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The fatty acid amide hydrolase 385 A/A (P129T) variant: haplotype analysis of an ancient missense mutation and validation of risk for drug addiction.

机译:脂肪酸酰胺水解酶385 A / A(P129T)变体:古代错义突变的单倍型分析和药物成瘾风险的验证。

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摘要

The human fatty acid amide hydrolase (FAAH) missense mutation c.385 C-->A, which results in conversion of a conserved proline residue to threonine (P129T), has been associated with street drug use and problem drug abuse. Although a link between the FAAH P129T variant and human drug abuse has been reported, the extent of risk and specific types of substance addiction vulnerability remain to be determined. Here, we investigated the relationship of the FAAH P129T variant to a number of linked single nucleotide polymorphisms to establish a haplotyping system, calculate the estimated age and origin of the FAAH 385 C-->A mutation and evaluate its association with clinically significant drug addiction in a case control study. The results showed a significant over-representation of the FAAH P129T homozygotes in 249 subjects with documented multiple different drug addictions compared to drug free individuals of the same ethnic backgrounds (P = 0.05) using logistic regression analysis controlling for ethnicity. To increase the logistic regression analysis power by increasing the sample size, the data from our previous study (Sipe et al. in Proc Natl Acad Sci USA 99:8394-8399, 2002) were pooled with the present cohort which increased the significance to P = 0.00003. Investigation of the FAAH chromosomal backgrounds of the P129T variant in both multiple different drug addicted and control subjects revealed a common ancestral haplotype, marked population differences in haplotype genetic diversity and an estimated P129T mutation age of 114,425-177,525 years. Collectively, these results show that the P129T mutation is the only common mutation in the FAAH gene and is significantly associated with addictive traits. Moreover, this mutation appears to have arisen early in human evolution and this study validates the previous link between the FAAH P129T variant and vulnerability to addiction of multiple different drugs.
机译:人脂肪酸酰胺水解酶(FAAH)错义突变c.385 C→A,导致保守的脯氨酸残基转化为苏氨酸(P129T),与街头吸毒和滥用毒品有关。尽管已经报道了FAAH P129T变体与滥用毒品之间的联系,但危险程度和特定类型的药物成瘾脆弱性仍有待确定。在这里,我们调查了FAAH P129T变异体与许多连锁的单核苷酸多态性的关系,以建立单倍型系统,计算FAAH 385 C-> A突变的估计年龄和起源,并评估其与临床上显着的药物成瘾的关联在案例对照研究中。结果显示,使用控制种族的逻辑回归分析,与具有相同种族背景的无毒品个体相比,在249名有多种不同的成瘾性的文献中,FAAH P129T纯合子的显着过多(P = 0.05)。为了通过增加样本量来增加逻辑回归分析能力,将我们先前的研究(Sipe等人,Proc Natl Acad Sci USA 99:8394-8399,2002)中的数据与本研究的研究对象进行了合并。 = 0.00003。在多个不同的药物成瘾者和对照对象中对P129T变体的FAAH染色体背景进行的调查显示,共有祖先单倍型,单倍型遗传多样性存在明显的群体差异,估计的P129T突变年龄为114,425-177,525岁。总的来说,这些结果表明,P129T突变是FAAH基因中唯一的常见突变,并且与成瘾性状显着相关。而且,这种突变似乎是在人类进化的早期出现的,这项研究证实了FAAH P129T变异体与多种不同药物成瘾的脆弱性之间的先前联系。

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