kynurenine has been researched along with Phenylketonurias in 11 studies
Kynurenine: A metabolite of the essential amino acid tryptophan metabolized via the tryptophan-kynurenine pathway.
kynurenine : A ketone that is alanine in which one of the methyl hydrogens is substituted by a 2-aminobenzoyl group.
Phenylketonurias: A group of autosomal recessive disorders marked by a deficiency of the hepatic enzyme PHENYLALANINE HYDROXYLASE or less frequently by reduced activity of DIHYDROPTERIDINE REDUCTASE (i.e., atypical phenylketonuria). Classical phenylketonuria is caused by a severe deficiency of phenylalanine hydroxylase and presents in infancy with developmental delay; SEIZURES; skin HYPOPIGMENTATION; ECZEMA; and demyelination in the central nervous system. (From Adams et al., Principles of Neurology, 6th ed, p952).
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 10 (90.91) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (9.09) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Ney, DM | 1 |
Murali, SG | 1 |
Stroup, BM | 1 |
Nair, N | 1 |
Sawin, EA | 1 |
Rohr, F | 1 |
Levy, HL | 1 |
FISCHL, J | 1 |
RABIAH, S | 1 |
Godin, C | 1 |
Dolan, G | 1 |
Kochen, W | 4 |
Byrd, DJ | 2 |
Bühner, R | 3 |
Bühlen, E | 1 |
Bührlen, E | 2 |
Jablonska, S | 1 |
Stachow, A | 1 |
Byrd, D | 1 |
Otting, W | 1 |
Machill, G | 1 |
Haufe, U | 1 |
Haufe, F | 1 |
Lubs, H | 1 |
Vassella, F | 1 |
Colombo, JP | 1 |
Humbel, R | 1 |
Rossi, E | 1 |
Heeley, AF | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Phase 2 Study of Glycomacropeptide vs. Amino Acid Diet for the Management of PKU[NCT01428258] | 32 participants (Actual) | Interventional | 2011-09-30 | Completed | |||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
Plasma concentration of BSAP was determined as a measure of bone turnover. (NCT01428258)
Timeframe: day 22 of each dietary treatment
Intervention | micro gram per liter (Mean) |
---|---|
GMP Diet/GMP Medical Foods | 17.0 |
AA Diet/AA Medical Foods | 17.0 |
Plasma will be collected at each base week and after 3 weeks on each of the dietary treatments, glycomacropeptide and amino acid, following an overnight fast. Plasma phenylalanine concentration (along with the complete profile of free amino acids) will be determined with an amino acid analyzer in the Wisconsin State Lab of Hygiene. Statistical analysis to determine the significance of the change in plasma phe concentration when comparing the 2 diets will consist of ANCOVA with covariates for baseline Phe and dietary Phe intake. The change in plasma Phe concentration from day 22 (final) to day 1 (baseline) was determined after adjusting for baseline Phe level and dietary Phe intake. (NCT01428258)
Timeframe: baseline to day 22 on each diet
Intervention | micro moles per liter plasma (Mean) |
---|---|
GMP Diet/GMP Medical Foods | 62 |
AA Diet/AA Medical Foods | -85 |
Concentrations of Phe in plasma and in dried blood spots collected simultaneously by subjects will be compared using 2 methodologies, regardless of intervention. At each of the 4 study visits (baseline and final for each dietary treatment): 1) venipuncture was used to collect blood and plasma was isolated and analyzed for Phe with ion exchange chromatography and 2) subjects were asked right after the venipuncture to spot their blood on filter paper for analysis of Phe with tandem mass spectroscopy (MS/MS). The discrepancy in Phe concentrations with these 2 methods was compared for each sample pair using Bland-Altman statistical analysis. Each subject should have had 4 sample pairs, 29 x 4 = 116, but we ended up with only 110 sample pairs, as explained below. (NCT01428258)
Timeframe: 4 times total, 2 per treatment
Intervention | micro moles per liter (Mean) |
---|---|
Phe Concentration in Plasma, Ion Exchange Chromatography | 731 |
Phe Concentration in Dried Blood Spots, Tandem Mass Spec | 514 |
