Abstract
Background: A recent study reported strong evidence for the involvement of a region on human chromosome 1 and genetic susceptibility to anorexia nervosa (AN). A more detailed analysis of this region has suggested 2 genes that may account for this 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 SNPs 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. © 2007 Society of Biological Psychiatry.
Original language | English |
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Pages (from-to) | 367-373 |
Number of pages | 7 |
Journal | Biological Psychiatry |
Volume | 61 |
Issue number | 3 |
DOIs | |
Publication status | Published - 1 Feb 2007 |
Keywords
- Adult
- Alleles
- Anorexia Nervosa
- DNA
- Female
- Gene Frequency
- Genotype
- Great Britain
- Humans
- Linkage Disequilibrium
- Odds Ratio
- Polymorphism, Genetic
- Psychiatric Status Rating Scales
- Receptor, Serotonin, 5-HT1D
- Receptors, Opioid, delta