Further evidence of association of OPRD1 & HTR1D Polymorphisms with susceptibility to anorexia nervosa

被引:61
作者
Brown, Kirsty M. O.
Bujac, Sarah R.
Mann, Evleen T.
Campbell, David A.
Stubbins, Michael J.
Blundell, John E.
机构
[1] Univ Dundee, Dept Publ Hlth, KMOB, Dundee, Scotland
[2] GlaxoSmithKline, Discovery & Pipeline Genet, Harlow, Essex, England
[3] Seacroft Hosp, Yorkshire Ctr Eating Disorders, Leeds, W Yorkshire, England
[4] Univ Leeds, Inst Psychol Sci, Leeds, W Yorkshire, England
基金
英国医学研究理事会;
关键词
anorexia nervosa; association; gene; opioid; serotonin; susceptibility;
D O I
10.1016/j.biopsych.2006.04.007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: A recent study reported strong evidence for the involvement of a region on human chromosome I and genetic susceptibility to anorexia nervosa (AN). A more detailed analysis of this region has suggested 2 genes that may account for Ibis susceptibility. These data suggest that polymorphisms in both the serotonin 1D (HTR1D) and opioid delta 1 (OPRD1) receptor genes show a significant association with restricting AN (RAN). Methods: In the current study, we have conducted an independent association study on 226 females meeting DSM-IV criteria for AN and 678 matched volunteers. Results. We genotyped 4 SNPs in HTR1D) and 6 SNTs in OPRD1.3 SNPs were found to be associated with both RAN and binge-purge AN (BPAN) within the gene for OPRD1. We also found evidence of association between 2 polymorphisms within HTR1D) and RAN. Conclusions: These data support the hypothesis that polymorphisms within this region form a component of the genetic basis to susceptibility to RAN. However, further work is required to understand the processes that may be mediated by these genes.
引用
收藏
页码:367 / 373
页数:7
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