performed better than average level of males at the physical test.
  30. ^ Yankov, Yanko (2023). How our brain evolved to become human. Fakel. p. 187. ISBN 9789544113278. Cultural factors also have a large influence. Although it is widely considered that males still outperform females on average, many women are much stronger than the average man. Studies by Western European scientists of 1,000 men and 1,000 women showed that 211 of the women performed better than the men's average, proving that the evolution of physical strength in humans is still uncharted territory.
  31. ^ Miller, A.E.; MacDougall, J.D.; Tarnopolsky, M.A.; Sale, D.G. (1993). "Gender differences in strength and muscle fiber characteristics". European Journal of Applied Physiology and Occupational Physiology. 66 (3): 254–62. doi:10.1007/BF00235103. hdl:11375/22586. PMID 8477683. S2CID 206772211.
  32. ^ Frontera, W.R.; Hughes, V.A.; Lutz, K.J.; Evans, W.J. (August 1991). "A cross-sectional study of muscle strength and mass in 45- to 78-yr-old men and women". Journal of Applied Physiology. 71 (2): 644–50. doi:10.1152/jappl.1991.71.2.644. PMID 1938738.
  33. ^ Holtz, Jan Leslie (2010). Applied Clinical Neuropsychology: An Introduction. Springer Publishing Company. p. 224. ISBN 978-0826104748.
  34. ^ World Report on Ageing and Health. World Health Organization. 2015. p. 53. ISBN 978-9241565042.
  35. ^ a b c Lomauro, Antonella; Aliboni, Lorenzo; Aliverti, Andrea (2021). "Sex Differences in the Anatomy of the Airways and the Lungs: Impact on Dysanapsis across the Lifespan". Sex-Based Differences in Lung Physiology. Physiology in Health and Disease. Springer Science+Business Media. pp. 13–38. doi:10.1007/978-3-030-63549-7_2. ISBN 978-3-030-63548-0. S2CID 234284090.
  36. ^ Cotes, John E.; Maynard, Robert L.; Pearce, Sarah J.; Nemery, Benoit B.; Wagner, Peter D.; Cooper, Brendan G. (2020). Lung Function. John Wiley & Sons. p. 450. ISBN 978-1-11-859735-4.
  37. ^ Heuer, Albert J. (2017). Wilkins' Clinical Assessment in Respiratory Care. Elsevier Health Sciences. p. 126. ISBN 978-0-32-351166-7.
  38. ^ Dunford, Marie; Doyle, Andrew (2021). Nutrition for Sport and Exercise. Cengage Learning. p. 98. ISBN 978-0-35-744827-4.
  39. ^ a b Glucksman, A. (1981). Sexual Dimorphism in Human and Mammalian Biology and Pathology. Academic Press. pp. 66–75.
  40. ^ Nait-Ali, Amine (2018). Biometrics under Biomedical Considerations. Springer. p. 121. ISBN 978-9-81-131144-4.
  41. ^ Vij, Krishan (2013). Textbook of Forensic Medicine & Toxicology: Principles & Practice - e-book. Elsevier Health Sciences. p. 171. ISBN 978-8-13-123623-9.
  42. ^ Malkinson, T.J.; Martin, S.; Simper, P.; Cooper, K.E. (August 1981). "Expired air volumes of males and females during cold water immersion". Canadian Journal of Physiology and Pharmacology. 59 (8): 843–6. doi:10.1139/y81-125. PMID 7296382.
  43. ^ Firooz, Alireza; Sadr, Bardia; Babakoohi, Shahab; Sarraf-Yazdy, Maryam; Fanian, Ferial; Kazerouni-Timsar, Ali; Nassiri-Kashani, Mansour; Naghizadeh, Mohammad Mehdi; Dowlati, Yahya (2012). "Variation of Biophysical Parameters of the Skin with Age, Gender, and Body Region". The Scientific World Journal. 2012: 386936. doi:10.1100/2012/386936. PMC 3317612. PMID 22536139.
  44. ^ a b Jablonski, N.G.; Chaplin, G. (July 2000). "The evolution of human skin coloration". Journal of Human Evolution. 39 (1): 57–106. Bibcode:2000JHumE..39...57J. doi:10.1006/jhev.2000.0403. PMID 10896812. S2CID 38445385.
