Kaze Arnaud D, Bertoni Alain G, Fox Ervin R, Hall Michael E, Mentz Robert J, Echouffo-Tcheugui Justin B
Department of Medicine, Division of Cardiology, Banner-University Medical Center Phoenix, The University of Arizona College of Medicine, Phoenix, AZ, USA.
Department of Epidemiology and Prevention, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Eur J Heart Fail. 2025 Mar;27(3):498-507. doi: 10.1002/ejhf.3447. Epub 2024 Sep 3.
The extent to which metabolic syndrome (MetS) severity influences subclinical myocardial remodelling, heart failure (HF) incidence and subtypes, remains unclear. We assessed the association of MetS with incident HF (including ejection fraction subtypes) among Black individuals.
We included 4069 Jackson Heart Study participants (mean age 54.4 years, 63.8% women, 37.2% with MetS) without HF. We categorized participants based on MetS status and MetS severity scores (based on waist circumference [MetS-Z-WC] and body mass index [MetS-Z-BMI]). We assessed the associations of MetS indices with echocardiographic parameters, biomarkers of myocardial damage (high-sensitivity cardiac troponin I [hs-cTnI] and B-type natriuretic peptide [BNP]) and incident HF hospitalizations including HF with preserved ejection fraction (HFpEF) and HF with reduced ejection fraction (HFrEF). MetS severity was associated with subclinical cardiac remodelling (assessed by echocardiographic measures and biomarkers of myocardial damage). Over a median of 12 years, 319 participants developed HF (157 HFpEF, 149 HFrEF and 13 HF of unknown type). MetS was associated with a twofold greater risk of HF (hazard ratio [HR] 2.07, 95% confidence interval [CI] 1.64-2.61). Compared to the lowest quartile (Q1) of MetS-Z-WC, the highest quartile (Q4) conferred a higher risk of HF (HR 2.35, 95% CI 1.67-3.30), with a stronger association for HFpEF (Q4 vs. Q1: HR 4.94, 95% CI 2.67-9.14) vs. HFrEF (HR 1.69, 95% CI 1.06-2.70).
Metabolic syndrome severity was associated with both HF subtypes among Black individuals, highlighting the importance of optimal metabolic health for preventing HF.
代谢综合征(MetS)的严重程度对亚临床心肌重塑、心力衰竭(HF)发病率及亚型的影响程度尚不清楚。我们评估了黑人个体中MetS与新发HF(包括射血分数亚型)之间的关联。
我们纳入了4069名杰克逊心脏研究参与者(平均年龄54.4岁,63.8%为女性,37.2%患有MetS),这些参与者均无HF。我们根据MetS状态和MetS严重程度评分(基于腰围[MetS-Z-WC]和体重指数[MetS-Z-BMI])对参与者进行分类。我们评估了MetS指标与超声心动图参数、心肌损伤生物标志物(高敏心肌肌钙蛋白I[hs-cTnI]和B型利钠肽[BNP])以及新发HF住院(包括射血分数保留的HF[HFpEF]和射血分数降低的HF[HFrEF])之间的关联。MetS严重程度与亚临床心脏重塑相关(通过超声心动图测量和心肌损伤生物标志物评估)。在中位12年的时间里,319名参与者发生了HF(157例HFpEF,149例HFrEF,13例类型不明的HF)。MetS与HF风险增加两倍相关(风险比[HR]2.07,95%置信区间[CI]1.64-2.61)。与MetS-Z-WC的最低四分位数(Q1)相比,最高四分位数(Q4)赋予更高的HF风险(HR 2.35,95%CI 1.67-3.30),与HFpEF的关联更强(Q4与Q1相比:HR 4.94,95%CI 2.67-9.14),而与HFrEF的关联较弱(HR 1.69,95%CI 1.06-2.70)。
代谢综合征严重程度与黑人个体的两种HF亚型均相关,突出了最佳代谢健康对预防HF的重要性。