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Glycemic response to newly initiated diabetes therapies
Andrew J Karter1, Howard H Moffet, Jennifer Liu
1Division of Research, Kaiser Permanente, 2000 Broadway, Oakland, CA 94612, USA. andy.j.karter@kp.org
Objective:
The glycemic response to antihyperglycemic therapies for type 2 diabetes has been thoroughly evaluated in randomized controlled trials, but inadequately studied in real-world settings.
Study Design:
We studied glycemic response among 15 126 type 2 diabetic patients who initiated any single new antihyperglycemic agent (metformin, sulfonylureas, thiazolidinediones, or insulin added to medical nutrition therapy or to existing diabetes therapies) during 1999-2000 within Kaiser Permanente of Northern California, an integrated healthcare delivery system.
Methods:
Pre-post (3-12 months after initiation) change in glycosylated hemoglobin (A1C) was analyzed using ANCOVA (analysis of covariance) models adjusted for baseline A1C, concurrent (ongoing) antihyperglycemic therapy, demographics, health behaviors, medication adherence, clinical factors, and processes of care.
Results:
Mean A1C was 9.01% (95% confidence interval [CI] 8.98%-9.04%) before therapy initiation and 7.87% (95% CI 7.85%-7.90%) 3 to 12 months after initiation (mean A1C reduction 1.14 percentage points; 95% CI 1.11-1.17). Overall, 30.2% (95% CI 29.2%-31.1%) of patients achieved glycemic target (A1C < 7%). Although baseline disease severity and concurrent therapies differed greatly across therapeutic classes, after adjustment for these baseline clinical characteristics, no significant differences were noted in glucose-lowering effect across therapeutic classes. Treatment effects did not differ by age, race, diabetes duration, obesity, or level of renal function.
Conclusions:
Metformin, sulfonylures, thiazolidinediones, and insulin were equally effective in improving glucose control. Nonetheless, most patients failed to achieve the glycemic target. Findings suggest that, to keep up with progressive worsening of glycemic control, patients and providers must commit to earlier, more aggressive therapy intensification, triggered promptly after A1C exceeds the recommended glycemic target.
Insights
Most type 2 diabetes medications like metformin and insulin showed similar effectiveness in lowering A1C. However, many patients still didn't reach their glycemic target, indicating a need for earlier, more aggressive treatment intensification.
Area of Science:
- Endocrinology
- Pharmacology
- Public Health
Background:
- Real-world glycemic response to antihyperglycemic therapies for type 2 diabetes is understudied.
- Randomized controlled trials provide limited insight into actual clinical practice.
Purpose of the Study:
- To evaluate the real-world effectiveness of initiating new antihyperglycemic agents in type 2 diabetes patients.
- To compare the glycemic response across different classes of antihyperglycemic medications.
Main Methods:
- A cohort of 15,126 type 2 diabetes patients initiating metformin, sulfonylureas, thiazolidinediones, or insulin was studied.
- Glycosylated hemoglobin (A1C) changes were analyzed 3-12 months post-initiation using ANCOVA.
- Analyses were adjusted for baseline A1C, concurrent therapies, demographics, and clinical factors.
Main Results:
- Mean A1C decreased from 9.01% to 7.87% after initiating new therapy.
- Only 30.2% of patients achieved a glycemic target of A1C < 7%.
- No significant differences in glucose-lowering effects were observed among metformin, sulfonylureas, thiazolidinediones, and insulin after adjustments.
Conclusions:
- Metformin, sulfonylureas, thiazolidinediones, and insulin demonstrate comparable efficacy in improving glycemic control.
- A majority of patients do not achieve target A1C levels, highlighting a gap in treatment.
- Earlier and more aggressive therapy intensification is recommended to manage progressive glycemic worsening.
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