  45. ^ Giacomoni, P.U.; Mammone, T.; Teri, M. (September 2009). "Gender-linked differences in human skin". Journal of Dermatological Science. 55 (3): 144–9. doi:10.1016/j.jdermsci.2009.06.001. PMID 19574028.
  46. ^ "Male pattern baldness". MedlinePlus. United States National Library of Medicine. Retrieved 25 August 2015.
  47. ^ Wennesland, R.; Brown, E.; Hopper, J (July 1959). "Red cell, plasma and blood volume in healthy men measured by radiochromium (Cr51) cell tagging and hematocrit: influence of age, somatotype and habits of physical activity on the variance after regression of volumes to height and weight combined". Journal of Clinical Investigation. 38 (7). etal: 1065–77. doi:10.1172/JCI103883. PMC 293254. PMID 13664782.
  48. ^ Fortney, S.M.; Nadel, E.R.; Wenger, C.B.; Bove, J.R. (December 1981). "Effect of blood volume on sweating rate and body fluids in exercising humans". Journal of Applied Physiology: Respiratory, Environmental and Exercise Physiology. 51 (6): 1594–600. doi:10.1152/jappl.1981.51.6.1594. PMID 7319888.
  49. ^ Jablonski, Nina (2012). Living Color. Berkeley, Los Angeles, London: University of California Press. ISBN 978-0-520-25153-3.[page needed]
  50. ^ Jablonski, Nina G. & Chaplin, George (2002). "Skin Deep" (PDF). Scientific American. 287 (4). University of Washington: 74–81. Bibcode:2002SciAm.287d..74J. doi:10.1038/scientificamerican1002-74. PMID 12271527. Archived from the original (PDF) on 24 October 2013. Retrieved 22 August 2014.
  51. ^ Frost P (1988). "Human skin color: a possible relationship between its sexual dimorphism and its social perception". Perspectives in Biology and Medicine. 32 (1): 38–58. doi:10.1353/pbm.1988.0010. PMID 3059317. S2CID 36144428.
  52. ^ Frost, P. (2006). "European hair and eye color - A case of frequency-dependent sexual selection?". Evolution and Human Behavior. 27 (2): 85–103. Bibcode:2006EHumB..27...85F. doi:10.1016/j.evolhumbehav.2005.07.002.
  53. ^ Duffy DL, Montgomery GW, Chen W, et al. (February 2007). "A Three–Single-Nucleotide Polymorphism Haplotype in Intron 1 of OCA2 Explains Most Human Eye-Color Variation". American Journal of Human Genetics. 80 (2): 241–52. doi:10.1086/510885. PMC 1785344. PMID 17236130.
  54. ^ a b Frost, P. (2007). "Sex linkage of human skin, hair, and eye color".
  55. ^ Sulem, Patrick; Gudbjartsson, Daniel F.; Stacey, Simon N.; Helgason, Agnar; Rafnar, Thorunn; Magnusson, Kristinn P.; Manolescu, Andrei; Karason, Ari; et al. (2007). "Genetic determinants of hair, eye and skin pigmentation in Europeans". Nature Genetics. 39 (12): 1443–52. doi:10.1038/ng.2007.13. PMID 17952075. S2CID 19313549.
  56. ^ Branicki, Wojciech; Brudnik, Urszula; Wojas-Pelc, Anna (2009). "Interactions Between HERC2, OCA2 and MC1R May Influence Human Pigmentation Phenotype". Annals of Human Genetics. 73 (2): 160–170. doi:10.1111/j.1469-1809.2009.00504.x. PMID 19208107. S2CID 5233533.
  57. ^ Interaction between loci affecting human pigmentation in Poland
  58. ^ Aoki, K. (2002). "Sexual selection as a cause of human skin colour variation: Darwin's hypothesis revisited". Annals of Human Biology. 29 (6): 589–608. doi:10.1080/0301446021000019144. PMID 12573076. S2CID 22703861.
  59. ^ "The Reproductive System | Loma Linda University Fertility". Loma Linda University Center for Fertility & IVF. Retrieved 2024-01-20.
  60. ^ Jones, Tiffany (2018). "Intersex Studies: A Systematic Review of International Health Literature". SAGE Open. 8 (2): 215824401774557. doi:10.1177/2158244017745577. ISSN 2158-2440.
  61. ^ "The Orgasm Wars". Psychology Today.
