carnitine has been researched along with BH4 Deficiency in 21 studies
Excerpt | Relevance | Reference |
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"Blood levels of amino acids and acylcarnitines (tandem mass spectrometry) were measured in 18,303 patients with suspected inherited metabolic diseases." | 3.81 | Spectrum analysis of common inherited metabolic diseases in Chinese patients screened and diagnosed by tandem mass spectrometry. ( Gao, X; Gu, X; Han, F; Han, L; Ji, W; Qiu, W; Wang, Y; Ye, J; Zhang, H, 2015) |
" Carnitine supplementation of AA-MFs shows reduced bioavailability due, in part, to bacterial degradation to TMAO, whereas the bioavailability of carnitine is greater with prebiotic GMP-MFs." | 2.87 | Metabolomic Markers of Essential Fatty Acids, Carnitine, and Cholesterol Metabolism in Adults and Adolescents with Phenylketonuria. ( Broniowska, K; Levy, HL; Murali, SG; Nair, N; Ney, DM; Rohr, F; Stroup, BM, 2018) |
"This disorder, known as phenylketonuria, produces profound mental retardation if not detected and treated early in life." | 2.43 | A biochemical perspective on the use of tandem mass spectrometry for newborn screening and clinical testing. ( Chace, DH; Kalas, TA, 2005) |
"The pathogenesis and the progression of phenylketonuria (PKU), an inborn error of phenylalanine (Phe) metabolism, have been associated with oxidative damage." | 1.42 | Protective effect of L-carnitine on Phenylalanine-induced DNA damage. ( Deon, M; Lamberty, JF; Landgraf, SS; Moura, DJ; Saffi, J; Vargas, CR; Wajner, M, 2015) |
"Patients with phenylketonuria (PKU) have to follow a lifelong phenylalanine restricted diet." | 1.38 | Metabolomics of dietary fatty acid restriction in patients with phenylketonuria. ( Beblo, S; Bruegel, M; Ceglarek, U; Kiess, W; Koletzko, B; Kortz, L; Matthies, C; Mütze, U; Rohde, C; Thiery, J, 2012) |
" Daily Phe intake, dosage of AA mixtures and body weight were recorded along with measurements of acylcarnitines in blood spots (by tandem mass spectrometry) and serum AA." | 1.35 | Carnitine status in early-treated children, adolescents and young adults with phenylketonuria on low phenylalanine diets. ( Kiener, C; Knerr, I; Meier, N; Rascher, W; Rauh, M; Schmid, P; Weigel, C, 2008) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (9.52) | 18.7374 |
1990's | 3 (14.29) | 18.2507 |
2000's | 4 (19.05) | 29.6817 |
2010's | 8 (38.10) | 24.3611 |
2020's | 4 (19.05) | 2.80 |
Authors | Studies |
---|---|
Schoen, MS | 1 |
Singh, RH | 1 |
Faverzani, JL | 3 |
Hammerschmidt, TG | 2 |
Mescka, CP | 2 |
Guerreiro, G | 3 |
Lopes, FF | 3 |
Delgado, CA | 1 |
de Moura Coelho, D | 2 |
Sitta, A | 5 |
Deon, M | 5 |
Wajner, M | 6 |
Vargas, CR | 6 |
Coelho, DM | 1 |
Bower, A | 1 |
Imbard, A | 1 |
Benoist, JF | 1 |
Pichard, S | 1 |
Rigal, O | 1 |
Baud, O | 1 |
Schiff, M | 1 |
Steinmetz, A | 1 |
Marchetti, DP | 1 |
Nascimento, LVM | 1 |
Steffens, L | 1 |
Henn, JG | 1 |
Ferro, MB | 1 |
Brito, VB | 1 |
Moura, DJ | 2 |
Stroup, BM | 1 |
Nair, N | 1 |
Murali, SG | 1 |
Broniowska, K | 1 |
Rohr, F | 1 |
Levy, HL | 1 |
Ney, DM | 1 |
Han, L | 1 |
Han, F | 1 |
Ye, J | 1 |
Qiu, W | 1 |
Zhang, H | 1 |
Gao, X | 1 |
Wang, Y | 1 |
Ji, W | 1 |
Gu, X | 1 |
