Challenges of Cardio-Kidney Composite Outcomes in Large-Scale Clinical Trials.


Journal

Circulation
ISSN: 1524-4539
Titre abrégé: Circulation
Pays: United States
ID NLM: 0147763

Informations de publication

Date de publication:
02 03 2021
Historique:
pubmed: 8 1 2021
medline: 4 1 2022
entrez: 7 1 2021
Statut: ppublish

Résumé

Patients with chronic cardiovascular or metabolic diseases, including diabetes, hypertension, obesity, and heart failure, often have comorbid kidney disease. Long-term outcomes are worse in the setting of both cardiac and kidney disease compared with either disease in isolation. In addition, the clinical presentations of certain acute cardiovascular events (such as heart failure) and worsening kidney function overlap and may be challenging to distinguish. Recently, certain novel treatments have demonstrated beneficial effects on both cardiac and kidney outcomes. Sodium-glucose cotransporter-2 inhibitors have exhibited concordant risk reduction and clinically important benefits in chronic kidney disease with and without diabetes, diabetes and established cardiovascular disease or multiple atherosclerotic vascular disease risk factors, and heart failure with reduced ejection fraction with and without diabetes. Primary trial results have revealed that sacubitril-valsartan therapy improves cardiovascular outcomes in patients with chronic heart failure with reduced ejection fraction and post hoc analyses suggest favorable kidney effects. A concordant pattern of kidney benefit with sacubitril-valsartan has also been observed in chronic heart failure with preserved ejection fraction. Given the complex interplay between cardiac and kidney disease and the possibility that treatments may show concordant cardio-kidney benefits, there has been recent interest in formally acknowledging, defining, and using composite cardio-kidney outcomes in future cardiovascular trials. This review describes potential challenges in use of such outcomes that should be considered and addressed before their incorporation into such trials.

Identifiants

pubmed: 33406882
doi: 10.1161/CIRCULATIONAHA.120.049514
pmc: PMC7920916
mid: NIHMS1664085
doi:

Substances chimiques

Aminobutyrates 0
Angiotensin Receptor Antagonists 0
Biphenyl Compounds 0
Drug Combinations 0
Sodium-Glucose Transporter 2 Inhibitors 0
Valsartan 80M03YXJ7I
sacubitril and valsartan sodium hydrate drug combination WB8FT61183

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

949-958

Subventions

Organisme : NCATS NIH HHS
ID : KL2 TR001424
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001422
Pays : United States

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Auteurs

Ravi B Patel (RB)

Division of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL (R.B.P., S.J.S.).

Jozine M Ter Maaten (JM)

Department of Cardiology, University of Groningen, University Medical Centre, the Netherlands (J.M.T.M.).

João Pedro Ferreira (JP)

Université de Lorraine, INSERM, Centre d'Investigations Cliniques, INI CRCT, and INSERM U1116, CHRU Nancy, France (J.P.F., P.R., F.Z.).

Finnian R McCausland (FR)

Renal Division, Department of Medicine (F.R.M.), Brigham and Women's Hospital and Harvard Medical School, Boston, MA.

Sanjiv J Shah (SJ)

Division of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL (R.B.P., S.J.S.).

Patrick Rossignol (P)

Université de Lorraine, INSERM, Centre d'Investigations Cliniques, INI CRCT, and INSERM U1116, CHRU Nancy, France (J.P.F., P.R., F.Z.).

Scott D Solomon (SD)

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

Muthiah Vaduganathan (M)

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

Milton Packer (M)

Baylor Heart and Vascular Institute, Baylor University Medical Center, Dallas, TX (M.P.).

Aliza Thompson (A)

Division of Cardiology and Nephrology, Office of New Drugs, Center for Drug Evaluation and Research, Food and Drug Administration, Silver Spring, MD (A.T., N.S.).

Norman Stockbridge (N)

Division of Cardiology and Nephrology, Office of New Drugs, Center for Drug Evaluation and Research, Food and Drug Administration, Silver Spring, MD (A.T., N.S.).

Faiez Zannad (F)

Université de Lorraine, INSERM, Centre d'Investigations Cliniques, INI CRCT, and INSERM U1116, CHRU Nancy, France (J.P.F., P.R., F.Z.).

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Classifications MeSH