Association of BMI and Change in Weight With Mortality in Patients With Fibrotic Interstitial Lung Disease.


Journal

Chest
ISSN: 1931-3543
Titre abrégé: Chest
Pays: United States
ID NLM: 0231335

Informations de publication

Date de publication:
05 2022
Historique:
received: 10 07 2021
revised: 31 10 2021
accepted: 03 11 2021
pubmed: 18 11 2021
medline: 11 5 2022
entrez: 17 11 2021
Statut: ppublish

Résumé

Mortality risk assessment in interstitial lung disease (ILD) is challenging. Our objective was to determine the prognostic significance of BMI and change in weight in the most common fibrotic ILD subtypes. Could BMI and weight loss over time be reliable prognostic indicators in patients with fibrotic ILD? This observational retrospective multicenter cohort study enrolled patients with fibrotic ILD from the six-center CAnadian REgistry for Pulmonary Fibrosis (CARE-PF, derivation) and the ILD registry at the University of California, San Francisco (UCSF, validation). Patients were subcategorized as underweight (BMI < 18.5), normal weight (BMI 18.5-24.9), overweight (BMI 25-29.9), or obese (BMI > 30). Annual change in weight was calculated for all years of follow-up as the slope of best fit using the least square method based on every available measurement. Separate multivariable analyses evaluated the associations of BMI and change in weight with mortality, adjusting for common prognostic variables. The derivation and validation cohorts included 1,786 and 1,779 patients, respectively. Compared with patients with normal BMI, mortality was highest in patients who were underweight (hazard ratio [HR], 3.19; 95% CI, 1.88-5.43; P < .001) and was lowest in those who were overweight (HR, 0.52; 95% CI, 0.36-0.75; P < .001) or obese (HR, 0.55; 95%CI, 0.37-0.83; P < .001) in the analysis adjusted for the ILD-GAP (gender, age, physiology) Index. Patients who had a weight loss of at least 2 kg within 1 year had increased risk of death in the subsequent year (HR, 1.41; 95% CI, 1.01-1.97; P = .04) after adjustment for the ILD-GAP Index and baseline BMI category, with a plateau in risk for patients with greater weight loss. Consistent results were observed in the validation cohort. Both BMI and weight loss are independently associated with 1-year mortality in fibrotic ILD. BMI and weight loss may be clinically useful prognostic indicators in fibrotic ILD.

Sections du résumé

BACKGROUND
Mortality risk assessment in interstitial lung disease (ILD) is challenging. Our objective was to determine the prognostic significance of BMI and change in weight in the most common fibrotic ILD subtypes.
RESEARCH QUESTION
Could BMI and weight loss over time be reliable prognostic indicators in patients with fibrotic ILD?
STUDY DESIGN AND METHODS
This observational retrospective multicenter cohort study enrolled patients with fibrotic ILD from the six-center CAnadian REgistry for Pulmonary Fibrosis (CARE-PF, derivation) and the ILD registry at the University of California, San Francisco (UCSF, validation). Patients were subcategorized as underweight (BMI < 18.5), normal weight (BMI 18.5-24.9), overweight (BMI 25-29.9), or obese (BMI > 30). Annual change in weight was calculated for all years of follow-up as the slope of best fit using the least square method based on every available measurement. Separate multivariable analyses evaluated the associations of BMI and change in weight with mortality, adjusting for common prognostic variables.
RESULTS
The derivation and validation cohorts included 1,786 and 1,779 patients, respectively. Compared with patients with normal BMI, mortality was highest in patients who were underweight (hazard ratio [HR], 3.19; 95% CI, 1.88-5.43; P < .001) and was lowest in those who were overweight (HR, 0.52; 95% CI, 0.36-0.75; P < .001) or obese (HR, 0.55; 95%CI, 0.37-0.83; P < .001) in the analysis adjusted for the ILD-GAP (gender, age, physiology) Index. Patients who had a weight loss of at least 2 kg within 1 year had increased risk of death in the subsequent year (HR, 1.41; 95% CI, 1.01-1.97; P = .04) after adjustment for the ILD-GAP Index and baseline BMI category, with a plateau in risk for patients with greater weight loss. Consistent results were observed in the validation cohort.
INTERPRETATION
Both BMI and weight loss are independently associated with 1-year mortality in fibrotic ILD. BMI and weight loss may be clinically useful prognostic indicators in fibrotic ILD.

Identifiants

pubmed: 34788669
pii: S0012-3692(21)04292-6
doi: 10.1016/j.chest.2021.11.008
pii:
doi:

Types de publication

Journal Article Multicenter Study Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1320-1329

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2021 American College of Chest Physicians. All rights reserved.

Auteurs

Alessia Comes (A)

Università Cattolica del Sacro Cuore, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy; Centre for Heart Lung Innovation, St. Paul's Hospital, Vancouver, BC, Canada. Electronic address: alessia.comes@gmail.com.

Alyson W Wong (AW)

Centre for Heart Lung Innovation, St. Paul's Hospital, Vancouver, BC, Canada; Department of Medicine, University of British Columbia, Vancouver, BC, Canada.

Jolene H Fisher (JH)

Department of Medicine, University of Toronto, Toronto, ON, Canada.

Julie Morisset (J)

Department of Medicine, Université de Montréal, Montreal, QC, Canada.

Kerri A Johannson (KA)

Department of Medicine, University of Calgary, Calgary, AB, Canada.

Erica Farrand (E)

Department of Medicine, University of California San Francisco, CA.

Charlene D Fell (CD)

Department of Medicine, University of Calgary, Calgary, AB, Canada.

Martin Kolb (M)

Department of Medicine, McMaster University, Hamilton, ON, Canada.

Hélène Manganas (H)

Department of Medicine, Université de Montréal, Montreal, QC, Canada.

Gerard Cox (G)

Department of Medicine, McMaster University, Hamilton, ON, Canada.

Andrea S Gershon (AS)

Department of Medicine, University of Toronto, Toronto, ON, Canada; Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON, Canada.

Andrew J Halayko (AJ)

Departments of Internal Medicine and Physiology and Pathophysiology, University of Manitoba, Winnipeg, MB, Canada.

Nathan Hambly (N)

Department of Medicine, McMaster University, Hamilton, ON, Canada.

Nasreen Khalil (N)

Department of Medicine, University of British Columbia, Vancouver, BC, Canada.

Mohsen Sadatsafavi (M)

Respiratory Evaluation Sciences Program, Collaboration for Outcomes Research and Evaluation, Faculty of Pharmaceutical Sciences, The University of British Columbia, Vancouver, BC, Canada.

Shane Shapera (S)

Department of Medicine, University of Toronto, Toronto, ON, Canada.

Teresa To (T)

Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON, Canada.

Pearce G Wilcox (PG)

Department of Medicine, University of British Columbia, Vancouver, BC, Canada.

Harold R Collard (HR)

Department of Medicine, University of California San Francisco, CA.

Christopher J Ryerson (CJ)

Centre for Heart Lung Innovation, St. Paul's Hospital, Vancouver, BC, Canada; Department of Medicine, University of British Columbia, Vancouver, BC, Canada.

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