AIMS: To investigate the influence of different LDL-receptor (LDLR) gene mutations on age at first cardiovascular event in familial hypercholesterolaemia (FH) patients. METHODS AND RESULTS: Dutch FH patients (n = 862) with known LDLR mutations from a retrospective cohort study were included. A gamma frailty Cox model was used. An event was defined as the first cardiovascular event. Gender, hypertension, smoking, diabetes, HDL cholesterol, LDL cholesterol (LDL-C), or triglycerides were included as covariates. Furthermore, the effect of LDLR mutation type on LDL and HDL cholesterol levels was investigated using mixed effects models, including gender, smoking, body mass index, and age at time of lipid measurement as covariates. A total of 86 different LDLR mutations were present in this cohort. Twenty-two percent of patients experienced an event (median age: 47.1 year; range: 25.6-85.8 years). The effect of LDLR mutation type on event-free survival is only significant in the models without LDL-C levels. Also, LDLR mutation type was significantly associated with LDL-C levels (P = 0.007), but not with HDL cholesterol levels (P = 0.12). CONCLUSION: In the present study, LDL-C levels are a more important risk factor of event-free survival than the type of LDLR mutation.
AIMS: To investigate the influence of different LDL-receptor (LDLR) gene mutations on age at first cardiovascular event in familial hypercholesterolaemia (FH) patients. METHODS AND RESULTS: Dutch FHpatients (n = 862) with known LDLR mutations from a retrospective cohort study were included. A gamma frailty Cox model was used. An event was defined as the first cardiovascular event. Gender, hypertension, smoking, diabetes, HDL cholesterol, LDL cholesterol (LDL-C), or triglycerides were included as covariates. Furthermore, the effect of LDLR mutation type on LDL and HDL cholesterol levels was investigated using mixed effects models, including gender, smoking, body mass index, and age at time of lipid measurement as covariates. A total of 86 different LDLR mutations were present in this cohort. Twenty-two percent of patients experienced an event (median age: 47.1 year; range: 25.6-85.8 years). The effect of LDLR mutation type on event-free survival is only significant in the models without LDL-C levels. Also, LDLR mutation type was significantly associated with LDL-C levels (P = 0.007), but not with HDL cholesterol levels (P = 0.12). CONCLUSION: In the present study, LDL-C levels are a more important risk factor of event-free survival than the type of LDLR mutation.
Authors: M Teresa Tejedor; Ana Cenarro; Diego Tejedor; Marianne Stef; Lourdes Palacios; Isabel de Castro; Angel L García-Otín; Luis V Monteagudo; Fernando Civeira; Miguel Pocovi Journal: Naturwissenschaften Date: 2011-09-21
Authors: Karen Broekhuizen; Mireille N M van Poppel; Lando L J Koppes; Johannes Brug; Willem van Mechelen Journal: BMC Public Health Date: 2010-02-15 Impact factor: 3.295
Authors: Roeland Huijgen; Iris Kindt; Sjoerd B J Verhoeven; Eric J G Sijbrands; Maud N Vissers; John J P Kastelein; Barbara A Hutten Journal: PLoS One Date: 2010-02-15 Impact factor: 3.240
Authors: Erik P A van Iperen; Suthesh Sivapalaratnam; S Matthijs Boekholdt; G Kees Hovingh; Stephanie Maiwald; Michael W Tanck; Nicole Soranzo; Jonathan C Stephens; Jennifer G Sambrook; Marcel Levi; Willem H Ouwehand; John Jp Kastelein; Mieke D Trip; Aeilko H Zwinderman Journal: Eur J Hum Genet Date: 2013-11-13 Impact factor: 4.246