Alpha-glucosidase inhibitor decreases the risk of colorectal adenoma in the aged with Type 2 diabetes

Abstract The rapidly aging population is fueling a surge in diabetes, especially Type 2, which heightens colorectal cancer (CRC) risk. Colorectal adenoma, a precursor, compounds this trend. Although alpha-glucosidase inhibitors are effective hypoglycemic drugs working in the GI tract, the link betwe...

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Main Authors: Dingchao Xia, Lanling Jin, Binfeng Wang, Yi Jin, Qun Zheng, Jie Xu, Senzhong Chen
Format: Article
Language:English
Published: Nature Portfolio 2025-01-01
Series:Scientific Reports
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Online Access:https://doi.org/10.1038/s41598-024-84294-3
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author Dingchao Xia
Lanling Jin
Binfeng Wang
Yi Jin
Qun Zheng
Jie Xu
Senzhong Chen
author_facet Dingchao Xia
Lanling Jin
Binfeng Wang
Yi Jin
Qun Zheng
Jie Xu
Senzhong Chen
author_sort Dingchao Xia
collection DOAJ
description Abstract The rapidly aging population is fueling a surge in diabetes, especially Type 2, which heightens colorectal cancer (CRC) risk. Colorectal adenoma, a precursor, compounds this trend. Although alpha-glucosidase inhibitors are effective hypoglycemic drugs working in the GI tract, the link between them and colorectal adenoma formation remains unexplored. A retrospective cross-sectional study was conducted on type 2 diabetes patients aged 60 and above using data from Wenzhou Central Hospital from January 2021 to May 2024. We used multivariable logistic regression and propensity score matching analysis (PSM) to calculate adjusted ORs for colorectal adenoma, controlling for potential confounders. A total of 311 subjects were enrolled in the study, with a mean age of 67.55 years. 138 (44.4%) were diagnosed with colorectal adenoma. Multivariate logistic regression analysis revealed that the AGI (Alpha-glucosidase inhibitor) Group had an adjusted OR of 0.399 (95% CI = 0.22–0.723, p = 0.002) compared to those with AGI free people. A similar trend was also observed in the PSM analysis (OR = 0.362, 95% CI = 0.176–0.744, p = 0.004). Subgroup analysis reveals hypertension as a potential modulator of the inverse relationship between AGI and colorectal adenoma occurrence post-PSM (p = 0.049). And AGI reduces serum iron levels, both before (p = 0.01) and after PSM (p = 0.028). In summary, our findings indicate that AGI significantly mitigates the risk of colorectal adenoma among individuals aged 60 and above, particularly among those afflicted with hypertension. Additionally, it substantially decreases serum iron levels.
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spelling doaj-art-e5843b7542c943338f1f29ab9a4a3a4f2025-01-05T12:16:48ZengNature PortfolioScientific Reports2045-23222025-01-0115111110.1038/s41598-024-84294-3Alpha-glucosidase inhibitor decreases the risk of colorectal adenoma in the aged with Type 2 diabetesDingchao Xia0Lanling Jin1Binfeng Wang2Yi Jin3Qun Zheng4Jie Xu5Senzhong Chen6Department of Infectious Diseases, Wenzhou Central HospitalDepartment of Neurology, Pujiang County People’s HospitalDepartment of Gastroenterology, Affiliated Yueqing Hospital,Wenzhou Medical UniversityDepartment of Rheumatology, The Second Affiliated Hospital of Wenzhou Medical UniversityDepartment of Rheumatology, The Second Affiliated Hospital of Wenzhou Medical UniversityDepartment of Rheumatology, The Second Affiliated Hospital of Wenzhou Medical UniversityDepartment of Gerontology, Wenzhou Central HospitalAbstract The rapidly aging population is fueling a surge in diabetes, especially Type 2, which heightens colorectal cancer (CRC) risk. Colorectal adenoma, a precursor, compounds this trend. Although alpha-glucosidase inhibitors are effective hypoglycemic drugs working in the GI tract, the link between them and colorectal adenoma formation remains unexplored. A retrospective cross-sectional study was conducted on type 2 diabetes patients aged 60 and above using data from Wenzhou Central Hospital from January 2021 to May 2024. We used multivariable logistic regression and propensity score matching analysis (PSM) to calculate adjusted ORs for colorectal adenoma, controlling for potential confounders. A total of 311 subjects were enrolled in the study, with a mean age of 67.55 years. 138 (44.4%) were diagnosed with colorectal adenoma. Multivariate logistic regression analysis revealed that the AGI (Alpha-glucosidase inhibitor) Group had an adjusted OR of 0.399 (95% CI = 0.22–0.723, p = 0.002) compared to those with AGI free people. A similar trend was also observed in the PSM analysis (OR = 0.362, 95% CI = 0.176–0.744, p = 0.004). Subgroup analysis reveals hypertension as a potential modulator of the inverse relationship between AGI and colorectal adenoma occurrence post-PSM (p = 0.049). And AGI reduces serum iron levels, both before (p = 0.01) and after PSM (p = 0.028). In summary, our findings indicate that AGI significantly mitigates the risk of colorectal adenoma among individuals aged 60 and above, particularly among those afflicted with hypertension. Additionally, it substantially decreases serum iron levels.https://doi.org/10.1038/s41598-024-84294-3AgedColorectal adenomaT2DMAlpha-glucosidase inhibitor
spellingShingle Dingchao Xia
Lanling Jin
Binfeng Wang
Yi Jin
Qun Zheng
Jie Xu
Senzhong Chen
Alpha-glucosidase inhibitor decreases the risk of colorectal adenoma in the aged with Type 2 diabetes
Scientific Reports
Aged
Colorectal adenoma
T2DM
Alpha-glucosidase inhibitor
title Alpha-glucosidase inhibitor decreases the risk of colorectal adenoma in the aged with Type 2 diabetes
title_full Alpha-glucosidase inhibitor decreases the risk of colorectal adenoma in the aged with Type 2 diabetes
title_fullStr Alpha-glucosidase inhibitor decreases the risk of colorectal adenoma in the aged with Type 2 diabetes
title_full_unstemmed Alpha-glucosidase inhibitor decreases the risk of colorectal adenoma in the aged with Type 2 diabetes
title_short Alpha-glucosidase inhibitor decreases the risk of colorectal adenoma in the aged with Type 2 diabetes
title_sort alpha glucosidase inhibitor decreases the risk of colorectal adenoma in the aged with type 2 diabetes
topic Aged
Colorectal adenoma
T2DM
Alpha-glucosidase inhibitor
url https://doi.org/10.1038/s41598-024-84294-3
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