腰臀比改变脂蛋白的心血管风险(a):来自MESA的见解

Muhammad Imtiaz Ahmad, Parag A Chevli, Saeid Mirzai, Rishi Rikhi, Harpeet Bhatia, Neha Pagidipati, Roger Blumenthal, Alexander C Razavi, Kathleen Ruddiman, Jared A Spitz, Khurram Nasir, Michael D Shapiro
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引用次数: 0

摘要

目的:评估腰臀比(WHR)等肥胖指标是否改变了脂蛋白(a) [Lp(a)]与动脉粥样硬化性心血管疾病(ASCVD)的关系。方法:来自多民族动脉粥样硬化研究(MESA)的4652名参与者分组如下:Lp(a) 结果:与对照组相比,孤立升高的Lp(a) ≥ 50 mg/dl或WHR≥90% pct与ASCVD风险无显著相关性(风险比(HR), 1.15, 95 %置信区间(CI): 0.94-1.39)和(HR, 1.14, 95 % CI: 0.92-1.41)。相反,Lp(a)≥50 mg/dl和WHR≥90%的合并升高与ASCVD风险相关(HR, 2.34, 95 % CI: 1.61-3.40)。Lp(a)≥50 mg/dl与第1和第2分位的ASCVD风险无显著相关性(HR, 1.06, 95 % CI: 0.72-1.48, HR, 1.08, 95 % CI: 0.79-1.48)。然而,在WHR最高分位数中,Lp(a)≥50 mg/dl与ASCVD风险显著相关(HR, 1.60, 95 % CI: 1.23-2.09)。(交互p = 0.01)。体重指数(BMI)和Lp(a)组合在最高风险类别中导致ASCVD的风险相似(HR, 1.33, 95 % CI: 1.00-1.77),没有显著的相互作用(p = 0.99)。结论:在MESA中,WHR显著改变与Lp相关的ASCVD的风险(a)。腹部脂肪的测量可能会进一步细化Lp(a)升高个体的心血管风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Waist to hip ratio modifies the cardiovascular risk of lipoprotein (a): Insights from MESA.

Aims: To assess if adiposity measures such as waist-to-hip ratio (WHR) modify the relationship of lipoprotein (a) [Lp(a)] with atherosclerotic cardiovascular disease (ASCVD).

Methods: 4652 participants from the Multi-Ethnic Study of Atherosclerosis (MESA) were grouped as follows: Lp(a) < 50 mg/dl and WHR <90th percentile(pct) (reference); Lp(a) < 50 mg/dl and WHR ≥90th pct; Lp(a) ≥ 50 mg/dl and WHR <90th pct; and Lp(a) ≥50 mg/dl and WHR ≥90th pct. Cox proportional hazard models assessed the relationship of Lp(a) and WHR with time to ASCVD events.

Results: Compared to the reference group, isolated elevated Lp(a) ≥ 50 mg/dl or WHR ≥90th pct were not significantly associated with risk of ASCVD (hazard ratio (HR), 1.15, 95 % confidence interval (CI): 0.94-1.39) and (HR, 1.14, 95 % CI: 0.92-1.41), respectively. In contrast, the combination of elevated Lp(a) ≥50 mg/dl and WHR ≥90th pct was associated with ASCVD risk (HR, 2.34, 95 % CI: 1.61-3.40). Lp(a) ≥50 mg/dl was not significantly associated with ASCVD risk in the 1st and 2nd tertile of WHR (HR, 1.06, 95 % CI: 0.72-1.48and HR, 1.08, 95 % CI: 0.79-1.48, respectively). However, Lp(a) ≥50 mg/dl was significantly associated with ASCVD risk in the highest tertile of WHR (HR, 1.60, 95 % CI: 1.23-2.09). (Interaction p = 0.01). Body mass index (BMI) and Lp(a) combinations resulted in similar greater risks of ASCVD in the highest risk category (HR, 1.33, 95 % CI: 1.00-1.77), without a significant interaction (p = 0.99).

Conclusions: In MESA, WHR significantly modifies the risk of ASCVD associated with Lp(a). Measures of abdominal adiposity may further refine the cardiovascular risk in individuals with elevated Lp(a).

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