Administration of Neutral Protamine Hagedorn Insulin at Bedtime versus with Dinner in Type 1 Diabetes Mellitus To Avoid Nocturnal Hypoglycemia and Improve Control
- 2 April 2002
- journal article
- research article
- Published by American College of Physicians in Annals of Internal Medicine
- Vol. 136 (7) , 504-514
- https://doi.org/10.7326/0003-4819-136-7-200204020-00007
Abstract
Background: intensive insulin treatment of type I diabetes mellitus increases the risk for nocturnal hypoglycemia. Objective: To demonstrate that splitting the evening insulin regimen reduces the risk for nocturnal hypoglycemia in intensive treatment of type 1 diabetes mellitus. Design: Randomized, open, two-treatment crossover trial in two 4-month periods. Setting: University research center in Italy. Patients: 22 C-peptide-negative persons with type I diabetes mellitus (mean age [+/-SD], 29 +/- 3 years). Interventions: Each patient was randomly assigned to one of two insulin regimens for 4 months and then switched to the other regimen for another 4 months. The two treatment regimens were 1) mixed treatment-a mixture of human regular and neutral protamine Hagedom (NPH) insulin administered before dinner and 2) split treatment-human regular insulin administered at dinner and NPH insulin administered at bedtime. Measurements: Frequency of nocturnal hypoglycemia. Secondary end points were levels of fasting blood glucose and hemoglobin A(1c) and responses to experimental hypoglycemia. Results: During the split-regimen treatment period, patients had fewer episodes of nocturnal hypoglycemia (mean [+/-SE], 0.10 +/- 0.02 episode/patient-day vs. 0.28 +/- 0.04 episode/patientday; P = 0.002), a lower fasting blood glucose level (mean [+/-SE], 7.6 +/- 0.2 mmol/L vs. 8,3 +/- 0.5 mmol/L [137 +/- 4 mg/dL vs. 160 +/- 8 mg/dL]; P = 0.030), less variable fasting blood glucose levels (SD range, 2.0 +/- 0.4 vs. 3.5 +/- 0.6; P = 0.001), and lower hemoglobin A(1c) value (mean [+/-SE], 7.0% +/- 0.11% vs. 7.5% +/- 0.15%; P = 0.004) than during the mixed regimen. Responses to experimental hypoglycemia were better preserved with the split regimen than with the mixed regimen. Conclusion: When the goal of insulin therapy in type 1 diabetes mellitus is near-normoglycemia, splitting the evening insulin treatment regimen into short-acting insulin at dinner and NPH insulin at bedtime reduces the risks for nocturnal hypoglycemia and hypoglycemia unawareness and decreases the hemoglobin A(1c) value compared with mixing short-acting insulin and NPH insulin at dinner.Keywords
This publication has 37 references indexed in Scilit:
- Pharmacokinetics and pharmacodynamics of subcutaneous injection of long-acting human insulin analog glargine, NPH insulin, and ultralente human insulin and continuous subcutaneous infusion of insulin lispro.Diabetes, 2000
- Insulin aspart vs. human insulin in the management of long‐term blood glucose control in Type 1 diabetes mellitus: a randomized controlled trialDiabetic Medicine, 2000
- Alterations in sleep physiology in young children with insulin-dependent diabetes mellitus: Relationship to nocturnal hypoglycemiaThe Journal of Pediatrics, 2000
- Less hypoglycemia with insulin glargine in intensive insulin therapy for type 1 diabetes. U.S. Study Group of Insulin Glargine in Type 1 Diabetes.Diabetes Care, 2000
- Efficacy and safety of HOE 901 versus NPH insulin in patients with type 1 diabetes. The European Study Group of HOE 901 in type 1 diabetes.Diabetes Care, 2000
- Insulin analogues and their potential in the management of diabetes mellitusDiabetologia, 1999
- Long-term intensive treatment of type 1 diabetes with the short-acting insulin analog lispro in variable combination with NPH insulin at mealtime.Diabetes Care, 1999
- Impact of nocturnal hypoglycemia on hypoglycemic cognitive dysfunction in type 1 diabetes.Diabetes, 1998
- A simple radioimmunoassay for plasma cortisolClinica Chimica Acta; International Journal of Clinical Chemistry, 1978
- Effects of arterial versus venous sampling on analysis of glucose kinetics in manJournal of Applied Physiology, 1976