Abstract
The initial injection in 1922 of a pancreatic extract, or insulin as it came to be
known, into a patient with diabetes mellitus has since been followed by the successive
introduction of longer-acting insulins, more highly purified insulins, and insulins
that have been modified to more closely match insulin activity to patients' physiologic
requirements. The recently introduced rapid-acting insulin analogues lispro and aspart
and the long-acting analogue glargine are further refinements of insulin therapy.
Current treatment strategies for severe insulin deficiency are based on the need to
provide 2 components of insulin replacement: basal and postprandial. Rapid-acting
insulin has been shown to provide superior postprandial glucose control compared with
regular insulin. Truly effective control of basal insulin has been achieved by the
introduction of the insulin pump in the 1980s and insulin glargine in 2001. Insulin
glargine is the first insulin analogue to provide, in a majority of patients, a continuous
level of insulin without a pronounced peak after a single daily injection, closely
mimicking the normal pancreatic release of basal insulin in healthy individuals. Clinical
experience is providing many insights into how basal and prandial components of insulin
therapy can be best combined, although evidence from controlled trials will take some
years to accumulate. Experience and observations since 2001 indicate that insulin
therapy should be introduced earlier in patients with type 2 diabetes to control blood
glucose levels. More importantly, the greatest benefit of insulin glargine has been
to change positively the way physicians and patients think about insulin therapy.
Newer insulin analogues, improved devices for home glucose monitoring, and pulmonary
inhaled insulin are other innovations that promise improvement of hemoglobin A1c levels.
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References
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© 2004 Excerpta Medica Inc. Published by Elsevier Inc. All rights reserved.