  62. ^ a b Korda JB; Goldstein SW; Sommer F (May 2010). "The history of female ejaculation". The Journal of Sexual Medicine. 7 (5): 1965–75. doi:10.1111/j.1743-6109.2010.01720.x. PMID 20233286.
  63. ^ MedlinePlus Encyclopedia: Semen analysis
  64. ^ Goetting-Minesky, M. Paula; Makova, Kateryna D. (2006). "Mammalian Male Mutation Bias: Impacts of Generation Time and Regional Variation in Substitution Rates". Journal of Molecular Evolution. 63 (4): 537–544. Bibcode:2006JMolE..63..537G. doi:10.1007/s00239-005-0308-8. PMID 16955237.
  65. ^ Graph Archived 2007-10-27 at the Wayback Machine @ FertilityLifelines.
  66. ^ Graph @ Epigee.org.
  67. ^ Karapanou, O.; Papadimitriou, A. (30 September 2010). "Determinants of menarche". Reproductive Biology and Endocrinology. 8: 115. doi:10.1186/1477-7827-8-115. PMC 2958977. PMID 20920296.
  68. ^ Schiebinger, Londa (1999). Has feminism changed science?. Cambridge, Massachusetts: Harvard University Press. pp. 120–121.
  69. ^ "Age and Fertility: A Guide for Patients" (PDF). American Society for Reproductive Medicine. 2003.
  70. ^ Montgomery, S.M.; Lambe, M.; Olsson, T.; Ekbom, A. (November 2004). "Parental age, family size, and risk of multiple sclerosis". Epidemiology. 15 (6): 717–23. doi:10.1097/01.ede.0000142138.46167.69. PMID 15475721. S2CID 14813112.
  71. ^ Reichenberg A, Gross R, Weiser M, et al. (September 2006). "Advancing paternal age and autism". Archives of General Psychiatry. 63 (9): 1026–32. doi:10.1001/archpsyc.63.9.1026. PMID 16953005.
  72. ^ Choi JY, Lee KM, Park SK, et al. (2005). "Association of paternal age at birth and the risk of breast cancer in offspring: a case control study". BMC Cancer. 5: 143. doi:10.1186/1471-2407-5-143. PMC 1291359. PMID 16259637.
  73. ^ Sipos A, Rasmussen F, Harrison G, et al. (November 2004). "Paternal age and schizophrenia: a population based cohort study". British Medical Journal. 329 (7474): 1070. doi:10.1136/bmj.38243.672396.55. PMC 526116. PMID 15501901.
  74. ^ Saha S, Barnett AG, Foldi C, et al. (March 2009). Brayne C (ed.). "Advanced Paternal Age Is Associated with Impaired Neurocognitive Outcomes during Infancy and Childhood". PLOS Medicine. 6 (3): e40. doi:10.1371/journal.pmed.1000040. PMC 2653549. PMID 19278291.
  75. ^ oldest birth parents
  76. ^ Goy, Robert W.; McEwen, Bruce S. (1980). Sexual Differentiation of the Brain: Based on a Work Session of the Neurosciences Research Program. Boston: MIT Press Classics. Archived from the original on 4 June 2011.
  77. ^ a b Joel, Daphna; Persico, Ariel; Salhov, Moshe; Berman, Zohar; Oligschläger, Sabine; Meilijson, Isaac; Averbuch, Amir (2018). "Analysis of Human Brain Structure Reveals that the Brain "Types" Typical of Males Are Also Typical of Females, and Vice Versa". Frontiers in Human Neuroscience. 12: 399. doi:10.3389/fnhum.2018.00399. ISSN 1662-5161. PMC 6204758. PMID 30405373.
  78. ^ "APA PsycNet". psycnet.apa.org. Retrieved 2024-01-20.
  79. ^ a b Eliot, Lise; Ahmed, Adnan; Khan, Hiba; Patel, Julie (2021-06-01). "Dump the "dimorphism": Comprehensive synthesis of human brain studies reveals few male-female differences beyond size". Neuroscience & Biobehavioral Reviews. 125: 667–697. doi:10.1016/j.neubiorev.2021.02.026. ISSN 0149-7634. PMID 33621637.
  80. ^ Joel, Daphna (2021-03-01). "Beyond the binary: Rethinking sex and the brain". Neuroscience & Biobehavioral Reviews. 122: 165–175. doi:10.1016/j.neubiorev.2020.11.018. ISSN 0149-7634. PMID 33440198.
