Effects of Liraglutide on Worsening Renal Function Among Patients With Heart Failure With Reduced Ejection Fraction: Insights From the FIGHT Trial.


Journal

Circulation. Heart failure
ISSN: 1941-3297
Titre abrégé: Circ Heart Fail
Pays: United States
ID NLM: 101479941

Informations de publication

Date de publication:
05 2020
Historique:
entrez: 5 5 2020
pubmed: 5 5 2020
medline: 18 11 2020
Statut: ppublish

Résumé

The FIGHT (Functional Impact of GLP-1 [glucagon-like peptide-1] for Heart Failure Treatment) trial randomized 300 patients with heart failure with reduced ejection fraction (HFrEF) and a recent hospitalization for heart failure to liraglutide versus placebo. While there was no difference in the primary outcome (rank score of time to death, time to rehospitalization for heart failure, and change in NT-proBNP [N-terminal pro-B-type natriuretic peptide]), there was a significant increase in cystatin C among patients randomized to liraglutide raising concern of adverse renal outcomes. We performed a post hoc analysis of FIGHT to investigate whether liraglutide was associated with worsening renal function (WRF). The relationship between randomization to liraglutide and WRF was evaluated using logistic regression models. Two hundred seventy-four patients (91%) had complete data to assess for WRF defined as: increase in SCr ≥0.3 mg/dL, or ≥25% decrease in estimated glomerular filtration rate, or an increase in cystatin C ≥0.3 mg/L from baseline to 180-days. Patients with WRF (n=113, 41%), compared with those without, were older, had more comorbidities, and lower utilization of guideline-directed medical treatment. Logistic regression models showed that age and baseline cystatin C levels were associated with WRF. In adjusted models, liraglutide was not associated with excess risk of WRF compared with placebo (odds ratio, 1.02 [95% CI, 0.62-1.67]). There was also no difference in the rank score when WRF was added as a fourth-tier outcome. Liraglutide was not associated with WRF among patients with HFrEF and a recent hospitalization for heart failure. These data support the relative renal safety profile of liraglutide among patients with HFrEF. Registration: URL: http://www.clinicaltrials.gov. Unique identifier: NCT01800968.

Sections du résumé

BACKGROUND
The FIGHT (Functional Impact of GLP-1 [glucagon-like peptide-1] for Heart Failure Treatment) trial randomized 300 patients with heart failure with reduced ejection fraction (HFrEF) and a recent hospitalization for heart failure to liraglutide versus placebo. While there was no difference in the primary outcome (rank score of time to death, time to rehospitalization for heart failure, and change in NT-proBNP [N-terminal pro-B-type natriuretic peptide]), there was a significant increase in cystatin C among patients randomized to liraglutide raising concern of adverse renal outcomes. We performed a post hoc analysis of FIGHT to investigate whether liraglutide was associated with worsening renal function (WRF).
METHODS
The relationship between randomization to liraglutide and WRF was evaluated using logistic regression models. Two hundred seventy-four patients (91%) had complete data to assess for WRF defined as: increase in SCr ≥0.3 mg/dL, or ≥25% decrease in estimated glomerular filtration rate, or an increase in cystatin C ≥0.3 mg/L from baseline to 180-days.
RESULTS
Patients with WRF (n=113, 41%), compared with those without, were older, had more comorbidities, and lower utilization of guideline-directed medical treatment. Logistic regression models showed that age and baseline cystatin C levels were associated with WRF. In adjusted models, liraglutide was not associated with excess risk of WRF compared with placebo (odds ratio, 1.02 [95% CI, 0.62-1.67]). There was also no difference in the rank score when WRF was added as a fourth-tier outcome.
CONCLUSIONS
Liraglutide was not associated with WRF among patients with HFrEF and a recent hospitalization for heart failure. These data support the relative renal safety profile of liraglutide among patients with HFrEF. Registration: URL: http://www.clinicaltrials.gov. Unique identifier: NCT01800968.

Identifiants

pubmed: 32362166
doi: 10.1161/CIRCHEARTFAILURE.119.006758
pmc: PMC7906045
mid: NIHMS1581987
doi:

Substances chimiques

GLP1R protein, human 0
Glucagon-Like Peptide-1 Receptor 0
Incretins 0
Liraglutide 839I73S42A

Banques de données

ClinicalTrials.gov
['NCT01800968']

Types de publication

Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

e006758

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR002541
Pays : United States

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Auteurs

Brahim Redouane (B)

McGill University Health Centre, McGill University, Montreal, QC, Canada (B.R., A.S.).

Stephen J Greene (SJ)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC (S.J.G., M.F., J.-L.S., A.D.D, S.E.M., R.J.M., A.F.H., G.M.F.).

Marat Fudim (M)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC (S.J.G., M.F., J.-L.S., A.D.D, S.E.M., R.J.M., A.F.H., G.M.F.).

Muthiah Vaduganathan (M)

Brigham and Women's Hospital Heart and Vascular Center, Harvard Medical School, Boston, MA (M.V.).

Andrew P Ambrosy (AP)

Division of Cardiology, The Permanente Medical Group, San Francisco, CA (A.P.A.).

Jie-Lena Sun (JL)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC (S.J.G., M.F., J.-L.S., A.D.D, S.E.M., R.J.M., A.F.H., G.M.F.).

Adam D DeVore (AD)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC (S.J.G., M.F., J.-L.S., A.D.D, S.E.M., R.J.M., A.F.H., G.M.F.).

Steven E McNulty (SE)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC (S.J.G., M.F., J.-L.S., A.D.D, S.E.M., R.J.M., A.F.H., G.M.F.).

Robert J Mentz (RJ)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC (S.J.G., M.F., J.-L.S., A.D.D, S.E.M., R.J.M., A.F.H., G.M.F.).

Adrian F Hernandez (AF)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC (S.J.G., M.F., J.-L.S., A.D.D, S.E.M., R.J.M., A.F.H., G.M.F.).

G Michael Felker (GM)

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC (S.J.G., M.F., J.-L.S., A.D.D, S.E.M., R.J.M., A.F.H., G.M.F.).

Lauren B Cooper (LB)

Inova Heart and Vascular Institute, Falls Church, VA (L.B.C.).

Barry A Borlaug (BA)

Division of Circulatory Failure, Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN (B.A.B.).

Eric J Velazquez (EJ)

Yale University School of Medicine, New Haven, CT (E.J.V.).

Kenneth B Margulies (KB)

Perelman School of Medicine, University of Pennsylvania, Philadelphia (K.B.M.).

Abhinav Sharma (A)

McGill University Health Centre, McGill University, Montreal, QC, Canada (B.R., A.S.).

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