Department of Neurology, Institute of Surgery Research, Daping Hospital, Third Military Medical University, Chongqing 400042, China.
Neurosci Lett. 2012 Aug 15;523(2):174-9. doi: 10.1016/j.neulet.2012.06.071. Epub 2012 Jul 7.
The association between Paraoxonase 1 (PON1) gene polymorphisms (Q192R, L55M) and Alzheimer's disease (AD) risk has been reported inconsistent results. To assess the association between PON1 polymorphisms and AD risk, a meta-analysis was performed. Based on comprehensive searches of the PubMed, Embase, Web of Science, Weipu, and CBM databases, a total of 10 studies including 3081 AD cases and 3054 controls were identified. The pooled odds ratio (OR) with 95% confidence interval (95% CI) were performed. There was no significant association between PON1 Q192R polymorphism and AD risk in all comparison models (R vs. Q, OR=0.89, 95% CI=0.82-0.96; RR vs. QQ, OR=0.83, 95% CI=0.68-1.01; RR+RQ vs. QQ, OR=0.86, 95% CI=0.75-0.97; and RR vs. QR+QQ, OR=0.94, 95% CI=0.81-1.11). For the PON1 L55M polymorphism, lack of an association was also found (L vs. M, OR=0.95, 95% CI=0.86-1.05; LL vs. MM, OR=0.67, 95% CI=0.51-0.88; LL vs. ML+MM, OR=0.82, 95% CI=0.69-0.98; and LL+ML vs. MM, OR=0.75, 95% CI=0.58-0.96). On subgroup analysis by ethnicity, similar results were found. Conclusively, the present meta-analysis revealed that PON1 gene polymorphisms (Q192R, L55M) were unlikely to contribute to AD susceptibility.
PON1 基因多态性(Q192R、L55M)与阿尔茨海默病(AD)风险之间的关联存在不一致的结果。为了评估 PON1 多态性与 AD 风险之间的关联,进行了荟萃分析。通过全面搜索 PubMed、Embase、Web of Science、维普和 CBM 数据库,共确定了 10 项研究,包括 3081 例 AD 病例和 3054 例对照。使用合并的优势比(OR)和 95%置信区间(95%CI)进行分析。在所有比较模型中,PON1 Q192R 多态性与 AD 风险均无显著关联(R 对 Q,OR=0.89,95%CI=0.82-0.96;RR 对 QQ,OR=0.83,95%CI=0.68-1.01;RR+RQ 对 QQ,OR=0.86,95%CI=0.75-0.97;RR 对 QR+QQ,OR=0.94,95%CI=0.81-1.11)。对于 PON1 L55M 多态性,也未发现关联(L 对 M,OR=0.95,95%CI=0.86-1.05;LL 对 MM,OR=0.67,95%CI=0.51-0.88;LL 对 ML+MM,OR=0.82,95%CI=0.69-0.98;LL+ML 对 MM,OR=0.75,95%CI=0.58-0.96)。按种族进行亚组分析,也得到了相似的结果。总之,本荟萃分析表明 PON1 基因多态性(Q192R、L55M)不太可能导致 AD 易感性。