GLP-1 medications were developed to treat diabetes and obesity — but emerging evidence shows they do much more. The landmark SELECT trial demonstrated that semaglutide reduces the risk of major cardiovascular events (heart attack, stroke, cardiovascular death) by 20% in overweight and obese adults,
At a glance
- GLP-1 medications were developed to treat diabetes and obesity — but emerging evidence shows they do much more.
- The landmark SELECT trial demonstrated that semaglutide reduces the risk of major cardiovascular events (heart attack, stroke, cardiovascular death) by 20% in overweight and obese adults, independent of diabetes status.
- This finding has profound implications for how we think about weight loss treatment — it's not just cosmetic; it's cardioprotective.
Introduction
GLP-1 medications were developed to treat diabetes and obesity — but emerging evidence shows they do much more. The landmark SELECT trial demonstrated that semaglutide reduces the risk of major cardiovascular events (heart attack, stroke, cardiovascular death) by 20% in overweight and obese adults, independent of diabetes status1. This finding has profound implications for how we think about weight loss treatment — it's not just cosmetic; it's cardioprotective.

The SELECT Trial: What It Found
The SELECT trial was a game-changer for the weight loss medication field, providing definitive evidence that GLP-1 treatment has cardiovascular benefits.
Study Design
- 17,604 adults aged 45+ with overweight/obesity and established cardiovascular disease
- Without diabetes (to isolate the cardiovascular effect from glucose-lowering benefits)
- Semaglutide 2.4 mg weekly vs placebo
- Mean follow-up: 39.8 months
Key Results
- 20% reduction in major adverse cardiovascular events (MACE: cardiovascular death, non-fatal MI, non-fatal stroke)
- Benefit observed regardless of baseline BMI
- Consistent across age groups, sex, and geographic regions
- Weight loss of approximately 9.4% with semaglutide vs 0.9% with placebo
Why This Matters
For overweight Singaporean men with cardiovascular risk factors, GLP-1 medications offer a dual benefit: weight loss AND direct cardiovascular protection. This changes the risk-benefit calculation significantly.
How GLP-1 Medications Protect the Heart
The cardiovascular benefits of GLP-1 medications appear to extend beyond weight loss alone. Multiple mechanisms contribute to this cardioprotective effect.
Weight-Loss-Mediated Benefits
- Reduced visceral fat → decreased inflammation and insulin resistance
- Lower blood pressure → reduced cardiac workload
- Improved lipid profile → less atherosclerosis progression
- Better glycaemic control → reduced vascular damage
Direct Cardiovascular Effects
Research suggests GLP-1 receptors are present in the heart and blood vessels, and GLP-1 agonists may directly:
- Reduce inflammation — lower levels of CRP and other inflammatory markers
- Improve endothelial function — better blood vessel health
- Reduce atherosclerotic plaque progression(Based on MOH guidelines and prescribing information)
- Protect against ischaemic damage — cardioprotective during low-oxygen events
Singapore Context: Why This Matters Here
Singapore's population faces specific cardiovascular risks that make these findings particularly relevant.
Singapore Cardiovascular Risk Profile
- Heart disease is the #2 cause of death in Singapore
- High diabetes prevalence — 8.5% of residents; diabetes is a major cardiovascular risk factor
- Metabolic syndrome is common — driven by sedentary lifestyles and dietary patterns
- Hypertension affects 1 in 4 adults — often inadequately controlled
- Dyslipidaemia is widespread — high-cholesterol diets and genetic factors
Practical Implications
For Singaporean men who are overweight with cardiovascular risk factors, GLP-1 medications offer evidence-based treatment that addresses multiple conditions simultaneously:
- Excess weight → weight loss
- Cardiovascular risk → direct risk reduction
- Diabetes risk → improved glucose metabolism
- Inflammation → anti-inflammatory effects
Who Benefits Most from Cardiovascular Protection?
The SELECT trial specifically enrolled individuals with established cardiovascular disease, but the findings likely have broader implications for at-risk populations.
Highest-Benefit Groups
- Men with established cardiovascular disease (prior MI, stroke, or peripheral vascular disease)
- Men with multiple cardiovascular risk factors (hypertension + diabetes + dyslipidaemia)
- Men with metabolic syndrome
- Men with strong family history of premature cardiovascular disease
Lower-Risk Men
For younger men without cardiovascular risk factors, the primary benefit of GLP-1 medications remains weight loss. The cardiovascular protection is an additional benefit that may become more relevant as they age.
Beyond Weight and Heart: Other Emerging Benefits
Ongoing research is exploring additional benefits of GLP-1 medications that extend well beyond their primary indications.
Kidney Protection
The FLOW trial demonstrated that semaglutide slowed kidney disease progression in patients with Type 2 diabetes and chronic kidney disease(Based on MOH guidelines and prescribing information).
Fatty Liver Disease (NAFLD/NASH)
GLP-1 medications reduce liver fat and inflammation, with potential benefits for non-alcoholic fatty liver disease — a common condition in overweight Singaporean men(Based on MOH guidelines and prescribing information).
Sleep Apnoea
Weight loss with GLP-1 medications has been shown to improve obstructive sleep apnoea severity, with some patients able to discontinue CPAP therapy(Based on MOH guidelines and prescribing information).
Cost in Singapore (SGD)
GLP-1 receptor agonist medications for weight management in Singapore typically cost SGD $200–500 per month depending on the specific medication and dosage. Costs vary by provider and whether branded or biosimilar options are available. noah™ offers structured weight loss plans with doctor oversight.
Prices are approximate and may vary. Updated April 2026.
FAQ
1. Do I need heart disease to benefit from the cardiovascular effects?
The SELECT trial enrolled patients with established cardiovascular disease. However, the weight loss, blood pressure reduction, and metabolic improvements benefit anyone at elevated cardiovascular risk — not just those with existing disease.
2. Does this mean GLP-1 medications replace heart medications?
No. GLP-1 medications are additive — they provide benefits alongside existing treatments (statins, antihypertensives, etc.), not as replacements. Continue all prescribed cardiovascular medications.
3. Is Ozempic or Mounjaro better for heart protection?
The SELECT trial used semaglutide. Cardiovascular outcome trials for tirzepatide are ongoing. At present, semaglutide has the strongest cardiovascular evidence, but tirzepatide may show similar benefits.
4. How long do I need to take GLP-1 for cardiovascular benefit?
The SELECT trial showed benefits over a mean follow-up of about 3 years, with effects emerging within the first year. Sustained use is likely needed for sustained cardiovascular protection.
5. Should I ask my cardiologist about GLP-1 medications?
If you're overweight with cardiovascular risk factors or established heart disease, absolutely. The SELECT trial evidence is compelling enough that many cardiologists are now actively recommending GLP-1 medications for eligible patients.
References
→ Return to pillar: Complete Guide to Medical Weight Loss in Singapore
This article is for informational purposes only and does not constitute medical advice. Always consult a licensed doctor before starting any treatment.
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Lincoff AM, Brown-Frandsen K, Colhoun HM, et al. Semaglutide and cardiovascular outcomes in obesity without diabetes. N Engl J Med. 2023;389(24):2221-2232. PMID: 29617641 ↩
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Written by our Editorial Team
Last updated 15 Jun 2026
Articles featured on Noah are for informational purposes only and should not be constituted as medical advice, diagnosis or treatment. If you have any medical questions or concerns, please talk to your healthcare provider. If you're looking for a healthcare provider, click here.