Cholesteryl ester transfer protein polymorphisms, statin use, and their impact on cholesterol levels and cardiovascular events

M. Leusink; N. C. Onland-Moret; F. W. Asselbergs; B. Ding; S. Kotti; N. R. Van Zuydam; A. C. Papp; N. Danchin; L. Donnelly; A. D. Morris; D. I. Chasman; P. A F M Doevendans; O. H. Klungel; P. M. Ridker; W. H. Van Gilst; T. Simon; F. Nyberg; C. N A Palmer; W. Sadee; P. Van Der Harst; P. I W De Bakker; A. De Boer; C. Verstuyft; A. H. Maitland-Van Der Zee

Cholesteryl ester transfer protein polymorphisms, statin use, and their impact on cholesterol levels and cardiovascular events

M. Leusink, N. C. Onland-Moret, F. W. Asselbergs, B. Ding, S. Kotti, N. R. Van Zuydam, A. C. Papp, N. Danchin, L. Donnelly, A. D. Morris, D. I. Chasman, P. A F M Doevendans, O. H. Klungel, P. M. Ridker, W. H. Van Gilst, T. Simon, F. Nyberg, C. N A Palmer, W. Sadee, P. Van Der HarstP. I W De Bakker, A. De Boer, C. Verstuyft, A. H. Maitland-Van Der Zee^*

^*Corresponding author for this work

Research output: Contribution to journal › Article › Academic › peer-review

Abstract

The association of nonfunctional variants of the cholesteryl ester transfer protein (CETP) with efficacy of statins has been a subject of debate. We evaluated whether three functional CETP variants influence statin efficacy. The effect of CETP genotype on achieved levels of high-density lipoprotein cholesterol (HDLc), low-density lipoprotein cholesterol (LDLc), and total cholesterol during statin treatment was estimated by meta-analysis of the linear regression outcomes of three studies (11,021 individuals). The effect of these single-nucleotide polymorphisms (SNPs) on statin response in protecting against myocardial infarction (MI) was estimated by meta-analysis of statin × SNP interaction terms from logistic regression in five studies (16,570 individuals). The enhancer SNP rs3764261 significantly increased HDLc by 0.02 mmol/l per T allele (P = 6 × 10^-5) and reduced protection against MI by statins (interaction odds ratio (OR) = 1.19 per T allele; P = 0.04). Focusing on functional CETP variants, we showed that in carriers of the rs3764261 T variant, HDLc increased more during statin treatment, and protection against MI by statins appeared to be reduced as compared with those in noncarriers.

Original language	English
Pages (from-to)	314-320
Number of pages	7
Journal	Clinical Pharmacology and Therapeutics
Volume	95
Issue number	3
Publication status	Published - 1 Mar 2014

Cite this

Leusink, M., Onland-Moret, N. C., Asselbergs, F. W., Ding, B., Kotti, S., Van Zuydam, N. R., Papp, A. C., Danchin, N., Donnelly, L., Morris, A. D., Chasman, D. I., Doevendans, P. A. F. M., Klungel, O. H., Ridker, P. M., Van Gilst, W. H., Simon, T., Nyberg, F., Palmer, C. N. A., Sadee, W., ... Maitland-Van Der Zee, A. H. (2014). Cholesteryl ester transfer protein polymorphisms, statin use, and their impact on cholesterol levels and cardiovascular events. Clinical Pharmacology and Therapeutics, 95(3), 314-320.

@article{7a04f27d4c574157a34bd9231f7a0113,

title = "Cholesteryl ester transfer protein polymorphisms, statin use, and their impact on cholesterol levels and cardiovascular events",

abstract = "The association of nonfunctional variants of the cholesteryl ester transfer protein (CETP) with efficacy of statins has been a subject of debate. We evaluated whether three functional CETP variants influence statin efficacy. The effect of CETP genotype on achieved levels of high-density lipoprotein cholesterol (HDLc), low-density lipoprotein cholesterol (LDLc), and total cholesterol during statin treatment was estimated by meta-analysis of the linear regression outcomes of three studies (11,021 individuals). The effect of these single-nucleotide polymorphisms (SNPs) on statin response in protecting against myocardial infarction (MI) was estimated by meta-analysis of statin × SNP interaction terms from logistic regression in five studies (16,570 individuals). The enhancer SNP rs3764261 significantly increased HDLc by 0.02 mmol/l per T allele (P = 6 × 10-5) and reduced protection against MI by statins (interaction odds ratio (OR) = 1.19 per T allele; P = 0.04). Focusing on functional CETP variants, we showed that in carriers of the rs3764261 T variant, HDLc increased more during statin treatment, and protection against MI by statins appeared to be reduced as compared with those in noncarriers.",

author = "M. Leusink and Onland-Moret, {N. C.} and Asselbergs, {F. W.} and B. Ding and S. Kotti and {Van Zuydam}, {N. R.} and Papp, {A. C.} and N. Danchin and L. Donnelly and Morris, {A. D.} and Chasman, {D. I.} and Doevendans, {P. A F M} and Klungel, {O. H.} and Ridker, {P. M.} and {Van Gilst}, {W. H.} and T. Simon and F. Nyberg and Palmer, {C. N A} and W. Sadee and {Van Der Harst}, P. and {De Bakker}, {P. I W} and {De Boer}, A. and C. Verstuyft and {Maitland-Van Der Zee}, {A. H.}",

