Abstract

ObjectiveMultiple daily injections (MDI) therapy is the most common treatment for type 1 diabetes (T1D), consisting of long-acting insulin to cover fasting conditions and rapid-acting insulin to cover meals. Titration of long-acting insulin is needed to achieve satisfactory glycemia but is challenging due to inter-and intra-individual metabolic variability. In this work, a novel titration algorithm for long-acting insulin leveraging continuous glucose monitoring (CGM) and smart insulin pens (SIP) data is proposed.MethodsThe algorithm is based on a glucoregulatory model that describes insulin and meal effects on blood glucose fluctuations. The model is individualized on patient’s data and used to extract the theoretical glucose curve in fasting conditions; the individualization step does not require any carbohydrate records. A cost function is employed to search for the optimal long-acting insulin dose to achieve the desired glycemic target in the fasting state. The algorithm was tested in two virtual studies performed within a validated T1D simulation platform, deploying different levels of metabolic variability (nominal and variance). The performance of the method was compared to that achieved with two published titration algorithms based on self-measured blood glucose (SMBG) records. The sensitivity of the algorithm to carbohydrate records was also analyzed.ResultsThe proposed method outperformed SMBG-based methods in terms of reduction of exposure to hypoglycemia, especially during the night period (0 am–6 am). In the variance scenario, during the night, an improvement in the time in the target glycemic range (70–180 mg/dL) from 69.0% to 86.4% and a decrease in the time in hypoglycemia (<70 mg/dL) from 10.7% to 2.6% was observed. Robustness analysis showed that the method performance is non-sensitive to carbohydrate records.ConclusionThe use of CGM and SIP in people with T1D using MDI therapy has the potential to inform smart insulin titration algorithms that improve glycemic control. Clinical studies in real-world settings are warranted to further test the proposed titration algorithm.SignificanceThis algorithm is a step towards a decision support system that improves glycemic control and potentially the quality of life, in a population of individuals with T1D who cannot benefit from the artificial pancreas system.

Highlights

  • In type 1 diabetes (T1D), life-long insulin replacement is required to compensate for the practically nonexistent insulin secretion due to the autoimmune destruction of the pancreatic beta-cells [1]

  • Comparing the last 15 days of the 120-day simulation to the baseline period, the Continuous glucose monitoring (CGM)-Opt did not change TIR in the nominal scenario (+1.0% confidence interval (CI)(-1.5% to 3.6%)), but increased TIR from 57.4% (±14.6%) to 63.6% (±15.4%) by +6.2% CI (3.6% to 8.8%) in the variance scenario

  • The CGM-Opt performed exceptionally well during the night period, where TIR increased by +16.1% CI(11.0% to 21.1%) in the nominal scenario and by +17.4% CI(13.8% to 21.0%) in the variance scenario, while TBR was decreased by -14.0% CI(-19.0% to -8.9%) in the nominal scenario and by -8.1% CI(-11.6% to -4.6%) in the variance scenario

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Summary

Introduction

In type 1 diabetes (T1D), life-long insulin replacement is required to compensate for the practically nonexistent insulin secretion due to the autoimmune destruction of the pancreatic beta-cells [1]. Glucose regulation is a challenging task, as it is heavily dependent on multiple daily treatment decisions by the patient to account for a wide variety of factors influencing insulin demand, e.g., circadian rhythms, physical activity, food, and stress. Most patients run the risk of developing longterm micro-/macro-vascular complications due to sustained hyperglycemia [2, 3]. Tight glucose control is key to avoiding long-term complications, but fear of hypoglycemia due to overdosing on insulin remains a limiting factor [4]. T1D patients are still not achieving their glycemic targets [9], with complication rates and excess mortality significantly higher in T1D compared to the general population [10]

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