posted on 2020-07-31, 16:43authored byAda AdminAda Admin, Carissa Vinovskis, Lu-Ping Li, Pottumarthi Prasad, Kalie Tommerdahl, Laura Pyle, Robert G. Nelson, Meda E. Pavkov, Daniel van Raalte, Marian Rewers, Marlon Pragnell, Farid H. Mahmud, David Z. Cherney, Richard J. Johnson, Kristen J. Nadeau, Petter Bjornstad
<a>The objective of this
study was to compare the ratio of renal oxygen availability (RO<sub>2</sub>) to
GFR (RO<sub>2</sub>: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). RO<sub>2</sub>
was estimated by blood oxygenation level dependent (BOLD) MRI, fat mass by </a>DXA, GFR and RPF by iohexol and <i>p</i>-aminohippurate
clearance, albuminuria by urine albumin-to-creatinine ratio (UACR), and M/I from
steady-state glucose infusion rate/insulin (mg/kg/min) by hyperglycemic clamp in
50 adolescents with T1D (16.1±3.0 years, HbA1c 8.6±1.2%) and 20 controls of
similar BMI (16.1±2.9 years, HbA1c 5.2±0.2%). <a>The RO<sub>2</sub>:GFR
(ms/ml/min) was calculated as renal oxygen availability (T2*, ms) divided by
GFR (ml/min). </a>Whole-kidney RO<sub>2</sub>:GFR was 25% lower in adolescents
with T1D vs. controls (<i>p<</i>0.0001). In adolescents with T1D, lower whole-kidney
RO<sub>2</sub>:GFR associated with higher UACR (r=-0.31, <i>p</i>=0.03), RPF
(r=-0.52, <i>p</i>=0.0009) and fat mass (r=-0.33, <i>p</i>=0.02). Lower
medullary RO<sub>2</sub>:GFR associated with lower M/I (r=0.31, <i>p</i>=0.03).
In conclusion, adolescents with T1D exhibited relative renal hypoxia that
associated with albuminuria, increased RPF, fat mass, and insulin resistance. These
data suggest a potential role of renal hypoxia in the development of DKD.
Funding
Financial support for this work provided by the NIDDK Diabetic Complications Consortium (RRID:SCR_001415, www.diacomp.org), grants DK076169 and DK115255 (18AU3871 [P.B.]), JDRF grant number 2-SRA-2018-627-M-B (P.B.), and NIH/NIDDK grant number K23-DK116720 (P.B.), K24-HL145076 (K.J.N.), UL1-RR025780 (University of Colorado Denver), support from Center for Women’s Health Research at University of Colorado, the Department of Pediatrics, Section of Endocrinology and Barbara Davis Center for Diabetes at University of Colorado School of Medicine, and by the Intramural Research Program of the NIDDK.