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Uromodulin as a protein and genetic biomarker for hypertension: A detailed systematic review and meta-analysis
Hash Brown Taha1, Nandhana Vivek2, Samuel Ogunsanya3
1Washington University in St. Louis, St. Louis, USA.
Insights
Uromodulin is not a clinically useful biomarker for hypertension, according to a meta-analysis. Further research may explore its potential for predicting other cardiovascular outcomes.
Area of Science:
- Nephrology
- Cardiology
- Biomarker Discovery
Background:
- Hypertension is a leading global cause of cardiovascular disease.
- There is a need for better biomarkers to manage hypertension.
- Uromodulin is associated with kidney function and blood pressure regulation.
Purpose of the Study:
- To systematically review and perform a meta-analysis on uromodulin as a biomarker for hypertension.
- To evaluate the clinical utility of uromodulin protein and genetic variants in hypertension.
Main Methods:
- Systematic review and meta-analysis of 35 human studies.
- Inclusion of studies on uromodulin protein levels and genome-wide association studies (GWAS) related to hypertension.
- Analysis using inverse variance weighted random effects models and assessment of publication bias.
Main Results:
- Uromodulin did not show clinically significant utility as a biomarker for hypertension or related outcomes across diagnostic, prognostic, and predictive studies.
- Analysis included data from 10,726 individuals with hypertension and 8,762 controls for protein levels.
- GWAS included over 450,000 hypertension cases and 150,000 controls.
Conclusions:
- Uromodulin is not a clinically useful protein or genetic biomarker for hypertension.
- Uromodulin may retain potential for predicting other cardiovascular outcomes.
Background:
Hypertension is a major global cause of cardiovascular morbidity and mortality, and improved biomarkers are needed to assess risk, disease progression, and treatment response. Uromodulin reflects tubular health and renal sodium handling and has been linked to hypertension. We performed a systematic review and meta-analysis to evaluate uromodulin as a biomarker for hypertension.
Methods:
We included human studies evaluating uromodulin protein levels or uromodulin-related genome-wide association study outcomes in relation to hypertension. Continuous outcomes were analyzed using inverse variance weighted random effects models, and publication bias was assessed with Begg's test, Egger's test, and funnel plots.
Results:
Thirty-five studies met the inclusion criteria. Across diagnostic, prognostic, and predictive biomarker studies, ∼10,726 individuals with hypertension (3,461 females) and ∼8,762 (3,605 females) normotensives were included. Genome-wide association studies included > 450,000 hypertension and > 150,000 normotensives. Across all analyses, uromodulin did not demonstrate clinically meaningful utility as a biomarker for hypertension or hypertension-related outcomes.
Conclusion:
Our meta-analysis shows that uromodulin is not a clinically useful protein or genetic biomarker for hypertension or hypertension-related outcomes. However, it may still have potential utility in predicting other cardiovascular outcomes.
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