How Does the Diabetes Drug, Pioglitazone, Reduce Protein Loss in the Urine?

NCT ID: NCT00749047

Last Updated: 2009-09-16

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE4
• Total Enrollment: 12 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-09-30
• Study Completion Date: 2010-03-31

Brief Summary

Pioglitazone is an insulin sensitising drug used in the treatment of patients with type 2 diabetes. In addition to its blood sugar lowering effect, pioglitazone also has a number of other beneficial effects, one of which is to reduce the loss of protein in the urine. The mechanism of this protein "sparing effect" of pioglitazone is not fully understood. The proposed study will investigate whether pioglitazone has beneficial effects on the filtration characteristics of filters in the kidney that are responsible for retaining protein in the body. The effect of pioglitazone on the size of the pores in the filters and also the electrostatic charge barriers that surround these pores will be investigated. The clinical study will involve 12 patients with type 2 diabetes with minimal urine protein loss, taking low dose pioglitazone for 3 months. Blood and urine samples will be collected at the beginning, mid point and end of the study and used to measure the concentration of specific proteins of different size and electrostatic charge. This data will be used to identify and characterise changes in the filtration properties of the kidney filters during the study.

Detailed Description

In addition to their insulin sensitising action, thiazolidinediones (TZDs) have beneficial effects on vascular function. These include a decrease in proteinuria and amelioration of diabetic nephropathy. Although the anti-proteinuric effect of TZDs is well established the mechanism(s) underlying these changes has yet to be determined. Possible mechanisms include altered renal haemodynamics, maintenance of anionic electrostatic filtration barriers in the glomerular basement membrane and pleiotropic effects.

The target of TZDs, the peroxisome proliferator-activated receptors (PPARs), directly modulate vessel wall function. The kidney differentially expresses all PPAR isoforms and there is evidence that TZDs have pleiotropic effects in the kidney over and above their metabolic and haemodynamic actions. These effects include a direct action on cultured mesangial cells, inhibition of in vivo mesangial expansion, reduction in podocyte injury, and decreased production of type IV collagen and urinary endothelin-1 levels in early stage diabetic nephropathy.

Glomerular ultrafiltration of plasma proteins is governed by the size of the filtration pores and the extent of anionic sites in the basement membrane and podocyte slit pore junction. It is possible that the anti-proteinuric effect of TZDs is attributable to an increase in size and/or charge selectivity in the glomerular filtration barrier. A Medline search showed there have been no studies on the effect of TZDs on protein ultrafiltration. The aim of the proposed study is to measure urinary protein size and charge selectivity in patients with early stage diabetic nephropathy before and after treatment with the TZD, pioglitazone.

Conditions

Diabetes Mellitus, Type 2

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: NONE

Study Groups

1

Open label arm

Group Type: EXPERIMENTAL

Pioglitazone

Intervention Type: DRUG

15-45 mg/day

Interventions

Pioglitazone

15-45 mg/day

Intervention Type: DRUG

Other Intervention Names

Actos; Batch number A490463

Eligibility Criteria

Inclusion Criteria

• Diabetes mellitus, Type 2
• Age 18-70 yrs

Exclusion Criteria

• Overt proteinuria (urine albumin:creatinine ratio >10.0
• Plasma creatinine 0.15 mmol/L
• HbA1c >10%
• Hear failure Class III or IV
• Peripheral oedema
• Abnormal liver function (serum AST >2.5 times upper limit of normal)
• Pregnancy or breastfeeding
• History of urinary tract infections
• Serious concomitant disorder

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Christchurch Hospital

OTHER

Sponsor Role: lead

Responsible Party

Lipid and Diabetes Research Group, Christchurch Hospital, New Zealand.

Locations

Christchurch Hospital

Christchurch, Canterbury, New Zealand

Countries

New Zealand

Other Identifiers

H6E-AY-O017

Identifier Type: -

Identifier Source: org_study_id