Urinary vitamin D binding protein: a marker of kidney tubular dysfunction in patients at risk for type 2 diabetes

Author:

Semnani-Azad Zhila12ORCID,Wang Windy Z N2,Cole David E C3456,Johnston Luke W7,Wong Betty Y L5,Fu Lei56ORCID,Retnakaran Ravi8910,Harris Stewart B11,Hanley Anthony J28912ORCID

Affiliation:

1. Department of Nutrition, Harvard T.H. Chan School of Public Health , Massachusetts , USA

2. Department of Nutritional Sciences, University of Toronto , Ontario , Canada

3. Department of Medicine, University of Toronto , Ontario , Canada

4. Department of Pediatrics (Genetics), University of Toronto , Ontario , Canada

5. Department of Laboratory Medicine and Molecular Diagnostics, Sunnybrook Health Sciences Centre

6. Department of Laboratory Medicine and Pathobiology, University of Toronto , Ontario , Canada

7. Department of Public Health, Aarhus University , Aarhus , Denmark

8. Division of Endocrinology and Metabolism, University of Toronto , Ontario , Canada

9. Leadership Sinai Centre for Diabetes, Mount Sinai Hospital , Toronto, Ontario , Canada

10. Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital , Toronto, Ontario , Canada

11. Schulich School of Medicine and Dentristy, Western University , London, Ontario , Canada

12. Dalla Lana School of Public Health, University of Toronto , Ontario , Canada

Abstract

Abstract Background Recent studies have reported elevated urinary vitamin D binding protein (uVDBP) concentrations in patients with diabetic kidney disease, although the utility of uVDBP to predict deterioration of kidney function over time has not been examined. Our objective was to assess the association of uVDBP with longitudinal changes in kidney function. Methods Adults at-risk for type 2 diabetes from the Prospective Metabolism and Islet Cell Evaluation (PROMISE) study had 3 assessments over 6 years (n = 727). Urinary albumin-to-creatinine ratio (ACR) and estimated glomerular filtration rate (eGFR) were used as measures of kidney function. Measurements of uVDBP were performed with ELISA and normalized to urine creatinine (uVDBP:cr). Generalized estimating equations (GEE) evaluated longitudinal associations of uVDBP and uVDBP:cr with measures of kidney function, adjusting for covariates. Results Renal uVDBP loss increased with ACR severity at baseline. Subjects with normoalbuminuria, microalbuminuria, and macroalbuminuria had median log uVDBP:cr concentrations of 1.62 μg/mmol, 2.63 μg/mmol, and 2.48 μg/mmol, respectively, and ACR positively correlated with uVDBP concentrations (r = 0.37, p < 0.001). There was no significant association between uVDBP and eGFR at baseline. Adjusted longitudinal GEE models indicated that each SD increase in both baseline and longitudinal uVDBP:cr was significantly associated with higher ACR over 6 years (β=30.67 and β=32.91, respectively). Conversely, neither baseline nor longitudinal uVDBP:cr measures showed a significant association with changes in eGFR over time. Significance These results suggest that loss of uVDBP:cr over time may be a useful marker for predicting renal tubular damage in subjects at risk for diabetes.

Publisher

The Endocrine Society

Subject

Endocrinology, Diabetes and Metabolism

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