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Published on: June 11, 2012
HbA1c variability in adults with type 1 diabetes on continuous subcutaneous insulin infusion (CSII) therapy compared
Emma S Scott1,2, Rachel T McGrath2,3, Andrzej S Januszewski1,4
1NHMRC Clinical Trials Centre, University of Sydney, Camperdown, New South Wales, Australia.
Insights
Continuous subcutaneous insulin infusion (CSII) therapy significantly lowers glycated haemoglobin (HbA1c) variability in adults with type 1 diabetes mellitus (T1DM) compared to multiple daily injections (MDI). This improvement is observed both in established users and those transitioning from MDI to CSII.
Area of Science:
- Endocrinology and Metabolism
- Diabetes Research
- Clinical Therapeutics
Background:
- Type 1 diabetes mellitus (T1DM) management requires precise glycemic control to mitigate long-term complications.
- Glycemic variability (GV), indicated by fluctuations in glycated haemoglobin (HbA1c), is a critical factor influencing diabetes outcomes.
- Continuous subcutaneous insulin infusion (CSII) and multiple daily injections (MDI) are primary treatment modalities for T1DM.
Purpose of the Study:
- To compare long-term glycemic variability (GV) between continuous subcutaneous insulin infusion (CSII) and multiple daily injection (MDI) therapies in adults with type 1 diabetes mellitus (T1DM).
- To assess the impact of transitioning from MDI to CSII on glycemic variability.
Main Methods:
- Retrospective audit of clinic records from 506 adults with T1DM at two Australian tertiary hospitals.
- Assessment of long-term GV using HbA1c standard deviation (SD) and coefficient of variation (CV).
- Analysis included patients on established MDI or CSII, and a subset who transitioned from MDI to CSII.
Main Results:
- CSII therapy was associated with significantly lower GV compared to MDI therapy (HbA1c SD: 0.5% vs 0.7%, p<0.001; HbA1c CV: 6.7% vs 9.3%, p<0.001).
- In a subset of 56 adults transitioning from MDI to CSII, mean HbA1c decreased by 0.4%.
- Glycemic variability significantly decreased post-transition to CSII (HbA1c SD: 0.7% to 0.4%, p<0.001; HbA1c CV: 9.2% to 6.1%, p<0.001).
Conclusions:
- Continuous subcutaneous insulin infusion (CSII) therapy is associated with reduced glycated haemoglobin (HbA1c) variability in adults with type 1 diabetes mellitus (T1DM) when compared to multiple daily injections (MDI).
- Transitioning from MDI to CSII leads to a significant reduction in glycemic variability.
- CSII represents a valuable therapeutic option for improving glycemic control and reducing variability in T1DM management.
Objective:
To determine if continuous subcutaneous insulin infusion (CSII) therapy is associated with lower glycated haemoglobin (HbA1c) variability (long-term glycaemic variability; GV) relative to multiple daily injection (MDI) treatment in adults with type 1 diabetes mellitus (T1DM).
Design:
Retrospective audit.
Setting And Participants:
Clinic records from 506 adults with T1DM from two tertiary Australian hospitals.
Outcome Measures:
Long-term GV was assessed by HbA1c SD and coefficient of variation (CV) in adults on established MDI or CSII therapy, and in a subset changing from MDI to CSII.
Results:
Adults (n=506, (164 CSII), 50% women, mean±SD age 38.0±15.3 years, 17.0±13.7 years diabetes, mean HbA1c 7.8%±1.2% (62±13 mmol/mol) on CSII, 8.0%±1.5% (64±16 mmol/mol) on MDI) were followed for 4.1±3.6 years. CSII use was associated with lower GV (HbA1c SD: CSII vs MDI 0.5%±0.41% (6±6 mmol/mol) vs 0.7%±0.7% (9±8 mmol/mol)) and CV: CSII vs MDI 6.7%±4.6% (10±10 mmol/mol) vs 9.3%±7.3% (14±13 mmol/mol), both p<0.001. Fifty-six adults (73% female, age 36±13 years, 16±13 years diabetes, HbA1c 7.8%±0.8% (62±9 mmol/mol)) transitioned from MDI to CSII. Mean HbA1c fell by 0.4%. GV from 1 year post-CSII commencement decreased significantly, HbA1c SD pre-CSII versus post-CSII 0.7%±0.5% (8±5 mmol/mol) vs 0.4%±0.4% (5±4 mmol/mol); p<0.001, and HbA1c CV 9.2%±5.5% (13±8 mmol/mol) vs 6.1%±3.9% (9±5 mmol/mol); p<0.001.
Conclusions:
In clinical practice with T1DM adults relative to MDI, CSII therapy is associated with lower HbA1c GV.
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