» Articles » PMID: 19684847

Improved Glycaemic Control with Biphasic Insulin Aspart 30 in Type 2 Diabetes Patients Failing Oral Antidiabetic Drugs: PRESENT Study Results

Overview
Journal Arch Drug Inf
Specialty Pharmacology
Date 2009 Aug 18
PMID 19684847
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

AIMS: This paper presents the treatment outcomes for patients intiated on biphasic insulin aspart 30 (BIAsp 30) treatment: BIAsp 30-only, BIAsp 30 + sulphonylureas (SU), BIAsp 30 + biguanides (BI), BIAsp 30 + SU + BI, BIAsp 30 + alpha-glucosidase inhibitors (GI), and BIAsp 30 + BI + thiazolidinediones (TZD) after failing oral antidiabetic drugs (OADs) treatment. METHODS: This was a multi-national, multi-centre, six-month, prospective, open-labelled, uncontrolled, clinical experience evaluation study, with the exception of a three-month study in one country (China) ("all exclude China" and "China"). Initiation and discontinuation of BIAsp 30 treatment were entirely at the discretion of the attending physicians. RESULTS: Mean HbA(1c), FPG and PPPG were significantly reduced from baseline at three and six months in all groups (P < 0.001). In "all exclude China", reductions in mean HbA(1c), FPG and PPPG at six months were as follows: BIAsp 30-only group (-2.12 +/- 1.76% points; -4.82 +/- 3.86 mmol/L; -6.89 +/- 4.74 mmol/L), BIAsp 30 + BI group (-2.24 +/- 1.77% points; -4.48 +/- 3.68 mmol/L; -6.66 +/- 4.55 mmol/L), BIAsp 30 + SU group (-1.95 +/- 1.59% points; -3.98 +/- 3.19 mmol/L; -6.25 +/- 4.45 mmol/L) and BIAsp 30 + SU + BI group (-1.78 +/- 1.20% points; -3.57 +/- 2.78 mmol/L; -5.89 +/- 3.98 mmol/L). The only serious adverse drug reaction was reported by the BIAsp 30-only group. In the "China" group, reductions in mean HbA(1c), FPG and PPPG at three months were: BIAsp 30-only group (-2.16 +/- 1.52% points; -3.34 +/- 2.49 mmol/L; -6.29 +/- 3.92 mmol/L), BIAsp 30 + BI group (-2.44 +/- 1.52% points; -4.01 +/- 2.50 mmol/L; -7.10 +/- 3.96 mmol/L), BIAsp 30 + GI group (-2.33 +/- 1.41% points; -4.34 +/- 2.52 mmol/L; -7.97 +/- 3.99 mmol/L) and BIAsp 30 + BI + TZD group (-1.21 +/- 1.60% points; -3.50 +/- 2.29 mmol/L; -5.97 +/- 3.39 mmol/L). No serious ADR were reported in China. The most frequent hypoglycaemic episodes were diurnal and minor in nature. CONCLUSIONS: BIAsp 30 treatment in a clinical setting improved glycaemic control in type 2 diabetes patients failing OADs.

Citing Articles

Drug-related risk of severe hypoglycaemia in observational studies: a systematic review and meta-analysis.

Czech M, Rdzanek E, Paweska J, Adamowicz-Sidor O, Niewada M, Jakubczyk M BMC Endocr Disord. 2015; 15:57.

PMID: 26458540 PMC: 4603823. DOI: 10.1186/s12902-015-0052-z.


Ten years of experience with biphasic insulin aspart 30: from drug development to the latest clinical findings.

Liebl A, Prusty V, Valensi P, Kawamori R, Christiansen J, Palmer A Drugs. 2012; 72(11):1495-520.

PMID: 22818015 PMC: 3590411. DOI: 10.2165/11635490-000000000-00000.


The impact of initiating biphasic human insulin 30 therapy in type 2 diabetes patients after failure of oral antidiabetes drugs.

Gu Y, Hou X, Zhang L, Pan J, Cai Q, Bao Y Diabetes Technol Ther. 2011; 14(3):244-50.

PMID: 22047050 PMC: 3284695. DOI: 10.1089/dia.2011.0168.

References
1.
. Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33). UK Prospective Diabetes Study (UKPDS) Group. Lancet. 1998; 352(9131):837-53. View

2.
Wright A, Burden A, Paisey R, Cull C, Holman R . Sulfonylurea inadequacy: efficacy of addition of insulin over 6 years in patients with type 2 diabetes in the U.K. Prospective Diabetes Study (UKPDS 57). Diabetes Care. 2002; 25(2):330-6. DOI: 10.2337/diacare.25.2.330. View

3.
Jacobsen L, Sogaard B, Riis A . Pharmacokinetics and pharmacodynamics of a premixed formulation of soluble and protamine-retarded insulin aspart. Eur J Clin Pharmacol. 2000; 56(5):399-403. DOI: 10.1007/s002280000159. View

4.
Boehm B, Home P, Behrend C, Kamp N, Lindholm A . Premixed insulin aspart 30 vs. premixed human insulin 30/70 twice daily: a randomized trial in Type 1 and Type 2 diabetic patients. Diabet Med. 2002; 19(5):393-9. DOI: 10.1046/j.1464-5491.2002.00733.x. View

5.
Garber A . Premixed insulin analogues for the treatment of diabetes mellitus. Drugs. 2006; 66(1):31-49. DOI: 10.2165/00003495-200666010-00003. View