Kidney function and size in diabetics before and during initial insulin treatment. 1982

J S Christiansen, and J Gammelgaard, and B Tronier, and P A Svendsen, and H H Parving

GFR, RPF, and kidney size were measured in nine young recently diagnosed insulin-dependent diabetics before (days 0) and 3 and 8 days after the beginning of the initial insulin treatment and in comparable control subjects. Kidney function was measured by a constant infusion technique using I-125-iothalamate and 131-I-hippuran. Kidney size was determined by means of ultrasound. Before insulin treatment elevated values for GFR (+44%, P less than 0.01), RPF (+18%, P less than 0.05), and kidney size (+29%, P less than 0.01) were found. Near-normal metabolic control was achieved in all patients using either multiple subcutaneous injections of insulin or an artificial betacell. GFR decreased from 160 +/- 9 SEM to 141 +/- 6 ml/min X 1.73 m2 (P less than 0.01) and further to 133 +/- 5 ml/min X 1.73 m2 (P less than 0.01, compared to day 0). Renal plasma flow was 601 +/- 33 and 588 +/- 44 ml x 1.73 m2 at days 0 and 3, respectively (NS) and decreased to 558 +/- 35 ml/min x 1.73 m2 at day 0 (P less than 0.01). By contrast no statistically significant changes in kidney volume were observed; the results on day 0, 3 and 8 were 145 +/- 7, 162 +/- 11 and 143 +/- 9 ml/1.73 m2, respectively. The present study demonstrates that kidney size and function are elevated at the onset of insulin-dependent diabetes. Near-normal metabolic control; for 8 days induces a reduction but not a complete normalization in kidney function. From the present observations it is suggested that the rapidly reversible part of the elevation in GFR cannot be explained by concomitant changes in kidney and glomerular size (morphological origin) but is probably due to a reduction in renal plasma flow and to a decreased transglomerular pressure (functional origin).

UI MeSH Term Description Entries
D007328 Insulin A 51-amino acid pancreatic hormone that plays a major role in the regulation of glucose metabolism, directly by suppressing endogenous glucose production (GLYCOGENOLYSIS; GLUCONEOGENESIS) and indirectly by suppressing GLUCAGON secretion and LIPOLYSIS. Native insulin is a globular protein comprised of a zinc-coordinated hexamer. Each insulin monomer containing two chains, A (21 residues) and B (30 residues), linked by two disulfide bonds. Insulin is used as a drug to control insulin-dependent diabetes mellitus (DIABETES MELLITUS, TYPE 1). Iletin,Insulin A Chain,Insulin B Chain,Insulin, Regular,Novolin,Sodium Insulin,Soluble Insulin,Chain, Insulin B,Insulin, Sodium,Insulin, Soluble,Regular Insulin
D007668 Kidney Body organ that filters blood for the secretion of URINE and that regulates ion concentrations. Kidneys
D008297 Male Males
D009929 Organ Size The measurement of an organ in volume, mass, or heaviness. Organ Volume,Organ Weight,Size, Organ,Weight, Organ
D012079 Renal Circulation The circulation of the BLOOD through the vessels of the KIDNEY. Kidney Circulation,Renal Blood Flow,Circulation, Kidney,Circulation, Renal,Blood Flow, Renal,Flow, Renal Blood
D001786 Blood Glucose Glucose in blood. Blood Sugar,Glucose, Blood,Sugar, Blood
D003920 Diabetes Mellitus A heterogeneous group of disorders characterized by HYPERGLYCEMIA and GLUCOSE INTOLERANCE.
D005260 Female Females
D005919 Glomerular Filtration Rate The volume of water filtered out of plasma through glomerular capillary walls into Bowman's capsules per unit of time. It is considered to be equivalent to INULIN clearance. Filtration Rate, Glomerular,Filtration Rates, Glomerular,Glomerular Filtration Rates,Rate, Glomerular Filtration,Rates, Glomerular Filtration
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

J S Christiansen, and J Gammelgaard, and B Tronier, and P A Svendsen, and H H Parving
July 1977, Acta endocrinologica,
J S Christiansen, and J Gammelgaard, and B Tronier, and P A Svendsen, and H H Parving
January 1974, Acta endocrinologica,
J S Christiansen, and J Gammelgaard, and B Tronier, and P A Svendsen, and H H Parving
December 1983, Science (New York, N.Y.),
J S Christiansen, and J Gammelgaard, and B Tronier, and P A Svendsen, and H H Parving
September 1988, Scandinavian journal of clinical and laboratory investigation,
J S Christiansen, and J Gammelgaard, and B Tronier, and P A Svendsen, and H H Parving
June 1965, Vrachebnoe delo,
J S Christiansen, and J Gammelgaard, and B Tronier, and P A Svendsen, and H H Parving
January 1986, Diabetic medicine : a journal of the British Diabetic Association,
J S Christiansen, and J Gammelgaard, and B Tronier, and P A Svendsen, and H H Parving
January 1987, Diabetes research and clinical practice,
J S Christiansen, and J Gammelgaard, and B Tronier, and P A Svendsen, and H H Parving
September 1985, Hiroshima journal of medical sciences,
J S Christiansen, and J Gammelgaard, and B Tronier, and P A Svendsen, and H H Parving
August 1980, Die Medizinische Welt,
J S Christiansen, and J Gammelgaard, and B Tronier, and P A Svendsen, and H H Parving
October 1989, Minerva stomatologica,
Copied contents to your clipboard!