TY - JOUR
T1 - Obesity as an independent risk factor for COVID-19 severity and mortality
AU - Tadayon Najafabadi, Borna
AU - Rayner, Daniel G.
AU - Shokraee, Kamyar
AU - Shokraie, Kamran
AU - Panahi, Parsa
AU - Rastgou, Paravaneh
AU - Seirafianpour, Farnoosh
AU - Momeni Landi, Feryal
AU - Alinia, Pariya
AU - Parnianfard, Neda
AU - Hemmati, Nima
AU - Banivaheb, Behrooz
AU - Radmanesh, Ramin
AU - Alvand, Saba
AU - Shahbazi, Parmida
AU - Dehghanbanadaki, Hojat
AU - Shaker, Elaheh
AU - Same, Kaveh
AU - Mohammadi, Esmaeil
AU - Malik, Abdullah
AU - Srivastava, Ananya
AU - Nejat, Peyman
AU - Tamara, Alice
AU - Chi, Yuan
AU - Yuan, Yuhong
AU - Hajizadeh, Nima
AU - Chan, Cynthia
AU - Zhen, Jamie
AU - Tahapary, Dicky
AU - Anderson, Laura
AU - Apatu, Emma
AU - Schoonees, Anel
AU - Naude, Celeste E.
AU - Thabane, Lehana
AU - Foroutan, Farid
N1 - Funding Information:
We would like to commemorate one of the authors of this review who we lost during the conduct of this review. Dr. Kamran Shokraee was a bright young man with great aspirations who contributed to this review with unparalleled enthusiasm and sincerity. Even though his departure was very sudden, saddening, and shocking to his family and friends, his great achievements in academic and social life will be remembered. He not only represented the true meaning of academic excellence but touched many lives through his compassion. Kamran was a caring teacher, curious researcher, compassionate doctor, and a loving brother and friend. Although his journey was short in this world, his memory will linger with us forever. This study was part of Dr. Borna Tadayon Najafabadi's thesis work for Ph.D. in Health Research Methodology at McMaster University. AS and CEN are partly supported by the Research, Evidence and Development Initiative (READ-It). READ-It (project number 300342-104) is funded by UK aid from the UK government; however, the views expressed do not necessarily reflect the UK government’s official policies. Cochrane Metabolic and Endocrine Disorders Groups upported the authors in the development of this review. The following people conducted the editorial process for this article Sign-off Editor (final editorial decision): Brenda Bongerts, Co-ordinating editor at the Cochrane Metabolic and Endocrine Disorders group Managing Editor (selected peer reviewers, provided comments, collated peer-reviewer comments, provided editorial guidance to authors, edited the article): Lara Kahale and Colleen Ovelman, Cochrane Central Editorial Service Editorial Assistant (conducted editorial policy checks and supported editorial team): Lisa Wydrzynski, Cochrane Central Editorial Service Copy Editor (copy-editing and production): [NAME, AFFILIATION] (will be identified later) Peer-reviewers (provided comments and recommended an editorial decision): Carmen Piernas, MSc PhD; University Research Lecturer, University of Oxford (content review), Robert Walton. Senior Fellow in General Practice, Cochrane UK (content review); Kerry Dwan, Cochrane Methods Support Unit (methods review); and Robin Featherstone, Cochrane Central Editorial Service (search review). Sign-off Editor (final editorial decision): Brenda Bongerts, Co-ordinating editor at the Cochrane Metabolic and Endocrine Disorders group Managing Editor (selected peer reviewers, provided comments, collated peer-reviewer comments, provided editorial guidance to authors, edited the article): Lara Kahale and Colleen Ovelman, Cochrane Central Editorial Service Editorial Assistant (conducted editorial policy checks and supported editorial team): Lisa Wydrzynski, Cochrane Central Editorial Service Copy Editor (copy-editing and production): [NAME, AFFILIATION] (will be identified later) Peer-reviewers (provided comments and recommended an editorial decision): Carmen Piernas, MSc PhD; University Research Lecturer, University of Oxford (content review), Robert Walton. Senior Fellow in General Practice, Cochrane UK (content review); Kerry Dwan, Cochrane Methods Support Unit (methods review); and Robin Featherstone, Cochrane Central Editorial Service (search review). One additional peer reviewer provided content peer review, but chose not to be publicly acknowledged
