Page last updated: 2024-09-03

caprylates and Lipid Metabolism, Inborn Error

caprylates has been researched along with Lipid Metabolism, Inborn Error in 19 studies

Research

Studies (19)

TimeframeStudies, this research(%)All Research%
pre-19907 (36.84)18.7374
1990's4 (21.05)18.2507
2000's3 (15.79)29.6817
2010's3 (15.79)24.3611
2020's2 (10.53)2.80

Authors

AuthorsStudies
Alatibi, KI; Ausserlechner, MJ; Grünert, SC; Hagenbuchner, J; Karall, D; Schilling, O; Tholen, S; Tucci, S; Vockley, J; Wehbe, Z1
Birkler, RID; Corydon, TJ; Fernandez-Guerra, P; Gregersen, N; Hansen, J; Nochi, Z; Olsen, RKJ; Wibrand, F1
Burchill, LJ; DeLany, JP; Deward, S; El-Gharbawy, AH; Gillingham, MB; Goldstein, A; Goodpaster, B; Harding, CO; Heitner, SB; Lasarev, MR; Martin, J; Matern, D; Pollaro, J; Rose, S; Shoemaker, J; Vockley, J1
Shoffner, JM1
Busanello, EN; Ferreira, GC; Moura, AP; Scaini, G; Schuck, PF; Simon, KR; Streck, EL; Tonin, AM; Wajner, M1
Bennett, MJ; Butt, Y; Jones, PM1
Bennett, MJ; Butt, YM; Jones, PM1
Borba Rosa, R; da Costa Ferreira, G; Dutra-Filho, CS; Duval Wannmacher, CM; Maria, Rde C; Reis de Assis, D; Ribeiro, CA; Santos Perry, ML; Schuck, PF; Terezinha de Souza Wyse, A; Wajner, M1
Amendt, BA; Felts, SJ; Fritchman, KS; Rhead, WJ1
Gregersen, N; Hobolth, N; Kølvraa, S; Lauritzen, R; Rasmussen, K; Rosleff, F1
Brivet, M; Duran, M; Heymans, HS; Ijlst, L; Niezen-Koning, KE; Reijngoud, DJ; Smit, GP; van Spronsen, FJ; Wanders, RJ1
Ijlst, L; Wanders, RJ1
de Klerk, JB; Ijlst, L; Przyrembel, H; van Elk, E; Wanders, RJ1
Bonnefont, JP; Cepanec, C; Colonna, M; Demaugre, F; Leroux, JP; Saudubray, JM1
Amendt, BA; Rhead, WJ1
Duran, M; Hofkamp, M; Rhead, WJ; Saudubray, JM; Wadman, SK1
Bruinvis, L; de Jager, JP; de Klerk, JB; Duran, M; Hofkamp, M; Ketting, D; Mitchell, G; Saudubray, JM; Wadman, SK1
Beckeringh, TE; Bruinvis, L; Dorland, L; Duran, M; Ketting, D; van Vossen, R; Wadman, SK1
Schwabe, AD; Valdivieso, VD1

Trials

1 trial(s) available for caprylates and Lipid Metabolism, Inborn Error

ArticleYear
Triheptanoin versus trioctanoin for long-chain fatty acid oxidation disorders: a double blinded, randomized controlled trial.
    Journal of inherited metabolic disease, 2017, Volume: 40, Issue:6

    Topics: Acyl-CoA Dehydrogenase, Long-Chain; Adolescent; Adult; Caprylates; Cardiomyopathies; Carnitine; Child; Dietary Fats; Double-Blind Method; Exercise; Fatty Acids; Female; Humans; Lipid Metabolism, Inborn Errors; Male; Middle Aged; Mitochondrial Myopathies; Mitochondrial Trifunctional Protein; Nervous System Diseases; Oxidation-Reduction; Rhabdomyolysis; Triglycerides; Young Adult

2017

Other Studies

18 other study(ies) available for caprylates and Lipid Metabolism, Inborn Error

ArticleYear
Lipidomic and Proteomic Alterations Induced by Even and Odd Medium-Chain Fatty Acids on Fibroblasts of Long-Chain Fatty Acid Oxidation Disorders.
    International journal of molecular sciences, 2021, Sep-29, Volume: 22, Issue:19

    Topics: Acyl-CoA Dehydrogenase, Long-Chain; Caprylates; Cardiolipins; Cell Line; Female; Fibroblasts; Genotype; Heptanoates; Humans; Lipid Metabolism, Inborn Errors; Lipidomics; Male; Mitochondria; Phosphatidylcholines; Phosphatidylethanolamines; Proteome; Proteomics; Sphingolipids

2021
Increased antioxidant response in medium-chain acyl-CoA dehydrogenase deficiency: does lipoic acid have a protective role?
    Pediatric research, 2020, Volume: 88, Issue:4

