Evidence map›Paper›PMID 41692868›Full record

ArticleAnnals of hematology2026

Laboratory and genetic characteristic associated with gallbladder-related outcomes in sickle cell disease in Brazil: results from the REDS-III multicenter cohort study.

André Rolim Belisário, Mina Cintho Ozahata, Isabel Cristina Gomes Moura, Carolina Miranda, Anna Bárbara Carneiro-Proietti, Ester Cerdeira Sabino, Alessandra Ferraz, Cláudia Máximo, Miriam V Flor-Park, Daniela de Oliveira Werneck Rodrigues and 5 more

Abstract readMulticenter Study
In one paragraph

Article in Annals of hematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

1 citing paper in PubMed.

  1. Article
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

15 authors.

André Rolim BelisárioFundação Hemominas, Belo Horizonte, Minas Gerais, Brazil. andrebelisario@yahoo.com.br.ORCID http://orcid.org/0000-0003-0166-4258
Mina Cintho OzahataDepartment of Computer Science - DCC, University of São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-1272-2380
Isabel Cristina Gomes MouraFaculdade Ciências Médicas, Minas Gerais, Brazil.ORCID http://orcid.org/0000-0002-5549-3426
Carolina MirandaFundação Hemominas, Belo Horizonte, Minas Gerais, Brazil.
Anna Bárbara Carneiro-ProiettiFundação Hemominas, Belo Horizonte, Minas Gerais, Brazil.ORCID http://orcid.org/0000-0003-4302-5817
Ester Cerdeira SabinoFaculdade de Medicina (FMUSP), Instituto de Medicina Tropical, Universidade de São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0003-2623-5126
Alessandra FerrazFundação Hemope, Pernambuco, Brazil.ORCID http://orcid.org/0000-0003-1849-0047
Cláudia MáximoHemorio, Rio de Janeiro, Brazil.ORCID http://orcid.org/0000-0002-9351-3766
Miriam V Flor-ParkITACI, Instituto da Criança, HCFMUSP, São Paulo, Brazil.ORCID http://orcid.org/0000-0001-5558-6166
Daniela de Oliveira Werneck RodriguesFundação Hemominas, Belo Horizonte, Minas Gerais, Brazil.ORCID http://orcid.org/0000-0003-3062-2954
Rosimere Afonso MotaFundação Hemominas, Belo Horizonte, Minas Gerais, Brazil.ORCID http://orcid.org/0000-0002-3955-6036
Brian CusterVitalant Research Institute, San Francisco, CA, USA.ORCID http://orcid.org/0000-0001-6251-366X
Shannon KellyUCSF Benioff Children's Hospital, Oakland, CA, USA.ORCID http://orcid.org/0000-0003-2049-3992
Carla Luana DinardoPró-Sangue, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-0453-7863
REDS-III Brazil SCD Cohort study and the TOPMed consortium

Funding

Fundação de Amparo à Pesquisa do Estado de Minas Gerais APQ-01764-16National Institutes of Health, National Heart, Lung, and Blood HHSN2682011NHLBI NIH HHS HHSN268201500015CNHLBI NIH HHS HHSN268201800001C
6 · The paper itself

Abstract

Sickle cell disease (SCD) is a hereditary disorder characterized by HBB variants, leading to chronic hemolytic anemia and vaso-occlusion. Hepatobiliary complications, including cholelithiasis, are common but underreported. This study investigated the rates and risk factors for cholelithiasis, cholecystitis, and cholecystectomy in a large Brazilian SCD cohort. Data from 2,778 individuals across six referral centers in the REDS-III Brazilian SCD cohort were analyzed. Clinical, laboratory, and genetic data were obtained retrospectively at enrollment and prospectively during follow-up. Gallbladder-related outcomes were assessed through medical records and imaging. Whole-genome sequencing was performed via the TOPMed program. Genome-wide association analyses used logistic mixed models adjusted for age, sex, genotype, and the first 10 principal components. Cholelithiasis, cholecystitis, and cholecystectomy occurred in 35.9%, 25.1%, and 10.6% of participants, respectively. Indirect bilirubin was consistently associated with all outcomes, while associations with other laboratory variables varied by genotype. Genetic analyses confirmed associations between UGT1A1 variants and bilirubin levels and identified genome-wide associations with cholecystectomy. Novel loci, including FER1L6, LRFN5, and SDK2, were also implicated. These findings indicate a high burden of gallbladder-related disease in Brazilian individuals with SCD and highlight both established and novel genetic pathways that may inform risk stratification and preventive strategies.

Indexed as

Anemia, Sickle CellCholecystitisCholelithiasisAdolescentAdultBilirubinBrazilCholecystectomyCohort StudiesFemaleGenome-Wide Association StudyGlucuronosyltransferaseHumansMaleMiddle AgedRetrospective StudiesBilirubinGlucuronosyltransferaseUGT1A1 EnzymeCholelithiasisGenome-wide association studyHemolysisSickle cell diseaseUGT1A1 variants

Identifiers

PMID41692868
PMCPMC12907275

What OpenQuestion holds

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Registered trials

None linked

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.