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trimethyloxamine and Inborn Errors of Metabolism

trimethyloxamine has been researched along with Inborn Errors of Metabolism in 20 studies

trimethyloxamine: used in manufacture of quaternary ammonium cpds; insect attractant; warming agent for gas; oxidant; structure
trimethylamine N-oxide : A tertiary amine oxide resulting from the oxidation of the amino group of trimethylamine.

Research Excerpts

ExcerptRelevanceReference
"The fish odour syndrome was diagnosed in 11 subjects: the percentage of total trimethylamine excreted in their urine samples that was oxidised to trimethylamine N-oxide was < 55% under normal dietary conditions and < 25% after oral challenge with trimethylamine (in normal subjects > 80% of trimethylamine was N-oxidised)."5.07The fish odour syndrome: biochemical, familial, and clinical aspects. ( Ayesh, R; Mitchell, SC; Smith, RL; Zhang, A, 1993)
"An oral trimethylamine challenge test has been used to confirm the heterozygous status of patients with 'fish-odour syndrome'."3.69Fish odour syndrome: verification of carrier detection test. ( Mitchell, S; Smith, R; Zhang, AQ, 1995)
" Beginning with a single propositus, who had been previously diagnosed at the age of 10 as suffering from trimethylaminuria (fish-odour syndrome), both her parents and two sisters were investigated biochemically with respect to their ability to N-oxidize trimethylamine (TMA), both when derived from the diet and when administered exogenously."3.67Trimethylaminuria ('fish-odour syndrome'): a study of an affected family. ( Al-Waiz, M; Ayesh, R; Idle, JR; Mitchell, SC; Smith, RL, 1988)
"Trimethylamine (TMA) is a tertiary amine with a characteristic fishy odour."2.53The complex metabolism of trimethylamine in humans: endogenous and exogenous sources. ( Bhargava, B; Chhibber-Goel, J; Gaur, A; Parakh, N; Sharma, A; Singhal, V, 2016)
"Trimethylamine (TMA) is a volatile substance produced in the gut, absorbed into the blood and further metabolized by healthy individuals into trimethylamine-N-oxide (TMAO) by TMA-oxidase and then excreted in urine."1.33Diagnosis of suspected trimethylaminuria by NMR spectroscopy. ( Arêas, JA; Lanfer-Marquez, UM; Podadera, P; Sipahi, AM, 2005)

Research

Studies (20)

TimeframeStudies, this research(%)All Research%
pre-19902 (10.00)18.7374
1990's7 (35.00)18.2507
2000's5 (25.00)29.6817
2010's4 (20.00)24.3611
2020's2 (10.00)2.80

Authors

AuthorsStudies
Fadhlaoui, K1
Arnal, ME1
Martineau, M1
Camponova, P1
Ollivier, B1
O'Toole, PW1
Brugère, JF1
Veyrat-Durebex, C1
Benz-de-Bretagne, I1
Clavier, V1
Bruno, C1
Andres, CR1
Antar, C1
Hennart, B1
Maillot, F1
Nadal-Desbarats, L1
Blasco, H1
Gao, C1
Catucci, G1
Castrignanò, S1
Gilardi, G1
Sadeghi, SJ1
D'Angelo, R1
Scimone, C1
Esposito, T1
Bruschetta, D1
Rinaldi, C1
Ruggeri, A1
Sidoti, A1
Oliveira, A1
Faria, A1
Oliva, M1
Chhibber-Goel, J1
Gaur, A1
Singhal, V1
Parakh, N1
Bhargava, B1
Sharma, A1
Fraser-Andrews, EA1
Manning, NJ1
Ashton, GH1
Eldridge, P1
McGrath, J1
Menagé, Hdu P1
Yamazaki, H1
Fujieda, M1
Togashi, M1
Saito, T1
Preti, G1
Cashman, JR1
Kamataki, T1
Podadera, P1
Sipahi, AM1
Arêas, JA1
Lanfer-Marquez, UM1
Hsu, WY1
Lo, WY1
Lai, CC1
Tsai, FJ1
Tsai, CH1
Tsai, Y1
Lin, WD1
Chao, MC1
Johnson, DW1
Hadidi, HF1
Cholerton, S1
Atkinson, S1
Irshaid, YM1
Rawashdeh, NM1
Idle, JR3
Ayesh, R3
Mitchell, SC4
Zhang, A1
Smith, RL4
Zhang, AQ2
Mitchell, S1
Smith, R1
Maschke, S1
Wahl, A1
Azaroual, N1
Boulet, O1
Crunelle, V1
Imbenotte, M1
Foulard, M1
Vermeersch, G1
Lhermitte, M1
Thithapandha, A1
Mamer, OA1
Choinière, L1
Treacy, EP1
al-Waiz, M2

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Phase II Study to Evaluate Oral Chlorophyllin in Hemorrhagic Cystitis Secondary to Radiation Therapy for Pelvic Malignancies[NCT05348239]Phase 224 participants (Anticipated)Interventional2022-03-26Recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Reviews

2 reviews available for trimethyloxamine and Inborn Errors of Metabolism

ArticleYear
Archaea, specific genetic traits, and development of improved bacterial live biotherapeutic products: another face of next-generation probiotics.
    Applied microbiology and biotechnology, 2020, Volume: 104, Issue:11

    Topics: Animals; Archaea; Biological Therapy; Cardiovascular Diseases; Diet; Gastrointestinal Microbiome; Hu

2020
The complex metabolism of trimethylamine in humans: endogenous and exogenous sources.
    Expert reviews in molecular medicine, 2016, Apr-29, Volume: 18

    Topics: Air Pollutants; Animals; Atherosclerosis; Diet; Humans; Metabolism, Inborn Errors; Methylamines; Neo

