Skip to main content
Top
Published in: Diabetologia 11/2009

Open Access 01-11-2009 | Short Communication

Contact frequency determines outcome of basal insulin initiation trials in type 2 diabetes

Authors: S. G. H. A. Swinnen, J. H. DeVries

Published in: Diabetologia | Issue 11/2009

Login to get access

Abstract

Aims/hypothesis

The aim of the present study was to investigate whether predetermined contact frequency with the study team and endpoint insulin dose are associated with study outcomes in basal insulin initiation trials in type 2 diabetes.

Methods

A systematic Medline search was performed. Using data from the selected studies, contact frequency was plotted against HbA1c reduction and endpoint insulin dose. The importance of face-to-face vs telephone contact was also analysed. Insulin dose was plotted against HbA1c reduction, hypoglycaemia rate and weight gain. To investigate non-specific study effects, the relationship between contact frequency and HbA1c was also assessed in dipeptidyl peptidase-4 (DPP-4) inhibitor trials.

Results

The reduction in HbA1c was highly correlated with contact frequency and endpoint insulin dose (r 2 = 0.751, p < 0.001 and r 2 = 0.433, p = 0.008, respectively). However, after adjusting for contact frequency, the relationship between insulin dose and HbA1c reduction was no longer significant (p = 0.270). The frequency of both clinical and telephone contacts were independent predictors of HbA1c improvement (p = 0.010 and p < 0.001, respectively). We found no dose–response relationship between end-of-study insulin dose and hypoglycaemia or weight gain. In DPP-4 inhibitor studies, contact frequency was not positively associated with HbA1c.

