National Institute for Nutrition and Health, Chinese Center for Disease Control and Prevention, Beijing 100050, China.
Nutrients. 2020 Dec 18;12(12):3880. doi: 10.3390/nu12123880.
Increasing studies have demonstrated that gene and famine may interact on type 2 diabetes risk. The data derived from the cross-sectional 2010-2012 China National Nutrition and Health Survey (CNNHS) was examined to explore whether gene and famine interacted to influence type 2 diabetes risk. In total, 2216 subjects were involved. The subjects born in 1960 and 1961 were selected as the famine-exposed group, whereas subjects born in 1963 were selected as the unexposed group. A Mass Array system was used to detect the genotypes of 50 related single-nucleotide polymorphisms (SNPs). Interactions were found between prenatal exposure to famine and ten SNPs (rs10401969, rs10886471, rs10946398, rs1470579, rs2796441, rs340874, rs3794991, rs5015480, rs7961581, and rs9470794) on type 2 diabetes risk after adjustments. The stratified results showed that famine exposure exacerbated the effect of CILP2-rs10401969 to fasting serum insulin (FINS), GRK5-rs10886471 to fasting plasma glucose (FPG) and FINS, IGF2BP2-rs1470579 to FINS, TLE1-rs2796441 to impaired fasting glucose (IFG), PROX1-rs340874 to impaired glucose tolerance (IGT), GATAD2A-rs3794991 to FINS, TSPAN8/LGR5-rs7961581 to FPG, and ZFAND3-rs9470794 to IGT and FINS. Famine exposure weakened the effect of CDKAL1-rs10946398 to type 2 diabetes. Famine exposure weakened the effect of HHEX-rs5015480 to IFG, but exacerbated the effect of HHEX-rs5015480 to FINS. The present study suggests that ten SNPs may affect type 2 diabetes risk in interaction with prenatal exposure to Chinese famine.
越来越多的研究表明,基因和饥荒可能相互作用影响 2 型糖尿病的发病风险。本研究利用 2010-2012 年中国居民营养与健康状况调查(CNNHS)的横断面数据,探讨基因与饥荒是否存在交互作用,从而影响 2 型糖尿病的发病风险。共纳入 2216 名研究对象,选择 1960 年和 1961 年出生的人群为饥荒暴露组,选择 1963 年出生的人群为非暴露组。采用 MassArray 系统检测 50 个相关单核苷酸多态性(SNP)的基因型。在调整了其他因素后,发现产前暴露于饥荒与 10 个 SNP(rs10401969、rs10886471、rs10946398、rs1470579、rs2796441、rs340874、rs3794991、rs5015480、rs7961581 和 rs9470794)在 2 型糖尿病发病风险上存在交互作用。分层分析结果显示,饥荒暴露增加了 CILP2-rs10401969 与空腹血清胰岛素(FINS)、GRK5-rs10886471 与空腹血糖(FPG)和 FINS、IGF2BP2-rs1470579 与 FINS、TLE1-rs2796441 与空腹血糖受损(IFG)、PROX1-rs340874 与糖耐量受损(IGT)、GATAD2A-rs3794991 与 FINS、TSPAN8/LGR5-rs7961581 与 FPG、以及 ZFAND3-rs9470794 与 IGT 和 FINS 之间的相关性;而饥荒暴露降低了 CDKAL1-rs10946398 与 2 型糖尿病之间的相关性。此外,饥荒暴露减弱了 HHEX-rs5015480 与 IFG 的相关性,但增强了 HHEX-rs5015480 与 FINS 的相关性。本研究提示,10 个 SNP 可能与中国饥荒的产前暴露相互作用影响 2 型糖尿病的发病风险。