[Mendelian randomization analysis: the causal relationship between the DNA methylation levels of JAK2 and obesity]

Zhonghua Liu Xing Bing Xue Za Zhi. 2022 Aug 10;43(8):1315-1320. doi: 10.3760/cma.j.cn112338-20220318-00200.
[Article in Chinese]

Abstract

Objective: Based on the Mendelian randomization analysis, to assess the causal relationship between DNA methylation levels of Janus kinase 2 (JAK2) and obesity. Methods: A case-control study was carried out, including 1 021 individuals [obesity (visceral fat index ≥10) vs. no obesity (visceral fat index <10) was 440 vs. 581] from the Henan Rural Cohort Study. MethylTargetTM target region methylation sequencing technology was used for testing the DNA methylation level of JAK2. logistic regression models were used to assess the association between the DNA methylation level of JAK2 and obesity. With SNP as the instrumental variable, the association between the DNA methylation level of JAK2 and obesity was explored by using the Mendelian randomization analysis method. Results: There was a positive association between Chr9:4984943 (one DNA methylation site in the promoter of JAK2) and obesity, and the OR (95%CI) was 1.22(1.04-1.42). Methylation level of five sites in the exon of JAK2 (Chr9:4985378, Chr9:4985404, Chr9:4985407, Chr9:4985409 and Chr9:4985435) were negatively associated with obesity, the corresponding OR (95%CI) were 0.53 (0.29-0.95), 0.58(0.36-0.93), 0.69 (0.49-0.97), 0.72 (0.53-0.99) and 0.58 (0.35-0.98) , respectively. Mendelian randomization analysis showed that there was a causal relationship between the DNA methylation levels of JAK2 and obesity, and the corresponding β (95%CI) were -1.985 (-3.520 - -0.450),-3.547 (-6.301 - -0.792) and -3.900 (-6.328 - -1.472) for Mendelian randomization method of inverse variance weighted, Mendelian randomization method of median based and Maximum-likelihood method, respectively. Conclusion: This study supported there was a causal relationship between the DNA methylation level of JAK2 and obesity.

目的: 采用孟德尔随机化法探讨酪氨酸激酶2(JAK2)基因甲基化水平与肥胖的因果关联。 方法: 从河南农村队列中选取1 021例研究对象,其中440例肥胖者(内脏脂肪指数≥10)和581例对照者(内脏脂肪指数<10)。采用MethylTargetTM目标区域甲基化测序技术检测JAK2基因甲基化水平;采用logistic回归模型分析JAK2基因甲基化水平与肥胖的关联;进一步以单核苷酸多态性为工具变量,采用孟德尔随机化法分析JAK2基因甲基化水平与肥胖的因果关联。 结果: JAK2基因的启动子区发现1个甲基化位点(Chr9:4984943)与肥胖呈正相关(OR=1.22,95%CI:1.04~1.42)。外显子区发现5个甲基化位点(Chr9:4985378、Chr9:4985404、Chr9:4985407、Chr9:4985409和Chr9:4985435)与肥胖呈负相关[OR值(95%CI)分别为0.53(0.29~0.95)、0.58(0.36~0.93)、0.69(0.49~0.97)、0.72(0.53~0.99)和0.58(0.35~0.98)]。3种孟德尔随机化法(逆方差加权孟德尔随机化法、基于中位数孟德尔随机化法和最大似然比法)的结果均显示JAK2基因甲基化水平与肥胖存在因果关联,其相应的β值(95%CI)分别为-1.985(-3.520~-0.450)、-3.547(-6.301~-0.792)和-3.900(-6.328~-1.472)。 结论: JAK2基因甲基化水平与肥胖存在因果关联。.

MeSH terms

  • Case-Control Studies
  • Cohort Studies
  • DNA Methylation*
  • Genome-Wide Association Study
  • Humans
  • Janus Kinase 2 / genetics
  • Mendelian Randomization Analysis* / methods
  • Obesity / complications
  • Obesity / genetics
  • Polymorphism, Single Nucleotide

Substances

  • JAK2 protein, human
  • Janus Kinase 2