Key result
Lower baseline basal disposition index and higher fasting plasma glucose predicted secondary sulfonylurea failure, while their combination with primary failure improved prediction.
Why the study?
Do baseline clinical characteristics predict primary and secondary sulfonylurea failure in patients with type 2 diabetes?
RCT (n=747)
Do baseline clinical characteristics predict primary and secondary sulfonylurea failure in patients with type 2 diabetes?
Baseline basal disposition index combined with initial glycemic response at one month can predict the long-term efficacy of sulfonylurea treatment in type 2 diabetes.
Answers are grounded in this paper and cite their sources.
May aid prediction of sulfonylurea failure; hypothesis-generating and should not yet change practice.
Background The aim of the present study was to investigate the value of clinical characteristics in predicting sulfonylurea ( SU ) treatment responses. Methods All 747 subjects in the present study were from the X iaoke P ill C linical T rial evaluating the safety and efficacy of SU . Subjects had the same initial dose of glibenclamide and drug doses were adjusted every 4 weeks during the 48‐week follow‐up period. Primary SU failure was defined as a <10% reduction in fasting plasma glucose ( FPG ) at the end of W eek 4 from randomization, whereas secondary SU failure was defined as a consecutive confirmed level of FPG >7 mmol/L. Results Kaplan– M eier survival analysis revealed that lower baseline basal disposition index ( DI b ) and higher FPG predict secondary SU failure. Inversely, higher baseline DI b and lower FPG predict primary SU failure. Primary SU failure can predict secondary SU failure. The combination of lower baseline DI b with primary SU failure is a better predictor of secondary SU failure than lower baseline DI b or primary SU failure alone. Conclusions Patients with good glycemic control and higher β‐cell reserve at entry are more likely to experience primary SU failure but are less likely to experience secondary SU failure. By combining baseline DI b with initial response at the first month of treatment, we can get quick information about the long‐term efficacy of SU treatment.
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Wang et al. (2017) conducted an RCT in Type 2 diabetes (n=747). Sulfonylurea (glibenclamide) was evaluated on Primary sulfonylurea failure (<10% reduction in FPG at Week 4) and secondary sulfonylurea failure (consecutive FPG >7 mmol/L). Lower baseline basal disposition index and higher fasting plasma glucose predicted secondary sulfonylurea failure, while their combination with primary failure improved prediction.
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