Landgraf, SS | 1 |
Lamberty, JF | 1 |
Saffi, J | 1 |
Barschak, AG | 1 |
de Mari, JF | 1 |
Barden, AT | 1 |
Vanzin, CS | 2 |
Biancini, GB | 2 |
Schwartz, IV | 2 |
Weigel, C | 1 |
Kiener, C | 1 |
Meier, N | 1 |
Schmid, P | 1 |
Rauh, M | 1 |
Rascher, W | 1 |
Knerr, I | 1 |
Sempere, A | 1 |
Arias, A | 1 |
Farré, G | 1 |
García-Villoria, J | 1 |
Rodríguez-Pombo, P | 1 |
Desviat, LR | 1 |
Merinero, B | 1 |
García-Cazorla, A | 1 |
Vilaseca, MA | 2 |
Ribes, A | 1 |
Artuch, R | 1 |
Campistol, J | 2 |
Manfredini, V | 1 |
de Oliveira, AB | 1 |
Wayhs, CA | 1 |
Ribas, GO | 1 |
Giugliani, L | 1 |
Bohrer, D | 1 |
Garcia, SC | 1 |
Mütze, U | 1 |
Beblo, S | 1 |
Kortz, L | 1 |
Matthies, C | 1 |
Koletzko, B | 1 |
Bruegel, M | 1 |
Rohde, C | 1 |
Thiery, J | 1 |
Kiess, W | 1 |
Ceglarek, U | 1 |
Scala, I | 1 |
Parenti, G | 1 |
Andria, G | 1 |
Chace, DH | 1 |
Kalas, TA | 1 |
Briones, P | 1 |
Ferrer, I | 1 |
Riverola, A | 1 |
Castillo, P | 1 |
Ramon, F | 1 |
Fischer, GM | 1 |
Nemeti, B | 1 |
Farkas, V | 1 |
Debreceni, B | 1 |
Laszlo, A | 1 |
Schaffer, Z | 1 |
Somogyi, C | 1 |
Sandor, A | 1 |
Broquist, HP | 1 |
Böhles, H | 1 |
Ullrich, K | 1 |
Endres, W | 1 |
Behbehani, AW | 1 |
Wendel, U | 1 |
Schulpis, KH | 1 |
Nounopoulos, C | 1 |
Scarpalezou, A | 1 |
Bouloukos, A | 1 |
Missiou-Tsagarakis, S | 1 |
Acosta, PB | 1 |
Stepnick-Gropper, S | 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 | |||
Etude de l'INflammation systémique de Bas GRade Chez Les Patients Adultes Atteints de PHénylcétonurie[NCT04879277] | 40 participants (Actual) | Interventional | 2021-05-26 | 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 |
3 reviews available for carnitine and BH4 Deficiency
Article | Year |
---|---|
Universal screening for inherited metabolic diseases in the neonate (and the fetus).
Topics: Acyl-CoA Dehydrogenase; Amino Acids; Carnitine; DNA; DNA Mutational Analysis; Female; Gestational Ag | 2012 |
A biochemical perspective on the use of tandem mass spectrometry for newborn screening and clinical testing.
Topics: Amino Acids; Carnitine; Humans; Infant, Newborn; Infant, Newborn, Diseases; Mass Spectrometry; Metab | 2005 |
Amino acid metabolism.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Biological Transport, Active; Carnitine; | 1976 |
1 trial available for carnitine and BH4 Deficiency
Article | Year |
---|---|
Metabolomic Markers of Essential Fatty Acids, Carnitine, and Cholesterol Metabolism in Adults and Adolescents with Phenylketonuria.
Topics: Adolescent; Adult; Amino Acids; Betaine; Biomarkers; Carnitine; Caseins; Cholesterol; Cross-Over Stu | 2018 |
Metabolomic Markers of Essential Fatty Acids, Carnitine, and Cholesterol Metabolism in Adults and Adolescents with Phenylketonuria.
Topics: Adolescent; Adult; Amino Acids; Betaine; Biomarkers; Carnitine; Caseins; Cholesterol; Cross-Over Stu | 2018 |
Metabolomic Markers of Essential Fatty Acids, Carnitine, and Cholesterol Metabolism in Adults and Adolescents with Phenylketonuria.
Topics: Adolescent; Adult; Amino Acids; Betaine; Biomarkers; Carnitine; Caseins; Cholesterol; Cross-Over Stu | 2018 |
Metabolomic Markers of Essential Fatty Acids, Carnitine, and Cholesterol Metabolism in Adults and Adolescents with Phenylketonuria.
