Evidence map›Paper›PMID 41204118›Full record

Observational studyBMC infectious diseases2025

Impact of long COVID phenotypes on quality of life following symptomatic omicron infection in Brazil: a machine learning analysis.

Fernando Luis Scolari, Julia Spinardi, Mariana Motta Dias da Silva, Geraldine Trott, Cristina de Oliveira Rodrigues, Marciane Maria Rover, Emanuel Maltempi de Souza, Josélia Larger Manfio, Nathan Iori Camargo, Ana Paula de Souza and 41 more

Abstract readObservational Study
In one paragraph

Observational study in BMC infectious diseases, 2025. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

51 authors.

Fernando Luis ScolariHospital Moinhos de Vento, Porto Alegre, RS, Brazil. fernando.scolari@hmv.org.br.
Julia SpinardiPfizer, Vaccines Medical and Scientific Affairs, Emerging Markets, Collegeville, PA, USA.
Mariana Motta Dias da SilvaHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Geraldine TrottHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Cristina de Oliveira RodriguesFaculdade de Medicina, Campus Toledo, Universidade Federal do Paraná (UFPR), Toledo, PR, Brazil.
Marciane Maria RoverHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Emanuel Maltempi de SouzaDepartamento de Bioquímica e Biologia Molecular, UFPR, Curitiba, PR, Brazil.
Josélia Larger ManfioHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Nathan Iori CamargoHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Ana Paula de SouzaHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Denise de SouzaHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Raíne Fogliati De CarliHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Emelyn de Souza RoldãoHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Duane MocellinHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Aline Paula MiozzoHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Gabrielle Nunes da SilvaHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Jennifer Menna Barreto de SouzaHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Rosa da Rosa Minho Dos SantosHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Carolina Rothmann ItaquiHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Gabriela Soares RechHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Vivian Menezes IrineuHospital Doutor Leo Orsi Bernardes de Itapetininga, Itapetininga, SP, Brazil.
Saionara Cristina FranciscoHospital Metropolitano Dr. Célio de Castro, Belo Horizonte, MG, Brazil.
Odilson SilvestreHospital Silvestre Santé, Rio Branco, AC, Brazil.
Precil Diego Miranda de Menezes NevesHospital Alemão Oswaldo Cruz, São Paulo, SP, Brazil.
Lucas TramujasInstituto de Pesquisa Hcor, São Paulo, SP, Brazil.
Vandack NobreFaculdade de Medicina, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG, Brazil.
Sidiclei Machado CarvalhoHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Carlos Delmar do Amaral FerreiraHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Jaqueline Carvalho de OliveiraDepartamento de Genética, UFPR, Curitiba, PR, Brazil.
Carla Adriane RoyerDepartamento de Genética, UFPR, Curitiba, PR, Brazil.
Rafael Messias LuizFaculdade de Medicina, Campus Toledo, Universidade Federal do Paraná (UFPR), Toledo, PR, Brazil.
Valter Antonio BauraDepartamento de Bioquímica e Biologia Molecular, UFPR, Curitiba, PR, Brazil.
Daniela Fiori GradiaDepartamento de Genética, UFPR, Curitiba, PR, Brazil.
Ana Paula Carneiro BrandalizeFaculdade de Medicina, Campus Toledo, Universidade Federal do Paraná (UFPR), Toledo, PR, Brazil.
Hellen Abreu PereiraDepartamento de Genética, UFPR, Curitiba, PR, Brazil.
Carolina Gracia PoitevinDepartamento de Genética, UFPR, Curitiba, PR, Brazil.
Caroline Cabral RobinsonHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Bruna Brandao BarretoFaculdade de Medicina, Universidade Federal da Bahia (UFBA), Salvador, BA, Brazil.
Paulo R SchvartzmanHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Milena MarcolinoFaculdade de Medicina, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG, Brazil.
Ana Carolina Peçanha AntonioHospital de Clínicas de Porto Alegre (HCPA), Porto Alegre, RS, Brazil.
Carisi Anne PolanczykHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Juçara Gasparetto MaccariHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Luiz Antonio NasiHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Srinivas Rao ValluriPfizer, Vaccines Medical and Scientific Affairs, Emerging Markets, Collegeville, PA, USA.
Viviane Wal JuliãoPfizer, Vaccines Medical and Scientific Affairs, Emerging Markets, Collegeville, PA, USA.
Florence Lefebvre d'HellencourtPfizer, Vaccines Medical and Scientific Affairs, Emerging Markets, Collegeville, PA, USA.
Moe H KyawPfizer, Vaccines Medical and Scientific Affairs, Emerging Markets, Collegeville, PA, USA.
Graciela Del Carmen Morales CastilloPfizer, Vaccines Medical and Scientific Affairs, Emerging Markets, Collegeville, PA, USA.
Maicon FalavignaHospital Moinhos de Vento, Porto Alegre, RS, Brazil.
Regis Goulart RosaHospital Moinhos de Vento, Porto Alegre, RS, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study aimed to identify phenotypes of long COVID symptoms in adults following Omicron infection and assess their association with health-related quality of life (HRQoL).

methodsWe analyzed three prospective observational studies in Brazil, enrolling adult patients who sought care for symptomatic Omicron infection between December 2021 and March 2023. The infection was confirmed by either an antigen test or reverse transcriptase polymerase chain reaction. Long COVID symptoms were assessed three months after enrollment through structured interviews. Phenotypes of Long COVID-19 were identified using a machine learning-based clustering approach. Exploratory analyses were conducted to examine predisposing factors and health-related quality of life utilities, measured by EQ-5D-3 L, associated with each phenotype.

resultsA total of 2,989 patients were analyzed (39% women, median age 41 years, and 96% had completed the primary series of COVID-19 vaccination). Long COVID symptoms at three months were reported by 1,155 (38.6%) patients. Three phenotypes were identified: cluster 1 (n = 459 [39.7%]), characterized by a median of three symptoms (IQR, 2-5) with memory loss (80.4%), concentration problems (38.3%) and fatigue (35.7%) being most common; cluster 2 (n = 549 [47.5%]), characterized by a median of two symptoms (IQR, 1-4) with fatigue (43.7%), other symptoms (42.3%), and cough (20.6%) being most common; and cluster 3 (n = 147, 12.7%), characterized by a higher number of symptoms (median, 8; IQR, 7-10), with fatigue (89.9%), memory loss (88.4%), and anxiety (64.6%) as the most common. The mean EQ-5D-3 L utility at 3 months was 0.75 for cluster 1, 0.73 for cluster 2, and 0.59 for cluster 3 (p < 0.001). After adjusted regression analysis, cluster 3 was independently associated with the lowest EQ-5D-3 L utilities (mean difference, -0.21; 95%CI, -0.24 to -0.18; p < 0.001).

conclusionsDistinct phenotypic presentations of Long COVID following Omicron infection in Brazil were identified, with significant differences in quality of life. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

COVID-19Machine LearningQuality of LifeAdultAgedBrazilFemaleHumansMaleMiddle AgedPhenotypeProspective StudiesSARS-CoV-2Cluster analysisCOVID-19EQ-5D-3LOmicronPhenotypeQuality of life

Identifiers

PMID41204118
PMCPMC12595840

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