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homovanillic acid and Deficiency, Mental

homovanillic acid has been researched along with Deficiency, Mental in 19 studies

Homovanillic Acid: A 3-O-methyl ETHER of (3,4-dihydroxyphenyl)acetic acid.
homovanillate : A hydroxy monocarboxylic acid anion which is obtained by deprotonation of the carboxy group of homovanillic acid.
homovanillic acid : A monocarboxylic acid that is the 3-O-methyl ether of (3,4-dihydroxyphenyl)acetic acid. It is a catecholamine metabolite.

Research Excerpts

ExcerptRelevanceReference
"In a patient with the Lesch-Nyhan syndrome we found decreased spinal fluid 5-hydroxyindole acetic acid (5-HIAA), the major metabolite of serotonin, and decreased homovanillic acid (HVA), the major metabolite of dopamine, indicating a decrease in monoamine metabolism."7.66Effects of L-5-hydroxytryptophan on monoamine and amino acids turnover in the Lesch-Nyhan syndrome. ( Castells, S; Chakrabarti, C; Hurwic, M; Nyhan, WL; Perel, JM; Winsberg, BG, 1979)
"In 8 cases of typical neuroleptic malignant syndrome (NMS), homovanillic acid (HVA), 5-hydroxyindole acetic acid (5-HIAA), noradrenaline (NA), and 3-methoxy-4-hydroxyphenylethyleneglycol (MHPG) levels in the cerebrospinal fluid (CSF) were assayed during both the active phase of NMS and after recovery."3.68Neuroleptic malignant syndrome: a study of CSF monoamine metabolism. ( Ishiguro, T; Nisijima, K, 1990)
"In a patient with the Lesch-Nyhan syndrome we found decreased spinal fluid 5-hydroxyindole acetic acid (5-HIAA), the major metabolite of serotonin, and decreased homovanillic acid (HVA), the major metabolite of dopamine, indicating a decrease in monoamine metabolism."3.66Effects of L-5-hydroxytryptophan on monoamine and amino acids turnover in the Lesch-Nyhan syndrome. ( Castells, S; Chakrabarti, C; Hurwic, M; Nyhan, WL; Perel, JM; Winsberg, BG, 1979)
"All AADCD patients were affected by intellectual disability and psychiatric disorders."1.72Long-term neurological and psychiatric outcomes in patients with aromatic l-amino acid decarboxylase deficiency. ( Battini, R; Carducci, C; Fusco, C; Leuzzi, V; Manti, F; Mastrangelo, M; Spagnoli, C; Tolve, M, 2022)
"The Fragile X syndrome, a common form of mental retardation in humans, is caused by silencing the fragile X mental retardation (FMR1) gene leading to the absence of the encoded fragile X mental retardation protein 1 (FMRP)."1.31Alterations of amino acids and monoamine metabolism in male Fmr1 knockout mice: a putative animal model of the human fragile X mental retardation syndrome. ( Braun, K; Gruss, M, 2001)
"In the group of 9 children with other psychoses, both the level of homovanillic acid and that of 5-hydroxy-indoleacetic acid was raised."1.27Childhood psychosis and monoamine metabolites in spinal fluid. ( Gillberg, C; Hamilton-Hellberg, C; Svennerholm, L, 1983)
"It is postulated that the seizures and neurological deterioration of the patient were related to a deficiency in the synthesis of biogenic amine neurotransmitters."1.26Biogenic amine synthesis defect in dihydropteridine reductase deficiency. ( Butler, IJ; Koslow, SH, 1977)

Research

Studies (19)

TimeframeStudies, this research(%)All Research%
pre-199011 (57.89)18.7374
1990's5 (26.32)18.2507
2000's2 (10.53)29.6817
2010's0 (0.00)24.3611
2020's1 (5.26)2.80

