Issues and strategies in the genetic analysis of alcoholism and related addictive behaviors

被引:19
作者
Schork, NJ
Schork, CM
机构
[1] Case Western Reserve Univ, Metrohlth Med Ctr, Dept Epidemiol & Biostat, Cleveland, OH 44109 USA
[2] Case Western Reserve Univ, Dept Genet, Cleveland, OH 44109 USA
[3] Harvard Univ, Sch Publ Hlth, Program Populat Genet, Boston, MA 02115 USA
[4] Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
[5] Jackson Lab, Bar Harbor, ME 04609 USA
关键词
alcoholism; genetic epidemiology; linkage mapping; association studies; DRD2; locus; behavior genetics;
D O I
10.1016/S0741-8329(97)00179-1
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Research into the genetics of alcoholism susceptibility and related behaviors has become highly contentious for a number of reasons: at issue is the identification of factors that may ultimately determine human behaviors, the limitations of the technologies being used to conduct relevant studies have not been assessed exhaustively, and independent studies have produced widely different results. Addressing these and other questions of relevance in the dissection of the genetic basis of alcoholism susceptibility will be nothing if not difficult. In this article, we consider issues related to one not-so-minor research angle being used more and more in investigations of alcoholism and related disorders: the identification of susceptibility loci through the use of anonymous (or seemingly anonymous) DNA markers. We also consider issues that might promote (or resist) the reconcilability of independent study results, and describe some basic strategies that might help make study results more compelling in light of the complexity of alcoholism and related behaviors. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:71 / 83
页数:13
相关论文
共 103 条
[71]   ASSOCIATION ANALYSIS OF THE DOPAMINE D-2 RECEPTOR GENE IN TOURETTES-SYNDROME USING THE HAPLOTYPE RELATIVE RISK METHOD [J].
NOTHEN, MM ;
HEBEBRAND, J ;
KNAPP, M ;
HEBEBRAND, K ;
CAMPS, A ;
VONGONTARD, A ;
WETTKESCHAFER, R ;
LISCH, S ;
CICHON, S ;
POUSTKA, F ;
SCHMIDT, M ;
LEHMKUHL, G ;
REMSCHMIDT, H ;
PROPPING, P .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1994, 54 (03) :249-252
[72]   A MOLECULAR INVESTIGATION SUGGESTS NO RELATIONSHIP BETWEEN OBSESSIVE-COMPULSIVE DISORDER AND THE DOPAMINE D-2 RECEPTOR [J].
NOVELLI, E ;
NOBILE, M ;
DIAFERIA, G ;
SCIUTO, G ;
CATALANO, M .
NEUROPSYCHOBIOLOGY, 1994, 29 (02) :61-63
[73]   Association of alcoholism with the N-glycosylation polymorphism of pseudodeficient human arylsulfatase A [J].
Park, DS ;
Poretz, RD ;
Stein, S ;
Nora, R ;
Manowitz, P .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1996, 20 (02) :228-233
[74]  
PARSIAN A, 1991, ARCH GEN PSYCHIAT, V48, P655
[75]   A manic depressive history [J].
Risch, N ;
Botstein, D .
NATURE GENETICS, 1996, 12 (04) :351-353
[76]   The future of genetic studies of complex human diseases [J].
Risch, N ;
Merikangas, K .
SCIENCE, 1996, 273 (5281) :1516-1517
[77]   [H-3]Naloxone binding in the human brain: Alcoholism and the TaqI A D-2 dopamine receptor polymorphism [J].
Ritchie, T ;
Noble, EP .
BRAIN RESEARCH, 1996, 718 (1-2) :193-197
[78]   DIRECT SEQUENCING OF THE DOPAMINE-D2 RECEPTOR (DRD2) IN SCHIZOPHRENICS REVEALS 3-POLYMORPHISMS BUT NO STRUCTURAL-CHANGE IN THE RECEPTOR [J].
SARKAR, G ;
KAPELNER, S ;
GRANDY, DK ;
MARCHIONNI, M ;
CIVELLI, O ;
SOBELL, J ;
HESTON, L ;
SOMMER, SS .
GENOMICS, 1991, 11 (01) :8-14
[79]  
SCHORK N, 1996, MOL GENETICS GENE TH, P79
[80]  
SCHORK NJ, 1993, AM J HUM GENET, V53, P1127