Abstract | BACKGROUND: AIM: METHODS: In a 3-month open-label pilot study including 25 patients with moderate overweight and secondary failure, we investigated whether nocturnal glycaemic control could be achieved with glimepiride administered at 20:00 hours. The starting dose was 1-2 mg, with subsequent titration up to a maximum of 6 mg. Rapid-acting insulin analogues were used three times daily to regain postprandial glucose control. RESULTS: Glycaemic control at 3 months was established with glimepiride in a dose of 4.4 +/- 0.3 mg/day (mean +/- standard error of the mean), and a total daily insulin dose of 24.1 +/- 2.6 IU. Fasting glucose levels decreased from 12.7 +/- 0.6 mmol/l to 8.1 +/- 0.3 mmol/l (p < 0.001), and target levels were reached in 14 of 25 patients (56%). Mean HbA1c decreased from 10.5 +/- 0.4 to 7.7 +/- 0.2% (p < 0.001). Symptomatic nocturnal hypoglycaemia was not reported. Body weight did not change (85.7 +/- 3.6 kg vs. 85.7 +/- 3.3 kg, p = 0.99). CONCLUSION: The data suggest that this new approach may be useful in about 50% of type 2 diabetes patients presenting with failure on maximal oral treatment.
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Authors | H de Boer, M Jansen, J Koerts, L Verschoor |
Journal | Diabetes, obesity & metabolism
(Diabetes Obes Metab)
Vol. 6
Issue 2
Pg. 114-9
(Mar 2004)
ISSN: 1462-8902 [Print] England |
PMID | 14746576
(Publication Type: Journal Article)
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Chemical References |
- Blood Glucose
- C-Peptide
- Hypoglycemic Agents
- Insulin
- Sulfonylurea Compounds
- glimepiride
- Metformin
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Topics |
- Blood Glucose
(analysis)
- C-Peptide
(blood)
- Diabetes Mellitus, Type 2
(blood, drug therapy)
- Drug Administration Schedule
- Drug Therapy, Combination
- Female
- Humans
- Hypoglycemic Agents
(therapeutic use)
- Insulin
(therapeutic use)
- Male
- Metformin
(therapeutic use)
- Middle Aged
- Pilot Projects
- Sulfonylurea Compounds
(therapeutic use)
- Weight Gain
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