Relative Hypoxia and Early Diabetic Kidney Disease in Type 1 Diabetes

Author:

Vinovskis Carissa1,Li Lu-Ping2,Prasad Pottumarthi2,Tommerdahl Kalie1ORCID,Pyle Laura1,Nelson Robert G.3ORCID,Pavkov Meda E.4ORCID,van Raalte Daniel5,Rewers Marian6,Pragnell Marlon7,Mahmud Farid H.8ORCID,Cherney David Z.9ORCID,Johnson Richard J.10,Nadeau Kristen J.1ORCID,Bjornstad Petter110ORCID

Affiliation:

1. Section of Endocrinology, Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO

2. Department of Radiology, NorthShore University HealthSystem, Evanston, IL

3. Chronic Kidney Disease Section, Phoenix Epidemiology and Clinical Research Branch, National Institute of Diabetes and Digestive and Kidney Diseases, Phoenix, AZ

4. Division of Diabetes Translation, Centers for Disease Control and Prevention, Atlanta, GA

5. Diabetes Center, Department of Internal Medicine, Amsterdam University Medical Centers, location VUmc, Amsterdam, the Netherlands

6. Barbara Davis Center for Diabetes, University of Colorado School of Medicine, Aurora, CO

7. JDRF, New York, NY

8. Division of Endocrinology, Department of Pediatrics, University of Toronto School of Medicine, Toronto, Ontario, Canada

9. Division of Nephrology, Department of Medicine, University of Toronto School of Medicine, Toronto, Ontario, Canada

10. Division of Nephrology, Department of Medicine, University of Colorado School of Medicine, Aurora, CO

Abstract

The objective of this study was to compare the ratio of renal oxygen availability (RO2) to glomerular filtration rate (GFR), a measure of relative renal hypoxia, in adolescents with and without type 1 diabetes (T1D) and relate the ratio to albuminuria, renal plasma flow (RPF), fat mass, and insulin sensitivity (M/I). RO2 was estimated by blood oxygen level–dependent MRI; fat mass was estimated by DXA; GFR and RPF were estimated by iohexol and p-aminohippurate clearance; albuminuria was estimated by urine albumin-to-creatinine ratio (UACR); and M/I was estimated from steady-state glucose infusion rate/insulin (mg/kg/min) by hyperglycemic clamp in 50 adolescents with T1D (age 16.1 ± 3.0 years, HbA1c 8.6 ± 1.2%) and 20 control patients of similar BMI (age 16.1 ± 2.9 years, HbA1c 5.2 ± 0.2%). The RO2:GFR (ms/mL/min) was calculated as RO2 (T2*, ms) divided by GFR (mL/min). Whole-kidney RO2:GFR was 25% lower in adolescents with T1D versus control patients (P < 0.0001). In adolescents with T1D, lower whole-kidney RO2:GFR was associated with higher UACR (r = −0.31, P = 0.03), RPF (r = −0.52, P = 0.0009), and fat mass (r = −0.33, P = 0.02). Lower medullary RO2:GFR was associated with lower M/I (r = 0.31, P = 0.03). In conclusion, adolescents with T1D exhibited relative renal hypoxia that was associated with albuminuria and with increased RPF, fat mass, and insulin resistance. These data suggest a potential role of renal hypoxia in the development of diabetic kidney disease.

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

JDRF International

NIDDK

National Heart, Lung, and Blood Institute

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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