Sabine E Hofer1, Kellee Miller2, Julia M Hermann3,4, Daniel J DeSalvo5, Michaela Riedl6, Irl B Hirsch7, Wolfram Karges8, Roy W Beck2, Reinhard W Holl3,4, David M Maahs9. 1. Department of Pediatrics, Medical University of Innsbruck, Innsbruck, Austria sabine.e.hofer@i-med.ac.at. 2. Jaeb Center for Health Research, Tampa, FL. 3. ZIBMT, Institute of Epidemiology and Medical Biometry, University of Ulm, Ulm, Germany. 4. German Center for Diabetes Research, München-Neuherberg, Germany. 5. Baylor College of Medicine, Houston, TX. 6. Department of Internal Medicine, Medical University of Vienna, Vienna, Austria. 7. University of Washington, Seattle, WA. 8. Division of Endocrinology and Diabetes, RWTH Aachen University, Aachen, Germany. 9. Lucile Packard Children's Hospital, Stanford University School of Medicine, Stanford, CA.
We thank the editors for the opportunity to respond to the comment made by Balkau et al. (1) on our recent article (2).Balkau et al. (1) were interested in detailed information about HbA1c in the overall group stratified by registry. As stated in the text, HbA1c was similar between the two registries. In the T1D Exchange Registry (TIDX), HbA1c was 8.6% (SE 0.06) in current smokers, 8.0% (0.05) in former smokers, and 7.9% (0.05) in never-smokers (P < 0.001). In the Prospective Diabetes Follow-up Registry (DPV), HbA1c was 8.5% (0.07) in current smokers, 8.2% (0.08) in former smokers, and 7.8% (0.06) in never-smokers (P < 0.001). The findings by Soulimane et al. (3) in a population without diabetes are of interest to the field as we try to better understand the best markers of glycemia. However, HbA1c is currently the best standardized and internationally comparable measurement of metabolic control in patients with diabetes. Our data describe significant differences in mean HbA1c between current smokers and never-smokers (8.5% and 7.9%, respectively, or a difference of 0.6%) in patients with type 1 diabetes versus a 0.1% difference in subjects who were not treated with glucose-lowering agents, as reported in the meta-analysis by Soulimane et al. (3). Further studies are required to investigate mechanistic explanations of whether this difference is due to nicotine, red blood cell turnover, or other physiological factors or to smoking-associated behavioral influences on metabolic control. The observation of significantly higher HbA1c levels in smokers is itself of concern. Data from a T1DX study investigating whether a racial difference exists in the relationship between continuous glucose monitoring glucose over 3 months and HbA1c were presented at the 2016 American Diabetes Association Scientific Sessions (4).
Authors: Sabine E Hofer; Kellee Miller; Julia M Hermann; Daniel J DeSalvo; Michaela Riedl; Irl B Hirsch; Wolfram Karges; Roy W Beck; Reinhard W Holl; David M Maahs Journal: Diabetes Care Date: 2016-08-16 Impact factor: 19.112
Authors: Soraya Soulimane; Dominique Simon; William H Herman; Celine Lange; Crystal M Y Lee; Stephen Colagiuri; Jonathan E Shaw; Paul Z Zimmet; Dianna Magliano; Sandra R G Ferreira; Yanghu Dong; Lei Zhang; Torben Jorgensen; Jaakko Tuomilehto; Viswanathan Mohan; Dirk L Christensen; Lydia Kaduka; Jacqueline M Dekker; Giel Nijpels; Coen D A Stehouwer; Olivier Lantieri; Wilfred Y Fujimoto; Donna L Leonetti; Marguerite J McNeely; Knut Borch-Johnsen; Edward J Boyko; Dorte Vistisen; Beverley Balkau Journal: Diabetologia Date: 2013-09-25 Impact factor: 10.122