Department of Epidemiology and Health Statistics, the College of Public Health of Qingdao University, Qingdao, Shandong Province, People's Republic of China.
Qingdao Municipal Center for Disease Control and Prevention, Qingdao, Shandong Province, People's Republic of China.
PLoS One. 2021 Feb 4;16(2):e0246436. doi: 10.1371/journal.pone.0246436. eCollection 2021.
Recently, new loci related to body mass index (BMI) or blood pressure (BP) have been identified respectively in genome-wide association studies (GWAS). However, limited studies focused on jointly associated genetic variance between systolic pressure (SBP), diastolic pressure (DBP) and BMI. Therefore, a bivariate twin study was performed to explore the genetic variants associated with BMI-SBP, BMI-DBP and SBP-DBP. A total of 380 twin pairs (137 dizygotic pairs and 243 monozygotic pairs) recruited from Qingdao Twin Registry system were used to access the genetic correlations (0.2108 for BMI-SBP, 0.2345 for BMI-DBP, and 0.6942 for SBP-DBP, respectively) by bivariate Cholesky decomposition model. Bivariate GWAS in 137 dizygotic pairs nominated 27 single identified 27 quantitative trait nucleotides (QTNs) for BMI and SBP, 27 QTNs for BMI and DBP, and 25 QTNs for SBP and DBP with the suggestive P-value threshold of 1×10-5. After imputation, we found eight SNPs, one for both BMI-SBP and SBP-DBP, and eight for SBP-DBP, exceed significant statistic level. Expression quantitative trait loci analysis identified rs4794029 as new significant eQTL in tissues related to BMI and SBP. Also, we found 6 new significant eQTLs (rs4400367, rs10113750, rs11776003, rs3739327, rs55978930, and rs4794029) in tissues were related to SBP and DBP. Gene-based analysis identified nominally associated genes (P < 0.05) with BMI-SBP, BMI-DBP, and SBP-DBP, respectively, such as PHOSPHO1, GNGT2, KEAP1, and S1PR5. In the pathway analysis, we found some pathways associated with BMI-SBP, BMI-DBP and SBP-DBP, such as prion diseases, IL5 pathway, cyclin E associated events during G1/S transition, TGF beta signaling pathway, G βγ signaling through PI3Kγ, prolactin receptor signaling etc. These findings may enrich the results of genetic variants related to BMI and BP traits, and provide some evidences to future study the pathogenesis of hypertension and obesity in the northern Chinese population.
最近,全基因组关联研究(GWAS)分别鉴定出与体重指数(BMI)或血压(BP)相关的新基因座。然而,有限的研究集中于收缩压(SBP)、舒张压(DBP)和 BMI 之间共同关联的遗传变异。因此,进行了一项双变量双胞胎研究,以探索与 BMI-SBP、BMI-DBP 和 SBP-DBP 相关的遗传变异。使用从青岛双胞胎登记系统招募的 380 对双胞胎(137 对双卵双胞胎和 243 对单卵双胞胎)来通过双变量 Cholesky 分解模型评估遗传相关性(BMI-SBP 为 0.2108,BMI-DBP 为 0.2345,SBP-DBP 为 0.6942)。在 137 对双卵双胞胎中进行的双变量 GWAS 鉴定了 27 个单核苷酸多态性(SNP)与 BMI 和 SBP 相关,27 个 SNP 与 BMI 和 DBP 相关,25 个 SNP 与 SBP 和 DBP 相关,其提示性 P 值阈值为 1×10-5。在进行了内插后,我们发现了 8 个 SNP,其中 1 个 SNP 与 BMI-SBP 和 SBP-DBP 相关,8 个 SNP 与 SBP-DBP 相关,并且有 8 个 SNP 达到了显著统计学水平。表达数量性状基因座分析确定了 rs4794029 是与 BMI 和 SBP 相关的组织中新的显著 eQTL。此外,我们还发现了 6 个新的显著 eQTL(rs4400367、rs10113750、rs11776003、rs3739327、rs55978930 和 rs4794029)与 SBP 和 DBP 相关。基于基因的分析确定了与 BMI-SBP、BMI-DBP 和 SBP-DBP 分别相关的基因(P < 0.05),例如 PHOSPHO1、GNGT2、KEAP1 和 S1PR5。在通路分析中,我们发现了一些与 BMI-SBP、BMI-DBP 和 SBP-DBP 相关的通路,例如朊病毒疾病、IL5 通路、G1/S 期过渡期间的周期蛋白 E 相关事件、TGF-β信号通路、Gβγ 通过 PI3Kγ 进行信号转导、催乳素受体信号等。这些发现可能丰富了与 BMI 和 BP 特征相关的遗传变异的结果,并为未来研究中国北方人群高血压和肥胖症的发病机制提供了一些证据。