  81. ^ Eliot, Lise (2021-04-22). "You don't have a male or female brain – the more brains scientists study, the weaker the evidence for sex differences". The Conversation. Retrieved 2024-01-20.
  82. ^ a b c O'Brien, Jodi (2009). Encyclopedia of Gender and Society. Los Angeles: SAGE. p. 343. ISBN 978-1412909167.
  83. ^ a b c Gould, Stephen Jay (1980). The Panda's Thumb. New York: Norton. pp. 152–159. ISBN 978-0393308198.
  84. ^ Fee, Elizabeth (1979). "Nineteenth-Century Craniology: The Study of the Female Skull". Bulletin of the History of Medicine. 53 (3): 415–53. PMID 394780.
  85. ^ Kimura, Doreen (1999). Sex and Cognition. MIT Press. pp. 127–8. ISBN 978-0-262-11236-9.
  86. ^ Rushton, J. Philippe (1993). "Corrections to a paper on race and sex differences in brain size and intelligence". Personality and Individual Differences. 15 (2): 229–231. doi:10.1016/0191-8869(93)90031-W.
  87. ^ Frederikse, M.E.; Lu, A.; Aylward, E.; Barta, P.; Pearlson, G. (December 1999). "Sex differences in the inferior parietal lobule". Cerebral Cortex. 9 (8): 896–901. doi:10.1093/cercor/9.8.896. PMID 10601007.
  88. ^ Ellis, Lee (2008). Sex differences: summarizing more than a century of scientific research. CRC Press.
  89. ^ Harasty, J.; Double, K.L.; Halliday, G.M.; Kril, J.J.; McRitchie, D.A. (February 1997). "Language-associated cortical regions are proportionally larger in the female brain". Archives of Neurology. 54 (2): 171–6. doi:10.1001/archneur.1997.00550140045011. PMID 9041858.
  90. ^ Brun, C.C.; Leporé, N.; Luders, E.; Chou, Y.Y.; Madsen, S.K.; Toga, A.W.; Thompson, P.M.; et al. (2009). "Sex differences in brain structure in auditory and cingulate regions". NeuroReport. 20 (10): 930–935. doi:10.1097/WNR.0b013e32832c5e65. PMC 2773139. PMID 19562831.
  91. ^ Carlson, Neil R. (2007). Physiology of Behavior. Boston: Pearson Allyn & Bacon. pp. 87–88. ISBN 978-0205467242.
  92. ^ Kitterle, F. L. (1995). Hemispheric communication: Mechanism and models. Hillsadale, N.J.: Lawrence Erlbaum Associates. ISBN 978-0805811445.
  93. ^ Hines, Melissa (2004). Brain gender. Oxford University Press. pp. 191–197. ISBN 9780195188363.
  94. ^ "Massive study reveals few differences between men's and women's brains". ScienceDaily. Retrieved 2024-01-20.
  95. ^ Bishop, K.; Wahlsten, D. (1997). "Sex Differences in the Human Corpus Callosum: Myth or Reality?" (PDF). Neuroscience & Biobehavioral Reviews. 21 (5): 581–601. doi:10.1016/S0149-7634(96)00049-8. PMID 9353793. S2CID 9909395.
  96. ^ Marner, L.; Nyengaard, J.R.; Tang, Y.; Pakkenberg, B. (2003). "Marked loss of myelinated nerve fibers in the human brain with age". The Journal of Comparative Neurology. 462 (2): 144–52. doi:10.1002/cne.10714. PMID 12794739. S2CID 35293796.
  97. ^ Gur, Ruben C.; Turetsky, Bruce I.; Matsui, Mie; Yan, Michelle; Bilker, Warren; Hughett, Paul; Gur, Raquel E. (15 May 1999). "Sex Differences in Brain Gray and White Matter in Healthy Young Adults: Correlations with Cognitive Performance". The Journal of Neuroscience. 19 (10): 4065–4072. doi:10.1523/JNEUROSCI.19-10-04065.1999. PMC 6782697. PMID 10234034.
  98. ^ Leonard, C. M.; Towler, S.; Welcome, S.; Halderman, L. L.; Otto, R. Eckert; Chiarello, C.; Chiarello, C. (2008). "Size Matters: Cerebral Volume Influences Sex Differences in Neuroanatomy". Cerebral Cortex. 18 (12): 2920–2931. doi:10.1093/cercor/bhn052. PMC 2583156. PMID 18440950.
