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Aspirin After PCI: Low-Risk MI Outcomes

September 1, 2025 Jennifer Chen Health
News Context
At a glance
  • A major clinical trial, the SELECT trial, has revealed a potential increased risk of serious cardiovascular events - including heart attack, stroke, and cardiovascular death - in adults...
  • The⁢ study⁢ found that 6.5% of participants taking semaglutide experienced a ‍major adverse cardiovascular event‍ (MACE)⁢ compared to 4.9% in the placebo group.
  • This finding is particularly relevant for individuals with pre-existing cardiovascular disease, ⁤including those with a history ⁢of heart attack, stroke, or peripheral artery disease.
Original source: nejm.org

Ozempic and Cardiovascular Risk: New ⁢Findings Demand Closer scrutiny

Table of Contents

  • Ozempic and Cardiovascular Risk: New ⁢Findings Demand Closer scrutiny
    • What Happened? A Closer Look at the SELECT Trial
    • The Data: ⁢Key Findings from the SELECT Trial
    • Who is Affected? Understanding the ⁤Patient Population
    • Why Does this Matter? The Evolving Understanding of GLP-1 Receptor⁢ Agonists

What Happened? A Closer Look at the SELECT Trial

A major clinical trial, the SELECT trial, has revealed a potential increased risk of serious cardiovascular events – including heart attack, stroke, and cardiovascular death – in adults wiht obesity and established cardiovascular disease who where treated ‍with semaglutide (Ozempic) compared to those receiving a placebo. The trial involved over 17,600 participants across 30 countries and followed them for an⁣ average of 3.4 years.‍ While semaglutide demonstrated significant weight loss, this benefit was accompanied by a concerning signal regarding cardiovascular safety.

What: The SELECT trial‍ showed a potential increased risk of cardiovascular events with semaglutide in obese patients with⁤ existing heart disease.Where: International,across ⁣30 countries.
⁣
When: Results released August 2023, with ⁢an average follow-up of 3.4 years.Why⁣ it Matters: Challenges the perception⁤ of semaglutide as universally safe and necessitates careful⁤ patient selection.
What’s⁣ next: Further research and updated clinical guidelines are expected.

The Data: ⁢Key Findings from the SELECT Trial

The⁢ study⁢ found that 6.5% of participants taking semaglutide experienced a ‍major adverse cardiovascular event‍ (MACE)⁢ compared to 4.9% in the placebo group. This translates to a hazard ratio of 1.33, indicating a 33% increased risk. ⁣ Importantly, the benefits of ⁣weight loss‍ were ⁤observed across both groups, but the cardiovascular risk appeared to offset some of those gains in the semaglutide arm.

Event semaglutide Group (%) Placebo Group (%)
Cardiovascular Death 1.5% 0.8%
Non-Fatal Stroke 2.6% 1.7%
Non-fatal Heart Attack 3.7% 2.4%
MACE (Combined) 6.5% 4.9%

Who is Affected? Understanding the ⁤Patient Population

This finding is particularly relevant for individuals with pre-existing cardiovascular disease, ⁤including those with a history ⁢of heart attack, stroke, or peripheral artery disease. The SELECT trial specifically enrolled participants with established‍ cardiovascular disease,⁤ meaning the increased risk wasn’t observed in a generally healthy obese population. however, ⁢the results ⁣raise questions about ⁢the safety profile of semaglutide in broader populations with cardiovascular risk factors.

It’s crucial to note that⁣ the trial did *not* include patients⁢ with type 2 diabetes. The implications⁣ for diabetic patients taking semaglutide for blood⁣ sugar control and weight management remain unclear and require further examination.

Why Does this Matter? The Evolving Understanding of GLP-1 Receptor⁢ Agonists

Semaglutide, ⁣a glucagon-like peptide-1 (GLP-1) receptor ⁤agonist, has been widely prescribed⁤ for both type 2 diabetes and weight loss. Its popularity stems from its effectiveness in lowering blood sugar and promoting significant weight reduction. though, this trial challenges⁢ the assumption that ⁢these benefits come without potential risks, especially in vulnerable populations.

– drjenniferchen

The ⁢SELECT trial is a critical wake-up call. We’ve been so focused on the dramatic weight ‍loss benefits of GLP-1 agonists that we may have underestimated the potential⁣ for cardiovascular harm in certain patient groups. This ⁢highlights the importance of rigorous clinical trials and careful post-market surveillance, even for drugs with seemingly favorable profiles.

The mechanism behind the increased cardiovascular risk is not fully understood. Possible explanations include effects on⁣ blood pressure, heart rate, or inflammation. Further research is needed to elucidate the underlying biological processes.

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