Cargando…

Risk of pancreatic cancer in individuals with celiac disease in the United States: A population-based matched cohort study

BACKGROUND: Celiac disease (CD) has been associated with gastrointestinal malignancies. However, the magnitude of the risk of pancreatic cancer (PC) associated with CD is much less clear, and risks have not been estimated from large populations. AIM: To assess the risk of PC in CD patients. METHODS:...

Descripción completa

Detalles Bibliográficos
Autores principales: Krishnan, Arunkumar, Hadi, Yousaf Bashir, Shabih, Sarah, Mukherjee, Diptasree, Patel, Ruhee A, Patel, Rushik, Singh, Shailendra, Thakkar, Shyam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10052666/
https://www.ncbi.nlm.nih.gov/pubmed/37009321
http://dx.doi.org/10.4251/wjgo.v15.i3.523
_version_ 1785015213057114112
author Krishnan, Arunkumar
Hadi, Yousaf Bashir
Shabih, Sarah
Mukherjee, Diptasree
Patel, Ruhee A
Patel, Rushik
Singh, Shailendra
Thakkar, Shyam
author_facet Krishnan, Arunkumar
Hadi, Yousaf Bashir
Shabih, Sarah
Mukherjee, Diptasree
Patel, Ruhee A
Patel, Rushik
Singh, Shailendra
Thakkar, Shyam
author_sort Krishnan, Arunkumar
collection PubMed
description BACKGROUND: Celiac disease (CD) has been associated with gastrointestinal malignancies. However, the magnitude of the risk of pancreatic cancer (PC) associated with CD is much less clear, and risks have not been estimated from large populations. AIM: To assess the risk of PC in CD patients. METHODS: We conducted a population-based, multicenter, propensity score-matched cohort study with consecutive patients diagnosed with CD using the TriNeTx research network platform. We examined the incidence of PC in patients with CD compared with a matched cohort of patients without CD (non-CD, controls). Each patient in the main group (CD) was matched to a patient in the control group using 1:1 propensity score matching to reduce confounding effects. The incidence of PC was estimated using a Cox proportional hazards model with a hazard ratio (HR) and 95% confidence interval (CI). RESULTS: A total of 389980 patients were included in this study. Among them, 155877 patients had a diagnosis of CD, and the remaining 234103 individuals without CD were considered a control cohort. The mean duration of follow-up for patients in the CD and control cohorts was 5.8 ± 1.8 and 5.9 ± 1.1 years, respectively. During the follow-up, 309 patients with CD developed PC, whereas 240 patients developed PC in the control group (HR = 1.29; 95%CI: 1.09-1.53). In the secondary analyses in the first year after diagnosis of CD, patients with CD were at a significant increase in risk for PC; 151 patients with CD had an incidence of PC compared with 96 incidences of PC among the patients in the non-CD control group (HR = 1.56; 95%CI: 1.20-2.01) and sensitivity analysis showed similar magnitude to the one generated in the primary and secondary analysis. CONCLUSION: Patients with CD are at increased risk of PC. Risk elevation persists beyond the first year after diagnosis to reference individuals without CD from the general population.
format Online
Article
Text
id pubmed-10052666
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Baishideng Publishing Group Inc
record_format MEDLINE/PubMed
spelling pubmed-100526662023-03-30 Risk of pancreatic cancer in individuals with celiac disease in the United States: A population-based matched cohort study Krishnan, Arunkumar Hadi, Yousaf Bashir Shabih, Sarah Mukherjee, Diptasree Patel, Ruhee A Patel, Rushik Singh, Shailendra Thakkar, Shyam World J Gastrointest Oncol Retrospective Cohort Study BACKGROUND: Celiac disease (CD) has been associated with gastrointestinal malignancies. However, the magnitude of the risk of pancreatic cancer (PC) associated with CD is much less clear, and risks have not been estimated from large populations. AIM: To assess the risk of PC in CD patients. METHODS: We conducted a population-based, multicenter, propensity score-matched cohort study with consecutive patients diagnosed with CD using the TriNeTx research network platform. We examined the incidence of PC in patients with CD compared with a matched cohort of patients without CD (non-CD, controls). Each patient in the main group (CD) was matched to a patient in the control group using 1:1 propensity score matching to reduce confounding effects. The incidence of PC was estimated using a Cox proportional hazards model with a hazard ratio (HR) and 95% confidence interval (CI). RESULTS: A total of 389980 patients were included in this study. Among them, 155877 patients had a diagnosis of CD, and the remaining 234103 individuals without CD were considered a control cohort. The mean duration of follow-up for patients in the CD and control cohorts was 5.8 ± 1.8 and 5.9 ± 1.1 years, respectively. During the follow-up, 309 patients with CD developed PC, whereas 240 patients developed PC in the control group (HR = 1.29; 95%CI: 1.09-1.53). In the secondary analyses in the first year after diagnosis of CD, patients with CD were at a significant increase in risk for PC; 151 patients with CD had an incidence of PC compared with 96 incidences of PC among the patients in the non-CD control group (HR = 1.56; 95%CI: 1.20-2.01) and sensitivity analysis showed similar magnitude to the one generated in the primary and secondary analysis. CONCLUSION: Patients with CD are at increased risk of PC. Risk elevation persists beyond the first year after diagnosis to reference individuals without CD from the general population. Baishideng Publishing Group Inc 2023-03-15 2023-03-15 /pmc/articles/PMC10052666/ /pubmed/37009321 http://dx.doi.org/10.4251/wjgo.v15.i3.523 Text en ©The Author(s) 2023. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Retrospective Cohort Study
Krishnan, Arunkumar
Hadi, Yousaf Bashir
Shabih, Sarah
Mukherjee, Diptasree
Patel, Ruhee A
Patel, Rushik
Singh, Shailendra
Thakkar, Shyam
Risk of pancreatic cancer in individuals with celiac disease in the United States: A population-based matched cohort study
title Risk of pancreatic cancer in individuals with celiac disease in the United States: A population-based matched cohort study
title_full Risk of pancreatic cancer in individuals with celiac disease in the United States: A population-based matched cohort study
title_fullStr Risk of pancreatic cancer in individuals with celiac disease in the United States: A population-based matched cohort study
title_full_unstemmed Risk of pancreatic cancer in individuals with celiac disease in the United States: A population-based matched cohort study
title_short Risk of pancreatic cancer in individuals with celiac disease in the United States: A population-based matched cohort study
title_sort risk of pancreatic cancer in individuals with celiac disease in the united states: a population-based matched cohort study
topic Retrospective Cohort Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10052666/
https://www.ncbi.nlm.nih.gov/pubmed/37009321
http://dx.doi.org/10.4251/wjgo.v15.i3.523
work_keys_str_mv AT krishnanarunkumar riskofpancreaticcancerinindividualswithceliacdiseaseintheunitedstatesapopulationbasedmatchedcohortstudy
AT hadiyousafbashir riskofpancreaticcancerinindividualswithceliacdiseaseintheunitedstatesapopulationbasedmatchedcohortstudy
AT shabihsarah riskofpancreaticcancerinindividualswithceliacdiseaseintheunitedstatesapopulationbasedmatchedcohortstudy
AT mukherjeediptasree riskofpancreaticcancerinindividualswithceliacdiseaseintheunitedstatesapopulationbasedmatchedcohortstudy
AT patelruheea riskofpancreaticcancerinindividualswithceliacdiseaseintheunitedstatesapopulationbasedmatchedcohortstudy
AT patelrushik riskofpancreaticcancerinindividualswithceliacdiseaseintheunitedstatesapopulationbasedmatchedcohortstudy
AT singhshailendra riskofpancreaticcancerinindividualswithceliacdiseaseintheunitedstatesapopulationbasedmatchedcohortstudy
AT thakkarshyam riskofpancreaticcancerinindividualswithceliacdiseaseintheunitedstatesapopulationbasedmatchedcohortstudy