What?

On Saturday, researchers shared the results of the STAREE trial at a cardiology congress in Munich, and the full paper appeared in the New England Journal of Medicine the same day. In this study, 9,971 adults aged 70 and older, who did not have heart disease, diabetes, or dementia at the start, received either 40 mg of atorvastatin or a placebo.

The trial set out to answer two main questions. First, it tracked heart attacks, strokes, cardiac deaths, and stent procedures. After about 5.9 years, 6.0% of people taking the drug had these events, compared to 8.3% on placebo. That 30% difference means 2.3 fewer people out of every 100 had these problems. Second, the study looked at whether the drug helped people live longer without dementia or physical disability. Here, those outcomes hit 12.8% of the drug group and 13.6% on placebo, a small difference that could have happened by chance.

So what?

Statins are among the most thoroughly studied drugs in medicine. Results from 27 randomized trials show they help prevent major vascular events, even for people at low risk. Even in that low-risk group, every 1 mmol/L drop in LDL cholesterol prevents about 11 events per 1,000 people over five years. The researchers concluded that the benefits are much greater than any known risks. If you already take a statin, there is no reason to stop based on this new study.

The real question is what benefit you personally might get. In Munich, that 2.3 in 100 came from adults with an average age of 74. In March, new US guidelines made 21.5 million more people eligible for statins. These people are younger and have a lower risk, with an average 3.1% risk over ten years. For them, the same 30% reduction means even fewer people benefit, but this is not always made clear. In Europe, the SCORE2 system is used, and the math works out the same.

The STAREE trial does not give information for people who are 50 years old. All participants were at least 70, and anyone with heart disease, diabetes, or dementia was excluded. So, you need to find out your own risk numbers.

Now what?

  • If you already take a statin, do not change your prescription until you talk with your doctor. Make sure to mention any symptoms or concerns at that visit.
  • Ask your doctor for your current risk estimate. In the US, learn about PREVENT and its 10-year and 30-year risk numbers. In Europe, ask which SCORE2 or SCORE2-OP estimate applies to you.
  • Review your ApoB and your one-time Lp(a) test result with your doctor. Try to keep ApoB below 80 mg/dL, or below 65 if you already have disease or a strong family history. Ask if a CAC score could change your risk category.
  • Ask your doctor this specific question: “With this dose, how many percentage points will my risk go down over the years I am likely to take it?”
  • At the same visit, ask about possible downsides. Serious side effects happened at the same rate in both groups, 2.7%. However, muscle, liver, and blood sugar problems were more common in people taking the drug.

You can find out your own risk number. Go and get it.

Stay healthy.

Andre

Editor's note

Editorial clarification and evidence update

The Upward ARC is an educational newsletter for a general audience, not a medical publication. It may use ordinary-language metaphors and simplifications to make complex evidence readable. Those phrases are not clinical terminology. The editorial standard remains unchanged: do not fabricate, cite falsely, hide important uncertainty, or simplify a point so far that it changes the practical meaning.

Updated September 3, 2026. The historical edition above remains unchanged.

A 30% relative result is not a personal estimate: STAREE's 30% relative reduction was observed in adults aged 70 or older without prior cardiovascular disease, diabetes or dementia. It should not be applied directly to younger or lower-risk people. Across statin trials, the relative reduction averages about 21% per 1 mmol/L reduction in LDL cholesterol, while the absolute benefit depends on starting risk, the LDL reduction achieved and time on treatment. [1]

Using PREVENT and SCORE2: PREVENT estimates primary-prevention risk for US adults aged 30 to 79. SCORE2 and SCORE2-OP are calibrated for European populations aged 40 to 89 without known cardiovascular disease. The European guideline advises against recalculating risk with on-treatment cholesterol values. People already taking lipid-lowering medication need interpretation based on their pretreatment risk and response. [2]

The ApoB numbers are editorial targets: The ApoB targets below 80 mg/dL, or below 65 mg/dL for higher-risk readers, are not universal goals in the 2026 US guideline. That guideline centers LDL and non-HDL cholesterol goals and uses ApoB selectively, especially when triglycerides exceed 200 mg/dL, diabetes is present or LDL is already below 70 mg/dL. [3]

What Lp(a) and a calcium scan add: Current US guidance supports measuring lipoprotein(a) at least once, with 125 nmol/L or 50 mg/dL as a risk-enhancing level. Coronary-artery calcium can reclassify risk when a treatment decision remains uncertain. The scan informs the decision; it does not prescribe treatment by itself. [3]

What the 2.7% safety number covered: In STAREE, serious adverse events occurred in 2.7% of each group. That figure does not cover every symptom or side effect. Musculoskeletal, hepatobiliary and diabetes-related adverse-event categories were reported more often with atorvastatin, so individual tolerability and monitoring still matter. [4]

References

  1. Cholesterol Treatment Trialists' Collaboration. Statins in people at low risk of vascular disease. The Lancet, 2012.
  2. European Society of Cardiology. 2025 Focused Update of the 2019 ESC/EAS Guidelines for the management of dyslipidaemias.
  3. American Heart Association and American College of Cardiology. 2026 Guideline on the Management of Dyslipidemia.
  4. STAREE Investigators. Atorvastatin in Healthy Older Persons. New England Journal of Medicine, 2026.

For informational and educational purposes only. This page does not provide individual medical advice, diagnosis, or treatment. Read the full medical disclaimer.