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Effect of urate-lowering therapy on all-cause and CVD-specific mortality in gout and hyperuricemia: a meta-analysis
1Department of Rheumatology, Korea University Anam Hospital, Korea University College of Medicine, 73, Goryeodae-ro, Seongbuk-gu, 02841, Seoul, Korea (Republic of). lyhcgh@korea.ac.kr.
Insights
Urate-lowering therapy (ULT) significantly reduces all-cause mortality in patients with gout or hyperuricemia. While ULT benefits overall survival, allopurinol did not significantly impact cardiovascular disease-specific mortality in this meta-analysis.
Area of Science:
- Rheumatology and Clinical Pharmacology
- Cardiovascular Epidemiology
- Public Health and Mortality Studies
Background:
- Gout and hyperuricemia are associated with increased mortality risks, particularly from cardiovascular causes.
- Urate-lowering therapy (ULT) aims to reduce serum uric acid levels, but its impact on long-term survival requires comprehensive evaluation.
- Understanding the differential effects of ULT on all-cause versus cardiovascular disease (CVD)-specific mortality is crucial for patient management.
Purpose of the Study:
- To investigate the association between urate-lowering therapy (ULT) and both all-cause and cardiovascular disease (CVD)-specific mortality in individuals with gout or hyperuricemia.
- To synthesize evidence from existing literature to quantify the mortality risks associated with ULT use in these patient populations.
Main Methods:
- A systematic meta-analysis was performed, including 11 comparative studies with a total of 38,396 ULT users and 47,530 controls.
- Literature search was conducted across PubMed, Embase, and Cochrane databases to identify relevant hazard ratios (HRs) for all-cause and CVD-specific mortality.
- Statistical analysis was employed to evaluate the pooled HRs and their corresponding confidence intervals (CIs) for mortality outcomes.
Main Results:
- ULT significantly reduced the risk of all-cause mortality in patients with gout or hyperuricemia (HR = 0.783, 95% CI = 0.702-0.874).
- Both ULT (HR = 0.651) and allopurinol (HR = 0.836) were associated with decreased all-cause mortality.
- ULT significantly lowered CVD-specific mortality in hyperuricemia patients (HR = 0.872) but not in gout patients (HR = 0.676).
Conclusions:
- Urate-lowering therapy (ULT) demonstrates a substantial benefit in reducing all-cause mortality for patients suffering from gout or hyperuricemia.
- Allopurinol, a common ULT, did not show a significant impact on cardiovascular disease-specific mortality in this meta-analysis.
- These findings highlight the significant potential of ULT in improving survival rates among specific patient groups with high uric acid levels.
Objective:
The aim of this study was to assess the relationships between urate-lowering therapy (ULT) and both all-cause and cardiovascular disease (CVD)-specific mortality in patients diagnosed with gout or hyperuricemia.
Methods:
The PubMed, Embase, and Cochrane databases were thoroughly searched to gather literature on overall and/or CVD-specific hazard ratios (HRs) of patients with gout or hyperuricemia. A meta-analysis was conducted to evaluate the mortality risks of UTL users in gout or hyperuricemia populations.
Results:
This meta-analysis included 11 comparative studies encompassing 38,396 ULT users and 47,530 controls for evaluating all-cause mortality in gout or hyperuricemia. ULT treatment in patients with gout or hyperuricemia led to a significantly lower risk of all-cause mortality compared to patients not receiving ULT (HR = 0.783, 95% confidence interval [CI] = 0.702-0.874; p < 0.001). Both ULT and allopurinol were associated with decreased all-cause mortality rates (ULT HR = 0.651, 95% CI = 0.520-0.816; p < 0.001; allopurinol HR = 0.836, 95% CI = 0.731-0.957; p = 0.009). ULT initiation significantly reduced CVD-specific mortality in hyperuricemia patients, although the same was not observed in gout patients (HR for hyperuricemia = 0.872, 95% CI = 0.796-0.955; p = 0.003; HR for gout = 0.676, 95% CI = 0.296-1.544; p = 0.353).
Conclusion:
This meta-analysis indicates that ULT substantially reduces all-cause mortality in patients with gout or hyperuricemia, although allopurinol does not significantly affect CVD-specific mortality. These results underscore the potential of ULT for enhancing survival rates in special patient populations.
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