Publisher Copyright:
Copyright © 2023 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
PY - 2023/5/24
Y1 - 2023/5/24
N2 - Background: Since December 2019, the world has struggled with the COVID-19 pandemic. Even after the introduction of various vaccines, this disease still takes a considerable toll. In order to improve the optimal allocation of resources and communication of prognosis, healthcare providers and patients need an accurate understanding of factors (such as obesity) that are associated with a higher risk of adverse outcomes from the COVID-19 infection. Objectives: To evaluate obesity as an independent prognostic factor for COVID-19 severity and mortality among adult patients in whom infection with the COVID-19 virus is confirmed. Search methods: MEDLINE, Embase, two COVID-19 reference collections, and four Chinese biomedical databases were searched up to April 2021. Selection criteria: We included case-control, case-series, prospective and retrospective cohort studies, and secondary analyses of randomised controlled trials if they evaluated associations between obesity and COVID-19 adverse outcomes including mortality, mechanical ventilation, intensive care unit (ICU) admission, hospitalisation, severe COVID, and COVID pneumonia. Given our interest in ascertaining the independent association between obesity and these outcomes, we selected studies that adjusted for at least one factor other than obesity. Studies were evaluated for inclusion by two independent reviewers working in duplicate. Data collection and analysis: Using standardised data extraction forms, we extracted relevant information from the included studies. When appropriate, we pooled the estimates of association across studies with the use of random-effects meta-analyses. The Quality in Prognostic Studies (QUIPS) tool provided the platform for assessing the risk of bias across each included study. In our main comparison, we conducted meta-analyses for each obesity class separately. We also meta-analysed unclassified obesity and obesity as a continuous variable (5 kg/m2 increase in BMI (body mass index)). We used the GRADE framework to rate our certainty in the importance of the association observed between obesity and each outcome. As obesity is closely associated with other comorbidities, we decided to prespecify the minimum adjustment set of variables including age, sex, diabetes, hypertension, and cardiovascular disease for subgroup analysis. Main results: We identified 171 studies, 149 of which were included in meta-analyses. As compared to 'normal' BMI (18.5 to 24.9 kg/m2) or patients without obesity, those with obesity classes I (BMI 30 to 35 kg/m2), and II (BMI 35 to 40 kg/m2) were not at increased odds for mortality (Class I: odds ratio [OR] 1.04, 95% confidence interval [CI] 0.94 to 1.16, high certainty (15 studies, 335,209 participants); Class II: OR 1.16, 95% CI 0.99 to 1.36, high certainty (11 studies, 317,925 participants)). However, those with class III obesity (BMI 40 kg/m2 and above) may be at increased odds for mortality (Class III: OR 1.67, 95% CI 1.39 to 2.00, low certainty, (19 studies, 354,967 participants)) compared to normal BMI or patients without obesity. For mechanical ventilation, we observed increasing odds with higher classes of obesity in comparison to normal BMI or patients without obesity (class I: OR 1.38, 95% CI 1.20 to 1.59, 10 studies, 187,895 participants, moderate certainty; class II: OR 1.67, 95% CI 1.42 to 1.96, 6 studies, 171,149 participants, high certainty; class III: OR 2.17, 95% CI 1.59 to 2.97, 12 studies, 174,520 participants, high certainty). However, we did not observe a dose-response relationship across increasing obesity classifications for ICU admission and hospitalisation. Authors' conclusions: Our findings suggest that obesity is an important independent prognostic factor in the setting of COVID-19. Consideration of obesity may inform the optimal management and allocation of limited resources in the care of COVID-19 patients.
AB - Background: Since December 2019, the world has struggled with the COVID-19 pandemic. Even after the introduction of various vaccines, this disease still takes a considerable toll. In order to improve the optimal allocation of resources and communication of prognosis, healthcare providers and patients need an accurate understanding of factors (such as obesity) that are associated with a higher risk of adverse outcomes from the COVID-19 infection. Objectives: To evaluate obesity as an independent prognostic factor for COVID-19 severity and mortality among adult patients in whom infection with the COVID-19 virus is confirmed. Search methods: MEDLINE, Embase, two COVID-19 reference collections, and four Chinese biomedical databases were searched up to April 2021. Selection criteria: We included case-control, case-series, prospective and retrospective cohort studies, and secondary analyses of randomised controlled trials if they evaluated associations between obesity and COVID-19 adverse outcomes including mortality, mechanical ventilation, intensive care unit (ICU) admission, hospitalisation, severe COVID, and COVID pneumonia. Given our interest in ascertaining the independent association between obesity and these outcomes, we selected studies that adjusted for at least one factor other than obesity. Studies were evaluated for inclusion by two independent reviewers working in duplicate. Data collection and analysis: Using standardised data extraction forms, we extracted relevant information from the included studies. When appropriate, we pooled the estimates of association across studies with the use of random-effects meta-analyses. The Quality in Prognostic Studies (QUIPS) tool provided the platform for assessing the risk of bias across each included study. In our main comparison, we conducted meta-analyses for each obesity class separately. We also meta-analysed unclassified obesity and obesity as a continuous variable (5 kg/m2 increase in BMI (body mass index)). We used the GRADE framework to rate our certainty in the importance of the association observed between obesity and each outcome. As obesity is closely associated with other comorbidities, we decided to prespecify the minimum adjustment set of variables including age, sex, diabetes, hypertension, and cardiovascular disease for subgroup analysis. Main results: We identified 171 studies, 149 of which were included in meta-analyses. As compared to 'normal' BMI (18.5 to 24.9 kg/m2) or patients without obesity, those with obesity classes I (BMI 30 to 35 kg/m2), and II (BMI 35 to 40 kg/m2) were not at increased odds for mortality (Class I: odds ratio [OR] 1.04, 95% confidence interval [CI] 0.94 to 1.16, high certainty (15 studies, 335,209 participants); Class II: OR 1.16, 95% CI 0.99 to 1.36, high certainty (11 studies, 317,925 participants)). However, those with class III obesity (BMI 40 kg/m2 and above) may be at increased odds for mortality (Class III: OR 1.67, 95% CI 1.39 to 2.00, low certainty, (19 studies, 354,967 participants)) compared to normal BMI or patients without obesity. For mechanical ventilation, we observed increasing odds with higher classes of obesity in comparison to normal BMI or patients without obesity (class I: OR 1.38, 95% CI 1.20 to 1.59, 10 studies, 187,895 participants, moderate certainty; class II: OR 1.67, 95% CI 1.42 to 1.96, 6 studies, 171,149 participants, high certainty; class III: OR 2.17, 95% CI 1.59 to 2.97, 12 studies, 174,520 participants, high certainty). However, we did not observe a dose-response relationship across increasing obesity classifications for ICU admission and hospitalisation. Authors' conclusions: Our findings suggest that obesity is an important independent prognostic factor in the setting of COVID-19. Consideration of obesity may inform the optimal management and allocation of limited resources in the care of COVID-19 patients.
UR - http://www.scopus.com/inward/record.url?scp=85159966426&partnerID=8YFLogxK
U2 - 10.1002/14651858.CD015201
DO - 10.1002/14651858.CD015201
M3 - Review article
C2 - 37222292
AN - SCOPUS:85159966426
SN - 1465-1858
VL - 2023
JO - Cochrane Database of Systematic Reviews
JF - Cochrane Database of Systematic Reviews
IS - 5
M1 - CD015201
ER -