Zhong Huimin, Magee Matthew J, Huang Yunfeng, Hui Qin, Gwinn Marta, Gandhi Neel R, Sun Yan V
Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, Georgia, USA.
Hubert Department of Global Health, Rollins School of Public Health, Emory University, Atlanta, Georgia, USA.
Open Forum Infect Dis. 2020 Mar 26;7(4):ofaa106. doi: 10.1093/ofid/ofaa106. eCollection 2020 Apr.
Understanding the link between tuberculosis (TB) and diabetes is increasingly important as public health responds to the growing global burden of noncommunicable diseases. Genetic association studies have identified numerous host genetic variants linked to TB; however, potential host genetic mechanisms linking TB and diabetes remain unexplored.
We used genetic and phenotypic data from the UK Biobank to evaluate the association of 6 previously reported TB-related host genetic variants (genome-wide significant associations from published studies) with diabetes. The study included 409692 adults of European ancestry including 2177 with type 1 diabetes mellitus (T1DM) and 13976 with type 2 diabetes mellitus (T2DM), defined by ICD-10 diagnosis codes.
Of the 6 TB-associated single nucleotide polymorphisms (SNPs), 2 were associated with T1DM and 3 with T2DM, after adjusting for age, sex, body mass index, smoking, alcohol use, and population structure. After correction for multiple testing, SNPs rs2894257 and rs3135359 () were associated with T1DM (rs2894257: odds ratio [OR], 1.32; 95% confidence interval [CI], 1.21-1.45; rs3135359: OR, 1.72; 95% CI, 1.57-1.88) and T2DM (rs2894257: OR, 1.11; 95% CI, 1.08-1.15; rs3135359: OR, 1.06; 95% CI, 1.025-1.096). The associations with T2DM weakened for rs2894257 and rs3135359 after further exclusion of probable T1DM cases defined by International Statistical Classification of Diseases and Related Health Problems (ICD-10) codes. SNP rs4733781 on chromosome 8 ( gene) was associated with T2DM after exclusion of T1DM cases.
Our findings suggest that common host genetic effects may play a role in the molecular mechanism linking TB and diabetes. Future large genetic studies of TB and diabetes should focus on developing countries with high burdens of infectious and chronic diseases.
随着公共卫生领域应对日益增长的全球非传染性疾病负担,了解结核病(TB)与糖尿病之间的联系变得愈发重要。基因关联研究已确定了众多与结核病相关的宿主基因变异;然而,将结核病与糖尿病联系起来的潜在宿主基因机制仍未得到探索。
我们使用了英国生物银行的基因和表型数据,以评估6个先前报道的与结核病相关的宿主基因变异(来自已发表研究的全基因组显著关联)与糖尿病之间的关联。该研究纳入了409692名欧洲血统的成年人,其中包括2177名1型糖尿病(T1DM)患者和13976名2型糖尿病(T2DM)患者,通过国际疾病分类第10版(ICD - 10)诊断编码进行定义。
在调整年龄、性别、体重指数、吸烟、饮酒和人群结构后,6个与结核病相关的单核苷酸多态性(SNP)中,2个与T1DM相关,3个与T2DM相关。在进行多重检验校正后,SNP rs2894257和rs3135359()与T1DM相关(rs2894257:比值比[OR],1.32;95%置信区间[CI],1.21 - 1.45;rs3135359:OR,1.72;95% CI,1.57 - 1.88),也与T2DM相关(rs2894257:OR,1.11;95% CI,1.08 - 1.15;rs3135359:OR,1.06;95% CI,1.025 - 1.096)。在进一步排除由国际疾病分类及相关健康问题统计分类(ICD - 10)编码定义的可能的TIDM病例后,rs2894257和rs3135359与T2DM的关联减弱。排除T1DM病例后,8号染色体上的SNP rs4733781(基因)与T2DM相关。
我们的研究结果表明,常见的宿主基因效应可能在将结核病与糖尿病联系起来的分子机制中起作用。未来关于结核病和糖尿病的大型基因研究应聚焦于传染病和慢性病负担较重的发展中国家。