Introduction & Objective: Obesity is becoming a frequent comorbidity not only in patients with type 2 but also with type 1 diabetes mellitus (T1D). The aim of this study was to compare glucose control and prevalence of diabetes-associated complications in patients with T1D according to the presence of overweight or obesity.

Methods: Using data from the diabetes registry of a tertiary center, patients with T1D were stratified according to BMI into normal weight (BMI<25 kg/m2: n=831, age 40 (29-52) years (yr), T1D duration 20 (11-29) yr), overweight (BMI 25-30 kg/m2, n=741, age 46 (35-60) yr, T1D duration 23 (15-33) yr) and obese (BMI ≥30 kg/m2, n=366, age 48 (39-59) yr, T1D duration 24 (16-34) yr) and compared based on glucose control parameters (HbA1c, continuous glucose sensor metrics) and prevalence of diabetic complications and metabolic comorbidities.

Results: Compared with overweight and obese, patients with normal weight had a significantly lower HbA1c (56 (49-64) vs. 57 (51-65) vs. 60 (52-67), mmol/l, p<0.001), time above target range of 3.9-10 mmol/l(25 (16-39) vs. 28 (18-41) vs 31 (17-43)%, p=0.004) and average sensor glycemia (8.2 (7.4-9.3) vs. 8.4 (7.6-9.6) vs 8.7 (7.7-9.7) mmol/l, p<0.001). No significant difference was found in time in range or glycemic variability, while time below range was slightly lower in patients with obesity (3 (1-7) vs. 3 (1-7) vs. 3 (1-6), %, p=0.024). Higher BMI was associated with increased prevalence of arterial hypertension (32.7 vs. 46.4 vs. 65.6%, p=<0.001), dyslipidemia (38.4 vs. 54.1 vs. 70.7%, p=<0.001) and cardiovascular complications (6.7 vs. 10.1 vs. 12.4%, p= 0.004), as well as diabetic retinopathy (35.8 vs. 45.2 vs. 53.0%, p <0.001) and diabetic foot disease (4.6 vs. 5.5 vs. 9.7%, p= 0.003).

Conclusion: Our data indicate that an increase in BMI in patients with T1D is associated with worse glucose control and higher rate of diabetes complications and metabolic comorbidities.

Disclosure

L. Horváth: None. M. Mraz: None. D. Vávra: None. K. Sochorova: Consultant; Medtronic, Ypsomed AG. R. Bem: Speaker's Bureau; Abbott, A.import (Dexcom, Tandem), Medtronic. Research Support; Ministry of Health - Czech republic. Speaker's Bureau; Novo Nordisk. J. Klouckova: None. M. Haluzik: Advisory Panel; Sanofi, Novo Nordisk, Eli Lilly and Company, AstraZeneca, Bayer Inc., Johnson & Johnson Medical Devices Companies. Consultant; Merck & Co., Inc., Sanofi, Novo Nordisk, Eli Lilly and Company, AstraZeneca, Bayer Inc., Boehringer-Ingelheim, Johnson & Johnson Medical Devices Companies, Novatin. Research Support; Sanofi. Speaker's Bureau; Sanofi, Novo Nordisk.

Funding

Supported by the project CarDia (Programme EXCELES, Project No. LX22NPO5104); Funded by the European Union; Next Generation EU and Funded by Ministry of Health, Czech Republic; Conceptual Development of Research Organization ("Institute for Clinical and Experimental Medicine – IKEM, IN 00023001").

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.