Interaction between interleukin 10 (IL-10) gene polymorphisms and obesity on susceptibility to polycystic ovary syndrome in Chinese women.

IF 1.8 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM
Ning Ding, Yi-Rou Chen, Rui-Juan Jia, Xi-Zhou Lu, Shu-Lin Xie, Hui-Ling Shang, Jian-Gang Shuai
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引用次数: 0

Abstract

Objectives: The pathogenesis of polycystic ovary syndrome (PCOS) was complex, and the incident PCOS involves both genetic and environmental factors. However, no study focused on the synergistic effect between interleukin 10 (IL-10) gene and obesity on PCOS risk yet. This study aimed to evaluate the correlation between IL-10 gene single nucleotide polymorphisms (SNPs) and PCOS susceptibility and impact of the interaction between IL-10 gene and obesity on PCOS risk.

Methods: A total of 540 participants consisted of 180 PCOS patients and 360 normal controls were enrolled in this study. Logistic regression model was employed to evaluate the association between IL-10 gene polymorphisms and PCOS susceptibility, odds ratios (ORs) and 95% confidence interval (CI) were calculated. Generalized multifactor dimensionality reduction (GMDR) was employed to screen the IL-10 gene-obesity interaction.

Results: Logistic regression also indicated that rs1800896-G allele was statistically significant correlated with increased risk of PCOS, the ORs (rs (95%CI) for AG, GG and AG+GG genotype was 1.75 (1.21-2.33), 1.93 (1.17-2.72) and 1.79 (1.26-2.35), respectively. However, no significant difference was observed on the distribution of genotypes and alleles within rs1800890, rs1800871, rs1800872 between PCOS patients and normal controls (all p values > 0.05). GMDR model found a significant interaction combination (two-locus model with p = 0.001) between rs1800896 and obesity, the cross-validation consistency was 10/10 and the prediction error was 0.641. Compared with those non-obese participants with rs1800896-AA genotype, OR (95% CI) was 1.62 (1.14-2.12), 1.46 (1.02-1.95) for non-obese participants with rs1800896-AG or GG genotype, obese participants with rs1800896-AA genotype, and obese participants with rs1800896-AG or GG genotype have the highest PCOS risk, OR (95% CI) = 3.58 (1.81-5.41), after covariates adjusting.

Conclusions: We found that rs1800896-G allele, gene-environment interaction between rs1800896 and obesity were all correlated with increased PCOS risk.

白介素10基因多态性与肥胖对中国女性多囊卵巢综合征易感性的相互作用
目的:多囊卵巢综合征(PCOS)发病机制复杂,多囊卵巢综合征的发生涉及遗传和环境因素。然而,目前尚未有研究关注白细胞介素10 (IL-10)基因与肥胖对PCOS风险的协同作用。本研究旨在探讨IL-10基因单核苷酸多态性(snp)与PCOS易感性的相关性,以及IL-10基因与肥胖相互作用对PCOS发病的影响。方法:540例PCOS患者180例,正常对照360例。采用Logistic回归模型评价IL-10基因多态性与PCOS易感性的相关性,计算比值比(ORs)和95%置信区间(CI)。采用广义多因素降维法(GMDR)筛选IL-10基因与肥胖的相互作用。结果:Logistic回归也显示rs1800896-G等位基因与PCOS风险增加有统计学意义,AG、GG和AG+GG基因型的or (95%CI)分别为1.75(1.21-2.33)、1.93(1.17-2.72)和1.79(1.26-2.35)。而PCOS患者与正常对照rs1800890、rs1800871、rs1800872基因型及等位基因分布差异无统计学意义(p值均为0.05)。GMDR模型发现rs1800896与肥胖存在显著交互作用组合(双位点模型p = 0.001),交叉验证一致性为10/10,预测误差为0.641。与rs1800896-AA基因型的非肥胖参与者相比,rs1800896-AG或GG基因型的非肥胖参与者、rs1800896-AA基因型的肥胖参与者和rs1800896-AG或GG基因型的肥胖参与者的PCOS风险最高,经协变量调整后OR (95% CI) = 3.58(1.81-5.41)。结论:我们发现rs1800896- g等位基因、rs1800896基因-环境互作与肥胖均与PCOS风险增加相关。
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来源期刊
Endocrine Research
Endocrine Research 医学-内分泌学与代谢
CiteScore
4.30
自引率
0.00%
发文量
10
审稿时长
>12 weeks
期刊介绍: This journal publishes original articles relating to endocrinology in the broadest context. Subjects of interest include: receptors and mechanism of action of hormones, methodological advances in the detection and measurement of hormones; structure and chemical properties of hormones. Invitations to submit Brief Reviews are issued to specific authors by the Editors.
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