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An estimate of amyotrophic lateral sclerosis heritability using twin data
BACKGROUND: Causative gene mutations have been identified in about 2% of those with amyotrophic lateral sclerosis (ALS), often, but not always, when there is a strong family history. There is an assumption that there is a genetic component to all ALS, but genome-wide association studies have yet to...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BMJ Group
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2988617/ https://www.ncbi.nlm.nih.gov/pubmed/20861059 http://dx.doi.org/10.1136/jnnp.2010.207464 |
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author | Al-Chalabi, A Fang, F Hanby, M F Leigh, P N Shaw, C E Ye, W Rijsdijk, F |
author_facet | Al-Chalabi, A Fang, F Hanby, M F Leigh, P N Shaw, C E Ye, W Rijsdijk, F |
author_sort | Al-Chalabi, A |
collection | PubMed |
description | BACKGROUND: Causative gene mutations have been identified in about 2% of those with amyotrophic lateral sclerosis (ALS), often, but not always, when there is a strong family history. There is an assumption that there is a genetic component to all ALS, but genome-wide association studies have yet to produce a robustly replicated result. A definitive estimate of ALS heritability is therefore required to determine whether ongoing efforts to find susceptibility genes are worth while. METHODS: The authors performed two twin studies, one population- and one clinic-based. The authors used structural equation modelling to perform a meta-analysis of data from these studies and an existing twin study to estimate ALS heritability, and identified 171 twin pairs in which at least one twin had ALS. RESULTS AND DISCUSSION: Five monozygotic twin pairs were concordant-affected, and 44 discordant-affected. No dizygotic twin pairs were concordant-affected, and 122 discordant-affected. The heritability of sporadic ALS was estimated as 0.61 (0.38 to 0.78) with the unshared environmental component 0.39 (0.22 to 0.62). ALS has a high heritability, and efforts to find causative genes should continue. |
format | Text |
id | pubmed-2988617 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BMJ Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-29886172010-12-06 An estimate of amyotrophic lateral sclerosis heritability using twin data Al-Chalabi, A Fang, F Hanby, M F Leigh, P N Shaw, C E Ye, W Rijsdijk, F J Neurol Neurosurg Psychiatry Research Paper BACKGROUND: Causative gene mutations have been identified in about 2% of those with amyotrophic lateral sclerosis (ALS), often, but not always, when there is a strong family history. There is an assumption that there is a genetic component to all ALS, but genome-wide association studies have yet to produce a robustly replicated result. A definitive estimate of ALS heritability is therefore required to determine whether ongoing efforts to find susceptibility genes are worth while. METHODS: The authors performed two twin studies, one population- and one clinic-based. The authors used structural equation modelling to perform a meta-analysis of data from these studies and an existing twin study to estimate ALS heritability, and identified 171 twin pairs in which at least one twin had ALS. RESULTS AND DISCUSSION: Five monozygotic twin pairs were concordant-affected, and 44 discordant-affected. No dizygotic twin pairs were concordant-affected, and 122 discordant-affected. The heritability of sporadic ALS was estimated as 0.61 (0.38 to 0.78) with the unshared environmental component 0.39 (0.22 to 0.62). ALS has a high heritability, and efforts to find causative genes should continue. BMJ Group 2010-09-22 2010-12 /pmc/articles/PMC2988617/ /pubmed/20861059 http://dx.doi.org/10.1136/jnnp.2010.207464 Text en © 2010, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode. |
spellingShingle | Research Paper Al-Chalabi, A Fang, F Hanby, M F Leigh, P N Shaw, C E Ye, W Rijsdijk, F An estimate of amyotrophic lateral sclerosis heritability using twin data |
title | An estimate of amyotrophic lateral sclerosis heritability using twin data |
title_full | An estimate of amyotrophic lateral sclerosis heritability using twin data |
title_fullStr | An estimate of amyotrophic lateral sclerosis heritability using twin data |
title_full_unstemmed | An estimate of amyotrophic lateral sclerosis heritability using twin data |
title_short | An estimate of amyotrophic lateral sclerosis heritability using twin data |
title_sort | estimate of amyotrophic lateral sclerosis heritability using twin data |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2988617/ https://www.ncbi.nlm.nih.gov/pubmed/20861059 http://dx.doi.org/10.1136/jnnp.2010.207464 |
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