Distribution of daily frequency of BGM

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Hyperinsulinemic-euglycemic clamp–derived insulin sensitivity (glucose disposal), model-derived insulin secretion parameters (sensitivity first-phase insulin.
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Time course of daily basal and mealtime insulin dose (A), glycated hemoglobin (B), laboratory-measured clinic FPG (C), prebreakfast SMPG (D), SMPG profiles.
A: Glucose levels during basal-bolus and SSI treatment.
Change in first-phase insulin response (A) and pancreas triglyceride content (B) in responders and nonresponders at baseline (hatched bars), after VLCD.
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Cumulative distributions of A1C and fasting plasma glucose values for the U.S. population aged ≥12 years without diabetes for each survey cycle: 1999–2000,
Four–time point diurnal profiles of plasma glucose concentrations (A) and AUCs (B) over quintiles of HbA1c. ○, AUC1; •, AUC2; ▴, AUC2 − AUC1 (differences.
Changes of major clinical and biochemical characteristics at baseline and during follow-up in different groups. Changes of major clinical and biochemical.
Cumulative mean numbers of confirmed (plasma glucose ≤3
Insulin secretion (hyperglycemic clamp) (A), insulin sensitivity (hyperinsulinemic-euglycemic clamp) (B), and glucose disposition index (GDI) (C) in adolescents.
Presentation transcript:

Distribution of daily frequency of BGM Distribution of daily frequency of BGM. Youth who remained on insulin pump therapy checked blood glucose levels significantly more often, both at pump initiation (χ2 = 5.93, P = 0.05) and after 1 year (χ2 = 6.99, P = 0.03), compared with youth who discontinued pump therapy. , remained on pump; ▪, discontinued therapy. Distribution of daily frequency of BGM. Youth who remained on insulin pump therapy checked blood glucose levels significantly more often, both at pump initiation (χ2 = 5.93, P = 0.05) and after 1 year (χ2 = 6.99, P = 0.03), compared with youth who discontinued pump therapy. , remained on pump; ▪, discontinued therapy. Jamie R. Wood et al. Dia Care 2006;29:2355-2360 ©2006 by American Diabetes Association