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Liraglutide reduces stroke recurrence from 18.1% to 5.8% in patients with high insulin resistanceLiraglutide reduces stroke risk for patients with insulin resistance

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Key Takeaway
Note that liraglutide significantly reduces stroke recurrence in patients with high insulin resistance (HOMA-IR ≥2.5).

This post hoc analysis of a randomized controlled trial evaluated 510 patients with minor ischemic stroke or high-risk transient ischemic attack and type 2 diabetes across 27 hospitals in China. The study compared liraglutide plus standard therapy against standard therapy alone over a 3 month follow-up period.

In patients with HOMA-IR ≥2.5, the addition of liraglutide reduced stroke recurrence from 18.1% to 5.8%, representing an absolute risk reduction of 12.3% (95% CI, 5.6%-19.0%; number needed to treat=8). Additionally, composite vascular events in this subgroup were reduced from 19.2% to 5.8% (absolute risk reduction, 13.4%; 95% CI, 6.6%-20.2%; number needed to treat=8). A significant interaction between treatment and insulin resistance was observed for both outcomes (p=0.02).

Safety data, including adverse events or discontinuations, were not reported. No significant benefit was observed in patients with HOMA-IR <2.5. Because this is a post hoc analysis, the results should be interpreted with caution. However, insulin resistance based stratification may help optimize glucagon-like peptide-1 receptor agonists for secondary stroke prevention and personalized risk management.

How this fits prior evidence

How this fits prior evidence: This finding addresses a gap in identifying specific patient phenotypes who benefit from GLP-1 receptor agonists in secondary stroke prevention. While previous coverage noted that lower aspirin doses combined with clopidogrel may reduce ischemic events in high risk patients, this study suggests that insulin resistance (HOMA-IR ≥2.5) identifies a specific subgroup where liraglutide provides significant reduction in recurrence from 18.1% to 5.8%.

Living with both type 2 diabetes and a recent minor stroke creates a complex challenge for managing long-term health. A study of 510 patients in China looked at how the medication liraglutide could help prevent another stroke or other vascular events in this specific group.

The researchers found that the medicine worked best for people with high insulin resistance (measured as HOMA-IR of 2.5 or higher). In these patients, the rate of stroke recurrence dropped from 18.1% to 5.8%. They also saw a significant drop in overall vascular events, which fell from 19.2% to 5.8%.

It is important to note that this was a post hoc analysis, which means researchers looked back at existing data to find these patterns. While the results were promising for those with high insulin resistance, no significant benefit was found in patients with lower insulin levels. Talk to your doctor about how these findings might apply to your specific health needs.

What this means for you:
Liraglutide significantly reduced stroke and vascular risks specifically for patients with high insulin resistance.

Common questions

Who specifically benefits from this treatment?

This finding specifically helps patients who have type 2 diabetes and have experienced a minor stroke or a high-risk transient ischemic attack. The benefit was most clear for those with high insulin resistance, measured as a HOMA-IR of 2.5 or higher.

How much did the risk of another stroke decrease?

For patients with high insulin resistance, the rate of stroke recurrence dropped from 18.1% to 5.8%. This represents an absolute risk reduction of 12.3%. The study found a significant interaction between the treatment and insulin levels.

What other health benefits were seen?

In addition to reducing stroke recurrence, the medication also lowered the rate of composite vascular events from 19.2% to 5.8% in patients with high insulin resistance. This was an absolute risk reduction of 13.4%.

Study Details

Study typeRct
EvidenceLevel 2
Follow-up780.0 mo
PublishedJul 2026
View Original Abstract ↓
BACKGROUND: Glucagon-like peptide-1 receptor agonists reduce major adverse cardiovascular events in type 2 diabetes. Although body mass index does not seem to modify these effects, whether insulin resistance influences treatment efficacy remains unclear. METHODS: This post hoc analysis of the LAMP trial (Liraglutide in Acute Minor Ischemic Stroke or High-Risk Transient Ischemic Attack Patients With Type 2 Diabetes Mellitus; a multicenter, open-label, randomized controlled trial conducted at 27 hospitals in China between June 25, 2019, and December 27, 2023) included patients with minor ischemic stroke or high-risk transient ischemic attack and type 2 diabetes. Participants were randomized (1:1) to liraglutide plus standard therapy or standard therapy alone. IR was assessed using the homeostasis model assessment of IR, with a cutoff of 2.5 based on prior studies in Asian populations. Treatment-by-IR interactions were evaluated using Cox models. Absolute risk reduction was calculated as the difference in event rates between groups and was based on crude estimates. RESULTS: Among 636 enrolled patients, 510 were included in this analysis (mean age, 65 years; 64.7% male; follow-up, 3 months). A significant interaction between treatment and insulin resistance was observed for both stroke recurrence and composite vascular events ( for interaction=0.02 for both). Among patients with homeostasis model assessment of IR ≥2.5, liraglutide reduced stroke recurrence (5.8% versus 18.1%; absolute risk reduction, 12.3% [95% CI, 5.6%-19.0%]; number needed to treat=8) and vascular events (5.8% versus 19.2%; absolute risk reduction, 13.4% [95% CI, 6.6%-20.2%]; number needed to treat=8). No significant benefit was observed in those with homeostasis model assessment of IR <2.5. CONCLUSIONS: IR may be an important determinant of the therapeutic efficacy of liraglutide in patients with acute minor ischemic stroke or high-risk transient ischemic attack and type 2 diabetes. IR-based stratification may help optimize the use of glucagon-like peptide-1 receptor agonists in secondary stroke prevention and guide personalized vascular risk management. REGISTRATION: URL: https://www.clinicaltrials.gov; Unique identifier: NCT03948347.
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