Deciphering the complex interplay between pancreatic cancer, diabetes mellitus subtypes and obesity/BMI through causal inference and mediation analyses.
Aged
Body Mass Index
C-Peptide
/ blood
Case-Control Studies
Causality
Diabetes Mellitus, Type 2
/ complications
Educational Status
Female
Glycated Hemoglobin
/ analysis
Humans
Male
Mediation Analysis
Middle Aged
Obesity
/ complications
Pancreatic Neoplasms
/ complications
Polymorphism, Single Nucleotide
/ genetics
Risk Factors
Sex Factors
Smoking
/ adverse effects
cancer epidemiology
diabetes mellitus
obesity
pancreatic cancer
Journal
Gut
ISSN: 1468-3288
Titre abrégé: Gut
Pays: England
ID NLM: 2985108R
Informations de publication
Date de publication:
02 2021
02 2021
Historique:
received:
03
10
2019
revised:
07
04
2020
accepted:
12
04
2020
pubmed:
16
5
2020
medline:
8
9
2021
entrez:
16
5
2020
Statut:
ppublish
Résumé
To characterise the association between type 2 diabetes mellitus (T2DM) subtypes (new-onset T2DM (NODM) or long-standing T2DM (LSDM)) and pancreatic cancer (PC) risk, to explore the direction of causation through Mendelian randomisation (MR) analysis and to assess the mediation role of body mass index (BMI). Information about T2DM and related factors was collected from 2018 PC cases and 1540 controls from the PanGenEU (European Study into Digestive Illnesses and Genetics) study. A subset of PC cases and controls had glycated haemoglobin, C-peptide and genotype data. Multivariate logistic regression models were applied to derive ORs and 95% CIs. T2DM and PC-related single nucleotide polymorphism (SNP) were used as instrumental variables (IVs) in bidirectional MR analysis to test for two-way causal associations between PC, NODM and LSDM. Indirect and direct effects of the BMI-T2DM-PC association were further explored using mediation analysis. T2DM was associated with an increased PC risk when compared with non-T2DM (OR=2.50; 95% CI: 2.05 to 3.05), the risk being greater for NODM (OR=6.39; 95% CI: 4.18 to 9.78) and insulin users (OR=3.69; 95% CI: 2.80 to 4.86). The causal association between T2DM (57-SNP IV) and PC was not statistically significant (OR Findings of this study do not support a causal effect of LSDM on PC, but suggest that PC causes NODM. The interplay between obesity, PC and T2DM is complex.
Identifiants
pubmed: 32409590
pii: gutjnl-2019-319990
doi: 10.1136/gutjnl-2019-319990
doi:
Substances chimiques
C-Peptide
0
Glycated Hemoglobin A
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
319-329Informations de copyright
© Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: None declared.