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CYP27B1基因多态性rs703842与多发性硬化症的关联:一项荟萃分析

The Association Between Genetic Polymorphism rs703842 in CYP27B1 and Multiple Sclerosis: A Meta-Analysis.

作者信息

Jiang Tao, Li Lizhuo, Wang Ying, Zhao Chuntao, Yang Jundong, Ma Dexuan, Guan Yanlei, Zhao Dan, Bao Yijun, Wang Yunjie, Yang Jingyun

机构信息

From the Department of Neurology (TJ, JY), Laizhou People's Hospital, Laizhou, Shandong; Department of Critical Care and Emergency Medicine (LL), The Affiliated Hospital of Hainan Medical University, Haikou, Hainan; Emergency Department (LL), Shengjing Hospital of China Medical University, Shenyang, Liaoning; Department of Neurosurgery (YW, DM), Huashan Hospital, Fudan University, Shanghai, China; Brain Tumor Center (CZ), Cancer and Blood Diseases Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA; Department of Neurosurgery (YG, DZ, YB, YW), The First Hospital of China Medical University, Shenyang, Liaoning; Rush Alzheimer's Disease Center (JY); and Department of Neurological Sciences (JY), Rush University Medical Center, Chicago, IL, USA.

出版信息

Medicine (Baltimore). 2016 May;95(19):e3612. doi: 10.1097/MD.0000000000003612.

Abstract

Multiple sclerosis (MS) is the most frequent nontraumatic disabling neurological disease among young adults. Previous studies have examined the association of rs703842 in CYP27B1 with MS susceptibility, with inconsistent results reported.The objective of this study is to conduct a systematic literature search and perform meta-analyses to examine whether rs703842 is associated with MS risk.We searched potential literature in PubMed, Cochrane Library, Embase, Google Scholar, Web of Science, and HuGE by using the following inclusion criteria: studies were on human subjects; the studies were case-control studies; studies included subjects who had MS and those who did not have MS; and the studies provided genotype data for rs703842 for subjects who had and did not have MS, or provided odds ratios (ORs) and the 95% confidence intervals (CIs) for assessing the association of rs703842 with MS, or provided sufficient data for the calculation of OR and the 95% CI. We used random-effects models to calculate the OR as a measure of association. We used I to assess between-study heterogeneity, and a funnel plot and Egger test to assess publication bias.Seven studies published since 2008 met the eligibility criteria and were included in the meta-analyses. We found that the C allele was significantly associated with reduced MS susceptibility (OR = 0.88, 95% CI: 0.80-0.89; P < 0.0001). We also found significant association of rs703842 with MS risk using a dominant and a recessive model (both P < 0.0002). Our results remain unchanged if our meta-analysis was limited to studies that included only Caucasian participants (OR = 0.85, 95% CI: 0.80-0.90; P < 0.0001).Our study has several limitations: The sample size is limited; We were unable to control for some important confounding factors as data for individual participant were not available; and Most of the included studies focus on MS risk in Caucasian. As a result, we could not perform meta-analysis for assessing the relationship in other ethnic groups.In summary, we found that the genetic variant rs703842 in CYP27B1 is associated with MS risk in Caucasians. More studies with larger sample size that control for important confounding factors are needed to validate the findings from this study.

摘要

多发性硬化症(MS)是年轻成年人中最常见的非创伤性致残性神经疾病。以往的研究探讨了CYP27B1基因中rs703842与MS易感性的关联,但报道的结果并不一致。本研究的目的是进行系统的文献检索并开展荟萃分析,以检验rs703842是否与MS风险相关。我们通过以下纳入标准在PubMed、Cochrane图书馆、Embase、谷歌学术、科学网和HuGE中检索潜在文献:研究对象为人类;研究为病例对照研究;研究纳入了患有MS的受试者和未患有MS的受试者;研究提供了患有和未患有MS的受试者的rs703842基因型数据,或提供了用于评估rs703842与MS关联的比值比(OR)和95%置信区间(CI),或提供了计算OR和95%CI的足够数据。我们使用随机效应模型计算OR作为关联度量。我们用I²评估研究间的异质性,并用漏斗图和Egger检验评估发表偏倚。2008年以来发表的7项研究符合纳入标准并被纳入荟萃分析。我们发现C等位基因与MS易感性降低显著相关(OR = 0.88,95%CI:0.80 - 0.89;P < 0.0001)。我们还使用显性和隐性模型发现rs703842与MS风险存在显著关联(P均< 0.0002)。如果我们的荟萃分析仅限于仅纳入白人参与者的研究,我们的结果保持不变(OR = 0.85,95%CI:0.80 - 0.90;P < 0.0001)。我们的研究有几个局限性:样本量有限;由于无法获取个体参与者的数据,我们无法控制一些重要的混杂因素;并且纳入的大多数研究关注白人中的MS风险。因此,我们无法进行荟萃分析来评估其他种族群体中的关系。总之,我们发现CYP27B1基因中的遗传变异rs703842与白人中的MS风险相关。需要更多样本量更大且能控制重要混杂因素的研究来验证本研究的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a5c/4902511/527e7a76b7f6/medi-95-e3612-g001.jpg

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