Literature DB >> 34148043

Association between Irritable Bowel Syndrome and Risk of Osteoporosis in Korean Premenopausal Women.

Sang-Yeoup Lee1,2, Hye-Rim Hwang3, Yu-Hyeon Yi2,3, Jin-Mi Kim4, Yun-Jin Kim2,3, Jeong-Gyu Lee2,3, Young-Hye Cho1,2, Young-Jin Tak2,3, Seung Hun Lee2,3, Eun Ju Park1,2, Youngin Lee1,2.   

Abstract

OBJECTIVE: The objective of this study is to evaluate irritable bowel syndrome (IBS) as a risk factor for osteoporosis and osteoporotic fracture in Korean women after controlling for basic confounding factors and considering detailed demographic and clinical information. SUBJECTS AND METHODS: We performed a nationwide population-based retrospective cohort analysis and matched every IBS case with a non-IBS case at a 1:4 frequency ratio based on age. The population consisted of female patients with data in the Health Insurance Review and Assessment (HIRA) database from 2002 to 2010. To determine the risk of osteoporosis and osteoporotic fracture in IBS and non-IBS patients, hazard ratios (HRs) with 95% confidence intervals (CI) were estimated using Cox proportional hazards regression models, adjusting for confounding variables, such as the area of residence, health insurance type, and economic status.
RESULTS: We identified 1,017,468 patients in the HIRA database with data from 2002 to 2010 who could potentially be included in the cohort. Among these, we identified 1,545 (11.4%) women (age >19 years) with newly diagnosed IBS (IBS group). Additionally, 6,180 patients without IBS and age-matched to the IBS group were selected. Cox modeling revealed that the crude HRs for osteoporosis and osteoporotic fractures in patients with IBS were 1.476 (95% CI, 1.241-1.754) and 1.427 (95% CI, 1.086-1.876), respectively.
CONCLUSION: Our data showed an increased incidence of osteoporosis and osteoporotic fractures in women with IBS compared with age-matched controls.
© 2021 The Author(s). Published by S. Karger AG, Basel.

Entities:  

Keywords:  Irritable bowel syndrome; Osteoporosis; Osteoporotic fracture

Mesh:

Year:  2021        PMID: 34148043      PMCID: PMC8738912          DOI: 10.1159/000517909

Source DB:  PubMed          Journal:  Med Princ Pract        ISSN: 1011-7571            Impact factor:   1.927


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