Obesity‐dependent molecular alterations in fatal COVID‐19: A retrospective postmortem study of metabolomic profile of adipose tissue

Author:

Pilger Bruna I.1,Castro Alex23,Vasconcellos Franciane F.1,Moura Karen F.1,Signini Étore De Favari4,Marqueze Luis Felipe B.1,Fiorenza‐Neto Edson A.1,Rocha Mateus T.1,Pedroso Giulia S.1,Cavaglieri Claudia R.5,Ferreira Antonio G.2,Figueiredo Caique6,Minuzzi Luciele G.6ORCID,Gatti da Silva Guilherme H.7,Castro Gabriela S.7,Lira Fábio S.6,Seelaender Marilia7,Pinho Ricardo A.1ORCID

Affiliation:

1. Graduate Program in Health Sciences, School of Medicine and Life Sciences Pontifícia Universidade Católica do Paraná Curitiba Brazil

2. Laboratory of Nuclear Magnetic Resonance, Department of Chemistry Universidade Federal de São Carlos São Carlos Brazil

3. Biosciences National Laboratory Brazilian Center for Research in Energy and Materials Campinas Brazil

4. Cardiovascular Physical Therapy Laboratory, Department of Physical Therapy Universidade Federal de São Carlos São Carlos Brazil

5. Exercise Physiology Laboratory, Faculty of Physical Education University of Campinas Campinas Brazil

6. Exercise and Immunometabolism Research Group, Post‐Graduation Program in Movement Sciences, Department of Physical Education Universidade Estadual Paulista Presidente Prudente Brazil

7. Cancer Metabolism Research Group, Department of Surgery and LIM 26, Hospital das Clínicas University of São Paulo São Paulo Brazil

Abstract

AbstractWe investigated the effects of obesity on metabolic, inflammatory, and oxidative stress parameters in the adipose tissue of patients with fatal COVID‐19. Postmortem biopsies of subcutaneous adipose tissue were obtained from 25 unvaccinated inpatients who passed from COVID‐19, stratified as nonobese (N‐OB; body mass index [BMI], 26.5 ± 2.3 kg m−2) or obese (OB BMI 34.2 ± 5.1 kg m−2). Univariate and multivariate analyses revealed that body composition was responsible for most of the variations detected in the metabolome, with greater dispersion observed in the OB group. Fifteen metabolites were major segregation factors. Results from the OB group showed higher levels of creatinine, myo‐inositol, O‐acetylcholine, and succinate, and lower levels of sarcosine. The N‐OB group showed lower levels of glutathione peroxidase activity, as well as higher content of IL‐6 and adiponectin. We revealed significant changes in the metabolomic profile of the adipose tissue in fatal COVID‐19 cases, with high adiposity playing a key role in these observed variations. These findings highlight the potential involvement of metabolic and inflammatory pathways, possibly dependent on hypoxia, shedding light on the impact of obesity on disease pathogenesis and suggesting avenues for further research and possible therapeutic targets.

Publisher

Wiley

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