Significance of Adipose Tissue Quantity and Distribution on Obesity Paradox in Heart Failure.


Journal

The American journal of cardiology
ISSN: 1879-1913
Titre abrégé: Am J Cardiol
Pays: United States
ID NLM: 0207277

Informations de publication

Date de publication:
15 11 2023
Historique:
received: 15 05 2023
revised: 12 08 2023
accepted: 20 08 2023
medline: 6 11 2023
pubmed: 30 9 2023
entrez: 29 9 2023
Statut: ppublish

Résumé

Obesity is a predictor of the development of systolic and diastolic heart failure (HF), but once established, patients with HF and obesity have better outcomes than their leaner counterparts, a phenomenon termed the "obesity paradox." We sought to investigate the impact of adipose tissue quantity and distribution, measured by way of computed tomography, on outcomes in patients with HF. Patients admitted for acute decompensated HF between January 2017 to December 2018 were retrospectively analyzed. Body composition measurements were made on computed tomography of the abdomen/pelvis. Visceral, subcutaneous, and intermuscular adipose tissues were measured at the mid-third lumbar vertebra, along with skeletal muscle and waist circumference. Paracardial (pericardial and epicardial) adipose tissue was measured at the mid-eight thoracic vertebra. Visceral adipose tissue index (VATI) and subcutaneous adipose tissue index (SATI), along with skeletal muscle index, were indexed for patient height. A total of 200 patients were included, 44.5% female. Body mass index and waist circumference did not significantly predict outcomes. Patients with high SATI (highest sex-stratified tertile) had significantly better survival (hazard ratio 0.58, 95% confidence interval 0.39 to 0.87, p = 0.009), whereas high VATI was nonsignificant. Patients were further divided into 4 groups based on both VATI and SATI. One- and 4-year mortality risks were lowest in those with low VATI high SATI compared with the other groups; this persisted after multivariable adjustment for covariates, including albumin and skeletal muscle index. In conclusion, the "obesity paradox" appears to be largely driven by subcutaneous adipose tissue, independent of nutrition or skeletal muscle.

Identifiants

pubmed: 37774476
pii: S0002-9149(23)00919-0
doi: 10.1016/j.amjcard.2023.08.136
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

339-348

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL146754
Pays : United States
Organisme : NHLBI NIH HHS
ID : T32 HL076132
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest Dr. Martens has received consultancy fees from AstraZeneca, Abbott, Bayer, Boehringer-Ingelheim, Daiichi Sankyo, Novartis, Novo Nordisk, and Vifor Pharma. Dr. Estep is a consultant and medical advisor for Abbott and Medtronic Inc. Dr. Tang served as a consultant for Sequana Medical, Cardiol Therapeutics, Genomics plc, Zehna Therapeutics, Renovacor, WhiteSwell, Kiniksa Pharmaceuticals, Boston Scientific, CardiaTec Biosciences, and has received an honorarium from Springer Nature and American Board of Internal Medicine. The remaining authors have no competing interests to declare.

Auteurs

Saeid Mirzai (S)

Section on Cardiovascular Medicine, Department of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina; Department of Internal Medicine.

Ian Persits (I)

Department of Internal Medicine.

Pieter Martens (P)

Kaufman Center for Heart Failure Treatment and Recovery, Heart Vascular and Thoracic Institute.

Po-Hao Chen (PH)

Section of Musculoskeletal Imaging, Imaging Institute, Cleveland Clinic, Cleveland, Ohio.

Jerry D Estep (JD)

Department of Cardiology, Cleveland Clinic Florida, Weston, Florida.

W H Wilson Tang (WHW)

Kaufman Center for Heart Failure Treatment and Recovery, Heart Vascular and Thoracic Institute. Electronic address: tangw@ccf.org.

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