Division of Cardiology, Children's Hospital of Cincinnati, Cincinnati, OH, USA.
Metabolism. 2012 Apr;61(4):531-41. doi: 10.1016/j.metabol.2011.08.010. Epub 2011 Oct 14.
The objective was to assess whether pediatric risk factors predict cardiovascular disease (CVD), impaired fasting glucose (IFG) + type 2 diabetes mellitus (T2DM), and high blood pressure (HBP) in young adulthood. We performed a prospective follow-up of 909 public-parochial suburban schoolchildren first studied at ages 6 to 18 years and 26 years later at a mean age of 38 years. Pediatric triglycerides (TGs), blood pressure, low-density lipoprotein cholesterol, body mass index, and glucose above and high-density lipoprotein cholesterol below established pediatric cutoffs, along with race, cigarette smoking, family history of CVD, T2DM, and HBP, were assessed as determinants of young adult CVD, a composite variable including IFG + T2DM and HBP. By stepwise logistic regression, adult CVD (19 yes, 862 no) was associated with pediatric high TG (odds ratio [OR], 5.85; 95% confidence interval [CI], 2.3-14.7). High TG in pediatric probands with young adult CVD was familial and was associated with early CVD in their high-TG parents. Adult IFG + T2DM (114 yes, 535 no) was associated with parental T2DM (OR, 2.2; 95% CI, 1.38-3.6), high childhood glucose (OR, 4.43; 95% CI, 2-9.7), and childhood cigarette smoking (OR, 1.64; 95% CI, 1.03-2.61). Adult HBP (133 yes, 475 no) was associated with pediatric high body mass index (OR, 2.7; 95% CI, 1.7-4.3) and HBP (OR, 2.5; 95% CI, 1.5-4.3). Pediatric risk factors are significantly, independently related to young adult CVD, IFG + T2DM, and HBP. Identification of pediatric risk factors for CVD, IFG + T2DM, and HBP facilitates initiation of primary prevention programs to reduce development of adult CVD, IFG + T2DM, and HBP.
目的在于评估儿科危险因素是否可预测心血管疾病(CVD)、空腹血糖受损(IFG)+2 型糖尿病(T2DM)以及青年期高血压(HBP)。我们对 909 名公私立郊区学童进行了前瞻性随访,这些学童首次在 6 岁至 18 岁之间接受研究,26 年后,即平均 38 岁时再次接受研究。儿科甘油三酯(TGs)、血压、低密度脂蛋白胆固醇、体重指数以及高于既定儿科标准的血糖和低于既定儿科标准的高密度脂蛋白胆固醇,以及种族、吸烟、CVD、T2DM 和 HBP 的家族史,被评估为青年期 CVD 的决定因素,青年期 CVD 是包括 IFG+T2DM 和 HBP 的一个综合变量。通过逐步逻辑回归,成人 CVD(19 例阳性,862 例阴性)与儿科高 TG(比值比[OR],5.85;95%置信区间[CI],2.3-14.7)相关。青年期 CVD 患儿的高 TG 与家族性高 TG 相关,且与高 TG 父母的早发性 CVD 相关。成人 IFG+T2DM(114 例阳性,535 例阴性)与父母 T2DM(OR,2.2;95%CI,1.38-3.6)、儿童期高血糖(OR,4.43;95%CI,2-9.7)和儿童期吸烟(OR,1.64;95%CI,1.03-2.61)相关。成人 HBP(133 例阳性,475 例阴性)与儿科高体重指数(OR,2.7;95%CI,1.7-4.3)和 HBP(OR,2.5;95%CI,1.5-4.3)相关。儿科危险因素与青年期 CVD、IFG+T2DM 和 HBP 显著独立相关。识别 CVD、IFG+T2DM 和 HBP 的儿科危险因素有助于启动初级预防计划,以减少成年期 CVD、IFG+T2DM 和 HBP 的发生。