Xie Li, Yan Huacheng, Shi Lei, Kong Yanying, Huang Mukun, Li Jian, Li Jin, Zheng Jiaqiang, Zhao Yongpan, Zhao Shujin
Guangzhou University of Traditional Chinese Medicine, Guangzhou 510006, China; Department of Pharmacy, Guangzhou General Hospital of Guangzhou Military Command, Guangzhou 510010, China.
Center for Disease Control and Prevention of Guangzhou Military Command, Guangzhou 510507, China; Department of Pharmacy, Guangzhou General Hospital of Guangzhou Military Command, Guangzhou 510010, China.
Neurosci Lett. 2016 Apr 8;618:77-82. doi: 10.1016/j.neulet.2016.02.053. Epub 2016 Mar 3.
The CYP17A1 gene encodes cytochrome P450c17α, an enzyme that catalyzes the formation of sex hormones, which have been linked to the pathogenesis of Alzheimer's disease (AD). An association between the CYP17A1 rs743572 single nucleotide polymorphism (SNP) and AD has been reported; however, the findings are controversial. In the present study, we investigated the association between rs743572 and another SNP, rs3824755, and AD risk in a Chinese Han population (n=207 patients and 239 controls), and their interaction with the apolipoprotein E (APOE) e4 allele. We found that the C allele and GC+CC genotypes of rs3824755 conferred protection against AD only in APOE e4 carriers. Both rs3824755 and rs743572 polymorphisms showed interactions with APOE e4. The C allele and GC+CC genotypes of rs3824755 acted as protective factors that decreased the risk of APOE e4 in AD. The CYP17A1 rs743572G allele and AG+GG genotypes were found to be potential risk factors that act synergetically with APOE e4. Moreover, the CA and GG haplotypes were protective and conferred a slight risk, respectively, in APOE e4 carriers. These results indicate that CYP17A1 rs3824755 and rs743572 are associated with AD in the Chinese Han population and act in combination with APOE e4.
CYP17A1基因编码细胞色素P450c17α,这是一种催化性激素形成的酶,而性激素已被证明与阿尔茨海默病(AD)的发病机制有关。已有报道称CYP17A1基因的rs743572单核苷酸多态性(SNP)与AD之间存在关联;然而,研究结果存在争议。在本研究中,我们调查了rs743572和另一个SNP rs3824755与中国汉族人群(207例患者和239例对照)AD风险之间的关联,以及它们与载脂蛋白E(APOE)e4等位基因的相互作用。我们发现,rs3824755的C等位基因和GC + CC基因型仅在APOE e4携带者中对AD具有保护作用。rs3824755和rs743572多态性均与APOE e4存在相互作用。rs3824755的C等位基因和GC + CC基因型作为保护因素,降低了AD中APOE e4的风险。发现CYP17A1 rs743572G等位基因和AG + GG基因型是与APOE e4协同作用的潜在风险因素。此外,CA和GG单倍型在APOE e4携带者中分别具有保护作用和轻微风险。这些结果表明,CYP17A1 rs3824755和rs743572与中国汉族人群的AD有关,并与APOE e4共同起作用。