Volume 373, Issue 9682, Pages (June 2009)

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Volume 373, Issue 9682, Pages 2215-2221 (June 2009) Trajectories of glycaemia, insulin sensitivity, and insulin secretion before diagnosis of type 2 diabetes: an analysis from the Whitehall II study  Dr Adam G Tabák, MD, Markus Jokela, PhD, Tasnime N Akbaraly, PhD, Eric J Brunner, PhD, Prof Mika Kivimäki, PhD, Daniel R Witte, MD  The Lancet  Volume 373, Issue 9682, Pages 2215-2221 (June 2009) DOI: 10.1016/S0140-6736(09)60619-X Copyright © 2009 Elsevier Ltd Terms and Conditions

Figure 1 Fasting (A) and 2-h postload (B) glucose trajectories before diagnosis of diabetes or the end of follow-up Numbers are 505 incident diabetes cases and 6033 non-diabetics. Time 0 is diagnosis for incident diabetes cases or end of follow-up for non-diabetics. Multilevel longitudinal modelling was done using linear growth model for non-diabetic and piecewise approach, including cubic terms for time, for incident diabetic individuals with oral glucose tolerance test fasting glucose (A) and 2-h glucose (B) as outcomes. Analysis was adjusted for age, sex, ethnic origin, and study phase. Estimations were done for a hypothetical population consisting of 71% male, 91% white individuals aged 63 years at time 0 years. Error bars show 95% CI for the fixed effects. Tables show the number of measurements for each year at and before diabetes diagnosis or the end of follow-up. The Lancet 2009 373, 2215-2221DOI: (10.1016/S0140-6736(09)60619-X) Copyright © 2009 Elsevier Ltd Terms and Conditions

Figure 2 Homoeostasis model assessment (HOMA) insulin sensitivity (A) and HOMA β-cell function trajectories (B) before diagnosis of diabetes or the end of follow-up Numbers are 505 incident diabetes cases and 6033 non-diabetics. Time 0 is diagnosis for incident diabetes cases or end of follow-up for non-diabetics. Multilevel longitudinal modelling was done using linear growth model for non-diabetic and non-piecewise or piecewise approach, including linear or quadratic terms for time, for incident diabetic individuals with HOMA2-%S (A) and HOMA2-%B (B) as outcomes. Analysis was adjusted for age, sex, ethnic origin, and study phase. Estimations were done for a hypothetical population consisting of 71% male, 91% white individuals aged 63 years at time 0 years. Error bars show 95% CI for the fixed effects. Tables show the number of measurements for each year at and before diabetes diagnosis or the end of follow-up. HOMA2-%S=homoeostasis model assessment insulin sensitivity. HOMA2-%B=homoeostasis model assessment β-cell function. The Lancet 2009 373, 2215-2221DOI: (10.1016/S0140-6736(09)60619-X) Copyright © 2009 Elsevier Ltd Terms and Conditions