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Age of onset

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For the criminological concept, see Age of onset (criminology).

The age of onset is the age at which an individual acquires, develops, or first experiences a condition or symptoms of a disease or disorder. For instance, the general age of onset for the spinal disease scoliosis is "10-15 years old,"[1] meaning that most people develop scoliosis when they are of age between ten and fifteen years.

Diseases are often categorized by their ages of onset as congenital, infantile, juvenile, or adult. Missed or delayed diagnosis often occurs if a disease that is typically diagnosed in juveniles (such as asthma) is present in adults, and vice versa (such as arthritis).[2] Depending on the disease, ages of onset may impact features such as phenotype, as is the case in Parkinson's and Huntington's diseases.[3][4] For example, the phenotype for juvenile Huntington's disease clearly differs from adult-onset Huntington's disease and late-onset Parkinson's exhibits more severe motor and non-motor phenotypes.[3][4]

Causes

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Germ-line mutations are often at least in part the cause of disease onset at an earlier age.[5][6] Though many germ-line mutations are deleterious, the genetic lens through which they may be viewed may provide insights to treatment, possibly through genetic counseling.[7][8]

In some cases, the age of onset may be the result of mutation accumulation.[9] If this is the case, it could be helpful to consider ages of onset as a product of the hypotheses depicted in theories of aging. Even some mental health disorders, whose ages of onset have been found to be harder to define than physical illnesses may have a mutated component.[10] The symptoms of standard mental disorders often start off non-specific. Pathological changes pertaining to disorders often become more detailed and less fickle before they can be defined in the American Psychiatric Association's DSM. The brain is a dynamic and complex system, it is constantly re-wiring itself and a major concern is what happens to the brain in earlier life that mirrors what occurs later in its psycho-pathological state.[11] The typical onset of many mental disorders in late adolescence may reflect the critical development that happens at this time.[12]

Theories of Aging

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The rate-of-living theory of aging states that senescence occurs because individuals accumulate damage to cells and tissues during cell division. This theory is not supported because its postulates that aging rate should be correlated with metabolic rate[13] and organisms cannot evolve longer lifespans[14][15] were not supported in trials.[14][15][16][17][18] The rate-of-living theory may not be used to draw conclusions about age of onset based on this.

There are two subsets to the evolutionary theory of aging: antagonistic pleiotropy hypothesis and the mutation accumulation hypothesis.

The antagonistic pleiotropy hypothesis was tested by monitoring the age-1 gene in C. elegans.[19] The age-1 gene plays a role in senescence; nematodes with mutations in this gene live up to 80% longer.[19] Mutants in the age-1 gene for allele hx546 seem to be otherwise normal until placed under stressful conditions.[19] Then, the carriers of the mutant gene appear to be at disadvantage—they do not lay eggs while being starved.[19] This evidence supports antagonistic pleiotropy as a theory of aging, and therefore as an onset cause in some cases.

The mutation accumulation hypothesis was tested by demonstrating how quickly deleterious mutations can accumulate in Musca domestica.[20] Reed and Bryant demonstrated this by limiting the lifespan of the flies to a few days, which made late-life mutations invisible to selection since they occurred after reproduction.[20] The lifespan of the flies was monitored by allowing them to carry out their complete lifespan every few generations, which was reported to decline substantially.[20] Mutation accumulation is supported as a theory of aging, and therefore an onset cause in cases of diseases resulting from mutation accumulation.

