Endotrophin, a Collagen VI Formation-Derived Peptide, in Heart Failure.


Journal

NEJM evidence
ISSN: 2766-5526
Titre abrégé: NEJM Evid
Pays: United States
ID NLM: 9918317485806676

Informations de publication

Date de publication:
Oct 2022
Historique:
medline: 30 8 2023
pubmed: 30 8 2023
entrez: 30 8 2023
Statut: ppublish

Résumé

Endotrophin, a collagen type VI-derived peptide, mediates metabolic dysregulation, inflammation, and fibrosis in animal models, but has not been studied in human heart failure (HF). We examined the association between circulating endotrophin and outcomes in participants suffering from HF with preserved ejection fraction (HFpEF) enrolled in the TOPCAT trial (n=205). Associations were validated in a participant-level meta-analysis (n=810) that included participants with HFpEF from the PHFS study (United States; n=174), PEOPLE cohort (New Zealand; n=168), a randomized trial of vasodilator therapy (United States; n=45), a cohort from Donostia University Hospital and University of Navarra (Spain; n=171), and the TRAINING-HF trial (Spain; n=47). We also assessed associations in HF with reduced ejection fraction in PHFS (n=1,642). Plasma endotrophin levels at baseline were associated with risk of future death (standardized hazard ratio [HR] = 1.74; 95% confidence interval [CI]=1.36-2.24; P<0.001) and death or HF-related hospital admission (DHFA; standardized HR=2.11; 95% CI= 1.67-2.67; P<0.001) in TOPCAT. Endotrophin improved reclassification and discrimination for these outcomes beyond the MAGGIC risk score and NT-proBNP (N-terminal pro b-type natriuretic peptide). Findings were confirmed in the participant-level meta-analysis. In participants with HF with reduced ejection fraction in PHFS, endotrophin levels were associated with death (standardized HR=1.82; 95% CI=1.66-2.00; P<0.001) and DHFA (standardized HR=1.40; 95% CI=1.31-1.50; P<0.001), but the strength of the latter association was substantially lower than for the MAGGIC risk score (standardized HR=1.93; 95% CI=1.76-2.12) and BNP (standardized HR=1.78; 95% CI=1.66-1.92). Circulating endotrophin levels are independently associated with future poor outcomes in patients with HF, particularly in HFpEF. (Funded by Bristol Myers Squibb; Instituto de Salud Carlos III [Spain] and European Regional Development Fund; European Commission CRUCIAL project; and the U.S. National Institutes of Health National Heart, Lung, and Blood Institute.).

Sections du résumé

BACKGROUND BACKGROUND
Endotrophin, a collagen type VI-derived peptide, mediates metabolic dysregulation, inflammation, and fibrosis in animal models, but has not been studied in human heart failure (HF).
METHODS METHODS
We examined the association between circulating endotrophin and outcomes in participants suffering from HF with preserved ejection fraction (HFpEF) enrolled in the TOPCAT trial (n=205). Associations were validated in a participant-level meta-analysis (n=810) that included participants with HFpEF from the PHFS study (United States; n=174), PEOPLE cohort (New Zealand; n=168), a randomized trial of vasodilator therapy (United States; n=45), a cohort from Donostia University Hospital and University of Navarra (Spain; n=171), and the TRAINING-HF trial (Spain; n=47). We also assessed associations in HF with reduced ejection fraction in PHFS (n=1,642).
RESULTS RESULTS
Plasma endotrophin levels at baseline were associated with risk of future death (standardized hazard ratio [HR] = 1.74; 95% confidence interval [CI]=1.36-2.24; P<0.001) and death or HF-related hospital admission (DHFA; standardized HR=2.11; 95% CI= 1.67-2.67; P<0.001) in TOPCAT. Endotrophin improved reclassification and discrimination for these outcomes beyond the MAGGIC risk score and NT-proBNP (N-terminal pro b-type natriuretic peptide). Findings were confirmed in the participant-level meta-analysis. In participants with HF with reduced ejection fraction in PHFS, endotrophin levels were associated with death (standardized HR=1.82; 95% CI=1.66-2.00; P<0.001) and DHFA (standardized HR=1.40; 95% CI=1.31-1.50; P<0.001), but the strength of the latter association was substantially lower than for the MAGGIC risk score (standardized HR=1.93; 95% CI=1.76-2.12) and BNP (standardized HR=1.78; 95% CI=1.66-1.92).
CONCLUSIONS CONCLUSIONS
Circulating endotrophin levels are independently associated with future poor outcomes in patients with HF, particularly in HFpEF. (Funded by Bristol Myers Squibb; Instituto de Salud Carlos III [Spain] and European Regional Development Fund; European Commission CRUCIAL project; and the U.S. National Institutes of Health National Heart, Lung, and Blood Institute.).