Conclusions/interpretation

The frequency of contact with the study team is highly correlated with the improvement in HbA1c achieved in basal insulin initiation trials in type 2 diabetic patients. This has important implications for trial design and interpretation, as well as for clinical care.
Literature
1.
go back to reference Nathan DM, Buse JB, Davidson MB et al (2009) Medical management of hyperglycemia in type 2 diabetes: a consensus algorithm for the initiation and adjustment of therapy: a consensus statement of the American Diabetes Association and the European Association for the Study of Diabetes. Diabetes Care 32:193–203CrossRefPubMed Nathan DM, Buse JB, Davidson MB et al (2009) Medical management of hyperglycemia in type 2 diabetes: a consensus algorithm for the initiation and adjustment of therapy: a consensus statement of the American Diabetes Association and the European Association for the Study of Diabetes. Diabetes Care 32:193–203CrossRefPubMed
2.
go back to reference Eliaschewitz FG, Calvo C, Valbuena H et al (2006) Therapy in type 2 diabetes: insulin glargine vs NPH insulin both in combination with glimepiride. Arch Med Res 37:495–501CrossRefPubMed Eliaschewitz FG, Calvo C, Valbuena H et al (2006) Therapy in type 2 diabetes: insulin glargine vs NPH insulin both in combination with glimepiride. Arch Med Res 37:495–501CrossRefPubMed
3.
go back to reference Fritsche A, Schweitzer MA, Häring HU (2003) Glimepiride combined with morning insulin glargine, bedtime neutral protamine hagedorn insulin, or bedtime insulin glargine in patients with type 2 diabetes. Ann Intern Med 138:952–959PubMed Fritsche A, Schweitzer MA, Häring HU (2003) Glimepiride combined with morning insulin glargine, bedtime neutral protamine hagedorn insulin, or bedtime insulin glargine in patients with type 2 diabetes. Ann Intern Med 138:952–959PubMed
4.
go back to reference Hermansen K, Davies M, Derezinski T et al (2006) A 26-week, randomized, parallel, treat-to-target trial comparing insulin detemir with NPH insulin as add-on therapy to oral glucose-lowering drugs in insulin-naive people with type 2 diabetes. Diabetes Care 29:1269–1274CrossRefPubMed Hermansen K, Davies M, Derezinski T et al (2006) A 26-week, randomized, parallel, treat-to-target trial comparing insulin detemir with NPH insulin as add-on therapy to oral glucose-lowering drugs in insulin-naive people with type 2 diabetes. Diabetes Care 29:1269–1274CrossRefPubMed
5.
go back to reference Riddle MC, Rosenstock J, Gerich J (2003) The treat-to-target trial: randomized addition of glargine or human NPH insulin to oral therapy of type 2 diabetic patients. Diabetes Care 26:3080–3086CrossRefPubMed Riddle MC, Rosenstock J, Gerich J (2003) The treat-to-target trial: randomized addition of glargine or human NPH insulin to oral therapy of type 2 diabetic patients. Diabetes Care 26:3080–3086CrossRefPubMed
6.
go back to reference Rosenstock J, Davies M, Home P, Larsen J, Koenen C, Schernthaner G (2008) A randomised, 52-week, treat-to-target trial comparing insulin detemir with insulin glargine when administered as add-on to glucose-lowering drugs in insulin-naïve people with type 2 diabetes. Diabetologia 51:408–416CrossRefPubMed Rosenstock J, Davies M, Home P, Larsen J, Koenen C, Schernthaner G (2008) A randomised, 52-week, treat-to-target trial comparing insulin detemir with insulin glargine when administered as add-on to glucose-lowering drugs in insulin-naïve people with type 2 diabetes. Diabetologia 51:408–416CrossRefPubMed
7.
go back to reference Yki-Järvinen H, Kauppinen-Mäkelin R, Tiikkainen M et al (2006) Insulin glargine or NPH combined with metformin in type 2 diabetes: the LANMET study. Diabetologia 49:442–451CrossRefPubMed Yki-Järvinen H, Kauppinen-Mäkelin R, Tiikkainen M et al (2006) Insulin glargine or NPH combined with metformin in type 2 diabetes: the LANMET study. Diabetologia 49:442–451CrossRefPubMed
8.
go back to reference Yki-Järvinen H, Dressler A, Ziemen M, HOE 901/3002 study group (2000) Less nocturnal hypoglycemia and better post-dinner glucose control with bedtime insulin glargine compared with bedtime NPH insulin during insulin combination therapy in type 2 diabetes. Diabetes Care 23:1130–1136CrossRefPubMed Yki-Järvinen H, Dressler A, Ziemen M, HOE 901/3002 study group (2000) Less nocturnal hypoglycemia and better post-dinner glucose control with bedtime insulin glargine compared with bedtime NPH insulin during insulin combination therapy in type 2 diabetes. Diabetes Care 23:1130–1136CrossRefPubMed
9.
go back to reference Esposito K, Ciotola M, Maiorino MI et al (2008) Addition of neutral protamine lispro insulin or insulin glargine to oral type 2 diabetes regimens for patients with suboptimal glycemic control: a randomized trial. Ann Intern Med 149:531–539PubMed Esposito K, Ciotola M, Maiorino MI et al (2008) Addition of neutral protamine lispro insulin or insulin glargine to oral type 2 diabetes regimens for patients with suboptimal glycemic control: a randomized trial. Ann Intern Med 149:531–539PubMed
10.
go back to reference Pan CY, Sinnassamy P, Chung KD, Kim KW (2007) Insulin glargine vs NPH insulin therapy in Asian type 2 diabetes patients. Diabetes Res Clin Pract 76:111–118CrossRefPubMed Pan CY, Sinnassamy P, Chung KD, Kim KW (2007) Insulin glargine vs NPH insulin therapy in Asian type 2 diabetes patients. Diabetes Res Clin Pract 76:111–118CrossRefPubMed
11.
go back to reference Standl E, Maxeiner S, Raptis S, HOE 901/4009 study group (2006) Once-daily insulin glargine administration in the morning compared to bedtime in combination with morning glimepiride in patients with type 2 diabetes: an assessment of treatment flexibility. Horm Metab Res 38:172–177CrossRefPubMed Standl E, Maxeiner S, Raptis S, HOE 901/4009 study group (2006) Once-daily insulin glargine administration in the morning compared to bedtime in combination with morning glimepiride in patients with type 2 diabetes: an assessment of treatment flexibility. Horm Metab Res 38:172–177CrossRefPubMed
12.
go back to reference Gale EAM, Beattie SD, Hu J, Koivisto V, Tan MH (2007) Recruitment to a clinical trial improves glycemic control in patients with diabetes. Diabetes Care 30:2989–2992CrossRefPubMed Gale EAM, Beattie SD, Hu J, Koivisto V, Tan MH (2007) Recruitment to a clinical trial improves glycemic control in patients with diabetes. Diabetes Care 30:2989–2992CrossRefPubMed
13.
go back to reference DeVries JH, Snoek FJ, Kostense PJ, Heine RJ (2003) Improved glycaemic control in type 1 diabetes patients following participation per se in a clinical trial—mechanisms and implications. Diabetes Metab Res Rev 19:357–362CrossRefPubMed DeVries JH, Snoek FJ, Kostense PJ, Heine RJ (2003) Improved glycaemic control in type 1 diabetes patients following participation per se in a clinical trial—mechanisms and implications. Diabetes Metab Res Rev 19:357–362CrossRefPubMed
14.
go back to reference Richter B, Bandeira-Echtler E, Bergerhoff K, Lerch CL (2008) Dipeptidyl peptidase-4 (DPP-4) inhibitors for type 2 diabetes mellitus. Cochrane Database Syst Rev, Issue 2, Art. no. CD006739. doi:10.1002/14651858.CD006739.pub2 Richter B, Bandeira-Echtler E, Bergerhoff K, Lerch CL (2008) Dipeptidyl peptidase-4 (DPP-4) inhibitors for type 2 diabetes mellitus. Cochrane Database Syst Rev, Issue 2, Art. no. CD006739. doi:10.​1002/​14651858.​CD006739.​pub2
15.
go back to reference Yki-Järvinen H (2001) Combination therapies with insulin in type 2 diabetes. Diabetes Care 24:758–767CrossRefPubMed Yki-Järvinen H (2001) Combination therapies with insulin in type 2 diabetes. Diabetes Care 24:758–767CrossRefPubMed
Metadata
Title
Contact frequency determines outcome of basal insulin initiation trials in type 2 diabetes
Authors
S. G. H. A. Swinnen
J. H. DeVries
Publication date
01-11-2009
Publisher
Springer-Verlag
Published in
Diabetologia / Issue 11/2009
Print ISSN: 0012-186X
Electronic ISSN: 1432-0428
DOI
https://doi.org/10.1007/s00125-009-1527-0