Authors

AuthorsStudies
Manti, F1
Mastrangelo, M1
Battini, R1
Carducci, C2
Spagnoli, C1
Fusco, C1
Tolve, M1
Leuzzi, V1
Gibson, KM1
Gupta, M1
Pearl, PL1
Tuchman, M1
Vezina, LG1
Snead, OC1
Smit, LM1
Jakobs, C1
Gillberg, C1
Svennerholm, L1
Hamilton-Hellberg, C1
Hameury, L1
Roux, S1
Barthélémy, C4
Adrien, JL1
Desombre, H1
Sauvage, D1
Garreau, B3
Lelord, G4
Lewis, MH1
Bodfish, JW1
Powell, SB1
Wiest, K1
Darling, M1
Golden, RN1
Gruss, M1
Braun, K1
Koslow, SH1
Butler, IJ1
Watts, RW1
Chalmers, RA1
Lawson, AM1
Castells, S1
Chakrabarti, C1
Winsberg, BG1
Hurwic, M1
Perel, JM1
Nyhan, WL1
Ritvo, ER1
Martineau, J2
Jouve, J2
Muh, JP3
Nisijima, K1
Ishiguro, T1
Zeman, J1
Böswart, J1
Percy, AK1
Zoghbi, H1
Riccardi, VM1
Nalini, K1
Aroor, AR1
Rao, A1
Bruneau, N2
Misionzhnik, EIu1
Kogan, RD1
Balandina, IuB1
Turova, NF1
Sazonova, NS1
Mrochek, JE1
Dinsmore, SR1
Ohrt, DW1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Stereotypies and Mental Retardation: Neurobiological Basis[NCT00491478]Phase 30 participants Interventional1992-09-30Recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Other Studies

19 other studies available for homovanillic acid and Deficiency, Mental

ArticleYear
Long-term neurological and psychiatric outcomes in patients with aromatic l-amino acid decarboxylase deficiency.
    Parkinsonism & related disorders, 2022, Volume: 103

    Topics: Adolescent; Adult; Amino Acids; Aromatic-L-Amino-Acid Decarboxylases; Biogenic Amines; Child; Dopami

2022
Significant behavioral disturbances in succinic semialdehyde dehydrogenase (SSADH) deficiency (gamma-hydroxybutyric aciduria).
    Biological psychiatry, 2003, Oct-01, Volume: 54, Issue:7

    Topics: Adult; Aldehyde Oxidoreductases; Atrophy; Cerebellum; Chromatography, High Pressure Liquid; Chromato

2003
Childhood psychosis and monoamine metabolites in spinal fluid.
    Journal of autism and developmental disorders, 1983, Volume: 13, Issue:4

    Topics: Adolescent; Age Factors; Autistic Disorder; Brain Diseases; Cerebral Palsy; Child; Child, Preschool;

1983
Quantified multidimensional assessment of autism and other pervasive developmental disorders. Application for bioclinical research.
    European child & adolescent psychiatry, 1995, Volume: 4, Issue:2

    Topics: 3,4-Dihydroxyphenylacetic Acid; Adolescent; Autistic Disorder; Brain; Child; Child Development Disor

1995
Plasma HVA in adults with mental retardation and stereotyped behavior: biochemical evidence for a dopamine deficiency model.
    American journal of mental retardation : AJMR, 1996, Volume: 100, Issue:4

    Topics: Adolescent; Adult; Dopamine; Female; Homovanillic Acid; Humans; Intellectual Disability; Male; Middl

1996
Alterations of amino acids and monoamine metabolism in male Fmr1 knockout mice: a putative animal model of the human fragile X mental retardation syndrome.
    Neural plasticity, 2001, Volume: 8, Issue:4

    Topics: 3,4-Dihydroxyphenylacetic Acid; Aging; Alanine; Amino Acids; Animals; Aspartic Acid; Brain; Brain St

2001
Biogenic amine synthesis defect in dihydropteridine reductase deficiency.
    Science (New York, N.Y.), 1977, Nov-04, Volume: 198, Issue:4316

