ReviewDiagnostics (Basel, Switzerland)2026
Prognostic Models for Incident Hypertension: Time to Move from Development to Implementation-An Umbrella Review.
Review in Diagnostics (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Authors and funding
2 authors.
Funding
Abstract
Hypertension represents a major modifiable cardiovascular risk factor with increasing global prevalence. While numerous prognostic models for incident hypertension have been developed, their clinical implementation remains limited, suggesting a gap between model development and practical application. This study aimed to synthesize evidence from systematic reviews on multivariable prognostic models estimating the future risk of incident hypertension among initially normotensive individuals, evaluating methodological quality, predictive performance, validation status, calibration reporting, and clinical utility. We conducted an umbrella review, searching six databases from January 2000 to March 2026. Systematic reviews (SRs) evaluating multivariable prognostic models for incident hypertension with documented external validation evidence were included; reviews mixing prognostic and cross-sectional diagnostic screening models were retained only when eligible prognostic evidence could be distinguished and were examined in sensitivity synthesis. Methodological quality was assessed using ROBIS, and primary-study risk of bias was extracted from PROBAST/CHARMS assessments reported by the included reviews. Six SRs (three with meta-analyses) identified 162 unique models reported as prognostic. Models were categorized as traditional statistical (60%), machine learning (30%), and genetic/polygenic risk score-based (10%). Reported pooled AUCs were 0.78 (95% CI 0.76-0.80) for traditional models and 0.82 (95% CI 0.77-0.86) for machine learning models, but all quantitative summaries showed extreme heterogeneity (I
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Registered trials
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