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白细胞介素-6 多态性与肥胖的关联:系统评价和荟萃分析。

Association of interleukin-6 polymorphisms with obesity: A systematic review and meta-analysis.

机构信息

Obesity and Eating Habits Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran; Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.

Elderly Health Research Center, Endocrinology and Metabolism Population Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Cytokine. 2019 Nov;123:154769. doi: 10.1016/j.cyto.2019.154769. Epub 2019 Aug 28.

Abstract

Obesity is a common metabolic disorder with increasing trend all around the world. Owing to the role of pro-inflammatory cytokines on obesity, we aimed to investigate the role of interleukin-6 (IL-6) polymorphisms on risk of obesity. Electronic literatures were searched in Web of Science, PubMed, Embase, and Scopus. The references of relevant reviews and included studies were also manually checked. All types of observational studies from 1 January 1992 to 28 February 2018 were included. Odds ratio (OR) was estimated by fixed and random effect model. Subgroup analysis was carried out based on age statues. Pooling analysis of eligible studies have been considered for rs2069845 and rs1800796, and no significant results were observed. Minor allele of IL-6 rs1800797polymorphism decreased the risk of obesity/overweight in allelic 0.74 (0.59-0.92), dominant 0.65 (0.49-0.85), and over-dominant 0.66 (0.51-0.87) models. Fourteen eligible studies were included for rs1800795. According to BMI, C allele showed increased risk of obesity in genetic models containing homozygote model 1.47 (1.02-2.12) for body mass index (BMI) ≥ 25 vs. BMI < 25, recessive model 1.32 (1.07-1.63) for BMI ≥ 30 vs. BMI < 25, and homozygote model 1.35 (1.10-1.66) for BMI ≥ 30 vs. BMI < 30. In overall definition of obesity more significant results were observed, including homozygote model in obese vs. normal 1.71 (1.14-2.56). Similarly, subgroups analysis revealed additional significant results. Minor alleles of rs1800795 raised and rs1800797 reduced the risk of obesity, while rs1800796 and rs2069845 may not be associated. However, more observational studies are recommended to confirm these results.

摘要

肥胖是一种常见的代谢紊乱疾病,在全球范围内呈上升趋势。由于促炎细胞因子在肥胖中的作用,我们旨在研究白细胞介素-6(IL-6)多态性与肥胖风险的关系。在 Web of Science、PubMed、Embase 和 Scopus 中检索电子文献。还手动检查了相关综述和纳入研究的参考文献。纳入了 1992 年 1 月 1 日至 2018 年 2 月 28 日的所有类型的观察性研究。采用固定效应模型和随机效应模型估计比值比(OR)。根据年龄状态进行亚组分析。对 rs2069845 和 rs1800796 进行了合格研究的汇总分析,未观察到显著结果。IL-6 rs1800797 多态性的次要等位基因降低了肥胖/超重的风险,杂合子 0.74(0.59-0.92),显性 0.65(0.49-0.85)和超显性 0.66(0.51-0.87)。rs1800795 纳入了 14 项合格研究。根据 BMI,C 等位基因在包含纯合子模型 1.47(1.02-2.12)的遗传模型中显示出肥胖的风险增加 BMI≥25 vs. BMI<25、隐性模型 1.32(1.07-1.63)BMI≥30 vs. BMI<25 和纯合子模型 1.35(1.10-1.66)BMI≥30 vs. BMI<30。在肥胖的总体定义中观察到更显著的结果,包括肥胖与正常的纯合子模型 1.71(1.14-2.56)。同样,亚组分析显示出额外的显著结果。rs1800795 的次要等位基因增加和 rs1800797 的降低与肥胖风险相关,而 rs1800796 和 rs2069845 可能没有关联。然而,建议进行更多的观察性研究来证实这些结果。

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