Increased Aortic Valve Calcification in Familial Hypercholesterolemia

Gert-Jan Kate, Sven Bos, Admir Dedic, Lisan Neefjes, Akira Kurata, Janneke Langendonk, A Liem, Adriaan Moelker, Gabriel Krestin, Pim Feijter, Jeanine Roeters van Lennep, Koen Nieman, E.J.G. Sijbrands

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Abstract

BACKGROUND Familial hypercholesterolemia is typically caused by LDL receptor (LDLR) mutations that result in elevated levels of LDL cholesterol (LDL-C). In homozygous FH, the prevalence of aortic valve calcification (AoVC) reaches 100% and is often symptomatic. OBJECTIVES The objective of this study was to investigate the prevalence, extent, and risk-modifiers of AoVC in heterozygous FH (he-FH) that are presently unknown. METHODS Asymptomatic patients with he-FH and 131 non-familial hypercholesterolemia controls underwent CT computed tomography calcium scoring. AoVC was defined as the presence of calcium at the aortic valve leaflets. The extent of AoVC was expressed in Agatston units, as the AoVC-score. We compared the prevalence and extent of AoVC between cases and controls. In addition, we investigated risk modifiers of AoVC, including the presence of LDLR mutations without residual function (LDLR-negative mutations), maximum untreated LDL-cholesterol (maxLDL), LDL-C, blood pressure, and coronary artery calcification (CAC). RESULTS We included 145 asymptomatic patients with he-FH (93 men; mean age 52 +/- 8 years) and 131 non-familial hypercholesterolemia controls. The prevalence (%) and AoVC-score (median, IQR) were higher in he-FH patients than in controls: 41%, 51 (9-117); and 21%, 21 (3-49) (p < 0.001 and p = 0.007). Age, untreated maxLDL, CAC, and diastolic blood pressure were independently associated with AoVC. LDLR-negative mutational he-FH was the strongest predictor of the AoVC-score (OR: 4.81; 95% CI: 2.22 to 10.40; p = < 0.001). CONCLUSIONS Compared to controls, he-FH is associated with a high prevalence and a large extent of subclinical AoVC, especially in patients with LDLR-negative mutations, highlighting the critical role of LDL-C metabolism in AoVC etiology. (C) 2015 by the American College of Cardiology Foundation.
Original languageUndefined/Unknown
Pages (from-to)2687-2695
Number of pages9
JournalJournal of the American College of Cardiology
Volume66
Issue number24
DOIs
Publication statusPublished - 2015

Research programs

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

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