Impact of high body mass index on hepatocellular carcinoma risk in chronic liver disease: A population-based prospective cohort study
- Abstract
- Background and aims: We investigated associations between body mass index (BMI) and hepatocellular carcinoma (HCC) in patients with hepatitis B (HBV) C (HCV) virus infection, alcoholic liver disease (ALD), non-alcoholic fatty liver disease (NAFLD), and liver cirrhosis (LC).
Methods: We followed 350,608 Korean patients with liver disease who underwent routine health examinations from 2003-2006 until December 2018 via national hospital discharge records. Multivariable adjusted hazard ratios (HRs) per 5-kg/m2 BMI increase (BMI ≥25 kg/m2) for HCC risk were calculated using Cox models. HCC developed in 17,752 patients.
Results: The HRs (95% CI) were 1.17 (1.06-1.28), 1.08 (0.87-1.34), 1.34 (1.14-1.58), 1.51 (1.17-1.94), and 1.11 (1.00-1.23) for HBV, HCV, ALD, NAFLD, and LC, respectively. The HRs for HBV were 1.45 (1.23-1.70) and 1.06 (0.95-1.19) in women and men, respectively; the corresponding HRs for LC were 1.27 (1.07-1.50) and 1.02 (0.90-1.16), respectively. In patients <65 years old with HBV, HCV, and NAFLD, the HRs were 1.17 (1.07-1.29), 1.33 (1.03-1.73), and 1.20 (0.87-1.64), respectively; the corresponding HRs were 1.05 (0.70-1.59), 0.74 (0.50-1.10), and 2.40 (1.62-3.54), respectively, in patients ≥65 years old. A BMI of 27.5-29.9 kg/m2 showed significantly higher HCC risks in patients with HBV, ALD, NAFLD, and LC.
Conclusions: Higher BMIs were associated with increased HCC risks in patients with HBV, ALD, NAFLD, and LC. Overweight status increased HCC risk. Women with HBV and LC had stronger BMI-HCC associations than men. The effect of high BMI was stronger in older patients with NAFLD and younger patients with viral hepatitis.
- All Author(s)
- Moonho Kim
; Baek Gyu Jun
; Hwang Sik Shin
; Jee-Jeon Yi
; Sang Gyune Kim
; Sang-Wook Yi
- Intsitutional Author(s)
- 신황식
- Issued Date
- 2025
- Type
- Article
- Publisher
- Public Library of Science
- ISSN
- 1932-6203
- Citation Title
- PloS one
- Citation Volume
- 20
- Citation Number
- 1
- Citation Start Page
- e0316175
- Citation End Page
- e0316175
- Language(ISO)
- eng
- DOI
- 10.1371/journal.pone.0316175
- URI
- http://schca-ir.schmc.ac.kr/handle/2022.oak/4776
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