Lipoprotein (a) and 10-year Cardiovascular Disease Incidence in Apparently Healthy Individuals: A Sex-based Sensitivity Analysis from ATTICA Cohort Study

Author:

Kouvari Matina1,Panagiotakos Demosthenes B.12ORCID,Chrysohoou Christina3,Georgousopoulou Ekavi N.145,Yannakoulia Mary1,Tousoulis Dimitrios3,Pitsavos Christos3

Affiliation:

1. Department of Nutrition and Dietetics, School of Health Science and Education, Harokopio University, Athens, Greece

2. Faculty of Health, University of Canberra, Canberra, Australia

3. First Cardiology Clinic, School of Medicine, University of Athens, Athens, Greece

4. School of Medicine, The University of Notre Dame, Sydney, Australia

5. Medical School, Australian National University, Canberra, Australia

Abstract

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.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine

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