    Topics: 5-Hydroxytryptophan; Biogenic Amines; Carbidopa; Dopamine; Homovanillic Acid; Humans; Hydroxyindolea

1977
Abnormal organic acidurias in mentally retarded patients.
    Lancet (London, England), 1975, Feb-15, Volume: 1, Issue:7903

    Topics: Acidosis; Acids; Adult; Benzoates; Child; Chromatography, Gas; Citrates; Female; Glycolates; Homovan

1975
Effects of L-5-hydroxytryptophan on monoamine and amino acids turnover in the Lesch-Nyhan syndrome.
    Journal of autism and developmental disorders, 1979, Volume: 9, Issue:1

    Topics: 5-Hydroxytryptophan; Amino Acids; Carbidopa; Dopamine; Homovanillic Acid; Humans; Hydroxyindoleaceti

1979
Biochemical studies of children with the syndromes of autism, childhood schizophrenia and related developmental disabilities: a review.
    Journal of child psychology and psychiatry, and allied disciplines, 1977, Volume: 18, Issue:4

    Topics: Autistic Disorder; Blood Platelets; Brain; Bufotenin; Child; Dopamine beta-Hydroxylase; Homovanillic

1977
Monoamines (serotonin and catecholamines) and their derivatives in infantile autism: age-related changes and drug effects.
    Developmental medicine and child neurology, 1992, Volume: 34, Issue:7

    Topics: 3,4-Dihydroxyphenylacetic Acid; Age Factors; Autistic Disorder; Catecholamines; Child; Child Develop

1992
Neuroleptic malignant syndrome: a study of CSF monoamine metabolism.
    Biological psychiatry, 1990, Feb-01, Volume: 27, Issue:3

    Topics: Adult; Biogenic Monoamines; Bipolar Disorder; Depressive Disorder; Female; Homovanillic Acid; Humans

1990
[Metabolites of neurotransmitters in the cerebrospinal fluid in children].
    Ceskoslovenska pediatrie, 1991, Volume: 46, Issue:5

    Topics: Adolescent; Child; Child, Preschool; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Infant; In

1991
Rett syndrome: initial experience with an emerging clinical entity.
    Brain & development, 1985, Volume: 7, Issue:3

    Topics: Adolescent; Biopsy; Child; Child Development; Child, Preschool; Electroencephalography; Female; Homo

1985
Urinary levels of biogenic amine metabolites in mentally retarded children.
    Journal of mental deficiency research, 1988, Volume: 32 ( Pt 5)

    Topics: Adolescent; Biogenic Amines; Child; Creatinine; Female; Homovanillic Acid; Humans; Hydroxyindoleacet

1988
Urinary homovanillic acid levels of autistic children.
    Developmental medicine and child neurology, 1988, Volume: 30, Issue:1

    Topics: Autistic Disorder; Child; Child, Preschool; Female; Homovanillic Acid; Humans; Intellectual Disabili

1988
Developmental changes in ERPs and monoamine metabolites in normal, mentally retarded and autistic children.
    Electroencephalography and clinical neurophysiology. Supplement, 1987, Volume: 40

    Topics: Autistic Disorder; Child; Child Development; Child, Preschool; Evoked Potentials, Auditory; Homovani

1987
[Clinico-pathogenetic correlations in intellectual deficiency in premature infants].
    Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952), 1985, Volume: 85, Issue:3

    Topics: Autoantibodies; Brain; Catecholamines; Child; Homovanillic Acid; Humans; Infant, Newborn; Infant, Pr

1985
Monitoring phenylalanine-tyrosine metabolism by high-resolution liquid chromatography of urine.
    Clinical chemistry, 1973, Volume: 19, Issue:8

    Topics: Aromatic Amino Acid Decarboxylase Inhibitors; Autistic Disorder; Carbidopa; Catechols; Child; Chroma

1973