Diabetes Care, Vol 23, Issue 11 1612-1618, Copyright © 2000 by American Diabetes Association
Appropriate insulin regimes for type 2 diabetes: a multicenter randomized crossover study
R Taylor, R Davies, C Fox, M Sampson, JU Weaver and L Wood
Diabetes Center, Newcastle upon Tyne, UK. roy.taylor@ncl.ac.uk
OBJECTIVE: To directly compare the rate of hypoglycemia and metabolic
control achieved on once-daily ultralente insulin administration with
twice-daily NPH insulin administration in patients with type 2 diabetes.
Patient treatment satisfaction and quality of life were also examined
before and during each treatment. RESEARCH DESIGN AND METHODS: A crossover
study was performed involving five centers and 79 patients with type 2
diabetes (fasting blood glucose > 8 mmol/l) with a 2-month run-in
followed by two 6-month periods of either NPH or ultralente insulin
administration. Patients were managed by a specialist nurse using a dosage
adjustment protocol. RESULTS: HbA1c was lower with NPH insulin therapy
during each of the 6-month periods (9.7 +/- 0.2 vs. 9.1 +/- 0.3 and 9.8 +/-
0.2 vs. 9.0 +/- 0.3 mmol/l; both P < 0.01). The difference was accounted
for by higher evening glucose levels with ultralente insulin (fasting 8.2
+/- 0.3 vs. 8.2 +/- 0.3 mmol/l, 6:00 P.M. 11.5 +/- 0.4 vs. 10.6 +/- 0.4
mmol/l). Despite worse control, the total number of hypoglycemic episodes
was greater with ultralente insulin (220 vs. 171), and hypoglycemic
episodes requiring third-party assistance occurred almost entirely with
ultralente (14 vs. 1). Treatment satisfaction scores increased more with
NPH insulin compared with ultralente and rose further upon changing to NPH
insulin, but fell upon changing to ultralente insulin. These changes were
highly significant (P < 0.001). Diabetes quality of life improved on
both regimens. CONCLUSIONS: These data clearly demonstrate the lower
hypoglycemia rate, better glucose control, and greater treatment
satisfaction accompanying therapy for type 2 diabetes with twice daily NPH
compared with once daily ultralente insulin.