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U-shaped relationship between uric acid levels and all-cause mortality in patients with hypertension
Yating Huang1, Jie Li2, Feifei Sun3
1Department of Cardiology, The Second Affiliated Hospital of Dalian Medical University, Dalian, China.
Insights
Uric acid (UA) levels show a U-shaped association with all-cause mortality in hypertension patients. Mortality risk decreases at lower UA levels but increases significantly above specific thresholds, which differ by sex.
Area of Science:
- Cardiovascular Medicine
- Nephrology
- Metabolic Disorders
Background:
- Elevated uric acid (UA) levels are linked to hypertension development.
- The impact of UA on all-cause mortality in hypertensive individuals is not well understood.
Purpose of the Study:
- To investigate the nonlinear association between serum UA levels and all-cause mortality in patients with hypertension.
- To determine sex-specific thresholds for UA's impact on mortality.
Main Methods:
- Utilized smoothed curve fitting to analyze nonlinear relationships.
- Employed threshold and saturation effect analysis and Cox regression models.
- Performed stratified analysis for interaction testing with comorbidities.
Main Results:
- Observed a U-shaped curve for UA and all-cause mortality in hypertensive patients.
- In males, mortality risk decreased below 7.2 mg/dL UA and increased above it.
- In females, UA was protective below 5.1 mg/dL and a risk factor above it.
Conclusions:
- The relationship between UA and all-cause mortality in hypertension is U-shaped.
- Sex-specific inflection points exist, indicating different risk profiles for men and women.
- UA management may require tailored approaches based on sex and baseline levels.
Abstract:
A correlation between UA levels and the development of hypertension has been demonstrated. However, the relationship between UA and all-cause mortality in patients with hypertension remains underexplored. A nonlinear association between UA and all-cause mortality across sexes was observed through smoothed curve fitting. The correlation between UA and all-cause mortality was calculated by threshold and saturation effect analysis, along with Cox regression models. The stability of the results in the presence of different comorbidities was verified through stratified analysis for interaction testing. Smoothed curve fitting was also used to examine the association between UA and various diseases. The association between UA and all-cause mortality in patients with hypertension exhibited a U-shaped curve, with inconsistent inflection points between the sexes. In male patients with hypertension, all-cause mortality gradually decreased with increasing UA levels when UA levels were ≤ 7.2 mg/dL (HR 0.975; 95% CI 0.929-1.024) and gradually increased with increasing UA levels when UA levels were > 7.2 mg/dL (HR 1.204; 95% CI 1.120-1.294). Similar findings were observed in female patients with hypertension, with UA as a protective factor when UA levels were ≤ 5.1 mg/dL (HR 0.902; 95% CI 0.820-0.991) and a risk factor when UA levels were > 5.1 mg/dL (HR 1.120; 95% CI 1.072-1.169). The association between UA and all-cause mortality in patients with hypertension exhibits a U-shaped curve. All-cause mortality tends to decrease and then increase with increasing UA levels, with the inflection point varying between sexes.
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