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首页> 外文期刊>Diabetes care >Aldosterone, C-reactive protein, and plasma B-type natriuretic Peptide are associated with the development of metabolic syndrome and longitudinal changes in metabolic syndrome components: findings from the jackson heart study.
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Aldosterone, C-reactive protein, and plasma B-type natriuretic Peptide are associated with the development of metabolic syndrome and longitudinal changes in metabolic syndrome components: findings from the jackson heart study.

机译:醛固酮,C反应蛋白和血浆B型利尿钠肽与代谢综合征的发展和代谢综合征成分的纵向变化有关:来自杰克逊心脏研究的发现。

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OBJECTIVE 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. RESEARCH DESIGN AND METHODS 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. RESULTS 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. CONCLUSIONS 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.
机译:目的代谢综合征(MetS)的发病机制涉及多种病理机制,尚未在非裔美国人(AAs)中进行研究。在这项研究的杰克逊心脏研究(JHS)参与者中,我们检查了一组选定的生物标记物对MetS发育的贡献。研究设计和方法我们评估了3019名JHS参与者(平均年龄,54岁; 64%的女性),测量了七个代表炎症的生物标志物(高敏感性C反应蛋白[CRP]),肥胖症(瘦素),利钠途径(B-利钠肽[BNP]),肾上腺途径(皮质醇和醛固酮)和内皮功能(内皮素和高半胱氨酸)。我们将生物标志物组与后续MetS的开发以及MetS组件的纵向变化相关联。结果基线时无MetS的1,215名参与者中有278名(22.9%)在随访中出现了新发MetS。 MetS的发生与血清醛固酮(P = 0.004),CRP(P = 0.03)和BNP(趋势P = 0.005)显着相关。对数生物标记物每SD增量的多变量校正比值比(95%CI)如下:醛固酮为1.25(1.07-1.45),CRP为1.20(1.02-1.43),1.54(1.07-2.23)和1.91(1.31) -2.80)分别用于低和高BNP四分位数。醛固酮与除低HDL胆固醇和腰围外的所有MetS危险因素的变化呈正相关。 CRP浓度与收缩压(SBP)和腰围的变化显着且直接相关,但与HDL胆固醇呈负相关。对于BNP,我们观察到与SBP和甘油三酸酯呈U形关系。结论我们的分析证实,在AA中,较高的循环醛固酮和CRP浓度可预测MetS事件。之前尚未报道BNP与MetS及其组分的非线性U形关系,因此值得重复。

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