Other articles of this Issue 11/2009

Diabetologia 11/2009 Go to the issue
Live Webinar | 27-06-2024 | 18:00 (CEST)

Keynote webinar | Spotlight on medication adherence

Live: Thursday 27th June 2024, 18:00-19:30 (CEST)

WHO estimates that half of all patients worldwide are non-adherent to their prescribed medication. The consequences of poor adherence can be catastrophic, on both the individual and population level.

Join our expert panel to discover why you need to understand the drivers of non-adherence in your patients, and how you can optimize medication adherence in your clinics to drastically improve patient outcomes.

Prof. Kevin Dolgin
Prof. Florian Limbourg
Prof. Anoop Chauhan
Developed by: Springer Medicine
Obesity Clinical Trial Summary

At a glance: The STEP trials

A round-up of the STEP phase 3 clinical trials evaluating semaglutide for weight loss in people with overweight or obesity.

Developed by: Springer Medicine

Highlights from the ACC 2024 Congress

Year in Review: Pediatric cardiology

Watch Dr. Anne Marie Valente present the last year's highlights in pediatric and congenital heart disease in the official ACC.24 Year in Review session.

Year in Review: Pulmonary vascular disease

The last year's highlights in pulmonary vascular disease are presented by Dr. Jane Leopold in this official video from ACC.24.

Year in Review: Valvular heart disease

Watch Prof. William Zoghbi present the last year's highlights in valvular heart disease from the official ACC.24 Year in Review session.

Year in Review: Heart failure and cardiomyopathies

Watch this official video from ACC.24. Dr. Biykem Bozkurt discusses last year's major advances in heart failure and cardiomyopathies.