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抵抗素与多发性骨髓瘤:两样本孟德尔随机化研究 被引量:2

Resistin and multiple myeloma:a two-sample Mendelian randomization study
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摘要 目的探讨抵抗素与多发性骨髓瘤(MM)发生风险之间是否存在因果关系。方法采用两样本孟德尔随机化分析方法,将抵抗素相关遗传变异数据作为工具变量,使用MM的全基因组关联研究数据作为结局事件,采用逆方差加权法(IVW)、MR-Egger、加权中位数、加权模式和简单模式5种方法分析抵抗素对MM发生风险的因果影响。结果5种分析方法均显示抵抗素与MM之间不存在因果关系(P>0.05)。敏感性分析显示,结果稳健,基因无水平多效性、异质性及离群值,无单独的SNPs影响结果。结论本研究不支持抵抗素与MM发生风险存在因果关系。 Objective To investigate the causal relationship between resistin and multiple myeloma(MM).Methods A two-sample Mendelian randomization analysis was conducted using genetic variants(SNPs)associated with resistin as instrumental variables and MM genome-wide association study(GWAS)data as the outcome event.Five analysis methods,including inverse-variance weighted(IVW),MR-Egger,weighted median,weighted model,and simple model were used to assess the causal impact of resistin on the risk of MM.Results None of the five analysis methods showed a causal relationship between resistin and multiple myeloma(P>0.05).Sensitivity analysis indicated consistent and robust results,with no evidence of horizontal pleiotropy,heterogeneity,outliers,or individual SNPs influencing the findings.Conclusion This Mendelian randomization study provides no support for a causal relationship between resistin and the risk of multiple myeloma.
作者 王洪波 王秀娟 郭新红 江明 WANG Hongbo;WANG Xiujuan;GUO Xinhong;JIANG Ming(Hematologic Disease Center,the First Affiliated Hospital of Xinjiang Medical University,Urumqi 830054,P.R.China;Institute of Hematology of Xinjiang Uygur Autonomous Region,Urumqi 830054,P.R.China)
出处 《中国循证医学杂志》 CSCD 北大核心 2023年第9期1005-1010,共6页 Chinese Journal of Evidence-based Medicine
基金 新疆维吾尔自治区自然科学基金项目(编号:2021D01C333)。
关键词 孟德尔随机化 多发性骨髓瘤 抵抗素 Mendelian randomization study Multiple myeloma Resistin
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  • 1Hardy J, Singleton A. Genomewide association studies and human disease. N Engl J Med,2009,360(17) : 1759-1768.
  • 2Zhang X J, Huang W, Yang S, et al. Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at lq21. Nat Genet,2009,41 (2) :205-210.
  • 3Han JW, Zheng HF, Cui Y, et al. Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. Nat Genet, 2009,41 ( 11 ) : 1234-1237.
  • 4Zhang FR, Huang W, Chen SM, et al. Genomewide association study of leprosy. N Engl J Med, 2009,361 (27) : 2609-2618.
  • 5Lei SF, Yang TL, Tan LJ, et al. Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci. Hum Genet, 2009,125( 1 ) ~ 1-9.
  • 6Guo Y, Tan LJ, Lei SF, et al. Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis. PLoS Genet, 2010,6( 1 ) : e1000806.
  • 7Bei JX, Li Y, Jia WH, et al. A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. Nat Genet, 2010,42 (7) : 599-603.
  • 8Wu C, Xu B, Yuan P, et al. Genome-wide examination of genetic variants associated with response to platinum-based chemotherapy in patients with small-cell lung cancer. Pharmacogenet Genomics, 2010,20(6) : 389-395.
  • 9Quan C, Ren YQ, Xiang LH, et al. Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC. Nat Genet,2010,42(7) :614-618.
  • 10Zhang H,Zhai Y,Hu Z,et al. Genome-wide association study identifies lp36.22 as a new susceptibility locus for hepatocellular carcinoma in chronic hepatitis B virus carriers. Nat Genet, 2010, 42(9) : 755-758.

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