4.7 Article

Renal Hyperfiltration Is Associated With Glucose-Dependent Changes in Fractional Excretion of Sodium in Patients With Uncomplicated Type 1 Diabetes

Journal

DIABETES CARE
Volume 37, Issue 10, Pages 2774-2781

Publisher

AMER DIABETES ASSOC
DOI: 10.2337/dc14-0798

Keywords

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Funding

  1. Kidney Foundation of Canada Scholarship
  2. Canadian Diabetes Association-Kidney Research Scientific Core Education and National Training (KRESCENT) Program Joint New Investigator Award
  3. Banting and Best Diabetes Centre Graduate Studentship
  4. Hilda and William Courtney Clayton Paediatric Research Fund Award
  5. Institute of Medical Science Graduate Student Award (University of Toronto)
  6. Peterborough K. M. Hunter Graduate Studentship

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OBJECTIVE Renal hyperfiltration is a common abnormality associated with diabetic nephropathy in patients with type 1 diabetes (T1D). In animal models, increased proximal tubular sodium reabsorption results in decreased distal sodium delivery, tubuloglomerular feedback activation, afferent vasodilatation, and hyperfiltration. The role of tubular factors is less well understood in humans. The aim of the current study was therefore to compare the fractional sodium excretion (FENa) in hyperfiltering (T1D-H) versus normofiltering (T1D-N) patients and healthy control (HC) subjects, as well as the role of ambient hyperglycemia on FENa. RESEARCH DESIGN AND METHODS Blood pressure, renal function (inulin for glomerular filtration rate [GFR], and paraaminohippurate for effective renal plasma flow), FENa, and circulating neurohormones were measured in T1D-H (n = 28, GFR >= 135 mL/min/1.73 m(2)), T1D-N (n = 30), and HC (n = 35) subjects during clamped euglycemia. Studies were repeated in a subset of patients during clamped hyperglycemia. RESULTS During clamped euglycemia, T1D-H exhibited lower FENa than T1D-N and HC subjects (0.64 +/- 0.06% vs. 0.91 +/- 0.12% and 0.90 +/- 0.10%, P < 0.05). During clamped hyperglycemia, FENa increased (Delta + 0.88 +/- 0.22% vs. Delta + 0.02 +/- 0.21%; between group effect, P = 0.01) significantly in T1D-H, whereas FENa did not change in T1D-N. When treated as continuous variables, elevated GFR values were associated with hyperglycemia-induced increases in FENa (R-2 = 0.20, P = 0.007). CONCLUSIONS Patients with uncomplicated T1D-H exhibit lower FENa under euglycemic conditions, which may help to identify patients with hyperfiltration outside of a controlled laboratory setting. Increased FENa in T1D-H but not T1D-N under clamped hyperglycemic conditions suggests that the mechanisms responsible for increased sodium reabsorption leading to hyperfiltration can be saturated.

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