Reduction in Mortality in Subjects With Homozygous Familial Hypercholesterolemia Associated With Advances in Lipid-Lowering Therapy
Author(s) -
Frederick J. Raal,
Gillian J. Pilcher,
Vanessa R. Panz,
Hendrick E. van Deventer,
Brigitte C. Brice,
Dirk Blom,
A. David Marais
Publication year - 2011
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.111.042523
Subject(s) - medicine , familial hypercholesterolemia , hazard ratio , proportional hazards model , confidence interval , statin , adverse effect , cholesterol , gastroenterology , cardiology , endocrinology
Homozygous familial hypercholesterolemia is an inherited disorder caused by mutations in both low-density lipoprotein receptor alleles, which results in extremely elevated plasma low-density lipoprotein cholesterol concentrations and very early morbidity and mortality due to cardiovascular disease.
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