  99. ^ Luders, E.; Steinmetz, H.; Jancke, L. (2002). "Brain size and grey matter volume in the healthy human brain". NeuroReport. 13 (17): 2371–2374. doi:10.1097/00001756-200212030-00040. PMID 12488829.
  100. ^ a b Haier, Richard J.; Jung, Rex E.; Yeo, Ronald A.; Head, Kevin; Alkire, Michael T. (March 2005). "The neuroanatomy of general intelligence: sex matters". NeuroImage. 25 (1): 320–327. doi:10.1016/j.neuroimage.2004.11.019. PMID 15734366. S2CID 4127512.
  101. ^ Haier, R.J.; Jung, R.E.; Yeo, R.A.; Head, K.; Alkire, M.T. (September 2004). "Structural brain variation and general intelligence" (PDF). NeuroImage. 23 (1): 425–33. doi:10.1016/j.neuroimage.2004.04.025. PMID 15325390. S2CID 29426973.
  102. ^ Sanchis-Segura, Carla; Ibañez-Gual, Maria Victoria; Adrián-Ventura, Jesús; Aguirre, Naiara; Gómez-Cruz, Álvaro Javier; Avila, César; Forn, Cristina (2019-07-01). "Sex differences in gray matter volume: how many and how large are they really?". Biology of Sex Differences. 10 (1): 32. doi:10.1186/s13293-019-0245-7. ISSN 2042-6410. PMC 6604149. PMID 31262342.
  103. ^ Marwha, Dhruv; Halari, Meha; Eliot, Lise (2017). "Meta-analysis reveals a lack of sexual dimorphism in human amygdala volume". NeuroImage. 147: 282–294. doi:10.1016/j.neuroimage.2016.12.021. PMID 27956206. S2CID 3479632.
  104. ^ Tan, Anh; Ma, Wenli; Vira, Amit; Marwha, Dhruv; Eliot, Lise (2016). "The human hippocampus is not sexually-dimorphic: Meta-analysis of structural MRI volumes". NeuroImage. 124 (Pt A): 350–366. doi:10.1016/j.neuroimage.2015.08.050. PMID 26334947. S2CID 26316768.
  105. ^ "Sex differences in brain anatomy". National Institutes of Health (NIH). 2020-07-27. Retrieved 2023-03-27.
  106. ^ Birke 2001, pp. 314–315.
  107. ^ "Study Reveals Reason Women Are More Sensitive To Pain Than Men". ScienceDaily. October 2005.
  108. ^ Defrin R, Shramm L, Eli I (September 2009). "Gender role expectations of pain is associated with pain tolerance limit but not with pain threshold". Pain. 145 (1–2): 230–6. doi:10.1016/j.pain.2009.06.028. PMID 19615821. S2CID 20186989.
  109. ^ McMahon SB, M Koltzenburg, A Holdcroft, and K Beckley. Wall and Melzack's textbook of pain. Churchill Livingstone. 2005. (pp. 1181-1197)
  110. ^ Kröner-Herwig, Birgit; Gaßmann, Jennifer; Tromsdorf, Marie; Zahrend, Elfi (2012). "The effects of sex and gender role on responses to pressure pain". GMS Psycho-Social-Medicine. 9: 1–10. doi:10.3205/psm000079. PMC 3290921. PMID 22400065.
  111. ^ a b Cahill, Larry (2005). "His Brain, Her Brain". Scientific American. 20 (3): 40–47. doi:10.1038/scientificamericanmind0509-40. Archived from the original on 17 March 2012.; Alexander, Gerianne M.; Hines, Melissa (2002). "Sex differences in response to children's toys in nonhuman primates (Cercopithecus aethiops sabaeus)". Evolution and Human Behavior. 23 (6): 467–479. Bibcode:2002EHumB..23..467A. doi:10.1016/s1090-5138(02)00107-1.
  112. ^ Klein, Sabra L.; Flanagan, Katie L. (2016). "Sex differences in immune responses". Nature Reviews Immunology. 16 (10): 626–638. doi:10.1038/nri.2016.90. ISSN 1474-1741. PMID 27546235.
  113. ^ Wilson, Clare (2023-02-04). "Are There Sex Differences in the Immune System?". New Scientist. 257 (3424): 40. Bibcode:2023NewSc.257...40W. doi:10.1016/S0262-4079(23)00214-2. ISSN 0262-4079. PMC 9897808. PMID 36776694.
