Diabetes Care, Vol 20, Issue 12 1870-1873, Copyright © 1997 by American Diabetes Association
Nighttime insulin kinetics and glycemic control in type 1 diabetes patients following administration of an intermediate-acting lispro preparation
MM Janssen, S Casteleijn, W Deville, C Popp-Snijders, P Roach and RJ Heine
Research Institute for Endocrinology, Reproduction, and Metabolism, Faculty of Medicine, Vrije Universiteit, Amsterdam, The Netherlands.
OBJECTIVE: To determine insulin kinetics and overnight glycemic control
after bedtime administration of a new intermediate-acting insulin
preparation called neutral protamine lispro (NPL). RESEARCH DESIGN AND
METHODS: We studied 12 patients with well-controlled type 1 diabetes. The
study had a double-blind, randomized, crossover design. After a lead-in
period of 10-14 days two experiments were carried out with an interval of
2-7 days. During these experiments overnight insulin kinetics and fasting
blood glucose levels were studied after evening administration of NPH
insulin and NPL. Blood glucose levels < 3.8 mmol/l were treated by means
of a variable infusion of a 20% glucose solution. RESULTS: A trend toward a
shorter time to peak insulin concentration was observed after
administration of NPL (P = 0.07). No differences between NPH and NPL were
detected in the total area under the curve (AUC) for insulin, in insulin
levels before breakfast, or in glucose levels before breakfast (P = 0.5,
0.6, and 0.4, respectively). CONCLUSIONS: We detected no major differences
between NPH and NPL in the total AUC for insulin, prebreakfast glucose
levels, or prebreakfast insulin levels. Therefore, we conclude that NPH and
NPL are equally effective in controlling overnight glycemia.