Topics: Adolescent; Adult; Amino Acids; Betaine; Biomarkers; Carnitine; Caseins; Cholesterol; Cross-Over Stu | 2018 |
17 other studies available for carnitine and BH4 Deficiency
Article | Year |
---|---|
Plasma metabolomic profile changes in females with phenylketonuria following a camp intervention.
Topics: Carnitine; Choline; Fatty Acids; Female; Humans; Male; Metabolomics; Phenylketonurias | 2022 |
Increased cytokine levels induced by high phenylalanine concentrations in late diagnosis PKU patients compared to early diagnosis: Anti-inflammatory effect of L-carnitine.
Topics: Carnitine; Cytokines; Delayed Diagnosis; Humans; Infant, Newborn; Interleukin-2; Interleukin-6; Inte | 2023 |
Increased peripheral of brain-derived neurotrophic factor levels in phenylketonuric patients treated with l-carnitine.
Topics: Antioxidants; Becaplermin; Brain-Derived Neurotrophic Factor; Carnitine; Dietary Supplements; Humans | 2023 |
Diagnostic contribution of metabolic workup for neonatal inherited metabolic disorders in the absence of expanded newborn screening.
Topics: Amino Acids; Carnitine; Female; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Intensiv | 2019 |
L-carnitine protects DNA oxidative damage induced by phenylalanine and its keto acid derivatives in neural cells: a possible pathomechanism and adjuvant therapy for brain injury in phenylketonuria.
Topics: Brain Injuries; Carnitine; Humans; Keto Acids; Oxidative Stress; Phenylalanine; Phenylketonurias | 2021 |
Spectrum analysis of common inherited metabolic diseases in Chinese patients screened and diagnosed by tandem mass spectrometry.
Topics: Acyl-CoA Dehydrogenase; Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Carbox | 2015 |
Protective effect of L-carnitine on Phenylalanine-induced DNA damage.
Topics: Adolescent; Carnitine; Dietary Supplements; DNA Damage; Female; Humans; Male; Phenylalanine; Phenylk | 2015 |
L-carnitine blood levels and oxidative stress in treated phenylketonuric patients.
Topics: Adolescent; Carnitine; Child; Diet, Protein-Restricted; Dietary Supplements; Down-Regulation; Female | 2009 |
Carnitine status in early-treated children, adolescents and young adults with phenylketonuria on low phenylalanine diets.
Topics: Adolescent; Adult; Analysis of Variance; Carnitine; Case-Control Studies; Child; Child, Preschool; C | 2008 |
Study of inborn errors of metabolism in urine from patients with unexplained mental retardation.
Topics: Adenylosuccinate Lyase; Adolescent; Adult; Aged; Carnitine; Child; Child, Preschool; Chromium; Cohor | 2010 |
Evidence that L-carnitine and selenium supplementation reduces oxidative stress in phenylketonuric patients.
Topics: Adolescent; Antioxidants; Carnitine; Dietary Supplements; Humans; Oxidative Stress; Phenylketonurias | 2011 |
Metabolomics of dietary fatty acid restriction in patients with phenylketonuria.
Topics: Blood Platelets; Carnitine; Child; Chromatography, Gas; Chromatography, Liquid; Eicosanoids; Fatty A | 2012 |
Controlled diet in phenylketonuria may cause serum carnitine deficiency.
Topics: Adolescent; Adult; Carnitine; Child; Child, Preschool; Diet; Humans; Infant; Phenylalanine; Phenylke | 1993 |
Metabolism of carnitine in phenylacetic acid-treated rats and in patients with phenylketonuria.
Topics: Adult; Animals; Betaine; Carnitine; Female; Glutamic Acid; Homogentisic Acid; Humans; Ketoglutaric A | 2000 |
Inadequate iron availability as a possible cause of low serum carnitine concentrations in patients with phenylketonuria.
Topics: Adolescent; Adult; Carnitine; Child; Child, Preschool; Ferritins; Hemoglobins; Humans; Infant; Iron; | 1991 |
Serum carnitine level in phenylketonuric children under dietary control in Greece.
Topics: Carnitine; Child, Preschool; Dietary Proteins; Female; Food, Formulated; Greece; Humans; Infant; Mal | 1990 |
Problems related to diet management of maternal phenylketonuria.
Topics: alpha-Linolenic Acid; Carnitine; Cations, Divalent; Cell Membrane Permeability; Cholesterol; Dietary | 1986 |