多种族动脉粥样硬化研究》中的脂蛋白(a)、高敏 c 反应蛋白、同型半胱氨酸与心血管疾病。

IF 4.3 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Sarah O. Nomura , Harpreet S. Bhatia , Parveen K. Garg , Amy B. Karger , Weihua Guan , Jing Cao , Michael D. Shapiro , Michael Y. Tsai
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引用次数: 0

摘要

背景和目的:脂蛋白(a) [Lp(a)]、高敏c反应蛋白(hs-CRP)和总同型半胱氨酸(tHcy)升高与动脉粥样硬化性心血管疾病(ASCVD)风险相关。本研究探讨了Lp(a)、hs-CRP和tHcy与冠心病(CHD)和脑卒中的个体和联合关系。方法:本研究在多民族动脉粥样硬化研究(MESA)队列(2000-2017)中进行(冠心病分析N = 6,676;中风分析N = 6,674名男性和女性)。结果:单独地,tHcy升高与冠心病和卒中发生率相关,Lp(a)仅与冠心病相关,hs-CRP仅与卒中相关。在联合分析中,当多种生物标志物升高时,冠心病的风险更高[hs-CRP+Lp(a),风险比(HR)=1.39, 95%可信区间(CI): 1.06, 1.82;hs-CRP+ tHcy, HR = 1.34, 95% CI: 1.02, 1.75;Lp(a)+ tHcy HR = 1.58, 95% CI: 1.08, 2.30;hs-CRP+Lp(a)+ tHcy HR = 2.02, 95% CI: 1.26, 3.24]。当hs-CRP和Lp(a) (HR = 1.51, 95% CI: 1.02, 2.23)或tHcy (HR = 2.10, 95% CI: 1.44, 3.06)也高时,当所有三种生物标志物均升高(HR = 2.99, 95% CI: 1.61, 5.58)或hs-CRP和tHcy (HR = 1.79, 95% CI: 1.16, 2.76)均高时,卒中风险升高。结论:伴有tHcy、hs-CRP和Lp升高的患者发生ASCVD的风险最高。纳入tHcy并考虑生物标志物组合而不是单个生物标志物水平,可能有助于更好地识别ASCVD事件风险最高的个体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Lipoprotein(a), high-sensitivity c-reactive protein, homocysteine and cardiovascular disease in the Multi-Ethnic Study of Atherosclerosis

Lipoprotein(a), high-sensitivity c-reactive protein, homocysteine and cardiovascular disease in the Multi-Ethnic Study of Atherosclerosis

Background and aims

Elevated lipoprotein(a) [Lp(a)], high-sensitivity C-Reactive Protein (hs-CRP), and total homocysteine (tHcy) are associated with atherosclerotic cardiovascular disease (ASCVD) risk. This study investigated the individual and joint associations of Lp(a), hs-CRP and tHcy with coronary heart disease (CHD) and stroke.

Methods

This study was conducted in the Multi-Ethnic Study of Atherosclerosis (MESA) cohort (2000–2017) (CHD analytic N = 6,676; stroke analytic N = 6,674 men and women). Associations between Lp(a) (<50 vs. ≥50 mg/dL), hs-CRP (<2 vs. ≥2 mg/L) and tHcy (<12 vs. ≥12 µmol/L) and CHD and stroke incidence were evaluated individually and jointly using Cox proportional hazards regression.

Results

Individually, elevated tHcy was associated with CHD and stroke incidence, Lp(a) with CHD only and hs-CRP with stroke only. In combined analyses, CHD risk was higher when multiple biomarkers were elevated [hs-CRP+Lp(a), hazard ratio (HR)=1.39, 95 % confidence interval (CI): 1.06, 1.82; hs-CRP+ tHcy, HR = 1.34, 95 % CI: 1.02, 1.75; Lp(a)+ tHcy HR = 1.58, 95 % CI: 1.08, 2.30; hs-CRP+Lp(a)+ tHcy HR = 2.02, 95 % CI: 1.26, 3.24]. Stroke risk was elevated when hs-CRP and either Lp(a) (HR = 1.51, 95 % CI: 1.02, 2.23) or tHcy (HR = 2.10, 95 % CI: 1.44, 3.06) was also high, when all three biomarkers were elevated (HR = 2.99, 95 % CI: 1.61, 5.58), or when hs-CRP and tHcy (HR = 1.79, 95 % CI: 1.16, 2.76) were both high.

Conclusions

Risk of ASCVD was highest with concomitant elevation of tHcy, hs-CRP and Lp(a). Inclusion of tHcy and consideration of biomarker combination rather than individual biomarker levels may help better identify individuals at greatest risk for ASCVD events.
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来源期刊
American journal of preventive cardiology
American journal of preventive cardiology Cardiology and Cardiovascular Medicine
CiteScore
6.60
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76 days
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