We examined the relationship between habitual daily activity and measures of GT, insulin sensitivity and β-cell responses in 230 adults (mean age 55 y; BMI 35 kg/m2) with IGT or drug-naïve, recently diagnosed T2D. Participants underwent a 3-h OGTT and hyperglycemic clamp. Wrist accelerometers worn for 7 days measured total activity counts (TAC; daily mean 233,461 {∼ 50th %ile for age}). We evaluated whether TAC predicted fasting plasma glucose (FPG); OGTT 2-h plasma glucose (2-h G) or glucose incremental area under the curve (G-iAUC); hyperglycemic clamp measures of insulin sensitivity (steady-state glucose infusion rate/insulin [M/I]) and β-cell responses (acute C-peptide response to glucose [ACPRg], steady-state C-peptide, maximal β-cell response [ACPRmax]); and OGTT C-peptide index (CPI, [ΔC-Peptide0-30/ΔGlucose0-30]). There was no association of TAC with FPG, 2-h G, or G-iAUC. Higher TAC was associated with higher insulin sensitivity. After adjusting for M/I, higher TAC was associated with lower CPI, but not with clamp-based β-cell responses. Despite similar post-load glucose values, adults with IGT or T2D who were more active demonstrated a greater than expected reduction in C-peptide response given their higher insulin sensitivity. Further studies are needed to understand this dissociation of activity effects on insulin sensitivity and β-cell function.
Disclosure

K.A. Temple: None. A.H. Tjaden: None. K.M. Atkinson: None. E. Barengolts: None. T.S. Hannon: Advisory Panel; Self; Eli Lilly and Company. K.J. Mather: Advisory Panel; Self; Roche Diabetes Care. Research Support; Self; Abbott, Merck & Co., Inc., Novo Nordisk A/S, Sanofi. K. Utzschneider: Consultant; Self; Novo Nordisk Inc. D.A. Ehrmann: None. B. Mokhlesi: None. R. Consortium: None.

Funding

National Heart, Lung, and Blood Institute; National Institute of Diabetes and Digestive and Kidney Diseases

Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. More information is available at http://www.diabetesjournals.org/content/license.