Evidence map›Paper›PMID 38947744›Full record

ArticleEndoscopic ultrasound

New-onset diabetes is a predictive risk factor for pancreatic lesions in high-risk individuals: An observational cohort study.

Seyda Baydogan, Chirayu Mohindroo, Merve Hasanov, Maria F Montiel, Pompeyo Quesada, Irina M Cazacu, Adrianna A Luzuriaga Chavez, Maureen E Mork, Wenli Dong, Lei Feng and 11 more

Abstract read
In one paragraph

Article in Endoscopic ultrasound. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
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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.

Seyda BaydoganDepartments of Clinical Cancer Prevention the University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Chirayu MohindrooDepartments of Clinical Cancer Prevention the University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Merve HasanovDepartments of Clinical Cancer Prevention the University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Maria F MontielDepartments of Clinical Cancer Prevention the University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Pompeyo QuesadaDepartments of Clinical Cancer Prevention the University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Irina M CazacuDepartment of Gastroenterology, Hepatology, and Nutrition, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Adrianna A Luzuriaga ChavezDepartment of Gastroenterology, Hepatology, and Nutrition, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Maureen E MorkClinical Cancer Genetics Program, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Wenli DongDepartments of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Lei FengDepartments of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Y Nancy YouClinical Cancer Genetics Program, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Banu ArunClinical Cancer Genetics Program, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Eduardo VilarDepartments of Clinical Cancer Prevention the University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Powel BrownDepartments of Clinical Cancer Prevention the University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Matthew H G KatzDepartment of Colon and Rectal Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Suresh T ChariDepartment of Gastroenterology, Hepatology, and Nutrition, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Anirban MaitraDepartment of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Eric P TammDepartments of Radiology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Michael P KimDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Manoop S BhutaniDepartment of Gastroenterology, Hepatology, and Nutrition, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Florencia McAllisterDepartments of Clinical Cancer Prevention the University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Funding

Dissecting the Source and Mechanisms of IL-17-Mediated Modulation of Pancreatic TumorigenesisR37CA237384 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MCALLISTER, FLORENCIA · 2020 to 2025
$2.6M
NCI NIH HHS R37 CA237384
6 · The paper itself

Abstract

Background and Objectives: Pancreatic cancer (PC) is the third cause of cancer-related deaths. Early detection and interception of premalignant pancreatic lesions represent a promising strategy to improve outcomes. We evaluated risk factors of focal pancreatic lesions (FPLs) in asymptomatic individuals at hereditary high risk for PC. Methods: This is an observational single-institution cohort study conducted over a period of 5 years. Surveillance was performed through imaging studies (EUS or magnetic resonance imaging/magnetic resonance cholangiopancreatography) and serum biomarkers. We collected demographic characteristics and used univariate and multivariate logistic regression models to evaluate associations between potential risk factors and odd ratios (ORs) for FPL development. Results: A total of 205 patients completed baseline screening. Patients were followed up to 53 months. We detected FPL in 37 patients (18%) at baseline; 2 patients had lesions progression during follow-up period, 1 of them to PC. Furthermore, 13 patients developed new FPLs during the follow-up period. Univariate and multivariate analyses revealed that new-onset diabetes (NOD) is strongly associated with the presence of FPL (OR, 10.94 [95% confidence interval, 3.01-51.79; Conclusions: In a PC high-risk cohort, NOD is significantly associated with presence of FPL at baseline and predictive of lesions progression or new lesions during surveillance.

Indexed as

Early detectionEUSFocal pancreatic lesionsGermline mutationsMRI/MRCPNew-onset diabetes

Identifiers

PMID38947744
PMCPMC11213578

What OpenQuestion holds

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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.