Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterolemia

Maurizio Averna, Paola Masturzo, Alfredo Cantafora, Sebastiano Calandra, Claudio Stefanutti, Lilla Di Scala, Silvia Langheim, Livia Pisciotta, Antonella Bellocchio, Gianni Pes, Stefano Bertolini, Maurizio Averna, Scipione Martini

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66 Citazioni (Scopus)


The clinical expression of heterozygous familial hypercholesterolemia (FH) is highly variable even in patients carrying the same LDL receptor (LDL-R) gene mutation. This variability might be due to environmental factors as well as to modifying genes affecting lipoprotein metabolism. We investigated Apo E (2, 3, 4), MTP (-493G/T), Apo B (-516C/T), Apo A-V (-1131T/C), HL (-514C/T and -250G/A), FABP-2 (A54T), LPL (D9N, N291S, S447X) and ABCA1 (R219K) polymorphisms in 221 unrelated FH index cases and 349 FH relatives with defined LDL-R gene mutations. We found a significant and independent effect of the following polymorphisms on: (i) plasma LDL-C (Apo E, MTP and Apo B); (ii) plasma HDL-C (HL, FABP-2 and LPL S447X); (iii) plasma triglycerides (Apo E and Apo A-V). In subjects with coronary artery disease (CAD+), the prevalence of FABP-2 54TT genotype was higher (16.5% versus 5.2%) and that of ABCA1 219RK and KK genotypes lower (33.0% versus 51.5%) than in subjects with no CAD. Independent predictors of increased risk of CAD were male sex, age, arterial hypertension, LDL-C level and FABP-2 54TT genotype, and of decreased risk the 219RK and KK genotypes of ABCA1. These findings show that several common genetic variants influence the lipid phenotype and the CAD risk in FH heterozygotes.
Lingua originaleEnglish
pagine (da-a)57-65
Numero di pagine9
Stato di pubblicazionePublished - 2004

All Science Journal Classification (ASJC) codes

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