Lipoprotein(a) levels are associated with aortic valve calcification in asymptomatic patients with familial hypercholesterolaemia

Ranitha Vongpromek, Sven Bos, Gert-Jan Kate, Reyhana Yahya , Adrie Verhoeven, Pim Feijter, F Kronenberg, Jeanine Roeters van Lennep, E.J.G. Sijbrands, Monique Mulder

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Abstract

ObjectivesLipoprotein(a) [Lp(a)] is an independent risk factor for aortic valve stenosis and aortic valve calcification (AVC) in the general population. In this study, we determined the association between AVC and both plasma Lp(a) levels and apolipoprotein(a) [apo(a)] kringle IV repeat polymorphisms in asymptomatic statin-treated patients with heterozygous familial hypercholesterolaemia (FH). MethodsA total of 129 asymptomatic heterozygous FH patients (age 40-69years) were included in this study. AVC was detected using computed tomography scanning. Lp(a) concentration and apo(a) kringle IV repeat number were measured using immunoturbidimetry and immunoblotting, respectively. Univariate and multivariate logistic regression were used to assess the association between Lp(a) concentration and the presence of AVC. ResultsAortic valve calcification was present in 38.2% of patients, including three with extensive AVC (>400Agatston units). Lp(a) concentration was significantly correlated with gender, number of apo(a) kringle IV repeats and the presence and severity of AVC, but not with coronary artery calcification (CAC). AVC was significantly associated with plasma Lp(a) level, age, body mass index, blood pressure, duration of statin use, cholesterol-year score and CAC score. After adjustment for all significant covariables, plasma Lp(a) concentration remained a significant predictor of AVC, with an odds ratio per 10-mgdL(-1) increase in Lp(a) concentration of 1.11 (95% confidence interval 1.01-1.20, P=0.03). ConclusionIn asymptomatic statin-treated FH patients, plasma Lp(a) concentration is an independent risk indicator for AVC.
Original languageUndefined/Unknown
Pages (from-to)166-173
Number of pages8
JournalJournal of Internal Medicine
Volume278
Issue number2
DOIs
Publication statusPublished - 2015

Research programs

  • EMC COEUR-09
  • EMC COEUR-09-39-01
  • EMC NIHES-03-30-01

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