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Lipoprotein (a) Levels and Abdominal Aortic Aneurysm. A Systematic Review and Meta-analysis

荟萃分析 腹主动脉瘤 医学 置信区间 内科学 脂蛋白(a) 严格标准化平均差 主动脉瘤 脂蛋白 动脉瘤 胃肠病学 心脏病学 外科 主动脉 胆固醇
作者
Evangelos Oikonomou,Stamatios Lampsas,Panteleimon Pantelidis,Panagiotis Theofilis,Konstantinos Grammatopoulos,Anastasios Marathonitis,Michael Vavuranakis,Gerasimos Siasos,Dimitris Tousoulis,Μanolis Vavuranakis
出处
期刊:Current Pharmaceutical Design [Bentham Science Publishers]
卷期号:28 (43): 3492-3499 被引量:13
标识
DOI:10.2174/1381612829666221124110920
摘要

Several studies have linked high Lipoprotein (a) (Lp(a)) concentrations to cardiovascular events, including the formation of Abdominal Aortic Aneurysms (AAA). We review and meta-analyze existing evidence on the association of Lp(a) levels with AAA.Studies evaluating the link of Lp(a) with AAA, up to December 27th 2021, were identified by a systematic search of PubMed, SCOPUS, and Web of Science databases. The results were qualitatively and quantitatively synthesized according to PRISMA guidelines. Results are presented as standardized mean differences (SMD) with 95% confidence intervals (CI).A total of 5,078 subjects (1,637 patients with AAA vs. 3,441 controls) from 11 studies were included in the meta-analysis, with a mean age of 69.9 years and a male sex prevalence of 85.8%. Based on the qualitative synthesis, high Lp(a) concentrations are linked to abdominal aortic wall degradation and extracellular matrix disarrangement. Moreover, despite the considerable variability among races, high Lp(a) levels are related to increased AAA risk, independently of race differences. Accordingly, patients with AAA displayed significantly higher Lp(a) levels compared to controls (SMD: 0.86, 95% CI: 0.55-1.17, p < 0.001). The outcome was not affected in a sensitivity analysis excluding three outlying studies (SMD: 0.40, 95% CI: 0.22-0.58, p < 0.001).This meta-analysis indicates the association between high Lp(a) levels and the presence of AAA, although existing literature presents high heterogeneity. Further studies are needed to standardize Lp(a) measurements and to conclude whether Lp(a) can be used as a sensitive biomarker of early presymptomatic AAA diagnosis.

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