Jansen Maria Ac, Dalmeijer Geertje W, Visseren Frank Lj, van der Ent Cornelis K, Leusink Maarten, Onland-Moret N Charlotte, Maitland-van der Zee Anke H, Grobbee Diederick E, Uiterwaal Cuno Spm
1 Julius Center for Health Sciences and Primary Care, University Medical Centre Utrecht, the Netherlands.
2 Department of Vascular Medicine, University Medical Centre Utrecht, the Netherlands.
Eur J Prev Cardiol. 2017 Feb;24(3):320-327. doi: 10.1177/2047487316679526. Epub 2016 Nov 19.
Aims Several genes are related to blood pressure (BP) levels in adults, but it is largely unknown whether these genes also determine BP early in life. Methods Systolic BP (SBP) and diastolic BP (DBP) were measured in 720 5-year-old children from the WHeezing-Illnesses-STudy-LEidsche-Rijn (WHISTLER) birth cohort in sitting and supine positions using a semi-automatic oscillometric device. Illumina chip technology was used to genotype 18, 19, 11 and 12 single nucleotide polymorphisms associated with adult SBP, DBP, mean arterial pressure (MAP) and hypertension, respectively, in the children's DNA and separate weighted genetic risk scores (GRSs) were constructed. The associations are reported as linear regression coefficients (mmHg BP in childhood/GRS score point) or odds ratios (highest childhood BP quintile/hypertension GRS score point). Results A higher GRS for SBP was related to higher supine SBP (0.37, 95% CI 0.01 to 0.7), but not to supine DBP (-0.05, 95% CI -0.4 to 0.3) or supine MAP (0.19, 95% CI -0.1 to 0.5). A higher GRS for DBP was related to a higher supine SBP (0.66, 95% CI 0.1 to 1.2), but not to supine DBP (-0.07, 95% CI -0.6 to 0.4) or supine MAP (0.28, 95% CI -0.2 to 0.7). With the sitting BP measurements, the GRSs for SBP and DBP were related to neither SBP nor DBP. No association was found between GRS for MAP and SBP, DBP or MAP. Hypertension GRS was not associated with a higher BP in children. Conclusions Higher scores for adult derived diastolic and systolic BP genes appear to be related to higher supine systolic BP at age 5 years.
目的 多个基因与成年人的血压(BP)水平相关,但这些基因是否也在生命早期就决定血压,目前很大程度上尚不清楚。方法 使用半自动示波装置,对来自惠更斯 - 莱顿莱茵河疾病研究(WHISTLER)出生队列的720名5岁儿童在坐位和仰卧位测量收缩压(SBP)和舒张压(DBP)。利用Illumina芯片技术对儿童DNA中分别与成人SBP、DBP、平均动脉压(MAP)和高血压相关的18、19、11和12个单核苷酸多态性进行基因分型,并构建单独的加权遗传风险评分(GRS)。关联结果以线性回归系数(儿童期mmHg血压/GRS评分点)或比值比(儿童期最高血压五分位数/高血压GRS评分点)报告。结果 较高的SBP遗传风险评分与较高的仰卧位SBP相关(0.37,95%可信区间0.01至0.7),但与仰卧位DBP(-0.05,95%可信区间-0.4至0.3)或仰卧位MAP(0.19,95%可信区间-0.1至0.5)无关。较高的DBP遗传风险评分与较高的仰卧位SBP相关(0.66,95%可信区间0.1至1.2),但与仰卧位DBP(-0.07,95%可信区间-0.6至0.4)或仰卧位MAP(0.28,95%可信区间-0.2至0.7)无关。对于坐位血压测量,SBP和DBP的遗传风险评分与SBP和DBP均无关。未发现MAP的遗传风险评分与SBP、DBP或MAP之间存在关联。高血压遗传风险评分与儿童较高血压无关。结论 源自成人的舒张压和收缩压基因的较高评分似乎与5岁时较高的仰卧位收缩压有关。