  114. ^ Lotter, Hanna; Altfeld, Marcus (1 March 2019). "Sex differences in immunity". Seminars in Immunopathology. 41 (2): 133–135. doi:10.1007/s00281-018-00728-x. ISSN 1863-2300. PMID 30742253.
  115. ^ Bren, Linda (July–August 2005). "Does Sex Make a Difference?". FDA Consumer Magazine. Archived from the original on 26 March 2009.
  116. ^ Ashcroft, Gillian S.; Dodsworth, Joanne; Boxtel, Egon Van; Tarnuzzer, Roy W.; Horan, Michael A.; Schultz, Gregory S.; Ferguson, Mark W.J. (November 1997). "Estrogen accelerates cutaneous wound healing associated with an increase in TGF-β1 levels". Nature Medicine. 3 (11): 1209–1215. doi:10.1038/nm1197-1209. ISSN 1078-8956. PMID 9359694. S2CID 23922583.
  117. ^ Ashcroft, Gillian S.; Mills, Stuart J. (1 September 2002). "Androgen receptor–mediated inhibition of cutaneous wound healing". Journal of Clinical Investigation. 110 (5): 615–624. doi:10.1172/JCI0215704. ISSN 0021-9738. PMC 151108. PMID 12208862.
  118. ^ Jorgensen, Lars Nannestad; Sorensen, Lars Tue; Kallehave, Finn; Vange, Jakob; Gottrup, Finn (March 2002). "Premenopausal women deposit more collagen than men during healing of an experimental wound". Surgery. 131 (3): 338–343. doi:10.1067/msy.2002.119986. PMID 11894040.
  119. ^ Shimizu, Tadamichi; Nishihira, Jun; Watanabe, Hirokazu; Abe, Riichiro; Honda, Ayumi; Ishibashi, Teruo; Shimizu, Hiroshi (2 April 2004). "Macrophage Migration Inhibitory Factor Is Induced by Thrombin and Factor Xa in Endothelial Cells". Journal of Biological Chemistry. 279 (14): 13729–13737. doi:10.1074/jbc.M400150200. ISSN 0021-9258. PMID 14736878. S2CID 41653014.
  120. ^ Gilliver, Stephen C.; Ashworth, Jason J.; Ashcroft, Gillian S. (January 2007). "The hormonal regulation of cutaneous wound healing". Clinics in Dermatology. 25 (1): 56–62. doi:10.1016/j.clindermatol.2006.09.012. PMID 17276202.
  121. ^ Engeland, Christopher G. (1 December 2006). "Mucosal Wound Healing: The Roles of Age and Sex". Archives of Surgery. 141 (12): 1193–7, discussion 1198. doi:10.1001/archsurg.141.12.1193. ISSN 0004-0010. PMID 17178961.
  122. ^ Benediktsdóttir, Ingibjörg S.; Wenzel, Ann; Petersen, Jens K.; Hintze, Hanne (April 2004). "Mandibular third molar removal: Risk indicators for extended operation time, postoperative pain, and complications". Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology. 97 (4): 438–446. doi:10.1016/j.tripleo.2003.10.018. PMID 15088029.
  123. ^ "Howstuffworks "Red Blood Cells"". April 2000.
  124. ^ Serpooshan, Vahid; Sheibani, Sara; Pushparaj, Pooja; Wojcik, Michal; Jang, Albert Y.; Santoso, Michelle R.; Jang, Joyce H.; Huang, Haina; Safavi-Sohi, Reihaneh; Haghjoo, Niloofar; Nejadnik, Hossein; Aghaverdi, Haniyeh; Vali, Hojatollah; Kinsella, Joseph Matthew; Presley, John; Xu, Ke; Chung-Ming Yang, Phillip; Mahmoudi, Morteza (2018). "Effect of Cell Sex on Uptake of Nanoparticles: The Overlooked Factor at the Nanobio Interface". ACS Nano. 12 (3): 2253–66. doi:10.1021/acsnano.7b06212. PMID 29536733.
  125. ^ Perevedentsev, Viktor (May 2006). "A Country of Widows". New Times. Archived from the original on 15 April 2006.
  126. ^ Birke 2001, pp. 307–322.
