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Updated: Jul 22, 2026

Assessment of Kidney Function in Mouse Models of Glomerular Disease
Published on: June 30, 2018
Predictors for the development of microalbuminuria and interaction with renal function
Christos Chatzikyrkou1, Jan Menne, Joseph Izzo
1aNephrology Section, Hanover Medical School, Hanover bClinic of Nephrology, Hypertension, Endocrinology and Diabetology, Otto-von-Guericke University Magdeburg, Magdeburg, Germany cDepartment of Medicine, Erie County Medical Center, Buffalo, New York, USA dKCL Guy's Hospital, London, UK eDepartment of Nephrology and Hypertension, Leiden University Medical Center, Leiden, The Netherlands fDivision of Hypertension, Universidad Autonome, Madrid, Spain gClinic of Nephrology, University Hospital, Düsseldorf, Germany.
Classical cardiovascular risk factors predict microalbuminuria in type 2 diabetes. Baseline urinary albumin-creatinine ratio (UACR) is a key predictor, while olmesartan
Area of Science:
- Nephrology
- Endocrinology
- Cardiology
Background:
- Microalbuminuria is a key indicator of diabetic kidney disease.
- Identifying predictors of microalbuminuria is crucial for early intervention in type 2 diabetes mellitus.
- Understanding the role of baseline albuminuria and estimated glomerular filtration rate (eGFR) is important for managing diabetic nephropathy.
Purpose of the Study:
- To identify predictors of new-onset microalbuminuria in patients with type 2 diabetes.
- To investigate the interaction between baseline albuminuria and eGFR.
- To evaluate the effects of olmesartan on microalbuminuria development and renal function.
Main Methods:
- Analysis of data from the Randomized Olmesartan and Diabetes Microalbuminuria Prevention Study.
- Randomization of 4447 patients to receive olmesartan or placebo for a median of 3.2 years.
- Assessment of baseline urinary albumin-creatinine ratio (UACR), eGFR, and other cardiovascular risk factors.
Main Results:
- Baseline UACR was the strongest predictor of microalbuminuria, followed by age, weight, HbA1C, glucose, cholesterol, SBP, antihypertensive drug count, and heart rate.
- Microalbuminuria incidence increased with higher baseline UACR tertiles across all eGFR tertiles.
- Olmesartan showed greater efficacy in preventing microalbuminuria in patients with higher baseline UACR, but led to a more significant eGFR decline, particularly in those with high baseline eGFR.
Conclusions:
- Classical cardiovascular risk factors, particularly baseline UACR, predict microalbuminuria development in type 2 diabetes.
- Olmesartan's effect on microalbuminuria prevention and eGFR decline may involve different mechanisms, as eGFR decrease was dependent on baseline eGFR, not UACR.
- The transition to microalbuminuria under olmesartan treatment was not associated with renal function preservation.
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