Hypoglycemia in Compensated Chronic Renal Insufficiency: Substrate Limitation of Gluconeogenesis

Author:

Garber Alan J1,Bier Dennis M1,Cryer Philip E1,Pagliara Anthony S1

Affiliation:

1. Metabolism Divisions, Departments of Medicine and Pediatrics, Washington University School of Medicine 660 S. Euclid, St. Louis, Missouri 63110

Abstract

A woman with diabetes mellitus, compensated chronic renal insufficiency, and multiple episodes of fasting hypoglycemia was studied. On fasting, despite appropriate insulin, glucagon and normal lactate levels, this patient developed early, profound hypoalaninemia followed by hypoglycemia. Glucose and alanine turnover rates were estimated after an overnight fast by the primed injection—continuous infusion of isotopically labeled alanine and glucose. Glucose production (mean ± S.E.) was 36.4 ± 2.8mg./kg. hr. (normal 129.0 ± 10.1 mg./kg. hr., n = 6). Glucose production from alanine was 3.1 ± 0.7 mg./kg. hr. (normal 18.0 ±1.0 mg./kg. hr.). Alanine turnover was 241 ± 11/μmoles/kg. hr. (normal 488 ± 48 μmoles/kg. hr.). These data suggest that an inadequate delivery of an important gluconeogenic substrate—alanine—can exert a significant rate limitation on glucose production thereby resulting in hypoglycemia during fasting.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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