Literature DB >> 9153292

Mechanisms permitting nephrotic patients to achieve nitrogen equilibrium with a protein-restricted diet.

B J Maroni1, C Staffeld, V R Young, A Manatunga, K Tom.   

Abstract

UNLABELLED: Clinical experience suggests nephrotic patients are at risk for malnutrition. To determine if nephrotic patients can adapt successfully to a protein-restricted diet, nephrotic (glomerular filtration rate, 52+/-15 ml/min; urinary protein [Uprot.], 7.2+/-2.2 grams/d) and control subjects completed a crossover comparison of diets providing 0.8 or 1.6 grams protein (plus 1 gram protein/gram Uprot.) and 35 kcal per kg per day. Nitrogen balance (BN) was determined and whole body protein turnover measured during fasting and feeding using intravenous -[1-13C]leucine and intragastric -[5,5, 5- 2H3]leucine. BN was positive in both nephrotic and control subjects consuming either diet and rates of whole-body protein synthesis, protein degradation, and leucine oxidation did not differ between groups. In both nephrotic and control subjects anabolism was due to a suppression of whole-body protein degradation and stimulation of protein synthesis during feeding. The principal compensatory response to dietary protein restriction was a decrease in amino acid oxidation and this response was the same in both groups. With the low protein diet leucine oxidation rates during feeding correlated inversely with Uprot. losses (r = -0.83; P < 0. 05).
CONCLUSIONS: (a) a diet providing 0.8 gram protein (plus 1 gram protein/gram Uprot.) and 35 kcal per kg per day maintains BN in nephrotic patients; (b) nephrotic patients activate normal anabolic responses to dietary protein restriction (suppression of amino acid oxidation) and feeding (stimulation of protein synthesis and inhibition of protein degradation); (c) the inverse correlation between leucine oxidation and Uprot. losses suggests that proteinuria is a stimulus to conserve dietary essential amino acids.

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Year:  1997        PMID: 9153292      PMCID: PMC508089          DOI: 10.1172/JCI119432

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  38 in total

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Journal:  Medicine (Baltimore)       Date:  1973-11       Impact factor: 1.889

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Journal:  J Chromatogr       Date:  1974-08-14

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Journal:  Metabolism       Date:  1981-09       Impact factor: 8.694

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Authors:  H Fisher; M K Brush; P Griminger; E R Sostman
Journal:  Am J Clin Nutr       Date:  1967-09       Impact factor: 7.045

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Journal:  Am J Physiol       Date:  1980-05

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Authors:  E A Oddoye; S Margen
Journal:  J Nutr       Date:  1979-03       Impact factor: 4.798

7.  Keto acids in tissues and biological fluids: O-t-butyldimethylsilyl quinoxalinols as derivatives for sensitive gas chromatographic/mass spectrometric determination.

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Journal:  Biomed Mass Spectrom       Date:  1985-09

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Authors:  B J Maroni; T I Steinman; W E Mitch
Journal:  Kidney Int       Date:  1985-01       Impact factor: 10.612

9.  Quantitation of 2-ketoacids in biological fluids by gas chromatography chemical ionization mass spectrometry of O-trimethylsilyl-quinoxalinol derivatives.

Authors:  F Rocchiccioli; J P Leroux; P Cartier
Journal:  Biomed Mass Spectrom       Date:  1981-04

10.  13C abundances of nutrients and the effect of variations in 13C isotopic abundances of test meals formulated for 13CO2 breath tests.

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Journal:  Am J Clin Nutr       Date:  1980-11       Impact factor: 7.045

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