Evidence map›Paper›PMID 38869458›Full record

ArticleEuropean thyroid journal2024

Thr92Ala-DIO2 heterozygosity is associated with skeletal muscle mass and myosteatosis in patients with COVID-19.

Fabyan Esberard de Lima Beltrão, Daniele Carvalhal de Almeida Beltrão, Giulia Carvalhal, Fabyanna Lethicia de Lima Beltrão, Jocyel de Brito Oliveira, Hatilla Dos Santos Silva, Helena Mariana Pitangueira Teixeira, Juliana Lopes Rodrigues, Camila Alexandrina Viana de Figueiredo, Ryan Dos Santos Costa and 5 more

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Article in European thyroid journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

15 authors.

Fabyan Esberard de Lima BeltrãoLauro Wanderley University Hospital, Federal University of Paraíba, João Pessoa, Paraíba, Brazil.
Daniele Carvalhal de Almeida BeltrãoUniversity Center of João Pessoa - UNIPE, João Pessoa, PB, Brazil.
Giulia CarvalhalCenter for Biological and Health Sciences, Federal University of Campina Grande, Campina Grande, Paraíba, Brazil.
Fabyanna Lethicia de Lima BeltrãoPost-Graduate Program in Medicine and Health, Medical School of Medicine, Federal University of Bahia, Salvador, Brazil.
Jocyel de Brito OliveiraBioregulation Department, Health and Science Institut, Federal University of Bahia, Salvador, Bahia, Brazil.
Hatilla Dos Santos SilvaBioregulation Department, Health and Science Institut, Federal University of Bahia, Salvador, Bahia, Brazil.
Helena Mariana Pitangueira TeixeiraBioregulation Department, Health and Science Institut, Federal University of Bahia, Salvador, Bahia, Brazil.
Juliana Lopes RodriguesLaboratory of Immunopharmacology and Molecular Biology, Health Sciences Institute, Federal University of Bahia, Brazil.
Camila Alexandrina Viana de FigueiredoLaboratory of Immunopharmacology and Molecular Biology, Health Sciences Institute, Federal University of Bahia, Brazil.
Ryan Dos Santos CostaLaboratory of Immunopharmacology and Molecular Biology, Health Sciences Institute, Federal University of Bahia, Brazil.
Fabio HechtThe Institute of Biophysics Carlos Chagas Filho, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Giciane Carvalho VieiraPost-Graduation Program in Cognitive Neuroscience and Behavior, Psychology Department of the Center of Human Sciences, Federal University of Paraíba, João Pessoa, Paraíba, Brazil.
Maria da Conceição Rodrigues GonçalvesLauro Wanderley University Hospital, Federal University of Paraíba, João Pessoa, Paraíba, Brazil.
Antonio C BiancoSection of Endocrinology and Metabolism, Division of the Biological Sciences, University of Chicago, Chicago, Illinois, USA.
Helton Estrela RamosPost-Graduate Program in Medicine and Health, Medical School of Medicine, Federal University of Bahia, Salvador, Brazil.ORCID 0000-0002-2900-2099

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The type 2 deiodinase and its Thr92Ala-DIO2 polymorphism have been linked to clinical outcomes in acute lung injury and coronavirus disease 2019 (COVID-19). Objective: The objective was to identify a potential association between Thr92Ala-DIO2 polymorphism and body composition (appendicular muscle mass, myosteatosis, and fat distribution) and to determine whether they reflect the severity or mortality associated with the disease. Methods: In this prospective cohort study (June-August 2020), 181 patients hospitalized with moderate-to-severe COVID-19 underwent a non-contrast-enhanced computed tomography (CT) of the thorax to assess body composition, laboratory tests, and genotyping for the Thr92Ala-DIO2 polymorphism. Results: In total, 181 consecutive patients were stratified into three subgroups according to the genotype: Thr/Thr (n = 64), Thr/Ala (n = 96), and Ala/Ala (n = 21). The prevalence of low muscle area (MA) (< 92 cm²) was 52.5%. Low MA was less frequent in Ala/Thr patients (44.8%) than in Thr/Thr (60.9%) or Ala/Ala patients (61.9%) (P = 0.027). Multivariate logistic regression analysis confirmed that the Thr/Ala allele was associated with a reduced risk of low MA (41% to 69%) and myosteatosis (62% to 72%) compared with Thr/Thr + Ala/Ala (overdominant model). Kaplan-Meier curves showed that patients with low muscle mass and homozygosity had lower survival rates than the other groups. Notably, the heterozygotes with MA ≥92 cm² exhibited the best survival rate. Conclusion: Thr92Ala-DIO2 heterozygosity is associated with increased skeletal MA and less myosteatosis in patients with COVID-19. The protective effect of Thr92Ala-DIO2 heterozygosity on COVID-19 mortality is restricted to patients with reduced MA.

Indexed as

COVID-19Muscle, SkeletalSARS-CoV-2AgedBody CompositionFemaleGenotypeHeterozygoteHumansIodothyronine Deiodinase Type IIMaleMiddle AgedProspective StudiesTomography, X-Ray ComputedDIO2 protein, humanIodothyronine Deiodinase Type IICOVID-19musclemyosteatosisThr92Ala-DIO2

Identifiers

PMID38869458
PMCPMC11301567

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.