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Do renin-angiotensin system inhibitors reduce risk for hepatocellular carcinoma?: A nationwide nested case-control
Kwang Min Kim1, Ji Hye Roh2, Sangjin Lee3
1Department of Medicine, Samsung Changwon Hospital, Sungkyunkwan University School of Medicine, Changwon, South Korea.
Background:
To date, there has been a renewed interest in renin-angiotensin system inhibitors (RASi) for HCC prevention because they may reduce potent angiogenic factors.
Objectives:
This study set out to investigate associations between RASi use and HCC development.
Methods:
We conducted a nested case-control study. A case was defined as a patient who was newly diagnosed with HCC. We selected 567 cases and controls using 1:1 propensity score matching. RASi exposure was classified into ever-user and never-user, then categorized according to cumulative dose and prescription period. Adjusted odds ratios (aORs) and 95% confidence intervals (CIs) for HCC incidence according to RASi use were analyzed.
Results:
Overall, no significant association was found between exposure to RASi and HCC incidence (ever-user vs. never-user: aOR, 0.77; 95% CI, 0.56-1.07). In subgroup analysis, women receiving RASi ≥30 cumulative defined daily doses (cDDDs) showed significantly lower aORs (0.49; 95% CI, 0.24-0.95. Angiotensin II receptor blockers only-use ≥30 cDDD was significantly associated with reduced risk of HCC (aOR, 0.65; 95% CI, 0.43-0.97). In cases where subjects did not have diabetes mellitus and where the cDDD of RASi was 1800 or more, the risk of HCC development was significantly reduced compared to that in subjects with no RASi exposure (aOR, 0.26; 95% CI, 0.08-0.72).
Conclusion:
The present study did not verify a significant overall association between RASi use and HCC but indicated lower HCC incidence in some subgroups. The possibility of a beneficial effect at a higher cumulative RASi dose was also presented.
Insights
Renin-angiotensin system inhibitors (RASi) showed no overall association with liver cancer (HCC) prevention. However, specific subgroups, particularly women and those with higher cumulative doses, experienced a reduced risk of HCC development.
Area of Science:
- Oncology
- Pharmacology
- Cardiovascular Medicine
Background:
- Growing interest in renin-angiotensin system inhibitors (RASi) for hepatocellular carcinoma (HCC) prevention due to potential anti-angiogenic effects.
- Previous research suggests a possible role for RASi in mitigating HCC development.
Purpose of the Study:
- To investigate the association between the use of renin-angiotensin system inhibitors (RASi) and the incidence of hepatocellular carcinoma (HCC).
Main Methods:
- A nested case-control study design involving 567 HCC cases and matched controls.
- Propensity score matching (1:1) was utilized to ensure comparability between cases and controls.
- RASi exposure was assessed based on ever-user/never-user status, cumulative dose, and prescription duration, with adjusted odds ratios (aORs) calculated.
Main Results:
- No significant overall association was observed between RASi use and HCC incidence (aOR, 0.77; 95% CI, 0.56-1.07).
- Subgroup analyses revealed a significant reduction in HCC risk for women receiving RASi (aOR, 0.49; 95% CI, 0.24-0.95) and with Angiotensin II Receptor Blocker (ARB)-only use (aOR, 0.65; 95% CI, 0.43-0.97) at higher cumulative doses (≥30 cDDDs).
- A notable decrease in HCC risk was observed in non-diabetic subjects with very high cumulative RASi doses (≥1800 cDDD) (aOR, 0.26; 95% CI, 0.08-0.72).
Conclusions:
- The study did not confirm a significant overall protective effect of RASi against HCC.
- A potential benefit of RASi in reducing HCC incidence was suggested in specific patient subgroups, particularly at higher cumulative doses.
- Further investigation into the dose-dependent effects and specific patient populations may be warranted.
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