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Mapping susceptibility loci for alcohol consumption using number of grams of alcohol consumed per day as a phenotype measure

BACKGROUND: There is substantial evidence for a significant genetic component to the risk for alcoholism. However, susceptibility loci or genes for alcohol dependence remain largely unknown. To identify susceptibility loci for alcohol dependence, we selected 329 extended families from the Framingham...

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Autores principales: Ma, Jennie Z, Zhang, Dong, Dupont, Randolph T, Dockter, Michael, Elston, Robert C, Li, Ming D
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866442/
https://www.ncbi.nlm.nih.gov/pubmed/14975172
http://dx.doi.org/10.1186/1471-2156-4-S1-S104
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author Ma, Jennie Z
Zhang, Dong
Dupont, Randolph T
Dockter, Michael
Elston, Robert C
Li, Ming D
author_facet Ma, Jennie Z
Zhang, Dong
Dupont, Randolph T
Dockter, Michael
Elston, Robert C
Li, Ming D
author_sort Ma, Jennie Z
collection PubMed
description BACKGROUND: There is substantial evidence for a significant genetic component to the risk for alcoholism. However, susceptibility loci or genes for alcohol dependence remain largely unknown. To identify susceptibility loci for alcohol dependence, we selected 329 extended families from the Framingham Heart Study population in which at least one family member reported alcohol consumption during the interview in 1970–1971, and performed genome-wide linkage analyses using various analytical methods. RESULTS: Multi-point sib-pair regression analysis using the SIBPAL program of S.A.G.E. provided strong evidence for linkage of alcohol dependence to chromosomes 9 (p-value < 0.0001) and weak evidence to chromosomes 15 and 16 (p-value < 0.005). To confirm these findings, we re-analyzed the same data set by various methods implemented in GENEHUNTER and found that only one region was significant with a LOD score > 2.0 by the variance-component method. This region is located on chromosome 9 between markers GATA21F05 and GATA81C04. CONCLUSION: Analyses of the Framingham Heart Study population provided evidence of genetic susceptibility loci for alcohol dependence on chromosomes 9, 15, and 16. The genomic region identified on chromosome 9 was particularly interesting because the region has also been previously reported to be linked to alcohol dependence in the American Indian population by another group.
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spelling pubmed-18664422007-05-11 Mapping susceptibility loci for alcohol consumption using number of grams of alcohol consumed per day as a phenotype measure Ma, Jennie Z Zhang, Dong Dupont, Randolph T Dockter, Michael Elston, Robert C Li, Ming D BMC Genet Proceedings BACKGROUND: There is substantial evidence for a significant genetic component to the risk for alcoholism. However, susceptibility loci or genes for alcohol dependence remain largely unknown. To identify susceptibility loci for alcohol dependence, we selected 329 extended families from the Framingham Heart Study population in which at least one family member reported alcohol consumption during the interview in 1970–1971, and performed genome-wide linkage analyses using various analytical methods. RESULTS: Multi-point sib-pair regression analysis using the SIBPAL program of S.A.G.E. provided strong evidence for linkage of alcohol dependence to chromosomes 9 (p-value < 0.0001) and weak evidence to chromosomes 15 and 16 (p-value < 0.005). To confirm these findings, we re-analyzed the same data set by various methods implemented in GENEHUNTER and found that only one region was significant with a LOD score > 2.0 by the variance-component method. This region is located on chromosome 9 between markers GATA21F05 and GATA81C04. CONCLUSION: Analyses of the Framingham Heart Study population provided evidence of genetic susceptibility loci for alcohol dependence on chromosomes 9, 15, and 16. The genomic region identified on chromosome 9 was particularly interesting because the region has also been previously reported to be linked to alcohol dependence in the American Indian population by another group. BioMed Central 2003-12-31 /pmc/articles/PMC1866442/ /pubmed/14975172 http://dx.doi.org/10.1186/1471-2156-4-S1-S104 Text en Copyright © 2003 Ma et al; licensee BioMed Central Ltd http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Proceedings
Ma, Jennie Z
Zhang, Dong
Dupont, Randolph T
Dockter, Michael
Elston, Robert C
Li, Ming D
Mapping susceptibility loci for alcohol consumption using number of grams of alcohol consumed per day as a phenotype measure
title Mapping susceptibility loci for alcohol consumption using number of grams of alcohol consumed per day as a phenotype measure
title_full Mapping susceptibility loci for alcohol consumption using number of grams of alcohol consumed per day as a phenotype measure
title_fullStr Mapping susceptibility loci for alcohol consumption using number of grams of alcohol consumed per day as a phenotype measure
title_full_unstemmed Mapping susceptibility loci for alcohol consumption using number of grams of alcohol consumed per day as a phenotype measure
title_short Mapping susceptibility loci for alcohol consumption using number of grams of alcohol consumed per day as a phenotype measure
title_sort mapping susceptibility loci for alcohol consumption using number of grams of alcohol consumed per day as a phenotype measure
topic Proceedings
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866442/
https://www.ncbi.nlm.nih.gov/pubmed/14975172
http://dx.doi.org/10.1186/1471-2156-4-S1-S104
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