2016

Trials

2 trials available for trimethyloxamine and Inborn Errors of Metabolism

ArticleYear
Effects of the dietary supplements, activated charcoal and copper chlorophyllin, on urinary excretion of trimethylamine in Japanese trimethylaminuria patients.
    Life sciences, 2004, Apr-16, Volume: 74, Issue:22

    Topics: Adult; Charcoal; Chlorophyllides; Diet; Dietary Supplements; Drug Therapy, Combination; Female; Huma

2004
The fish odour syndrome: biochemical, familial, and clinical aspects.
    BMJ (Clinical research ed.), 1993, Sep-11, Volume: 307, Issue:6905

    Topics: Adolescent; Adult; Animals; Female; Fishes; Humans; Infant; Male; Mental Disorders; Metabolism, Inbo

1993

Other Studies

16 other studies available for trimethyloxamine and Inborn Errors of Metabolism

ArticleYear
Quality consideration for the validation of urine TMA and TMAO measurement by nuclear magnetic resonance spectroscopy in Fish Odor Syndrome.
    Analytical biochemistry, 2021, 10-01, Volume: 630

    Topics: Calibration; Female; Humans; Magnetic Resonance Spectroscopy; Metabolism, Inborn Errors; Methylamine

2021
Inactivation mechanism of N61S mutant of human FMO3 towards trimethylamine.
    Scientific reports, 2017, 11-07, Volume: 7, Issue:1

    Topics: Computer Simulation; Humans; In Vitro Techniques; Metabolism, Inborn Errors; Methylamines; Mutation;

2017
Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report.
    Journal of medical case reports, 2014, Oct-06, Volume: 8

    Topics: Biomarkers; Child; Down-Regulation; Female; Genetic Markers; Humans; Metabolism, Inborn Errors; Meth

2014
Fish Malodour syndrome in a child.
    BMJ case reports, 2015, Apr-13, Volume: 2015

    Topics: Child, Preschool; Diagnosis, Differential; Diet Therapy; Female; Humans; Hygiene; Metabolism, Inborn

2015
Fish odour syndrome with features of both primary and secondary trimethylaminuria.
    Clinical and experimental dermatology, 2003, Volume: 28, Issue:2

    Topics: Biomarkers; Female; Humans; Metabolism, Inborn Errors; Methylamines; Middle Aged; Odorants

2003
Diagnosis of suspected trimethylaminuria by NMR spectroscopy.
    Clinica chimica acta; international journal of clinical chemistry, 2005, Volume: 351, Issue:1-2

    Topics: Adult; Amines; Animals; Choline; Diet; Dogfish; Humans; Magnetic Resonance Spectroscopy; Male; Metab

2005
Rapid screening assay of trimethylaminuria in urine with matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.
    Rapid communications in mass spectrometry : RCM, 2007, Volume: 21, Issue:12

    Topics: Child, Preschool; Female; Humans; Infant; Metabolism, Inborn Errors; Methylamines; Reproducibility o

2007
A flow injection electrospray ionization tandem mass spectrometric method for the simultaneous measurement of trimethylamine and trimethylamine N-oxide in urine.
    Journal of mass spectrometry : JMS, 2008, Volume: 43, Issue:4

    Topics: Humans; Metabolism, Inborn Errors; Methylamines; Odorants; Spectrometry, Mass, Electrospray Ionizati

2008
The N-oxidation of trimethylamine in a Jordanian population.
    British journal of clinical pharmacology, 1995, Volume: 39, Issue:2

    Topics: Adult; Ethnicity; Female; Humans; Jordan; Male; Metabolism, Inborn Errors; Methylamines; Middle Aged

1995
Fish odour syndrome: verification of carrier detection test.
    Journal of inherited metabolic disease, 1995, Volume: 18, Issue:6

    Topics: Adult; Female; Genetic Carrier Screening; Humans; Male; Metabolism, Inborn Errors; Methylamines; Odo

1995
Discontinuous distribution of N-oxidation of dietary-derived trimethylamine in a British population.
    Xenobiotica; the fate of foreign compounds in biological systems, 1996, Volume: 26, Issue:9

    Topics: Adult; Diet; Female; Humans; Male; Metabolism, Inborn Errors; Methylamines; Middle Aged; Odorants; O

1996
1H-NMR analysis of trimethylamine in urine for the diagnosis of fish-odour syndrome.
    Clinica chimica acta; international journal of clinical chemistry, 1997, Jul-25, Volume: 263, Issue:2

    Topics: Amine Oxidase (Copper-Containing); Female; Humans; Liver; Magnetic Resonance Spectroscopy; Male; Met

1997
A pharmacogenetic study of trimethylaminuria in Orientals.
    Pharmacogenetics, 1997, Volume: 7, Issue:6

    Topics: Adult; Asian People; Female; Humans; Male; Metabolism, Inborn Errors; Methylamines; Middle Aged; Odo

1997
Measurement of trimethylamine and trimethylamine N-oxide independently in urine by fast atom bombardment mass spectrometry.
    Analytical biochemistry, 1999, Dec-15, Volume: 276, Issue:2

    Topics: Case-Control Studies; Female; Humans; Male; Metabolism, Inborn Errors; Methylamines; Reference Value

1999
Trimethylaminuria: the detection of carriers using a trimethylamine load test.
    Journal of inherited metabolic disease, 1989, Volume: 12, Issue:1

    Topics: Administration, Oral; Adult; Genetic Carrier Screening; Humans; Male; Metabolism, Inborn Errors; Met

1989
Trimethylaminuria ('fish-odour syndrome'): a study of an affected family.
    Clinical science (London, England : 1979), 1988, Volume: 74, Issue:3

    Topics: Adult; Female; Humans; Male; Metabolism, Inborn Errors; Methylamines; Syndrome

1988