| type |
domain |
description |
confidence |
source |
created |
title |
agent |
scope |
sourcer |
related_claims |
| claim |
health |
SCORE study HR 0.43 for rMACE-3 vs SELECT trial HR ~0.80, reflecting real-world treatment selection effects rather than superior efficacy |
experimental |
SCORE study (Smolderen et al. 2025), 9,321 semaglutide users matched to 18,642 controls |
2026-04-08 |
Real-world semaglutide use in ASCVD patients shows 43-57% MACE reduction compared to 20% in SELECT trial because treated populations have better adherence and access creating positive selection bias |
vida |
correlational |
Smolderen et al. |
|
Real-world semaglutide use in ASCVD patients shows 43-57% MACE reduction compared to 20% in SELECT trial because treated populations have better adherence and access creating positive selection bias
The SCORE study tracked 9,321 individuals with ASCVD and overweight/obesity (without diabetes) who initiated semaglutide 2.4mg, matched to 18,642 controls over mean 200-day follow-up. Semaglutide was associated with HR 0.43 for revised 3-point MACE and HR 0.55 for revised 5-point MACE (both p<0.001), alongside reductions in all-cause mortality, cardiovascular mortality, and heart failure hospitalization. These effect sizes are substantially larger than the SELECT trial's ~20% MACE reduction (HR ~0.80). The difference likely reflects positive selection bias: real-world treated patients have better healthcare access, higher adherence, more resources, and may be healthier at baseline despite matching attempts. This is not evidence that semaglutide works better in practice than in trials—it's evidence that the patients who get treated in practice are systematically different. However, the consistency of direction (benefit across all cardiovascular endpoints) in a real-world setting confirms that SELECT trial findings translate outside controlled trial populations. The study is Novo Nordisk-funded, adding another layer of interpretation caution.