Literature DB >> 31617858

Association of Low-Density Lipoprotein Cholesterol With Risk of Aortic Valve Stenosis in Familial Hypercholesterolemia.

Liv J Mundal1, Anders Hovland2,3, Jannicke Igland4,5, Marit B Veierød6, Kirsten B Holven7,8, Martin Prøven Bogsrud8,9, Grethe S Tell5,10, Trond P Leren9, Kjetil Retterstøl1,7.   

Abstract

Importance: Aortic valve stenosis (AS) is the most common valve disease. Elevated levels of low-density lipoprotein (LDL) cholesterol are a risk factor; however, lipid-lowering treatment seems not to prevent progression of AS. The importance of LDL cholesterol in the development of AS thus remains unclear. People with familial hypercholesterolemia (FH) have elevated LDL cholesterol levels from birth and until lipid-lowering treatment starts. Thus, FH may serve as a model disease to study the importance of LDL cholesterol for the development of AS. Objective: To compare the incidence of AS per year in all genetically proven patients with FH in Norway with the incidence of these diseases in the total Norwegian population of about 5 million people. Design, Setting, and Participants: This is a registry-based prospective cohort study of all Norwegian patients with FH with regard to first-time AS between 2001 and 2009. All genotyped patients with FH in Norway were compared with the total Norwegian populations through linkage with the Cardiovascular Disease in Norway project and the Norwegian Cause of Death Registry regarding occurrence of first-time AS. Data were analyzed between January 1, 2018, and December 31, 2018. Main Outcomes and Measures: Standardized incidence ratios.
Results: In total, 53 cases of AS occurred among 3161 persons (1473 men [46.6%]) with FH during 18 300 person-years of follow-up. Mean age at inclusion and at time of AS were 39.9 years (range, 8-91 years) and 65 years (range, 44-88 years), respectively. Total standardized incidence ratios were 7.9 (95% CI, 6.1-10.4) for men and women combined, 8.5 (95% CI, 5.8-12.4) in women, and 7.4 (95% CI, 5.0-10.9) in men, respectively, indicating marked increased risk of AS compared with the general Norwegian population. Conclusions and Relevance: In this prospective registry study, we demonstrate a marked increase in risk of AS in persons with FH.

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Year:  2019        PMID: 31617858      PMCID: PMC6802245          DOI: 10.1001/jamacardio.2019.3903

Source DB:  PubMed          Journal:  JAMA Cardiol            Impact factor:   14.676


  11 in total

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3.  Risk of Ischemic Stroke and Total Cerebrovascular Disease in Familial Hypercholesterolemia.

Authors:  Anders Hovland; Liv J Mundal; Jannicke Igland; Marit B Veierød; Kirsten B Holven; Martin Prøven Bogsrud; Grethe S Tell; Trond P Leren; Kjetil Retterstøl
Journal:  Stroke       Date:  2018-11-21       Impact factor: 7.914

4.  LDL-cholesterol goal achievement, cardiovascular disease, and attributed risk of Lp(a) in a large cohort of predominantly genetically verified familial hypercholesterolemia.

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5.  Clinical and molecular characteristics of homozygous familial hypercholesterolemia patients: Insights from SAFEHEART registry.

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8.  Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: consensus statement of the European Atherosclerosis Society.

Authors:  Børge G Nordestgaard; M John Chapman; Steve E Humphries; Henry N Ginsberg; Luis Masana; Olivier S Descamps; Olov Wiklund; Robert A Hegele; Frederick J Raal; Joep C Defesche; Albert Wiegman; Raul D Santos; Gerald F Watts; Klaus G Parhofer; G Kees Hovingh; Petri T Kovanen; Catherine Boileau; Maurizio Averna; Jan Borén; Eric Bruckert; Alberico L Catapano; Jan Albert Kuivenhoven; Päivi Pajukanta; Kausik Ray; Anton F H Stalenhoef; Erik Stroes; Marja-Riitta Taskinen; Anne Tybjærg-Hansen
Journal:  Eur Heart J       Date:  2013-08-15       Impact factor: 29.983

9.  Impact of age on excess risk of coronary heart disease in patients with familial hypercholesterolaemia.

Authors:  Liv J Mundal; Jannicke Igland; Marit B Veierød; Kirsten Bjørklund Holven; Leiv Ose; Randi Marie Selmer; Torbjorn Wisloff; Ivar S Kristiansen; Grethe S Tell; Trond P Leren; Kjetil Retterstøl
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Review 10.  Calcific aortic valve stenosis: hard disease in the heart: A biomolecular approach towards diagnosis and treatment.

Authors:  Frederique E C M Peeters; Steven J R Meex; Marc R Dweck; Elena Aikawa; Harry J G M Crijns; Leon J Schurgers; Bas L J H Kietselaer
Journal:  Eur Heart J       Date:  2018-07-21       Impact factor: 29.983

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5.  An Exploratory Analysis of Proprotein Convertase Subtilisin/Kexin Type 9 Inhibition and Aortic Stenosis in the FOURIER Trial.

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6.  Aortic Valvular Disease in Elderly Subjects with Heterozygous Familial Hypercholesterolemia: Impact of Lipid-Lowering Therapy.

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7.  Menaquinone 4 increases plasma lipid levels in hypercholesterolemic mice.

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8.  Large-Scale Screening for Monogenic and Clinically Defined Familial Hypercholesterolemia in Iceland.

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