Evidence map›Paper›PMID 41014487›Full record

ArticleClinical genetics2026

Mapping the Prevalence of Lynch Syndrome in the Ceará-Northeast of Brazil.

Maria Claudia Dos Santos Luciano, Paulo Goberlanio de Barros Silva, Rosane Oliveira de Sant'Ana, Clarissa Gondim Picanço de Albuquerque, Francisca Fernanda Barbosa Oliveira, Flavio da Silveira Bitencourt, Isabelle Joyce de Lima Silva Fernandes, José Fernando Bastos Moura, Maria Júlia Barbosa Bezerra

Abstract read
In one paragraph

Article in Clinical genetics, 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

9 authors.

Maria Claudia Dos Santos LucianoInstituto Do Câncer Do Ceará/Faculdade Rodolfo Teófilo, Fortaleza, Brazil.ORCID 0000-0002-7871-2513
Paulo Goberlanio de Barros SilvaInstituto Do Câncer Do Ceará/Faculdade Rodolfo Teófilo, Fortaleza, Brazil.
Rosane Oliveira de Sant'AnaInstituto Do Câncer Do Ceará/Faculdade Rodolfo Teófilo, Fortaleza, Brazil.
Clarissa Gondim Picanço de AlbuquerqueInstituto Do Câncer Do Ceará/Faculdade Rodolfo Teófilo, Fortaleza, Brazil.
Francisca Fernanda Barbosa OliveiraInstituto Do Câncer Do Ceará/Faculdade Rodolfo Teófilo, Fortaleza, Brazil.ORCID 0000-0003-3060-1395
Flavio da Silveira BitencourtInstituto Do Câncer Do Ceará/Faculdade Rodolfo Teófilo, Fortaleza, Brazil.
Isabelle Joyce de Lima Silva FernandesInstituto Do Câncer Do Ceará/Faculdade Rodolfo Teófilo, Fortaleza, Brazil.
José Fernando Bastos MouraInstituto Do Câncer Do Ceará/Faculdade Rodolfo Teófilo, Fortaleza, Brazil.
Maria Júlia Barbosa BezerraInstituto Do Câncer Do Ceará/Faculdade Rodolfo Teófilo, Fortaleza, Brazil.

Funding

National Oncology Care Support Program (PRONON) 25000.083638/2015-93
6 · The paper itself

Abstract

Lynch syndrome (LS) is an autosomal dominant hereditary disorder that increases the risk of various cancers, especially colorectal (CRC) and endometrial cancer (EC). It results from pathogenic variants in mismatch repair (MMR) genes-primarily MLH1, MSH2, MSH6, and PMS2. Population-specific variant frequencies emphasize the need for localized genetic studies. Methods This study investigated LS prevalence in Ceará, Northeast Brazil, analyzing 150 patients: 130 with CRC, 13 with endometrial cancer, and 7 with other tumors but a family history of LS-associated cancers. Researchers used next-generation sequencing (NGS) to examine 131 genes linked to hereditary cancer syndromes. Variants were classified as Lynch-syndrome associated (MMR genes) or non-Lynch-associated (non-MMR genes). Detection rates varied from 1.18 to 5.07 per 100,000 people; pathogenic variant prevalence ranged from 0 to 1.96 per 100,000 across microregions. Overall, the prevalence of MMR variants was 0.56 per 100,000, and 0.34 for non-MMR variants. MSH2 showed the highest number of pathogenic or likely pathogenic variants, followed by MSH6, PMS2, and MLH1. The study found a particular geographic distribution of LS-related variants. One novel MSH6 variant and two unreported non-Lynch variants (APC and SMAD4) were identified. Conclusions These findings highlight three novel variants in MSH6, APC, and SMAD4, and indicate that Ceará has a higher diversity and a unique spectrum of variants. This reinforces the importance of regional genetic screening and suggests the need to expand testing access, especially in high-risk areas, to improve the early detection and prevention of hereditary cancers in Northeast Brazil.

Indexed as

Colorectal Neoplasms, Hereditary NonpolyposisGenetic Predisposition to DiseaseAdultAgedBrazilDNA-Binding ProteinsDNA Mismatch RepairFemaleHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedMismatch Repair Endonuclease PMS2MutL Protein Homolog 1MutS Homolog 2 ProteinPrevalenceDNA-Binding ProteinsMismatch Repair Endonuclease PMS2MutL Protein Homolog 1MutS Homolog 2 ProteinPMS2 protein, humancolorectal cancergenetic evaluationnovel variant

Identifiers

PMID41014487
PMCPMC12958010

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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.