Corresponding author: Solomon K. Musani,
Diabetes Care. 2013 Oct;36(10):3084-92. doi: 10.2337/dc12-2562. Epub 2013 Jun 11.
Several pathomechanisms are implicated in the pathogenesis of metabolic syndrome (MetS), most of which have not been investigated in African Americans (AAs). We examined the contribution of a selected panel of biomarkers to the development of MetS in Jackson Heart Study (JHS) participants in this investigation.
We evaluated 3,019 JHS participants (mean age, 54 years; 64% women) with measurements for seven biomarkers representing inflammation (high-sensitivity C-reactive protein [CRP]), adiposity (leptin), natriuretic pathway (B-natriuretic peptide [BNP]), adrenal pathway (cortisol and aldosterone), and endothelial function (endothelin and homocysteine). We related the biomarker panel to the development of MetS on follow-up and to longitudinal changes in MetS components.
There were 278 (22.9%) of 1,215 participants without MetS at baseline who had development of new-onset MetS at follow-up. The incidence of MetS was significantly associated with serum aldosterone (P=0.004), CRP (P=0.03), and BNP (P for trend=0.005). The multivariable-adjusted odds ratios (95% CI) per SD increment of log biomarker were as follows: 1.25 (1.07-1.45) for aldosterone, 1.20 (1.02-1.43) for CRP, and 1.54 (1.07-2.23) and 1.91 (1.31-2.80) for low and high BNP quartiles, respectively. Aldosterone was positively associated with change in all MetS risk components, except low HDL cholesterol and waist circumference. CRP concentration was significantly and directly associated with change in systolic blood pressure (SBP) and waist circumference but inversely associated with HDL cholesterol. For BNP, we observed a U-shape relation with SBP and triglycerides.
Our analysis confirms that, in AAs, higher circulating aldosterone and CRP concentrations predict incident MetS. The nonlinear U-shape relation of BNP with MetS and its components has not been reported before and thus warrants replication.
多种病理机制与代谢综合征(MetS)的发病机制有关,其中大多数在非裔美国人(AA)中尚未得到研究。我们在这项研究中检查了一组选定的生物标志物对 Jackson Heart 研究(JHS)参与者 MetS 发展的贡献。
我们评估了 3019 名 JHS 参与者(平均年龄 54 岁;64%为女性),这些参与者的七项生物标志物测量值代表炎症(高敏 C 反应蛋白[CRP])、肥胖(瘦素)、利钠肽途径(B 型利钠肽[BNP])、肾上腺途径(皮质醇和醛固酮)和内皮功能(内皮素和同型半胱氨酸)。我们将生物标志物组与随访期间 MetS 的发展以及 MetS 成分的纵向变化相关联。
在基线时没有 MetS 的 1215 名参与者中,有 278 名(22.9%)在随访期间出现新发生的 MetS。MetS 的发生率与血清醛固酮(P=0.004)、CRP(P=0.03)和 BNP(P 趋势=0.005)显著相关。每 SD 增加 log 生物标志物的多变量校正比值比(95%CI)如下:醛固酮增加 1.25(1.07-1.45),CRP 增加 1.20(1.02-1.43),BNP 低和高四分位数分别增加 1.54(1.07-2.23)和 1.91(1.31-2.80)。醛固酮与除低 HDL 胆固醇和腰围外的所有 MetS 风险成分的变化呈正相关。CRP 浓度与收缩压(SBP)和腰围的变化显著且直接相关,但与 HDL 胆固醇呈负相关。对于 BNP,我们观察到与 SBP 和甘油三酯呈 U 形关系。
我们的分析证实,在 AA 中,循环醛固酮和 CRP 浓度升高可预测 MetS 的发生。BNP 与 MetS 及其成分的非线性 U 形关系以前尚未报道过,因此需要进一步验证。