Twin studies and the heritability of MS: a conclusion

Objective The classical twin study has the potential to evaluate the relative contribution of genes and environment and guide further research strategies, provided the sampling and methods of analysis are correct. We wish to review all the more informative twin studies on multiple sclerosis (MS). Me...

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Veröffentlicht in:Multiple sclerosis 2009-06, Vol.15 (6), p.661-667
Hauptverfasser: Hawkes, CH, Macgregor, AJ
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container_title Multiple sclerosis
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creator Hawkes, CH
Macgregor, AJ
description Objective The classical twin study has the potential to evaluate the relative contribution of genes and environment and guide further research strategies, provided the sampling and methods of analysis are correct. We wish to review all the more informative twin studies on multiple sclerosis (MS). Methods We examined six large population-based twin studies in MS and calculated indices of heritability (h2), which is the traditional method of assessing genetic contribution to disease and to allow comparison between studies. Results This index was found to vary widely from 0.25 to 0.76 with large confidence intervals that reflect small sample size and prevent robust interpretation. Conclusion Overall the studies support a genetic contribution to disease; however, the imprecision of the heritability estimates and potential biases that they contain mean that very little inference can be drawn its exact size. Given that the magnitude of genetic effect cannot be measured because of the relative infrequency of MS; the consequent difficulty in collecting an informative sample; and in many countries, the lack of a comprehensive twin register, we suggest that further twin prevalence surveys should not be undertaken. Twin studies could be used more effectively in other ways, such as the co-twin case–control approach.
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We wish to review all the more informative twin studies on multiple sclerosis (MS). Methods We examined six large population-based twin studies in MS and calculated indices of heritability (h2), which is the traditional method of assessing genetic contribution to disease and to allow comparison between studies. Results This index was found to vary widely from 0.25 to 0.76 with large confidence intervals that reflect small sample size and prevent robust interpretation. Conclusion Overall the studies support a genetic contribution to disease; however, the imprecision of the heritability estimates and potential biases that they contain mean that very little inference can be drawn its exact size. Given that the magnitude of genetic effect cannot be measured because of the relative infrequency of MS; the consequent difficulty in collecting an informative sample; and in many countries, the lack of a comprehensive twin register, we suggest that further twin prevalence surveys should not be undertaken. Twin studies could be used more effectively in other ways, such as the co-twin case–control approach.</description><identifier>ISSN: 1352-4585</identifier><identifier>EISSN: 1477-0970</identifier><identifier>DOI: 10.1177/1352458509104592</identifier><identifier>PMID: 19482860</identifier><identifier>CODEN: MUSCFZ</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Biological and medical sciences ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. 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We wish to review all the more informative twin studies on multiple sclerosis (MS). Methods We examined six large population-based twin studies in MS and calculated indices of heritability (h2), which is the traditional method of assessing genetic contribution to disease and to allow comparison between studies. Results This index was found to vary widely from 0.25 to 0.76 with large confidence intervals that reflect small sample size and prevent robust interpretation. Conclusion Overall the studies support a genetic contribution to disease; however, the imprecision of the heritability estimates and potential biases that they contain mean that very little inference can be drawn its exact size. Given that the magnitude of genetic effect cannot be measured because of the relative infrequency of MS; the consequent difficulty in collecting an informative sample; and in many countries, the lack of a comprehensive twin register, we suggest that further twin prevalence surveys should not be undertaken. Twin studies could be used more effectively in other ways, such as the co-twin case–control approach.</description><subject>Biological and medical sciences</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Genetic Predisposition to Disease - epidemiology</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Multiple Sclerosis - epidemiology</subject><subject>Multiple Sclerosis - genetics</subject><subject>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. 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Leukodystrophies. Prion diseases</topic><topic>Genetic Predisposition to Disease - epidemiology</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Multiple Sclerosis - epidemiology</topic><topic>Multiple Sclerosis - genetics</topic><topic>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. 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Given that the magnitude of genetic effect cannot be measured because of the relative infrequency of MS; the consequent difficulty in collecting an informative sample; and in many countries, the lack of a comprehensive twin register, we suggest that further twin prevalence surveys should not be undertaken. Twin studies could be used more effectively in other ways, such as the co-twin case–control approach.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>19482860</pmid><doi>10.1177/1352458509104592</doi><tpages>7</tpages></addata></record>
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subjects Biological and medical sciences
Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
Genetic Predisposition to Disease - epidemiology
Humans
Medical sciences
Multiple Sclerosis - epidemiology
Multiple Sclerosis - genetics
Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis
Neurology
Prevalence
Sample Size
Twin Studies as Topic
Twins
title Twin studies and the heritability of MS: a conclusion
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