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Genotype-Dependent Effects of Dalcetrapib on Cholesterol Efflux and Inflammation Concordance With Clinical Outcomes

Tardif, Jean-Claude (author)
Montreal Heart Institute, Canada; University of Montreal, Canada
Rhainds, David (author)
Montreal Heart Institute, Canada
Brodeur, Mathieu (author)
Montreal Heart Institute, Canada
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Feroz Zada, Yassamin (author)
University of Montreal, Canada
Fouodjio, Rene (author)
University of Montreal, Canada
Provost, Sylvie (author)
University of Montreal, Canada
Boule, Marie (author)
Montreal Heart Institute, Canada
Alem, Sonia (author)
Montreal Heart Institute, Canada
Gregoire, Jean C. (author)
Montreal Heart Institute, Canada; University of Montreal, Canada
LAllier, Philippe L. (author)
Montreal Heart Institute, Canada; University of Montreal, Canada
Ibrahim, Reda (author)
Montreal Heart Institute, Canada; University of Montreal, Canada
Guertin, Marie-Claude (author)
Montreal Health Innovat Coordinating Centre, Canada
Mongrain, Ian (author)
University of Montreal, Canada
Olsson, Anders (author)
Linköpings universitet,Medicinska fakulteten,Avdelningen för kardiovaskulär medicin,Region Östergötland, Endokrinmedicinska kliniken
Schwartz, Gregory G. (author)
Vet Affairs Medical Centre, CO USA; University of Colorado, CO USA
Rheaume, Eric (author)
Montreal Heart Institute, Canada; University of Montreal, Canada
Dube, Marie-Pierre (author)
Montreal Heart Institute, Canada; University of Montreal, Canada; University of Montreal, Canada
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 (creator_code:org_t)
LIPPINCOTT WILLIAMS & WILKINS, 2016
2016
English.
In: Circulation. - : LIPPINCOTT WILLIAMS & WILKINS. - 1942-325X .- 1942-3268. ; 9:4, s. 340-348
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background-Dalcetrapib effects on cardiovascular outcomes are determined by adenylate cyclase 9 gene polymorphisms. Our aim was to determine whether these clinical end point results are also associated with changes in reverse cholesterol transport and inflammation. Methods and Results-Participants of the dal-OUTCOMES and dal-PLAQUE-2 trials were randomly assigned to receive dalcetrapib or placebo in addition to standard care. High-sensitivity C-reactive protein was measured at baseline and at end of study in 5243 patients from dal-OUTCOMES also genotyped for the rs1967309 polymorphism in adenylate cyclase 9. Cholesterol efflux capacity of high-density lipoproteins from J774 macrophages after cAMP stimulation was determined at baseline and 12 months in 171 genotyped patients from dal-PLAQUE-2. Treatment with dalcetrapib resulted in placebo-adjusted geometric mean percent increases in high-sensitivity C-reactive protein from baseline to end of trial of 18.1% (P=0.0009) and 18.7% (P=0.00001) in participants with the GG and AG genotypes, respectively, but the change was -1.0% (P=0.89) in those with the protective AA genotype. There was an interaction between the treatment arm and the genotype groups (P=0.02). Although the mean change in cholesterol efflux was similar among study arms in patients with GG genotype (mean: 7.8% and 7.4%), increases were 22.3% and 3.5% with dalcetrapib and placebo for those with AA genotype (P=0.005). There was a significant genetic effect for change in efflux for dalcetrapib (P=0.02), but not with placebo. Conclusions-Genotype-dependent effects on C-reactive protein and cholesterol efflux are supportive of dalcetrapib benefits on atherosclerotic cardiovascular outcomes in patients with the AA genotype at polymorphism rs1967309.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

Keyword

reactive protein; cholesterol efflux; dalcetrapib; HDL; pharmacogenetics

Publication and Content Type

ref (subject category)
art (subject category)

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