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Digital Treatment & Global Tobacco Use Reduction

October 12, 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 patients taking ‍semaglutide experienced a major adverse cardiovascular event (MACE) compared⁣ to 4.9% in the placebo group.
  • These findings primarily affect adults with ⁢obesity *and* pre-existing cardiovascular 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 Patient Risk
    • Why ⁤Does This Matter? The Shifting Landscape 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 with obesity and ⁣established cardiovascular disease who were 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 notable weight loss, the cardiovascular safety signal is prompting a reassessment of its use in this specific patient population.

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: Trial results released August 17, 2023, with ongoing analysis.

Why it Matters: Challenges the perception of semaglutide as universally cardio-protective and necessitates careful patient selection.
What’s Next: Further⁣ inquiry into the underlying mechanisms and refinement of patient selection criteria.

The Data: Key Findings from the SELECT Trial

The study found that 6.5% of patients 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 weight⁢ loss achieved with semaglutide⁢ – an average⁤ of approximately 15% of initial body weight – did *not* appear to offset this cardiovascular ⁢risk. The findings⁢ were consistent across various subgroups, although some signals were more pronounced in patients with prior heart failure.

Event Semaglutide‍ Group (%) Placebo Group (%)
Cardiovascular Death 1.5% 1.2%
non-Fatal Stroke 1.7% 1.3%
Non-Fatal‍ Heart Attack 3.4% 2.4%
MACE (Combined) 6.5% 4.9%

Who is Affected? Understanding Patient Risk

These findings primarily affect adults with ⁢obesity *and* pre-existing cardiovascular disease. This⁣ includes individuals with⁤ a history of heart attack, stroke, peripheral artery disease, or heart failure. The trial did *not* include patients ⁤with type 2⁤ diabetes, so the results cannot be directly extrapolated to that population. However, given that many individuals with type‍ 2 diabetes also have cardiovascular risk factors, these findings warrant caution and further research in that group‍ as well.

It’s crucial to differentiate between this population and individuals using semaglutide for weight loss *without* established cardiovascular disease. The risk-benefit profile may ‍be different ⁢for these individuals, but ongoing monitoring ⁤remains essential.

Why ⁤Does This Matter? The Shifting Landscape of GLP-1 Receptor agonists

Semaglutide, like⁣ other GLP-1 receptor agonists, has been widely touted for its weight loss benefits and, in ⁢some earlier trials, potential cardiovascular protection – notably in patients with type 2 diabetes. The SELECT trial challenges ⁣this narrative,⁢ highlighting the importance of considering the specific patient population and underlying health conditions.This isn’t necessarily a condemnation of semaglutide, but a call for more nuanced prescribing practices.

– drjenniferchen
⁣

The⁤ SELECT⁢ trial is a critical reminder that medications are not one-size-fits-all. The⁤ initial enthusiasm surrounding GLP-1 receptor agonists for weight loss and cardiovascular health needs to be tempered with a rigorous assessment of individual patient risk. We’re ‍seeing a shift ‍from a broad-spectrum approach to a more personalized one

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