Evidence map›Paper›PMID 39115133›Full record

ArticleThe Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology2024

Clinical and Molecular Analysis in Patients with Peutz-Jeghers Syndrome.

Pınar Güney Aslan, Ahmet Okay Çağlayan, Elçin Bora, Altuğ Koç, Hilal Yücel, Ayfer Ülgenalp, Yeşim Öztürk, Gül Şeker, Mesut Akarsu

Abstract read
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Article in The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology, 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
–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

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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

2 citing papers in PubMed.

  1. Article
  2. 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

9 authors.

Pınar Güney AslanDepartment of Internal Medicine, Dokuz Eylül University School of Medicine, İzmir, Turkey.
Ahmet Okay ÇağlayanDepartment of Medical Genetics, Dokuz Eylül University School of Medicine, İzmir, Turkey.
Elçin BoraDepartment of Medical Genetics, Dokuz Eylül University School of Medicine, İzmir, Turkey.
Altuğ KoçDepartment of Medical Genetics, Dokuz Eylül University School of Medicine, İzmir, Turkey.
Hilal YücelDepartment of Medical Genetics, Dokuz Eylül University School of Medicine, İzmir, Turkey.
Ayfer ÜlgenalpDepartment of Medical Genetics, Dokuz Eylül University School of Medicine, İzmir, Turkey.
Yeşim ÖztürkDivision of Pediatric Gastroenterology, Department of Pediatrics, Dokuz Eylül University School of Medicine, İzmir, Turkey.
Gül ŞekerDivision of Pediatric Gastroenterology, Department of Pediatrics, Dokuz Eylül University School of Medicine, İzmir, Turkey.
Mesut AkarsuDivision of Gastroenterology, Department of Internal Medicine, Dokuz Eylül University School of Medicine, İzmir, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peutz-Jeghers syndrome (PJS) is a rare hereditary disorder linked to increased cancer risk due to specific genetic variants in the STK11 gene. This study aimed to assess disease manifestations, genetic profiles, and genotype-phenotype correlations in PJS patients. Twenty patients from 14 families with PJS who were followed up at our clinic between 2011 and 2021 were included. Genetic susceptibility to hereditary cancers was assess-ed using targeted next-generation sequencing (NGS) and multiplex ligation-dependent probe amplification (MLPA) of the STK11 gene. Clinical data were also collected and analyzed in conjunction with the genetic findings. Initial symptoms appeared around 18.9 years, predominantly abdominal pain and intussusception. Mucocutaneous lesions were found in 85%, and hamartomatous polyps in 90%. Dysplastic polyps were found in 4 patients, with 3 cases of malignancy. Nextgeneration sequencing identified 11 pathogenic and 3 likely pathogenic mutations, including 3 novel STK11 variants (LRG_319: c.598- 8_601del, LRG_319: c.708_718del, and LRG_319: c.146_147del). Next-generation sequencing diagnostic rate was 78.5% (11/14), and the overall diagnostic rate with NGS and MLPA studies was 85.7% (12/14). Patients without STK11 mutations had later symptom onset and potentially lower cancer risk. Truncated mutations are associated with earlier symptoms and elevated cancer risk. This is the first PJS case series in Turkey using the NGS and MLPA methods. It reports 3 novel mutations and emphasizes the genotype-phenotype relationship of PJS. With further studies, the genotype-phenotype relationship of STK11 variants will be better understood.

Indexed as

AMP-Activated Protein Kinase KinasesGenetic Predisposition to DiseaseHigh-Throughput Nucleotide SequencingPeutz-Jeghers SyndromeProtein Serine-Threonine KinasesAbdominal PainAdolescentAdultChildFemaleGenetic Association StudiesHumansMaleMiddle AgedMultiplex Polymerase Chain ReactionMutationAMP-Activated Protein Kinase KinasesProtein Serine-Threonine KinasesSTK11 protein, human

Identifiers

PMID39115133
PMCPMC11181252

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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.