SNP-based and haplotype-based genome-wide association on drug dependence in Han Chinese
Drug addiction is a serious problem worldwide and is influenced by genetic factors. The present study aimed to investigate the association between genetics and drug addiction among Han Chinese. A total of 1000 Chinese users of illicit drugs and 9693 healthy controls were enrolled and underwent singl...
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Veröffentlicht in: | BMC genomics 2024-03, Vol.25 (1), p.255-255, Article 255 |
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Sprache: | eng |
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Zusammenfassung: | Drug addiction is a serious problem worldwide and is influenced by genetic factors. The present study aimed to investigate the association between genetics and drug addiction among Han Chinese.
A total of 1000 Chinese users of illicit drugs and 9693 healthy controls were enrolled and underwent single nucleotide polymorphism (SNP)-based and haplotype-based association analyses via whole-genome genotyping.
Both single-SNP and haplotype tests revealed associations between illicit drug use and several immune-related genes in the major histocompatibility complex (MHC) region (SNP association: log
BF = 15.135, p = 1.054e-18; haplotype association: log
BF = 20.925, p = 2.065e-24). These genes may affect the risk of drug addiction via modulation of the neuroimmune system. The single-SNP test exclusively reported genome-wide significant associations between rs3782886 (SNP association: log
BF = 8.726, p = 4.842e-11) in BRAP and rs671 (SNP association: log
BF = 7.406, p = 9.333e-10) in ALDH2 and drug addiction. The haplotype test exclusively reported a genome-wide significant association (haplotype association: log
BF = 7.607, p = 3.342e-11) between a region with allelic heterogeneity on chromosome 22 and drug addiction, which may be involved in the pathway of vitamin B12 transport and metabolism, indicating a causal link between lower vitamin B12 levels and methamphetamine addiction.
These findings provide new insights into risk-modeling and the prevention and treatment of methamphetamine and heroin dependence, which may further contribute to potential novel therapeutic approaches. |
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ISSN: | 1471-2164 1471-2164 |
DOI: | 10.1186/s12864-024-10117-4 |