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Person-reported and continuous glucose monitoring (CGM) recorded hypoglycaemia in people with insulin-treated type 2 diabetes and mild to moderate chronic kidney disease; post hoc analysis from the Hypo-METRICS study

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Abstract

Background & aims People with diabetes and chronic kidney disease (CKD) may be at increased risk of iatrogenic hypoglycaemia. We compared rates of sensor-detected (SDH) and person-reported hypoglycaemia (PRH) in people with insulin-treated type 2 diabetes (T2D) with and without CKD in the Hypo-METRICS study. Materials & Method Insulin-treated T2D patients with >1 hypoglycaemic episode within the last three months wore a blinded continuous glucose monitor (CGM) and recorded PRH on the bespoke Hypo-METRICS app for ten weeks. SDH was defined as per consensus guidelines. The participants were grouped based on estimated glomerular filtration rate (eGFR), i.e. CKD 1 (eGFR≥90 ml/min; n=117), CKD 2 (eGFR 60-89 ml/min; n=140), and CKD 3 (eGFR 30-59 ml/min; n=56). We used descriptive statistics, Kruskal-Wallis rank sum tests, and a negative binomial models to control for confounders. Results In total, 313 participants with T2DM were included. Median age increased with declining eGFR (p < 0.001). Median (IQR) events per week for SDH <3.9 mmol/L were 1.72 (0.66–3.43) in CKD 1, 2.12 (0.85–4.55) in CKD 2, and 2.22 (1.09–4.57) in CKD 3 (p=0.12). For SDH <3.0 mmol/L, these rates were 0.20 (0.00–0.50), 0.21 (0.10–0.61), and 0.20 (0.00–0.71), respectively (p=0.88). PRH events had medians of 1.05 (0.40–2.12), 1.31 (0.61–2.42), and 1.28 (0.68–2.25) for CKD 1, CKD 2, and CKD 3 (p=0.24). Conclusion In people with insulin-treated T2DM and CKD stages 2 or 3, the rates of SDH and PRH do not significantly differ from those in people without CKD. The study was registered on ClinicalTRials.gov (NCT04304963).

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Journal Title

Diabetes, Obesity and Metabolism

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Journal ISSN

1462-8902
1463-1326

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Publisher

Wiley

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Except where otherwised noted, this item's license is described as Attribution 4.0 International
Sponsorship
This work was supported by the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement 777460. JU receives support from the European Union’s Horizon 2020 Research and Innovation Programme and European Federation of Pharmaceutical Industries and Associations and T1D Exchange, Juvenile Diabetes Research Foundation, International Diabetes Federation, and The Leona M. and Harry B. Helmsley Charitable Trust. The industry partners supporting JU include Abbott Diabetes Care, Eli Lilly, Medtronic, Novo Nordisk, and Sanofi-Aventis. Abbott Diabetes Care provided the continuous glucose monitors used in the study.