    Topics: Acyl-CoA Dehydrogenase; Antioxidants; Caprylates; Carnitine; Cell Death; Fibroblasts; Genotype; Glycolysis; Humans; Lipid Metabolism, Inborn Errors; Lipid Peroxidation; Mitochondria; Oxidative Stress; Phenotype; Superoxides; Thioctic Acid

2020
Concerning "Triheptanoin vs trioctanoin for long-chain fatty acid oxidation disorders: A double blinded, randomized controlled trial" by Gillingham et al.
    Journal of inherited metabolic disease, 2019, Volume: 42, Issue:3

    Topics: Caprylates; Fatty Acids; Humans; Lipid Metabolism, Inborn Errors; Oxidation-Reduction; Triglycerides

2019
Toxicity of octanoate and decanoate in rat peripheral tissues: evidence of bioenergetic dysfunction and oxidative damage induction in liver and skeletal muscle.
    Molecular and cellular biochemistry, 2012, Volume: 361, Issue:1-2

    Topics: Acyl-CoA Dehydrogenase; Animals; Caprylates; Creatine Kinase; Decanoates; Electron Transport; Electron Transport Complex IV; Glutathione; Lipid Metabolism, Inborn Errors; Liver; Male; Mitochondria; Muscle, Skeletal; Oxidation-Reduction; Oxidative Stress; Protein Carbonylation; Rats; Rats, Wistar; Thiobarbituric Acid Reactive Substances

2012
Accumulation of 3-hydroxy-fatty acids in the culture medium of long-chain L-3-hydroxyacyl CoA dehydrogenase (LCHAD) and mitochondrial trifunctional protein-deficient skin fibroblasts: implications for medium chain triglyceride dietary treatment of LCHAD d
    Pediatric research, 2003, Volume: 53, Issue:5

    Topics: 3-Hydroxyacyl CoA Dehydrogenases; Caprylates; Cells, Cultured; Decanoates; Fibroblasts; Humans; In Vitro Techniques; Lipid Metabolism, Inborn Errors; Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase; Mitochondrial Trifunctional Protein; Multienzyme Complexes; Oxidation-Reduction; Palmitates; Point Mutation; Skin

2003
Effects of odd-numbered medium-chain fatty acids on the accumulation of long-chain 3-hydroxy-fatty acids in long-chain L-3-hydroxyacyl CoA dehydrogenase and mitochondrial trifunctional protein deficient skin fibroblasts.
    Molecular genetics and metabolism, 2004, Volume: 81, Issue:2

    Topics: 3-Hydroxyacyl CoA Dehydrogenases; Caprylates; Cell Line; Culture Media; Decanoates; Fatty Acids; Fibroblasts; Heptanoates; Humans; Lipid Metabolism, Inborn Errors; Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase; Mitochondrial Diseases; Skin

2004
Inhibition of energy metabolism in cerebral cortex of young rats by the medium-chain fatty acids accumulating in MCAD deficiency.
    Brain research, 2004, Dec-24, Volume: 1030, Issue:1

    Topics: Acetates; Acyl-CoA Dehydrogenase; Age Factors; Animals; Antifungal Agents; Antihypertensive Agents; Caprylates; Carbon Radioisotopes; Cerebral Cortex; Citrate (si)-Synthase; Creatine Kinase; Decanoic Acids; Electron Transport; Energy Metabolism; Fatty Acids; Lipid Metabolism, Inborn Errors; Rats; Rats, Wistar

2004
Dicarboxylic aciduria: deficient [1-14C]octanoate oxidation and medium-chain acyl-CoA dehydrogenase in fibroblasts.
    Science (New York, N.Y.), 1983, Jul-01, Volume: 221, Issue:4605

    Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Butyrates; Butyric Acid; Caprylates; Dicarboxylic Acids; Fibroblasts; Humans; Lipid Metabolism, Inborn Errors; Mitochondria; Oxidation-Reduction

1983
Non-ketotic C6-C10-dicarboxylic aciduria: biochemical investigations of two cases.
    Clinica chimica acta; international journal of clinical chemistry, 1980, Mar-28, Volume: 102, Issue:2-3

    Topics: Adipates; Caproates; Caprylates; Child, Preschool; Chromatography, Gas; Decanoic Acids; Dicarboxylic Acids; Fatty Acid Desaturases; Fatty Acids; Glycine; Humans; Hydroxy Acids; Hydroxybutyrates; Hypoglycemia; Infant; Lipid Metabolism, Inborn Errors; Male; Mass Spectrometry; Valerates

1980
A patient with lethal cardiomyopathy and a carnitine-acylcarnitine translocase deficiency.
    Journal of inherited metabolic disease, 1995, Volume: 18, Issue:2

    Topics: Caprylates; Cardiomyopathies; Carnitine Acyltransferases; Carnitine O-Palmitoyltransferase; Cells, Cultured; Fatal Outcome; Female; Fibroblasts; Humans; Infant, Newborn; Leukocytes; Lipid Metabolism, Inborn Errors; Oxidation-Reduction; Palmitates

1995
Fatty acid beta-oxidation in leukocytes from control subjects and medium-chain acyl-CoA dehydrogenase deficient patients.
    Biochimica et biophysica acta, 1992, Jan-16, Volume: 1138, Issue:1

    Topics: 3-Hydroxybutyric Acid; Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Caprylates; Fatty Acids; Humans; Hydroxybutyrates; Leukocytes; Lipid Metabolism, Inborn Errors; Mitochondria; Oxidation-Reduction; Palmitates; Time Factors

1992
Octanoate and palmitate beta-oxidation in human leukocytes: implications for the rapid diagnosis of fatty acid beta-oxidation disorders.
    Journal of inherited metabolic disease, 1991, Volume: 14, Issue:3

    Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenase, Long-Chain; Caprylates; Fatty Acid Desaturases; Fatty Acids; Fibroblasts; Humans; In Vitro Techniques; Infant; Leukocytes; Lipid Metabolism, Inborn Errors; Oxidation-Reduction; Palmitic Acid; Palmitic Acids

1991
Infantile form of carnitine palmitoyltransferase II deficiency with hepatomuscular symptoms and sudden death. Physiopathological approach to carnitine palmitoyltransferase II deficiencies.
    The Journal of clinical investigation, 1991, Volume: 87, Issue:3

    Topics: Blotting, Western; Butyrates; Caprylates; Carnitine O-Palmitoyltransferase; Death, Sudden; Humans; Infant; Ketone Bodies; Lipid Metabolism, Inborn Errors; Liver Diseases; Male; Molecular Weight; Palmitates

1991
The multiple acyl-coenzyme A dehydrogenation disorders, glutaric aciduria type II and ethylmalonic-adipic aciduria. Mitochondrial fatty acid oxidation, acyl-coenzyme A dehydrogenase, and electron transfer flavoprotein activities in fibroblasts.
    The Journal of clinical investigation, 1986, Volume: 78, Issue:1

    Topics: Acyl Coenzyme A; Acyl-CoA Dehydrogenases; Adipates; Animals; Caprylates; Electron Transport; Electron-Transferring Flavoproteins; Fatty Acids; Fibroblasts; Flavin-Adenine Dinucleotide; Flavoproteins; Glutarates; Lipid Metabolism, Inborn Errors; Liver; Malonates; Mitochondria; Palmitoyl Coenzyme A; Succinates; Succinic Acid; Swine

1986
Sudden child death and 'healthy' affected family members with medium-chain acyl-coenzyme A dehydrogenase deficiency.
    Pediatrics, 1986, Volume: 78, Issue:6

    Topics: Acyl-CoA Dehydrogenase; Caproates; Caprylates; Decanoic Acids; Fatty Acid Desaturases; Fatty Acids; Fatty Acids, Nonesterified; Female; Humans; Infant; Lipid Metabolism, Inborn Errors; Male; Mitochondria, Liver; Oxidation-Reduction; Sudden Infant Death

1986
Octanoic acidemia and octanoylcarnitine excretion with dicarboxylic aciduria due to defective oxidation of medium-chain fatty acids.
    The Journal of pediatrics, 1985, Volume: 107, Issue:3

    Topics: Acyl-CoA Dehydrogenases; Caprylates; Carnitine; Cells, Cultured; Decanoic Acids; Dicarboxylic Acids; Fatty Acids; Fatty Acids, Nonesterified; Female; Fibroblasts; Humans; Infant; Lipid Metabolism, Inborn Errors; Male; Oxidation-Reduction

1985
Octanoylglucuronide excretion in patients with a defective oxidation of medium-chain fatty acids.
    Clinica chimica acta; international journal of clinical chemistry, 1985, Nov-15, Volume: 152, Issue:3

    Topics: Acyl-CoA Dehydrogenase; Acyl-CoA Dehydrogenases; Caprylates; Carnitine; Fatty Acids; Gas Chromatography-Mass Spectrometry; Humans; Hydrogen-Ion Concentration; Lipid Metabolism, Inborn Errors

1985
Absorption of medium-chain lipids from the rat cecum.
    The American journal of digestive diseases, 1966, Volume: 11, Issue:6

    Topics: Animals; Caprylates; Cecum; Chromatography, Thin Layer; Intestinal Absorption; Intestine, Large; Lipid Metabolism, Inborn Errors; Rats

1966