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Endotrophin, a Collagen VI Formation-Derived Peptide, in Heart Failure.
Chirinos, Julio A; Zhao, Lei; Reese-Petersen, Alexander L; Cohen, Jordana B; Genovese, Federica; Richards, A Mark; Doughty, Robert N; Díez, Javier; González, Arantxa; Querejeta, Ramón; Zamani, Payman; Nuñez, Julio; Wang, Zhaoqing; Ebert, Christina; Kammerhoff, Karl; Maranville, Joseph; Basso, Michael; Qian, Chenao; Rasmussen, Daniel G K; Schafer, Peter H; SeifFert, Dietmar; Karsdal, Morten A; Gordon, David A; Ramirez-Valle, Francisco; Cappola, Thomas P.
Affiliation
  • Chirinos JA; Hospital of the University of Pennsylvania, Philadelphia.
  • Zhao L; University of Pennsylvania, Perelman School of Medicine, Philadelphia.
  • Reese-Petersen AL; Bristol Myers Squibb Company, Princeton, NJ.
  • Cohen JB; Nordic Bioscience, Herlev, Denmark.
  • Genovese F; Hospital of the University of Pennsylvania, Philadelphia.
  • Richards AM; Nordic Bioscience, Herlev, Denmark.
  • Doughty RN; Cardiovascular Research Institute, National University of Singapore, Singapore.
  • Díez J; Christchurch Heart Institute, University of Otago, Dunedin, New Zealand.
  • González A; University of Auckland, Auckland, New Zealand.
  • Querejeta R; Program of Cardiovascular Diseases, CIMA Universidad de Navarra, IdiSNA and CIBERCV, Pamplona, Navarra, Spain.
  • Zamani P; Departments of Cardiology and Nephrology, Clínica Universidad de Navarra, Pamplona, Navarra, Spain.
  • Nuñez J; Program of Cardiovascular Diseases, CIMA Universidad de Navarra, IdiSNA and CIBERCV, Pamplona, Navarra, Spain.
  • Wang Z; Department of Cardiology, Hospital Universitario Donostia, San Sebastián, Guipúzcoa, Spain.
  • Ebert C; Hospital of the University of Pennsylvania, Philadelphia.
  • Kammerhoff K; University of Pennsylvania, Perelman School of Medicine, Philadelphia.
  • Maranville J; Hospital Clínico Universitario de Valencia, Universidad de Valencia, INCLIVA, CIBER Cardiovascular, Valencia, Spain.
  • Basso M; Bristol Myers Squibb Company, Princeton, NJ.
  • Qian C; Bristol Myers Squibb Company, Princeton, NJ.
  • Rasmussen DGK; Bristol Myers Squibb Company, Princeton, NJ.
  • Schafer PH; Bristol Myers Squibb Company, Princeton, NJ.
  • SeifFert D; Bristol Myers Squibb Company, Princeton, NJ.
  • Karsdal MA; University of Pennsylvania, Perelman School of Medicine, Philadelphia.
  • Gordon DA; Nordic Bioscience, Herlev, Denmark.
  • Ramirez-Valle F; Bristol Myers Squibb Company, Princeton, NJ.
  • Cappola TP; Bristol Myers Squibb Company, Princeton, NJ.
NEJM Evid ; 1(10)2022 Oct.
Article in En | MEDLINE | ID: mdl-37645406
ABSTRACT

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:

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:

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:

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.).

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Prognostic_studies Language: En Journal: NEJM Evid Year: 2022 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Prognostic_studies Language: En Journal: NEJM Evid Year: 2022 Document type: Article