The first purpose of this project is to design an optimal dietary supplement for patients with chronic renal failure in the pre-dialysis stage. Criteria to be optimized (in descending order of importance) are progression of renal insufficiency, protein nutrition, PTH levels, and plasma levels of amino acids and electrolytes. A 20-25 gm mixed quality protein diet low in phosphorus will be used, and the composition of a supplement containing amino acids and N-free analogues will be varied. Short-term N balance plus long-term (three months) out-patient studies will be used. We will first compare the """"""""best"""""""" supplement identified to date, """"""""EE"""""""", with another containing different proportions and including serine (""""""""FF""""""""). Second, we will determine whether ornithine is more or less effective on short-term N balance than in equinitrogenous glycine and if so, whether this is because it inhibits oxidation of ketoleucine as suggested by in vitro data. Third, we will determine the effects of keto-leucine alone (added to a diet containing 35 gm of mostly high biological value protein), or keto-leucine plus smaller amounts of ketovaline and ketoisoleucine, first on N balance and if effective, long-term. At or about this point, we expect to have designed a nearly optimal supplement. We will then document its advantages by comparison in a cross-over desing with whatever amino acid formulation is then available. In study 2 we will continue to pursue continuous nasogastric alimentation with a mixture containing these same constituents plus oligosaccharides, in patients with end-stage renal failure. We have shown that highly efficient N conservation and improved protein nutrition results from this regimen. To explore why, we will (1) change the infusion schedule from essentially continuous to nocturnal only (12-16 hours) (2) replace ornithine with isonitrogenous alanine (3) later, vary other constituents. In each case, the comparison between two regimens will be made by treating individual patients first with one (for one week or more) followed by the other (for the same interval). N balance, plasma amino acid levels and serum chemistries will be the methods for evaluating the results.

Project Start
1983-04-01
Project End
1987-03-31
Budget Start
1985-04-01
Budget End
1986-03-31
Support Year
3
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Walser, M (1990) Progression of chronic renal failure in man. Kidney Int 37:1195-210
Goodship, T H; Mitch, W E (1988) Nutritional approaches to preserving renal function. Adv Intern Med 33:337-55
Druml, W; Mitch, W E (1988) Protein-restricted diets and progression of renal failure. Blood Purif 6:285-98
LaFrance, N D; Drew, H H; Walser, M (1988) Radioisotopic measurement of glomerular filtration rate in severe chronic renal failure. J Nucl Med 29:1927-30
Walser, M (1987) Creatinine excretion as a measure of protein nutrition in adults of varying age. JPEN J Parenter Enteral Nutr 11:73S-78S
Walser, M; LaFrance, N; Ward, L et al. (1987) Progression of chronic renal failure in patients given keto acids following amino acids. Infusionsther Klin Ernahr 14 Suppl 5:17-20
Mitch, W E; Steinman, T I (1987) Treatment of progressive chronic renal failure. Implications for changing the composition of amino acid and ketoacid supplements. Contrib Nephrol 55:28-35
Walser, M; Swain, L M; Alexander, V (1987) Measurement of branched-chain ketoacids in plasma by high-performance liquid chromatography. Anal Biochem 164:287-91
Walser, M; LaFrance, N D; Ward, L et al. (1987) Progression of chronic renal failure in patients given ketoacids following amino acids. Kidney Int 32:123-8
Kelly, R A; O'Hara, D S; Mitch, W E et al. (1986) Endogenous digitalis-like factors in hypertension and chronic renal insufficiency. Kidney Int 30:723-9

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