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Effect of prolonged oral terbutaline therapy on glucose tolerance in pregnancy
Journal article   Peer reviewed

Effect of prolonged oral terbutaline therapy on glucose tolerance in pregnancy

Michael R. Foley, Mark B. Landon, Steven G. Gabbe, Thomas M. O’Dorisio, Michael Waxman, Rita Leard and Jay D. lams
American journal of obstetrics and gynecology, Vol.168(1), pp.100-105
1993
PMID: 8420308

Abstract

gestational diabetes glucose intolerance Terbutaline tocolysis
Objective: Our objective was to elucidate the pathophysiologic effects and potential reversibility of terbutaline-induced changes in carbohydrate metabolism. Study Design: We prospectively evaluated serum glucose, insulin, glucagon, C-peptide, and pancreatic polypeptide levels in response to a 100 gm glucose challenge (oral 3-hour glucose tolerance test) in 17 obstetric patients without complications who were given terbutaline (5 mg orally every 4 hours) for 5 consecutive days between 24 and 32 weeks' gestation. Each patient served as her own control, with day 1 representing pretreatment, day 7 the treatment phase, and day 14 the posttreatment evaluation. Body mass index and posttreatment serum terbutaline levels were also measured. Results: A significant initial treatment effect (day 1 versus 7) was observed for glucose (elevated), insulin (elevated), insulin/glucose ratio (elevated), and pancreatic polypeptide (elevated). A significant delayed treatment effect (day 1 versus 14) was also observed for insulin (elevated), insulin/glucose ratio (elevated), and pancreatic polypeptide (elevated). Body mass index directly correlated with postchallenge measures of insulin, insulin/glucose ratio, pancreatic polypeptide, and C-peptide. Posttreatment serum terbutaline levels directly correlated with pancreatic polypeptide, but not with other parameters. Conclusions: Our data support a dose-independent, terbutaline-induced glucose intolerance mediated by glucagon and caused by diminished insulin sensitivity. © 1993, Mosby. All rights reserved.

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