References

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  1. ^ "National Scoliosis Foundation".
  2. ^ Kirkpatrick, Susan; Locock, Louise; Farre, Albert; Ryan, Sara; Salisbury, Helen; McDonagh, Janet E. (2018-02-09). "Untimely illness: When diagnosis does not match age-related expectations". Health Expectations. 21 (4): 730–740. doi:10.1111/hex.12669. ISSN 1369-6513. PMC 6117493. PMID 29424066.
  3. ^ a b Pagano, Gennaro; Ferrara, Nicola; Brooks, David J.; Pavese, Nicola (2016-02-10). "Age at onset and Parkinson disease phenotype". Neurology. 86 (15): 1400–1407. doi:10.1212/wnl.0000000000002461. ISSN 0028-3878. PMC 4831034. PMID 26865518.
  4. ^ a b Sipilä, Jussi O. T.; Kauko, Tommi; Päivärinta, Markku; Majamaa, Kari (2017-08-28). "Comparison of mid-age-onset and late-onset Huntington's disease in Finnish patients". Journal of Neurology. 264 (10): 2095–2100. doi:10.1007/s00415-017-8600-2. ISSN 0340-5354. PMID 28849405. S2CID 37872535.
  5. ^ Lewinsohn, M.; Brown, A. L.; Weinel, L. M.; Phung, C.; Rafidi, G.; Lee, M. K.; Schreiber, A. W.; Feng, J.; Babic, M. (2015-12-28). "Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies". Blood. 127 (8): 1017–1023. doi:10.1182/blood-2015-10-676098. ISSN 0006-4971. PMC 4968341. PMID 26712909.
  6. ^ Zhang, Zhongqiu; Wang, Yian; Lantry, Laura E; Kastens, Elizabeth; Liu, Gongjie; Hamilton, Andrew D; Sebti, Said M; Lubet, Ronald A; You, Ming (September 2003). "Farnesyltransferase inhibitors are potent lung cancer chemopreventive agents in A/J mice with a dominant-negative p53 and/or heterozygous deletion of Ink4a/Arf". Oncogene. 22 (40): 6257–6265. doi:10.1038/sj.onc.1206630. ISSN 0950-9232. PMID 13679864.
  7. ^ Smith, Karen Lisa; Isaacs, Claudine (2011). "BRCA Mutation Testing in Determining Breast Cancer Therapy". The Cancer Journal. 17 (6): 492–499. doi:10.1097/ppo.0b013e318238f579. ISSN 1528-9117. PMC 3240813. PMID 22157293.
  8. ^ Fanen, Pascale; Wohlhuter-Haddad, Adeline; Hinzpeter, Alexandre (July 2014). "Genetics of cystic fibrosis: CFTR mutation classifications toward genotype-based CF therapies" (PDF). The International Journal of Biochemistry & Cell Biology. 52: 94–102. doi:10.1016/j.biocel.2014.02.023. ISSN 1357-2725. PMID 24631642.
  9. ^ Campisi, Judith (February 1996). "Replicative Senescence: An Old Lives' Tale?". Cell. 84 (4): 497–500. doi:10.1016/s0092-8674(00)81023-5. ISSN 0092-8674. PMID 8598035. S2CID 10751319.
  10. ^ Kandaswamy, Radhika; McQuillin, Andrew; Sharp, Sally I.; Fiorentino, Alessia; Anjorin, Adebayo; Blizard, Robert A.; Curtis, David; Gurling, Hugh M. D. (2013-06-01). "Genetic Association, Mutation Screening, and Functional Analysis of a Kozak Sequence Variant in the Metabotropic Glutamate Receptor 3 Gene in Bipolar Disorder". JAMA Psychiatry. 70 (6): 591–8. doi:10.1001/jamapsychiatry.2013.38. ISSN 2168-622X. PMID 23575746.
  11. ^ Jones, P. B. (2013-01-01). "Adult mental health disorders and their age at onset". The British Journal of Psychiatry. 202 (s54): s5–s10. doi:10.1192/bjp.bp.112.119164. ISSN 0007-1250. PMID 23288502.
  12. ^ Gogtay, N.; Vyas, N. S.; Testa, R.; Wood, S. J.; Pantelis, C. (2011-04-19). "Age of Onset of Schizophrenia: Perspectives From Structural Neuroimaging Studies". Schizophrenia Bulletin. 37 (3): 504–513. doi:10.1093/schbul/sbr030. ISSN 0586-7614. PMC 3080674. PMID 21505117.
  13. ^ Austad, S. N.; Fischer, K. E. (1991-03-01). "Mammalian Aging, Metabolism, and Ecology: Evidence From the Bats and Marsupials". Journal of Gerontology. 46 (2): B47–B53. doi:10.1093/geronj/46.2.b47. ISSN 0022-1422. PMID 1997563.
  14. ^ a b Rose, Michael R. (September 1984). "Laboratory Evolution of Postponed Senescence in Drosophila melanogaster". Evolution. 38 (5): 1004–1010. doi:10.2307/2408434. ISSN 0014-3820. JSTOR 2408434. PMID 28555803.
  15. ^ a b Luckinbill, Leo S.; Arking, Robert; Clare, Michael J.; Cirocco, William C.; Buck, Steven A. (September 1984). "Selection for Delayed Senescence in Drosophila Melanogaster". Evolution. 38 (5): 996–1003. doi:10.1111/j.1558-5646.1984.tb00369.x. ISSN 0014-3820. PMID 28555795.
  16. ^ Partridge, Linda; Fowler, Kevin (February 1992). "Direct and Correlated Responses to Selection on Age at Reproduction in Drosophila melanogaster". Evolution. 46 (1): 76–91. doi:10.1111/j.1558-5646.1992.tb01986.x. ISSN 0014-3820. JSTOR 2409806. PMID 28564973.
  17. ^ Partridge, L. (1987). "Is Accelerated Senescence a Cost of Reproduction?". Functional Ecology. 1 (4): 317–320. doi:10.2307/2389786. ISSN 0269-8463. JSTOR 2389786.
  18. ^ Roper, Caroline; Pignatelli, Patricia; Partridge, Linda (April 1993). "Evolutionary Effects of Selection on Age at Reproduction in Larval and Adult: Drosophila Melanogaster". Evolution. 47 (2): 445–455. doi:10.1111/j.1558-5646.1993.tb02105.x. ISSN 0014-3820. PMID 28568728.
  19. ^ a b c d Walker, David W.; McColl, Gawain; Jenkins, Nicole L.; Harris, Jennifer; Lithgow, Gordon J. (May 2000). "Evolution of lifespan in C. elegans". Nature. 405 (6784): 296–297. doi:10.1038/35012693. ISSN 0028-0836. PMID 10830948. S2CID 4402039.
  20. ^ a b c Reed, David H; Bryant, Edwin H (2000). "The evolution of senescence under curtailed life span in laboratory populations of Musca domestica (the housefly)". Heredity. 85 (2): 115–121. doi:10.1046/j.1365-2540.2000.00737.x. ISSN 0018-067X. PMID 11012712.
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