Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/149226
Title: KIF6 gene as a pharmacogenetic marker for lipid-lowering effect in statin treatment
Author: Ruiz Iruela, Cristina
Padró i Miquel, Ariadna
Pintó Sala, Xavier
Baena Díez, Neus
Caixàs i Pedragós, Assumpta
Güell Miró, Roser
Navarro Badal, Rosa
Jusmet Miguel, Xavier
Calmarza, Pilar
Puzo Foncilla, José Luis
Alía Ramos, Pedro
Candás Estébanez, Beatriz
Keywords: Malalties cardiovasculars
Colesterol
Agents antilipèmics
Cardiovascular diseases
Cholesterol
Antilipemic agents
Issue Date: 10-Oct-2018
Publisher: Public Library of Science (PLoS)
Abstract: Introduction: The therapeutic response to statins has a high interindividual variability with respect to reductions in plasma LDL-cholesterol (c-LDL) and increases in HDL cholesterol (c-HDL). Many studies suggest that there is a relationship between the rs20455 KIF6 gene variant (c.2155T> C, Trp719Arg) and a lower risk of cardiovascular disease in patients being treated with statins. Aim: The aim of this study was to investigate whether or not the c.2155T> C KIF6 gene variant modulates the hypercholesteremic effects of treatment with simvastatin, atorvastatin, or rosuvastatin. Materials and methods: This was a prospective, observational and multicenter study. Three hundred and forty-four patients who had not undergone prior lipid-lowering treatment were recruited. Simvastatin, atorvastatin or rosuvastatin were administered. Lipid profiles and multiple clinical and biochemical variables were assessed before and after treatment. Results: The c.2155T> C variant of the KIF6 gene was shown to influence physiological responses to treatment with simvastatin and atorvastatin. Patients who were homozygous for the c.2155T> C variant (CC genotype, ArgArg) had a 7.0% smaller reduction of LDL cholesterol levels (p = 0.015) in response to hypolipidemic treatment compared to patients with the TT (TrpTrp) or CT (TrpArg) genotype. After pharmacological treatment with rosuvastatin, patients carrying the genetic variant had an increase in c-HDL that was 21.9% lower compared to patients who did not carry the variant (p = 0.008). Conclusion: Being a carrier of the c.2155T> C variant of the KIF6 gene negatively impacts patient responses to simvastatin, atorvastatin or rosuvastatin in terms of lipid lowering effect. Increasing the intensity of hypolipidemic therapy may be advisable for patients who are positive for the c.2155T> C variant.
Note: Reproducció del document publicat a: https://doi.org/10.1371/journal.pone.0205430
It is part of: PLoS One, 2018, vol. 13, num. 10, p. e0205430
URI: http://hdl.handle.net/2445/149226
Related resource: https://doi.org/10.1371/journal.pone.0205430
ISSN: 1932-6203
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
Articles publicats en revistes (Ciències Clíniques)

Files in This Item:
File Description SizeFormat 
688134.pdf1.52 MBAdobe PDFView/Open


This item is licensed under a Creative Commons License Creative Commons