Evidence map›Paper›PMID 38911040›Full record

ArticleFrontiers in endocrinology2024

The Thr92Ala polymorphism in the type 2 deiodinase gene is linked to depression in patients with COVID-19 after hospital discharge.

Daniele Carvalhal de Almeida Beltrão, Fabyan Esberard de Lima Beltrão, Giulia Carvalhal, Fabyanna Lethicia de Lima Beltrão, Amanda da Silva Brito, Hatilla Dos Santos Silva, Helena Mariana Pitangueira Teixeira, Juliana Lopes Rodrigues, Camila Alexandrina Viana de Figueiredo, Ryan Dos Santos Costa and 3 more

Abstract read
In one paragraph

Article in Frontiers in endocrinology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Daniele Carvalhal de Almeida Beltrão *Postgraduate Program in Cognitive Neuroscience and Behavior, Center for Health Sciences, Federal University of Paraíba, João Pessoa, Paraíba, Brazil.
Fabyan Esberard de Lima Beltrão *Department of Internal Medicine, University Centre of João Pessoa (UNIPE), João Pessoa, Paraíba, 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.
Amanda da Silva BritoDepartment of Internal Medicine, Royal Portuguese Hospital of Beneficence, Recife, Pernambuco, 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, Salvador, Bahia, Brazil.
Camila Alexandrina Viana de FigueiredoLaboratory of Immunopharmacology and Molecular Biology, Health Sciences Institute, Federal University of Bahia, Salvador, Bahia, Brazil.
Ryan Dos Santos CostaLaboratory of Immunopharmacology and Molecular Biology, Health Sciences Institute, Federal University of Bahia, Salvador, Bahia, Brazil.
Liana Clebia De Morais PordeusPostgraduate Program in Cognitive Neuroscience and Behavior, Center for Health Sciences, Federal University of Paraíba, João Pessoa, Paraíba, Brazil.
Giciane Carvalho Vieira *Postgraduate Program in Cognitive Neuroscience and Behavior, Center for Health Sciences, Federal University of Paraíba, João Pessoa, Paraíba, Brazil.
Helton Estrela Ramos *Post-Graduate Program in Medicine and Health, Medical School of Medicine, Federal University of Bahia, Salvador, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The Thr92Ala-DIO2 polymorphism has been associated with clinical outcomes in hospitalized patients with COVID-19 and neuropsychiatric diseases. This study examines the impact of the Thr92Ala-DIO2 polymorphism on neuropsychological symptoms, particularly depressive symptoms, in patients who have had moderate to severe SARS-CoV-2 infection and were later discharged. Methods: Our prospective cohort study, conducted from June to August 2020, collected data from 273 patients hospitalized with COVID-19. This included thyroid function tests, inflammatory markers, hematologic indices, and genotyping of the Thr92Ala-DIO2 polymorphism. Post-discharge, we followed up with 68 patients over 30 to 45 days, dividing them into depressive (29 patients) and non-depressive (39 patients) groups based on their Beck Depression Inventory scores. Results: We categorized 68 patients into three groups based on their genotypes: Thr/Thr (22 patients), Thr/Ala (41 patients), and Ala/Ala (5 patients). Depressive symptoms were less frequent in the Thr/Ala group (29.3%) compared to the Thr/Thr (59.1%) and Ala/Ala (60%) groups ( Conclusion: Our findings appear to be the first to show that heterozygosity for Thr92Ala-DIO2 in patients with COVID-19 may protect against post-COVID-19 depression symptoms up to 2 months after the illness.

Indexed as

COVID-19DepressionPatient DischargeAdultAgedFemaleGenotypeHumansIodide PeroxidaseIodothyronine Deiodinase Type IIMaleMiddle AgedPolymorphism, Single NucleotideProspective StudiesSARS-CoV-2DIO2 protein, humanIodide PeroxidaseIodothyronine Deiodinase Type IIbiomarkersdepressionpost-COVID-19Thr92Ala-DIO2 polymorphismthyroid function

Identifiers

PMID38911040
PMCPMC11190161

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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.