HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Contribution of the dawn phenomenon to the fasting and postbreakfast hyperglycemia in type 1 diabetes treated with once-nightly insulin glargine.

AbstractOBJECTIVE:
To observe the effect of the dawn phenomenon on basal glucose and postbreakfast hyperglycemia in patients with type 1 diabetes treated with once-nightly insulin glargine and premeal insulin lispro.
METHODS:
In 49 study subjects consuming a fixed isocaloric (50% carbohydrate) diet of usual food, the insulin glargine dose was titrated from daily continuous glucose monitoring downloads to achieve a basal glucose goal of <130 mg/dL 4 hours after meals and during serial meal omissions but with fewer than 10% of readings at <70 mg/dL during 24 hours. Patients also performed self-monitoring of plasma glucose 7 times a day (before and 2 hours after each meal or omitted meal and at bedtime).
RESULTS:
The target mean basal glucose level was achieved only during the non-dawn phenomenon period (1400 hours to 0400 hours). During the dawn phenomenon, the mean (standard deviation) basal glucose level increased from 118 (57) mg/dL at 0400 hours to 156 (67) mg/dL before the breakfast meal, a 32% increase (P = .00149). The mean self-monitored plasma glucose level with meal omission was 63.8% of that increase with a breakfast meal.
CONCLUSION:
The fasting morning glucose concentration is considerably elevated because of the dawn phenomenon. Targeting insulin titration to this glucose level may result in excessive basal insulin dosing for the non-dawn phenomenon periods of the day. The dawn phenomenon is a large component of the postbreakfast hyperglycemia. Rather than increasing the morning premeal insulin bolus, consideration should be given to pretreating the earlier dawn phenomenon with an insulin pump with use of a variable basal insulin rate.
AuthorsAllen B King, Dawn Clark, Gary S Wolfe
JournalEndocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists (Endocr Pract) 2012 Jul-Aug Vol. 18 Issue 4 Pg. 558-62 ISSN: 1934-2403 [Electronic] United States
PMID22548951 (Publication Type: Clinical Trial, Journal Article)
Chemical References
  • Blood Glucose
  • Hypoglycemic Agents
  • Insulin Lispro
  • Insulin, Long-Acting
  • Insulin Glargine
Topics
  • Adolescent
  • Adult
  • Aged
  • Blood Glucose (analysis)
  • Blood Glucose Self-Monitoring
  • Breakfast
  • California
  • Diabetes Mellitus, Type 1 (blood, diet therapy, drug therapy)
  • Diet, Diabetic
  • Drug Chronotherapy
  • Drug Therapy, Combination
  • Female
  • Humans
  • Hyperglycemia (etiology)
  • Hypoglycemia (prevention & control)
  • Hypoglycemic Agents (administration & dosage, therapeutic use)
  • Insulin Glargine
  • Insulin Lispro (administration & dosage, therapeutic use)
  • Insulin, Long-Acting (administration & dosage, therapeutic use)
  • Male
  • Middle Aged
  • Postprandial Period
  • Young Adult

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: