Comparison of Lantus (Insulin Glargine) and Tresiba (Insulin Degludec) for Hypoglycemia Risk and Driving Safety
Tresiba (insulin degludec) is superior to Lantus (insulin glargine U-100) for reducing hypoglycemia risk, which directly impacts driving safety, with a 40% reduction in severe hypoglycemia rates and 35% reduction in nocturnal hypoglycemia—the episodes most likely to impair driving ability.
Direct Hypoglycemia Comparison: The DEVOTE Trial Evidence
The FDA label for Tresiba provides the highest-quality head-to-head comparison from the DEVOTE trial, which enrolled 7,637 patients with type 2 diabetes and cardiovascular disease 1:
- Severe hypoglycemia occurred in 4.9% of Tresiba patients vs 6.6% of Lantus patients (odds ratio 0.73,95% CI 0.60-0.89, p<0.001) 1
- Event rates were 3.70 per 100 patient-years with Tresiba vs 6.25 per 100 patient-years with Lantus (rate ratio 0.60,95% CI 0.48-0.76, p<0.001) 1
- This represents a 40% reduction in severe hypoglycemia rates with Tresiba compared to Lantus 1
Type 1 Diabetes Evidence: SWITCH 1 Trial
For patients with type 1 diabetes at higher risk for hypoglycemia, the SWITCH 1 trial demonstrated even more pronounced benefits 2:
- Overall symptomatic hypoglycemia: 2200.9 episodes per 100 person-years with Tresiba vs 2462.7 with Lantus (rate ratio 0.89, p<0.001 for superiority) 2
- Nocturnal hypoglycemia: 277.1 episodes per 100 person-years with Tresiba vs 428.6 with Lantus (rate ratio 0.64, p<0.001 for superiority) 2
- Severe hypoglycemia during maintenance: 10.3% with Tresiba vs 17.1% with Lantus (p=0.002) 2
Direct Connection to Driving Safety
The American Diabetes Association guidelines explicitly recognize that hypoglycemia is the primary diabetes-related driving risk 3:
- Severe hypoglycemia can lead to coma or death, and episodes occurring while driving create exponential risk increases 3
- Patients with two episodes of severe hypoglycemia in the preceding 12 months have a 12% increased risk of driving mishaps 3
- Nocturnal hypoglycemia is particularly relevant because residual cognitive impairment can persist into morning driving hours 3
Clinical Guideline Context
The 2024 American Diabetes Association Standards of Care establish the framework for choosing between these insulins 3:
- Longer-acting basal analogs (including degludec) convey lower nocturnal hypoglycemia risk compared with U-100 glargine 3
- Long-acting basal analogs reduce the risk of level 2 hypoglycemia and nocturnal hypoglycemia compared with NPH insulin 3
- Both insulins work primarily by restraining hepatic glucose production and limiting hyperglycemia overnight and between meals 3, 4
Real-World Confirmation
The EU-TREAT prospective observational study confirmed these findings in routine clinical practice 5:
- Type 1 diabetes patients switching to Tresiba experienced rate ratios of 0.61 for nocturnal hypoglycemia (p<0.001) 5
- Type 2 diabetes patients had rate ratios of 0.35 for nocturnal hypoglycemia (p<0.001) 5
- Severe hypoglycemia rate ratio was 0.28 in type 1 diabetes patients (p<0.001) 5
Practical Implications for Patient Selection
Choose Tresiba over Lantus for patients who:
- Have a history of severe or nocturnal hypoglycemia 3, 2
- Drive regularly for work or have occupations requiring sustained attention 3
- Have experienced hypoglycemia-related driving mishaps or near-misses 3
- Are at high cardiovascular risk (DEVOTE showed cardiovascular non-inferiority with superior hypoglycemia outcomes) 1
Important Caveats
- Both insulins provide similar glycemic control (HbA1c reduction), so the choice is driven by hypoglycemia risk rather than efficacy 1, 2
- Tresiba has a 42-hour duration of action compared to Lantus's 24-hour profile, providing more consistent coverage 6
- Cost considerations may favor human NPH insulin in resource-limited settings, though with higher hypoglycemia risk 3
- The concentrated U-300 glargine formulation (Toujeo) also shows lower nocturnal hypoglycemia than U-100 glargine, though direct comparisons with Tresiba are limited 3
Dosing Considerations When Switching
When converting between these insulins 4: