SynthesisBMC nephrology2025
Effect of statin therapy on renal and lipid outcomes in CKM syndrome stage 2: a meta-analysis of randomized controlled trials.
Synthesis in BMC nephrology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Cardiovascular-kidney-metabolic syndrome: a comprehensive review of pathophysiology, epidemiology, diagnosis, and management.Cardiovascular diabetology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
Abstract
Cardiovascular-kidney-metabolic (CKM) syndrome is a recently defined multisystem disorder integrating metabolic, renal, and cardiovascular dysfunction. CKM syndrome stage 2 represents an early, potentially reversible phase that offers a critical window for intervention. This meta-analysis evaluated the effects of statin therapy on renal and lipid outcomes in this population. 7 randomized controlled trials involving 490 participants were included. In the primary analysis, statin therapy showed a directionally favorable but non-significant trend toward improved estimated glomerular filtration rate (eGFR) and reduced 24-hour urinary total protein excretion (24h UTP), with no significant change in serum creatinine (Scr). Statins significantly reduced LDL-C (MD = - 52.18) and total cholesterol (MD = - 52.70), while changes in HDL-C and triglycerides were not significant. Subgroup analyses indicated numerically greater renal and lipid benefits with high-intensity regimens, longer treatment duration (≥ 26 weeks), and lower baseline eGFR, though no significant subgroup interactions were detected. Sensitivity analysis including a borderline CKM syndrome 2-3 trial characterized by higher renal risk, longer duration, and high-intensity atorvastatin rendered both renal and lipid outcomes statistically significant without altering effect direction. These findings suggest that statin therapy confers robust lipid-lowering efficacy and potential renoprotective effects in early CKM syndrome stages, particularly under conditions of greater baseline metabolic or renal burden. Statins may therefore serve as an early metabolic-renal intervention, warranting further validation in larger, stage-specific clinical trials.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.