Clinical trial
JUPITER — Rosuvastatin in Healthy Adults with Elevated hsCRP
Last updated Sun May 17 2026 00:00:00 GMT+0000 (Coordinated Universal Time)
Design
JUPITER randomised 17,802 adults with LDL <130 mg/dL and hsCRP ≥2 mg/L to rosuvastatin 20 mg/day or placebo. Median follow-up was 1.9 years; the trial was halted early for efficacy.
Findings
- Primary composite endpoint (MI, stroke, hospitalisation for unstable angina, revascularisation, cardiovascular death): 44% relative reduction.
- Individually: MI down 54%, stroke down 48%.
- All-cause mortality: 20% reduction.
- Numerically small increase in incident diabetes (now considered a real, modest statin side effect).
Why it matters
JUPITER established two things:
- Statins benefit primary-prevention populations with normal LDL who are at elevated risk by an alternative marker (hsCRP).
- Inflammation matters in cardiovascular biology, complementing lipid pathways — a precursor to CANTOS years later.
Criticisms
- Stopped early; effect sizes may be overstated.
- Generalisability to lower-risk populations.
- Number needed to treat was relatively high for some endpoints.
Despite the debate, JUPITER changed practice: hsCRP became an accepted risk-reclassification tool, and statin prescribing thresholds broadened.
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References
- Ridker, P. M. et al. Rosuvastatin to prevent vascular events in men and women with elevated C-reactive protein. N. Engl. J. Med. 359, 2195–2207 (2008).