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Lipoprotein (a) and 10-year Cardiovascular Disease Incidence in Apparently Healthy Individuals: A Sex-based Sensitivity Analysis from ATTICA Cohort Study
Author(s) -
Kouvari Matina,
Panagiotakos Demosthenes B.,
Chrysohoou Christina,
Georgousopoulou Ekavi N.,
Yannakoulia Mary,
Tousoulis Dimitrios,
Pitsavos Christos
Publication year - 2019
Publication title -
angiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 65
eISSN - 1940-1574
pISSN - 0003-3197
DOI - 10.1177/0003319719854872
Subject(s) - medicine , hazard ratio , lipoprotein(a) , confidence interval , prospective cohort study , apolipoprotein b , incidence (geometry) , lipoprotein , proportional hazards model , cohort study , gastroenterology , cholesterol , physics , optics
The association between lipoprotein (a) (Lp(a)) and 10-year first fatal/nonfatal cardiovascular disease (CVD) risk in apparently healthy men and women was evaluated. The ATTICA prospective study was conducted during 2001-2012 and included n = 1514 men and n = 1528 women (age >18 years) from the greater Athens area, Greece. Follow-up CVD assessment (2011-2012) was achieved in n = 2020 participants (n = 317 cases); baseline Lp(a) was measured in n = 1890 participants. The recommended threshold of 50 mg/dL was used to define abnormal Lp(a) status. Ten-year CVD-event rate was 14% and 24% in participants with Lp(a) <50 and Lp(a) ≥50 mg/dL, respectively. Multivariate analysis revealed that participants with Lp(a) ≥50 mg/dL versus Lp(a) <50 mg/dL had about 2 times higher CVD risk (hazard ratio (HR) = 2.18, 95% confidence interval (CI) 1.11, 4.28). The sex-based analysis revealed that the independent Lp(a) effect was retained only in men (HR = 2.00, 95% CI 1.19, 2.56); in women, significance was lost after adjusting for lipid markers. Sensitivity analyses revealed that Lp(a) increased CVD risk only in case of abnormal high-density lipoprotein cholesterol, apolipoprotein A1, and triglycerides as well as low adherence to Mediterranean diet. Certain patient characteristics may be relevant when considering Lp(a) as a therapeutic or risk-prediction target.

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