Literature DB >> 17117961

A joint genomewide linkage analysis of symptoms of alcohol dependence and conduct disorder.

Kenneth S Kendler1, Po-Hsiu Kuo, B Todd Webb, Gursharan Kalsi, Michael C Neale, Patrick F Sullivan, Dermot Walsh, Diana G Patterson, Brien Riley, Carol A Prescott.   

Abstract

BACKGROUND: A large linkage peak for alcohol dependence (AD) was detected on chromosome 4q in the Irish Affected Sib Pair Study of Alcohol Dependence (IASPSAD). Are the susceptibility genes underlying this peak specific for AD or do they increase risk for externalizing disorders more generally? Can we, in the IASPSAD, replicate prior evidence for linkage to conduct disorder (CD)?
METHODS: The 733 all possible sibling pairs in IASPSAD were typed for 1,020 short-tandem-repeat genetic markers. Univariate and bivariate linkage analyses were conducted by the program sequential oligogenic linkage analysis routines (SOLAR), for both the raw and the transformed number of symptoms of AD (ADsx) and number of symptoms of CD (CDsx). In the bivariate analyses, specificity was assessed by the ratio of the variance accounted for in ADsx and CDsx by the quantitative trait locus.
RESULTS: In the univariate linkage analyses, no evidence for linkage to CDsx was found under the 4q peak for ADsx and the largest peaks for CDsx were seen on chromosomes 1q (LOD=3.16) and 14p (LOD=2.36). In the bivariate linkage analysis, the 4q peak had high specificity for AD (AD/CD ratio of 39.9). Several smaller peaks, on chromosomes 1, 7, and 10, had moderate specificity for CD but also impacted on risk for AD, with AD/CD ratios of 0.18 to 0.32.
CONCLUSIONS: Genes under the 4q linkage peak for AD in the IASPSAD impact specifically on risk for AD rather than more broadly on risk for externalizing syndromes. Suggestive linkages were found in several locations for CD, 2 of which broadly replicate prior findings. The bivariate analyses identified genomic locations containing susceptibility loci that impacted on risk for both CDsx and ADsx.

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Year:  2006        PMID: 17117961     DOI: 10.1111/j.1530-0277.2006.00243.x

Source DB:  PubMed          Journal:  Alcohol Clin Exp Res        ISSN: 0145-6008            Impact factor:   3.455


  16 in total

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Journal:  Neurosci Biobehav Rev       Date:  2016-06-24       Impact factor: 8.989

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Review 3.  Conduct disorder in adolescent females: current state of research and study design of the FemNAT-CD consortium.

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4.  Single nucleotide polymorphisms in the REG-CTNNA2 region of chromosome 2 and NEIL3 associated with impulsivity in a Native American sample.

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Review 6.  A comparison of selected quantitative trait loci associated with alcohol use phenotypes in humans and mouse models.

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8.  Externalizing disorders in American Indians: comorbidity and a genome wide linkage analysis.

Authors:  Cindy L Ehlers; David A Gilder; Wendy S Slutske; Penelope A Lind; Kirk C Wilhelmsen
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2008-09-05       Impact factor: 3.568

9.  Alcohol consumption indices of genetic risk for alcohol dependence.

Authors:  Julia D Grant; Arpana Agrawal; Kathleen K Bucholz; Pamela A F Madden; Michele L Pergadia; Elliot C Nelson; Michael T Lynskey; Richard D Todd; Alexandre A Todorov; Narelle K Hansell; John B Whitfield; Nicholas G Martin; Andrew C Heath
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10.  Sociodemographic and psychopathologic predictors of first incidence of DSM-IV substance use, mood and anxiety disorders: results from the Wave 2 National Epidemiologic Survey on Alcohol and Related Conditions.

Authors:  B F Grant; R B Goldstein; S P Chou; B Huang; F S Stinson; D A Dawson; T D Saha; S M Smith; A J Pulay; R P Pickering; W J Ruan; W M Compton
Journal:  Mol Psychiatry       Date:  2008-04-22       Impact factor: 15.992

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