UZ Leuven
Clinical and Experimental Endocrinology
Ms. Jolien De Meulemeester obtained a master’s degree in Biomedical Sciences at the KU Leuven (Belgium) in 2021. She then started a PhD at the department of Endocrinology, University Hospitals Leuven. Her PhD focuses on the use of hybrid closed-loop devices in people with type 1 diabetes, and is supervised by Prof. Pieter Gillard.

Presenter of 1 Presentation

THE RELATIONSHIP BETWEEN CHRONIC COMPLICATIONS AND TIME IN RANGE IN PEOPLE WITH TYPE 1 DIABETES: A RETROSPECTIVE CROSS-SECTIONAL REAL-WORLD STUDY

Session Type
Oral Presentations Session
Date
Sat, 30.04.2022
Session Time
11:00 - 12:30
Room
Hall 119
Lecture Time
11:00 - 11:08

Abstract

Background and Aims

Time in range (TIR; glucose of 70-180 mg/dL) overcomes some of the limitations of HbA1c in the individual assessment of glycemic control. This study evaluates whether TIR is associated with the presence of chronic complications in a real-world population of people with type 1 diabetes (T1D).

Methods

Sensor-measured TIR and the occurrence of microvascular (diabetic retinopathy [DR], diabetic nephropathy [DN], diabetic peripheral neuropathy [DPN]) and macrovascular complications in 812 people with T1D were analyzed cross-sectionally. Binary logistic regression was used to evaluate the contribution of TIR to the presence of chronic complications, after correction for sex, age, diabetes duration, BMI, blood pressure, lipid profile, smoking, lipid lowering and antihypertensive therapy.

Results

Mean TIR was 52.7 ± 15.2%. Overall, 46.1% had at least one microvascular complication (34.5% DR, 23.9% DN, 16% DPN) and 16.6% suffered from any macrovascular complication. The prevalence of at least one microvascular complication (p for trend <0.001), DR (p for trend <0.001) and DN (p for trend =0.036) decreased with increasing TIR quartiles (figure 1). The odds ratio of having at least one microvascular complication, DR, DN, DPN or any macrovascular complication per 1% increase in TIR was 0.969 (95%CI: 0.957-0.982, p<0.001), 0.959 (95%CI: 0.945-0.974, p<0.001), 0.981 (95%CI: 0.967-0.995, p=0.008), 0.980 (95%CI: 0.964-0.997, p=0.019) and 0.975 (95%CI: 0.958-0.992, p=0.005) respectively.

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Conclusions

TIR is inversely associated with the presence of chronic diabetes complications. These data add validity to the use of TIR as key measure of glycemic control and endpoint of clinical trials, in addition to HbA1c.

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