Compliance with the glycomacropeptide and amino acid dietary treatments will be assessed by comparison of the intake of medical food in grams of protein from medical food per day based on subject completion of 3-day food records prior to the final study visit on day 22. Statistical analysis for a dietary treatment effect will consist of ANOVA. (NCT01428258)
Timeframe: 3 week dietary treatment
Intervention | g protein from MF/kg/day (Mean) |
---|---|
GMP Diet | 0.74 |
AA Diet/AA Medical Foods | 0.76 |
Completion of a standardized test, the Behavior Rating Inventory of Executive Function (BRIEF), by each subject for the GMP diet and the AA diet. Values are T-scores which have a mean of 50 points and a SD of 10 points. A T score of <50 is considered within the normative range. Data are analyzed with a paired t-test. (NCT01428258)
Timeframe: day 22 of each dietary treatment
Intervention | T score (Mean) |
---|---|
GMP Diet/GMP Medical Foods | 49.0 |
AA Diet/AA Medical Foods | 48.8 |
Plasma concentration of NTX was determined as a measure of bone resorption; higher levels indicate greater bone breakdown (NCT01428258)
Timeframe: day 22 of each dietary treatment
Intervention | nmol per liter bone collagen equivalents (Mean) |
---|---|
GMP Diet/GMP Medical Foods | 17.5 |
AA Diet/AA Medical Foods | 17.1 |
Vitamin D was measured as a measure of the capacity for calcium absorption. Higher levels of plasma vitamin D are consistent with higher calcium absorption. (NCT01428258)
Timeframe: day 22 of each dietary treatment
Intervention | ng per ml (Mean) |
---|---|
GMP Diet/GMP Medical Foods | 33.8 |
AA Diet/AA Medical Foods | 33.6 |
1 trial available for kynurenine and Phenylketonurias
Article | Year |
---|---|
Metabolomic changes demonstrate reduced bioavailability of tyrosine and altered metabolism of tryptophan via the kynurenine pathway with ingestion of medical foods in phenylketonuria.
Topics: Adolescent; Adult; Amino Acids; Biological Availability; Caseins; Catecholamines; Cross-Over Studies | 2017 |
10 other studies available for kynurenine and Phenylketonurias
Article | Year |
---|---|
DETERMINATION OF FREE AND TOTAL INDOLE-3-ACETIC ACID AND OF THE INDOLE INDEX.
Topics: Friedreich Ataxia; Humans; Indoleacetic Acids; Indoles; Intestines; Kynurenine; Metabolism; Myotonia | 1964 |
Tryptophan metabolism in normal and phenylketonuric rats.
Topics: Animals; Carbon Dioxide; Carbon Isotopes; Humans; Indoleacetic Acids; Injections, Intravenous; Kynur | 1966 |
[Studies on tryptophan metabolism in untreated phenylketonuric patients].
Topics: Acetophenones; Adolescent; Adult; Biotransformation; Child; Child, Preschool; Chromatography, Ion Ex | 1975 |
Tryptophan metabolism in untreated phenylketonuria.
Topics: Adolescent; Adult; Age Factors; Child; Child, Preschool; Humans; Indoles; Kynurenine; Phenylketonuri | 1975 |
[Pseudoscleroderma or scleroderma coexisting with phenylketonuria].
Topics: Child; Diagnosis, Differential; Female; Humans; Kynurenine; Phenylketonurias; Scleroderma, Localized | 1972 |
[Proceedings: Tryptophan metabolism in untreated phenylketonuria and in vitamin B6 dependent cramps].
Topics: 3-Hydroxyanthranilic Acid; Adolescent; Adult; Carboxylic Acids; Child; Child, Preschool; Humans; Hyd | 1972 |
[Identification of oxindole and 3-indolecarbaldehyde in the urine of patients with untreated phenylketonuria].
Topics: Aldehydes; Carbamates; Chromatography, Thin Layer; Humans; Indoles; Kynurenine; Mass Spectrometry; N | 1972 |
[Kynureninase activity and pyridoxine elimination in rats with experimental phenylketonuria].
Topics: Animals; Disease Models, Animal; Humans; Hydrolases; Kynurenine; Liver; Phenylketonurias; Pyridoxine | 1971 |
[L-tryptophan metabolism in phenylketonuria].
Topics: Adolescent; Adult; Child; Diet Therapy; Female; Humans; Indoles; Kynurenine; Male; Phenylalanine; Ph | 1968 |
The effect of pyridoxine on tryptophan metabolism in phenylketonuria.
Topics: Child; Child, Preschool; Chromatography, Ion Exchange; Diet Therapy; Humans; In Vitro Techniques; In | 1965 |