year = "2014",

month = mar,

day = "1",

language = "English",

volume = "95",

pages = "314--320",

journal = "Clinical Pharmacology and Therapeutics",

issn = "0009-9236",

publisher = "Wiley-Blackwell",

number = "3",

}

Leusink, M, Onland-Moret, NC, Asselbergs, FW, Ding, B, Kotti, S, Van Zuydam, NR, Papp, AC, Danchin, N, Donnelly, L, Morris, AD, Chasman, DI, Doevendans, PAFM, Klungel, OH, Ridker, PM, Van Gilst, WH, Simon, T, Nyberg, F, Palmer, CNA, Sadee, W, Van Der Harst, P, De Bakker, PIW, De Boer, A, Verstuyft, C & Maitland-Van Der Zee, AH 2014, 'Cholesteryl ester transfer protein polymorphisms, statin use, and their impact on cholesterol levels and cardiovascular events', Clinical Pharmacology and Therapeutics, vol. 95, no. 3, pp. 314-320.

TY - JOUR

T1 - Cholesteryl ester transfer protein polymorphisms, statin use, and their impact on cholesterol levels and cardiovascular events

AU - Leusink, M.

AU - Onland-Moret, N. C.

AU - Asselbergs, F. W.

AU - Ding, B.

AU - Kotti, S.

AU - Van Zuydam, N. R.

AU - Papp, A. C.

AU - Danchin, N.

AU - Donnelly, L.

AU - Morris, A. D.

AU - Chasman, D. I.

AU - Doevendans, P. A F M

AU - Klungel, O. H.

AU - Ridker, P. M.

AU - Van Gilst, W. H.

AU - Simon, T.

AU - Nyberg, F.

AU - Palmer, C. N A

AU - Sadee, W.

AU - Van Der Harst, P.

AU - De Bakker, P. I W

AU - De Boer, A.

AU - Verstuyft, C.

AU - Maitland-Van Der Zee, A. H.

PY - 2014/3/1

Y1 - 2014/3/1

N2 - The association of nonfunctional variants of the cholesteryl ester transfer protein (CETP) with efficacy of statins has been a subject of debate. We evaluated whether three functional CETP variants influence statin efficacy. The effect of CETP genotype on achieved levels of high-density lipoprotein cholesterol (HDLc), low-density lipoprotein cholesterol (LDLc), and total cholesterol during statin treatment was estimated by meta-analysis of the linear regression outcomes of three studies (11,021 individuals). The effect of these single-nucleotide polymorphisms (SNPs) on statin response in protecting against myocardial infarction (MI) was estimated by meta-analysis of statin × SNP interaction terms from logistic regression in five studies (16,570 individuals). The enhancer SNP rs3764261 significantly increased HDLc by 0.02 mmol/l per T allele (P = 6 × 10-5) and reduced protection against MI by statins (interaction odds ratio (OR) = 1.19 per T allele; P = 0.04). Focusing on functional CETP variants, we showed that in carriers of the rs3764261 T variant, HDLc increased more during statin treatment, and protection against MI by statins appeared to be reduced as compared with those in noncarriers.

AB - The association of nonfunctional variants of the cholesteryl ester transfer protein (CETP) with efficacy of statins has been a subject of debate. We evaluated whether three functional CETP variants influence statin efficacy. The effect of CETP genotype on achieved levels of high-density lipoprotein cholesterol (HDLc), low-density lipoprotein cholesterol (LDLc), and total cholesterol during statin treatment was estimated by meta-analysis of the linear regression outcomes of three studies (11,021 individuals). The effect of these single-nucleotide polymorphisms (SNPs) on statin response in protecting against myocardial infarction (MI) was estimated by meta-analysis of statin × SNP interaction terms from logistic regression in five studies (16,570 individuals). The enhancer SNP rs3764261 significantly increased HDLc by 0.02 mmol/l per T allele (P = 6 × 10-5) and reduced protection against MI by statins (interaction odds ratio (OR) = 1.19 per T allele; P = 0.04). Focusing on functional CETP variants, we showed that in carriers of the rs3764261 T variant, HDLc increased more during statin treatment, and protection against MI by statins appeared to be reduced as compared with those in noncarriers.

UR - http://www.scopus.com/inward/record.url?scp=84894487302&partnerID=8YFLogxK

M3 - Article

C2 - 24080640

AN - SCOPUS:84894487302

SN - 0009-9236

VL - 95

SP - 314

EP - 320

JO - Clinical Pharmacology and Therapeutics

JF - Clinical Pharmacology and Therapeutics

IS - 3

ER -

Cholesteryl ester transfer protein polymorphisms, statin use, and their impact on cholesterol levels and cardiovascular events

Abstract

Other files and links

Fingerprint

Cite this