Department of Pharmacy, University of Asia Pacific, Dhaka, 1205, Bangladesh.
Department of Pharmacy, Noakhali Science and Technology University, Noakhali, 3814, Bangladesh.
J Mol Neurosci. 2021 Apr;71(4):675-690. doi: 10.1007/s12031-020-01696-4. Epub 2020 Sep 5.
Schizophrenia (SCZ) is a destructive neuropsychiatric illness affecting millions of people worldwide. The correlation between RELN gene polymorphisms and SCZ was investigated by previous researches, though the results remained conflicting. Based on the available studies, we conducted this meta-analysis to provide a more comprehensive outcome on whether the RELN gene polymorphisms (rs7341475 and rs262355) are associated with SCZ. A total of 15 studies with 25,403 subjects (9047 cases and 16,356 controls) retrieved from PubMed, ScienceDirect, EMBASE, Wiley, BMC, Cochrane, Springer, MDPI, SAGE, and Google Scholar up to June 2020 were included. Meta-analysis was performed using Review Manager 5.3. The heterogeneity was checked using I statistics and Q-test, whereas publication bias was also measured. The rs7341475 polymorphism showed a significantly lower risk for SCZ for the allele (A vs. G: OR = 0.93, 95%CI = 0.87-0.99), codominant 1 (AG vs. GG: OR = 0.92, 95%CI = 0.85-0.99), dominant model (AA+AG vs. GG: OR = 0.92, 95%CI = 0.86-0.98), and over dominant model (AG vs. AA+GG: OR = 0.92, 95%Cl = 0.86-0.99). The allele, codominant model 1, and dominant models remained statistically significant after the correction of the Bonferroni (p < 0.025). Subgroup analysis confirmed the association of allele and dominant models in the Caucasian after Bonferroni correction. For rs262355 polymorphism, a significantly increased risk of SCZ was found only in Caucasians for codominant 2, dominant, and allele models, but significance exists only for the allele model after Bonferroni correction. Publication bias was found in the case of codominant 2 and recessive models for rs7341475 in the overall population, but this publication was not found after performing the Bonferroni correction or after performing the subgroup analysis. No such publication was found for rs262355. The results suggest that RELN rs7341475 is associated with a lower risk of SCZ in the overall population and Caucasian population, but rs262355 is associated with an increased risk of SCZ only in the Caucasian population.
精神分裂症(SCZ)是一种破坏性的神经精神疾病,影响着全球数百万人。先前的研究调查了 RELN 基因多态性与 SCZ 之间的相关性,但结果仍存在争议。基于现有研究,我们进行了这项荟萃分析,以提供更全面的结果,即 RELN 基因多态性(rs7341475 和 rs262355)是否与 SCZ 相关。从 2020 年 6 月之前的 PubMed、ScienceDirect、EMBASE、Wiley、BMC、Cochrane、Springer、MDPI、SAGE 和 Google Scholar 中检索到了 15 项研究,共有 25403 名受试者(9047 例病例和 16356 例对照)纳入本研究。使用 Review Manager 5.3 进行荟萃分析。使用 I 统计量和 Q 检验检查异质性,同时还测量了发表偏倚。rs7341475 多态性的等位基因(A 对 G:OR=0.93,95%CI=0.87-0.99)、共显性 1(AG 对 GG:OR=0.92,95%CI=0.85-0.99)、显性模型(AA+AG 对 GG:OR=0.92,95%CI=0.86-0.98)和超显性模型(AG 对 AA+GG:OR=0.92,95%CI=0.86-0.99)与 SCZ 的风险呈显著降低相关。等位基因、共显性模型 1 和显性模型在经过 Bonferroni 校正(p<0.025)后仍然具有统计学意义。在对 Bonferroni 进行校正后,在白种人中亚组分析证实了等位基因和显性模型的相关性。对于 rs262355 多态性,仅在白种人中发现了共显性 2、显性和等位基因模型与 SCZ 风险显著增加,但在经过 Bonferroni 校正后,仅在等位基因模型中存在显著性。在总体人群中,rs7341475 的共显性 2 和隐性模型存在发表偏倚,但在进行 Bonferroni 校正或进行亚组分析后,这种发表偏倚就不存在了。对于 rs262355,未发现这种发表偏倚。结果表明,RELN rs7341475 与 SCZ 的总体人群和白种人群的低风险相关,但 rs262355 仅与白种人群的 SCZ 高风险相关。