Institute of Clinical Medicine and Cardiovascular Research Center, National Yang-Ming University, Taipei, Taiwan.
Healthcare and Service Center, Taipei Veterans General Hospital, Taipei, Taiwan.
Sci Rep. 2019 Dec 5;9(1):18405. doi: 10.1038/s41598-019-54938-w.
The interaction of genetic susceptibility and dietary habits in cardiovascular disease (CVD) remains undetermined. The purpose of this study was to investigate whether a Mediterranean dietary style modified the genetic risk of developing CVD in a Chinese cohort. A total of 2098 subjects with dietary information from a Chinese community cohort (CVDFACTS) were enrolled. Candidate genes, including SNP markers rs1333049 (CDKN2B, 9p21.3), rs17465637 (MIA3, 1q41) and rs501120 (CXCL12, 10q11.21), were genotyped to analyze the association with future CVD. The impact of dietary pattern was also analyzed according to adherence to the diet using the Mediterranean Diet Score (MDS). After an average follow-up of 7.8 years, only the C risk allele of rs1333049 at chromosome 9p21.3 was associated with a higher risk of MI with either an additive [HR = 1.78, 95% CI:1.23-2.5] or a recessive model [HR = 2.40, 95% CI: 1.42-4.04], and the CC genotype had a higher risk of developing MI (p = 0.009, log-rank test). There was no significant difference in the association of the lipid profile with future CV outcomes among the MDS tertiles. However, the high MI risk of the CC genotype in individuals consuming a less healthy diet (MDS1) (HR: 6.39, 95% CI: 1.74-23.43) significantly decreased to 2.38 (95% CI: 0.57-10.04) in individuals consuming a healthier diet (MDS3), indicating that a healthier dietary pattern (higher MDS) modified the risk of developing MI in carriers of variants in CDKN2B. In conclusion, genetic variants of CDKN2B at 9p21 were significantly associated with future MI risk in a Chinese cohort, and the genetic risk of MI could be modified by a healthier diet.
遗传易感性和饮食习惯在心血管疾病(CVD)中的相互作用仍未确定。本研究旨在探讨地中海饮食方式是否能改变中国队列中发生 CVD 的遗传风险。共纳入了来自中国社区队列(CVDFACTS)的 2098 名具有饮食信息的受试者。候选基因,包括 SNP 标记 rs1333049(CDKN2B,9p21.3)、rs17465637(MIA3,1q41)和 rs501120(CXCL12,10q11.21),进行了基因分型,以分析与未来 CVD 的关联。还根据地中海饮食评分(MDS)的依从性分析了饮食模式的影响。在平均 7.8 年的随访后,只有 9p21.3 染色体上 rs1333049 的 C 风险等位基因与 MI 的更高风险相关,无论是加性模型 [HR=1.78,95%CI:1.23-2.5]还是隐性模型 [HR=2.40,95%CI:1.42-4.04],CC 基因型发生 MI 的风险更高(p=0.009,对数秩检验)。在 MDS 三分位数中,血脂谱与未来 CV 结局的相关性没有差异。然而,在饮食不健康(MDS1)的个体中,CC 基因型的 MI 高风险(HR:6.39,95%CI:1.74-23.43)显著降低至 2.38(95%CI:0.57-10.04)在饮食更健康的个体(MDS3)中,这表明更健康的饮食模式(更高的 MDS)改变了 CDKN2B 变异携带者发生 MI 的风险。总之,中国队列中 9p21 的 CDKN2B 遗传变异与未来 MI 风险显著相关,MI 的遗传风险可以通过更健康的饮食来改变。