Identifiants

pubmed: 37645406
doi: 10.1056/evidoa2200091
pmc: PMC10465122
mid: NIHMS1874972
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : NHLBI NIH HHS
ID : K23 HL130551
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL157264
Pays : United States

Références

J Card Fail. 2013 Mar;19(3):156-62
pubmed: 23482075
Ann Intern Med. 2014 Feb 18;160(4):267-70
pubmed: 24727843
Circulation. 2015 Jan 6;131(1):34-42
pubmed: 25406305
Matrix Biol. 2018 Oct;71-72:348-367
pubmed: 29277723
Circulation. 2015 Feb 10;131(6):550-9
pubmed: 25552356
J Am Heart Assoc. 2017 Feb 20;6(2):
pubmed: 28219917
Am J Cardiol. 2020 Feb 15;125(4):575-582
pubmed: 31843232
PLoS One. 2015 Dec 07;10(12):e0144525
pubmed: 26641456
J Am Coll Cardiol. 2020 Mar 24;75(11):1281-1295
pubmed: 32192654
EBioMedicine. 2021 Jun;68:103391
pubmed: 34044221
J Am Coll Cardiol. 2021 Sep 14;78(11):1166-1187
pubmed: 34503685
N Engl J Med. 2014 Apr 10;370(15):1383-92
pubmed: 24716680
Am J Physiol Endocrinol Metab. 2016 Dec 1;311(6):E952-E963
pubmed: 27729337
JACC Basic Transl Sci. 2020 Mar 23;5(3):211-225
pubmed: 32215346
J Biol Chem. 2019 Sep 13;294(37):13769-13780
pubmed: 31346034
Circulation. 2020 Mar 24;141(12):1001-1026
pubmed: 32202936
Eur Heart J. 2013 May;34(19):1404-13
pubmed: 23095984
Circulation. 2020 May 5;141(18):1463-1476
pubmed: 32237898
N Engl J Med. 2017 Apr 27;376(17):1690-1692
pubmed: 28445660
Am J Cardiol. 2014 Apr 1;113(7):1211-6
pubmed: 24507172
ESC Heart Fail. 2018 Apr;5(2):262-270
pubmed: 28967709
Circulation. 2009 Jul 28;120(4):310-7
pubmed: 19597049
ESC Heart Fail. 2021 Aug;8(4):2698-2712
pubmed: 33991175
J Am Coll Cardiol. 2011 Jul 19;58(4):386-94
pubmed: 21757116
JACC Heart Fail. 2020 Mar;8(3):172-184
pubmed: 31926856
Circulation. 2014 Jun 10;129(23):2380-7
pubmed: 24799515
Nat Commun. 2014 Mar 19;5:3485
pubmed: 24647224
Circ Heart Fail. 2018 Dec;11(12):e005266
pubmed: 30562095
Stat Med. 2000 Jul 15;19(13):1793-819
pubmed: 10861779
J Am Heart Assoc. 2018 Oct 16;7(20):e009594
pubmed: 30371285

Auteurs

Julio A Chirinos (JA)

Hospital of the University of Pennsylvania, Philadelphia.
University of Pennsylvania, Perelman School of Medicine, Philadelphia.

Lei Zhao (L)

Bristol Myers Squibb Company, Princeton, NJ.

Alexander L Reese-Petersen (AL)

Nordic Bioscience, Herlev, Denmark.

Jordana B Cohen (JB)

Hospital of the University of Pennsylvania, Philadelphia.

Federica Genovese (F)

Nordic Bioscience, Herlev, Denmark.

A Mark Richards (AM)

Cardiovascular Research Institute, National University of Singapore, Singapore.
Christchurch Heart Institute, University of Otago, Dunedin, New Zealand.

Robert N Doughty (RN)

University of Auckland, Auckland, New Zealand.

Javier Díez (J)

Program of Cardiovascular Diseases, CIMA Universidad de Navarra, IdiSNA and CIBERCV, Pamplona, Navarra, Spain.
Departments of Cardiology and Nephrology, Clínica Universidad de Navarra, Pamplona, Navarra, Spain.

Arantxa González (A)

Program of Cardiovascular Diseases, CIMA Universidad de Navarra, IdiSNA and CIBERCV, Pamplona, Navarra, Spain.

Ramón Querejeta (R)

Department of Cardiology, Hospital Universitario Donostia, San Sebastián, Guipúzcoa, Spain.

Payman Zamani (P)

Hospital of the University of Pennsylvania, Philadelphia.
University of Pennsylvania, Perelman School of Medicine, Philadelphia.

Julio Nuñez (J)

Hospital Clínico Universitario de Valencia, Universidad de Valencia, INCLIVA, CIBER Cardiovascular, Valencia, Spain.

Zhaoqing Wang (Z)

Bristol Myers Squibb Company, Princeton, NJ.

Christina Ebert (C)

Bristol Myers Squibb Company, Princeton, NJ.

Karl Kammerhoff (K)

Bristol Myers Squibb Company, Princeton, NJ.

Joseph Maranville (J)

Bristol Myers Squibb Company, Princeton, NJ.

Michael Basso (M)

Bristol Myers Squibb Company, Princeton, NJ.

Chenao Qian (C)

University of Pennsylvania, Perelman School of Medicine, Philadelphia.

Daniel G K Rasmussen (DGK)

Nordic Bioscience, Herlev, Denmark.

Peter H Schafer (PH)

Bristol Myers Squibb Company, Princeton, NJ.

Dietmar SeifFert (D)

Bristol Myers Squibb Company, Princeton, NJ.

Morten A Karsdal (MA)

Nordic Bioscience, Herlev, Denmark.

David A Gordon (DA)

Bristol Myers Squibb Company, Princeton, NJ.

Francisco Ramirez-Valle (F)

Bristol Myers Squibb Company, Princeton, NJ.

Thomas P Cappola (TP)

Hospital of the University of Pennsylvania, Philadelphia.
University of Pennsylvania, Perelman School of Medicine, Philadelphia.

Classifications MeSH