Evidence map›Paper›PMID 37564037›Full record

ArticleFrontiers in medicine2023

Prediction of the occurrence of leprosy reactions based on Bayesian networks.

Rafael Saraiva de Andrade Rodrigues, Eduardo Ferreira José Heise, Luis Felipe Hartmann, Guilherme Eduardo Rocha, Marcia Olandoski, Mariane Martins de Araújo Stefani, Ana Carla Pereira Latini, Cleverson Teixeira Soares, Andrea Belone, Patrícia Sammarco Rosa and 11 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% of its field
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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
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

21 authors at 8 institutions in 2 countries.

Rafael Saraiva de Andrade RodriguesSchool of Medicine and Life Sciences, Graduate Program in Health Sciences, Pontifícia Universidade Católica do Paraná - PUCPR, Curitiba, Paraná, Brazil.
Eduardo Ferreira José HeiseSchool of Medicine and Life Sciences, Graduate Program in Health Sciences, Pontifícia Universidade Católica do Paraná - PUCPR, Curitiba, Paraná, Brazil.
Luis Felipe HartmannGraduate Program in Health Technology, PUCPR, Curitiba, Paraná, Brazil.
Guilherme Eduardo RochaGraduate Program in Health Technology, PUCPR, Curitiba, Paraná, Brazil.
Marcia OlandoskiSchool of Medicine and Life Sciences, Graduate Program in Health Sciences, Pontifícia Universidade Católica do Paraná - PUCPR, Curitiba, Paraná, Brazil.
Mariane Martins de Araújo StefaniTropical Pathology and Public Health Institute, Federal University of Goiás, Goiania, Brazil.
Ana Carla Pereira LatiniInstituto Lauro de Souza Lima, Bauru, São Paulo, Brazil.
Cleverson Teixeira SoaresInstituto Lauro de Souza Lima, Bauru, São Paulo, Brazil.
Andrea BeloneInstituto Lauro de Souza Lima, Bauru, São Paulo, Brazil.
Patrícia Sammarco RosaInstituto Lauro de Souza Lima, Bauru, São Paulo, Brazil.
Maria Araci de Andrade PontesDona Libânia Dermatology Centre, Ceará, Brazil.
Heitor de Sá GonçalvesDona Libânia Dermatology Centre, Ceará, Brazil.
Rossilene CruzTropical Dermatology and Venerology Alfredo da Matta Foundation, Amazonas, Brazil.
Maria Lúcia Fernandes PennaEpidemiology and Biostatistics Department, Federal University Fluminense, Rio de Janeiro, Brazil.
Deborah Ribeiro CarvalhoGraduate Program in Health Technology, PUCPR, Curitiba, Paraná, Brazil.
Vinicius Medeiros FavaProgram in Infectious Diseases and Immunity in Global Health, Research Institute of the McGill University Health Centre, and The McGill International TB Centre, Departments of Human Genetics and Medicine, McGill University, Montreal, QC, Canada.
Samira Bührer-SékulaTropical Pathology and Public Health Institute, Federal University of Goiás, Goiania, Brazil.
Gerson Oliveira PennaTropical Medicine Centre, University of Brasília, and Fiocruz School of Government - Brasilia, Brasília, Brazil.
Claudia Maria Cabral MoroGraduate Program in Health Technology, PUCPR, Curitiba, Paraná, Brazil.
Julio Cesar NievolaGraduate Program in Informatics, PUCPR, Curitiba, Paraná, Brazil.
Marcelo Távora MiraSchool of Medicine and Life Sciences, Graduate Program in Health Sciences, Pontifícia Universidade Católica do Paraná - PUCPR, Curitiba, Paraná, Brazil.
Pontifícia Universidade Católica do Paraná · BRInstituto Lauro de Souza Lima · BRInstituto de Dermatologia Dona Libania · BRUniversidade Federal de Goiás · BRBrazilian Society of Tropical Medicine · BRFundação de Medicina Tropical · BRMcGill University Health Centre · CAUniversidade Federal Fluminense · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Leprosy reactions (LR) are severe episodes of intense activation of the host inflammatory response of uncertain etiology, today the leading cause of permanent nerve damage in leprosy patients. Several genetic and non-genetic risk factors for LR have been described; however, there are limited attempts to combine this information to estimate the risk of a leprosy patient developing LR. Here we present an artificial intelligence (AI)-based system that can assess LR risk using clinical, demographic, and genetic data. Methods: The study includes four datasets from different regions of Brazil, totalizing 1,450 leprosy patients followed prospectively for at least 2 years to assess the occurrence of LR. Data mining using WEKA software was performed following a two-step protocol to select the variables included in the AI system, based on Bayesian Networks, and developed using the NETICA software. Results: Analysis of the complete database resulted in a system able to estimate LR risk with 82.7% accuracy, 79.3% sensitivity, and 86.2% specificity. When using only databases for which host genetic information associated with LR was included, the performance increased to 87.7% accuracy, 85.7% sensitivity, and 89.4% specificity. Conclusion: We produced an easy-to-use, online, free-access system that identifies leprosy patients at risk of developing LR. Risk assessment of LR for individual patients may detect candidates for close monitoring, with a potentially positive impact on the prevention of permanent disabilities, the quality of life of the patients, and upon leprosy control programs.

Indexed as

artificial intelligenceBayesian networksleprosyleprosy reactionsrisk

Identifiers

PMID37564037
PMCPMC10411956
OpenAlexW4385281785

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.