SEX DIFFERENCES IN MYOCARDIAL INFARCTION RISK AMONG INDIVIDUALS WITH HIGH LIPOPROTEIN(A): A META-ANALYSIS

IF 5.9 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Sneha Annie Sebastian MD , Inderbir Padda MD, MPH
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引用次数: 0

Abstract

Therapeutic Area

ASCVD/CVD Risk Assessment

Background

Lipoprotein(a) [Lp(a)] is a well-established causal risk factor for cardiovascular morbidity and mortality. Despite this, little is known about how sex influences the risk of myocardial infarction (MI) in individuals with high Lp(a) levels.

Methods

We conducted a comprehensive search of multiple databases up to March 25, 2025. Statistical analysis was performed using RevMan 5.4, applying a random-effects model to pool dichotomous outcomes as risk ratios (RR) with corresponding 95% confidence intervals (CI). The degree of heterogeneity among studies was assessed using Higgins I2 statistic. High Lp(a) levels were defined as median levels of ≥30 mg/dL. The protocol for this study has been submitted to PROSPERO for registration (CRD 1022715).

Results

Our final analysis included 14 observational studies examining the influence of sex on Lp(a) levels and the risk of MI, with a total of 66,124 patients (46% females), an average age of 57 years, and an average follow-up period of 7.6 years. The narrative synthesis of the included studies indicated a positive association between elevated Lp(a) levels and an increased risk of MI in both females and males. However, the pooled analysis showed no statistically significant difference in the risk of MI between females and males with high Lp(a) levels, with an RR of 1.01 (95% CI: 0.77–1.31; p = 0.96; I2 = 98%), and high heterogeneity was observed. Additionally, some studies reported a significant increase in Lp(a) levels in women after the age of 50.

Conclusions

Our analysis found no sex-based difference in the risk of MI associated with high Lp(a) levels. However, further studies are needed to explore sex-specific thresholds in the clinical evaluation of cardiovascular disease risk based on Lp(a) levels, which could improve personalized cardiovascular risk assessment.
高脂蛋白人群心肌梗死风险的性别差异(a):一项荟萃分析
治疗领域ascvd /CVD风险评估背景脂蛋白(a) [Lp(a)]是心血管发病率和死亡率的一个公认的因果危险因素。尽管如此,对于性别如何影响高脂蛋白(a)水平个体的心肌梗死(MI)风险知之甚少。方法对截至2025年3月25日的多个数据库进行综合检索。采用RevMan 5.4进行统计分析,采用随机效应模型,将二分类结果作为风险比(RR),相应的95%置信区间(CI)。采用Higginsⅱ统计量评估各研究间的异质性程度。高Lp(a)水平定义为中位数水平≥30 mg/dL。本研究方案已提交普洛斯彼罗注册(CRD 1022715)。结果我们的最终分析包括14项观察性研究,研究性别对Lp(a)水平和心肌梗死风险的影响,共有66124例患者(46%为女性),平均年龄57岁,平均随访时间7.6年。对纳入研究的叙述综合表明,在女性和男性中,Lp(a)水平升高与心肌梗死风险增加之间存在正相关。然而,合并分析显示,高Lp(a)水平的女性和男性发生心肌梗死的风险无统计学差异,RR为1.01 (95% CI: 0.77-1.31; p = 0.96;I2 = 98%),异质性较高。此外,一些研究报告了50岁以后女性Lp(a)水平的显著增加。结论sour分析发现,与高Lp(a)水平相关的心肌梗死风险无性别差异。然而,基于Lp(a)水平的心血管疾病风险临床评价的性别特异性阈值有待进一步研究,以完善个性化的心血管风险评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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
自引率
0.00%
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审稿时长
76 days
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