  127. ^ a b c Rall-Scharpf, Melanie; Friedl, Thomas W.P.; Biechonski, Shahar; Denkinger, Michael; Milyavsky, Michael; Wiesmüller, Lisa (2021). "Sex-specific differences in DNA double-strand break repair of cycling human lymphocytes during aging". Aging. 13 (17): 21066–21089. doi:10.18632/aging.203519. PMC 8457596. PMID 34506302.
  128. ^ "X-linked recessive disorders." . GP notebook, n.d. Web. 4 Dec 2011. <http://www.gpnotebook.co.uk/simplepage.cfm?ID=-1341784030>.
  129. ^ "X-linked dominant disorders." . GP notebook, n.d. Web. 4 Dec 2011. <https://gpnotebook.co.uk/simplepage.cfm?ID=-1382416350>.
  130. ^ a b "Gender, women, and health, Reports from WHO 2002–2005". World Health Organization. Archived from the original on 2 January 2004.
  131. ^ "Women's increased risk of depression". Mayo Clinic. Retrieved 2024-01-20.
  132. ^ Quigley, Jacqueline A.; Logsdon, Molly K.; Turner, Christopher A.; Gonzalez, Ivette; Leonardo, Noah; Becker, Jill B. (2021-04-01). "Sex differences in vulnerability to addiction". Neuropharmacology. 187: 108491. doi:10.1016/j.neuropharm.2021.108491. ISSN 0028-3908. PMC 7979496. PMID 33567305.
  133. ^ Jousilahti, Pekka; Vartiainen, Erkki; Tuomilehto, Jaakko; Puska, Pekka (1999-03-09). "Sex, Age, Cardiovascular Risk Factors, and Coronary Heart Disease: A Prospective Follow-Up Study of 14 786 Middle-Aged Men and Women in Finland". Circulation. 99 (9): 1165–1172. doi:10.1161/01.CIR.99.9.1165. ISSN 0009-7322. PMID 10069784.
  134. ^ Ryczkowska, Kamila; Adach, Weronika; Janikowski, Kamil; Banach, Maciej; Bielecka-Dabrowa, Agata (2022-12-10). "Menopause and women's cardiovascular health: is it really an obvious relationship?". Archives of Medical Science. 19 (2): 458–466. doi:10.5114/aoms/157308. ISSN 1734-1922. PMC 10074318. PMID 37034510.
  135. ^ "Gender Disparities in Health and Mortality". PRB. Retrieved 2024-01-20.
  136. ^ "Women Face Higher Risk of Blindness Than Men". American Academy of Ophthalmology. 2017-04-24. Retrieved 2024-01-20.
  137. ^ "Gender". The International Agency for the Prevention of Blindness. Retrieved 2024-01-20.
  138. ^ Birke 2001, p. 316.
  139. ^ "ACL Tears in Female Athletes: Q&A with a Sports Medicine Expert". www.hopkinsmedicine.org. 2022-10-03. Retrieved 2024-01-20.
  140. ^ Marlow, Neil; Wolke, Dieter; Bracewell, Melanie A.; Samara, Muthanna; Epicure Study, Group (January 2005). "Neurologic and Developmental Disability at Six Years of Age after Extremely Preterm Birth". New England Journal of Medicine. 352 (1): 9–19. doi:10.1056/NEJMoa041367. PMID 15635108. {{cite journal}}: |first5= has generic name (help)
  141. ^ Kraemer, S. (2000). "The fragile male: Male zygotes are often formed at suboptimal times in fertile cycle". British Medical Journal. 321 (7276): 1609–1612. doi:10.1136/bmj.321.7276.1609. PMC 1119807. PMID 11124200.
  142. ^ Wade, Nicholas (10 April 2007). "Pas De Deux of Sexuality is Written in the Genes". The New York Times.
  143. ^ Bribiescas, Richard (2008). Men: Evolutionary and Life History. Harvard University Press. ISBN 978-0-674-03034-3.

Sources

  • Birke, Lydia (2001). Lederman, Muriel; Bartsch, Ingrid (eds.). The Gender and Science Reader. New York: Routledge.
  • Merry, Clare V. (2005). "Pelvic Shape". Mind - Primary Cause of Human Evolution. Trafford Publishing. ISBN 1-4120-5457-5.
  • Schuenke, Michael; Schulte, Erik; Schumacher, Udo (2006). Thieme Atlas of Anatomy: General Anatomy and Musculoskeletal System. Thieme. ISBN 978-1-58890-419-5.

Further reading

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