Literature DB >> 25860816

(1)H-MRS in glutaric aciduria type 1: impact of biochemical phenotype and age on the cerebral accumulation of neurotoxic metabolites.

Inga Harting1, Nikolas Boy, Jana Heringer, Angelika Seitz, Martin Bendszus, Petra J W Pouwels, Stefan Kölker.   

Abstract

BACKGROUND: In glutaric aciduria type 1 (GA1) the neurotoxic metabolites glutaric acid (GA) and 3-hydroxyglutaric acid (3-OH-GA) accumulate within the brain. Due to limited efflux across the blood-brain-barrier biochemical monitoring of intracerebrally accumulating toxic metabolites is as yet not possible. AIMS: To investigate brain metabolic patterns in glutaric aciduria type 1 using (1)H magnetic resonance spectroscopy ((1)H-MRS) with focus on detecting the disease-related neurotoxic metabolites GA and 3-OH-GA. PATIENTS AND METHODS: Short echo time (1)H-MRS was performed in 13 treated metabolically stable patients. Twenty-one white matter and 16 basal ganglia spectra from 12 patients (age range 7 months - 22 years) were included. Subgroups based on age, biochemical phenotype and/or associated MRI changes were compared with control spectra.
RESULTS: GA was elevated in white matter of patients. 3-OH-GA was elevated in white matter of older patients with associated signal changes on MRI, which was structurally characterized by decreased creatine and phosphocreatine (tCr) and elevated choline (Cho). Metabolite changes differed with biochemical phenotype and disease duration: Low excretors with up to 30% residual enzyme activity had only mildly, non-significantly elevated GA and mildly subnormal N-acetylaspartate (tNAA). High excretors with complete lack of enzyme activity had significantly increased GA, tNAA was mildly subnormal in younger and decreased in older high excretors.
CONCLUSIONS: GA and 3-OH-GA are detectable by in vivo (1)H-MRS, which might finally allow biochemical follow-up monitoring of intracerebrally accumulating neurotoxic metabolites in GA1. A high excreting phenotype appears to be a risk factor for cerebral GA accumulation and progressive neuroaxonal compromise despite a similar clinical course in younger high and low excreting patients. This might have consequences for long-term outcome.

Entities:  

Mesh:

Substances:

Year:  2015        PMID: 25860816     DOI: 10.1007/s10545-015-9826-8

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  46 in total

1.  Glutaric aciduria type I: a neuroimaging diagnosis?

Authors:  Cesar C Santos; E Steve Roach
Journal:  J Child Neurol       Date:  2005-07       Impact factor: 1.987

2.  Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I).

Authors:  S Kölker; E Christensen; J V Leonard; C R Greenberg; A B Burlina; A P Burlina; M Dixon; M Duran; S I Goodman; D M Koeller; E Müller; E R Naughten; E Neumaier-Probst; J G Okun; M Kyllerman; R A Surtees; B Wilcken; G F Hoffmann; P Burgard
Journal:  J Inherit Metab Dis       Date:  2007-01-03       Impact factor: 4.982

3.  Bioenergetics in glutaryl-coenzyme A dehydrogenase deficiency: a role for glutaryl-coenzyme A.

Authors:  Sven W Sauer; Jürgen G Okun; Marina A Schwab; Linda R Crnic; Georg F Hoffmann; Stephen I Goodman; David M Koeller; Stefan Kölker
Journal:  J Biol Chem       Date:  2005-04-19       Impact factor: 5.157

Review 4.  Striatal degeneration and spongy myelinopathy in glutaric acidemia.

Authors:  D Soffer; N Amir; O N Elpeleg; J M Gomori; R S Shalev; S Gottschalk-Sabag
Journal:  J Neurol Sci       Date:  1992-02       Impact factor: 3.181

5.  Neuropathological, biochemical and molecular findings in a glutaric acidemia type 1 cohort.

Authors:  Christopher B R Funk; Asuri N Prasad; Patrick Frosk; Sven Sauer; Stefan Kölker; Cheryl R Greenberg; Marc R Del Bigio
Journal:  Brain       Date:  2005-02-02       Impact factor: 13.501

6.  3-Hydroxyglutaric acid is transported via the sodium-dependent dicarboxylate transporter NaDC3.

Authors:  Franziska Stellmer; Britta Keyser; Birgitta C Burckhardt; Hermann Koepsell; Thomas Streichert; Markus Glatzel; Sabrina Jabs; Joachim Thiem; Wilhelm Herdering; David M Koeller; Stephen I Goodman; Zoltan Lukacs; Kurt Ullrich; Gerhard Burckhardt; Thomas Braulke; Chris Mühlhausen
Journal:  J Mol Med (Berl)       Date:  2007-03-14       Impact factor: 4.599

7.  Glutaric aciduria type I and methylmalonic aciduria: simulation of cerebral import and export of accumulating neurotoxic dicarboxylic acids in in vitro models of the blood-brain barrier and the choroid plexus.

Authors:  Sven W Sauer; Silvana Opp; Anne Mahringer; Marcin M Kamiński; Christian Thiel; Jürgen G Okun; Gert Fricker; Marina A Morath; Stefan Kölker
Journal:  Biochim Biophys Acta       Date:  2010-03-17

8.  Dynamic changes of striatal and extrastriatal abnormalities in glutaric aciduria type I.

Authors:  Inga Harting; Eva Neumaier-Probst; Angelika Seitz; Esther M Maier; Birgit Assmann; Ivo Baric; Monica Troncoso; Chris Mühlhausen; Johannes Zschocke; Nikolas P S Boy; Georg F Hoffmann; Sven F Garbade; Stefan Kölker
Journal:  Brain       Date:  2009-05-11       Impact factor: 13.501

9.  Decline of acute encephalopathic crises in children with glutaryl-CoA dehydrogenase deficiency identified by newborn screening in Germany.

Authors:  Stefan Kölker; Sven F Garbade; Nikolas Boy; Esther M Maier; Thomas Meissner; Chris Mühlhausen; Julia B Hennermann; Thomas Lücke; Johannes Häberle; Jochen Baumkötter; Wolfram Haller; Edith Muller; Johannes Zschocke; Peter Burgard; Georg F Hoffmann
Journal:  Pediatr Res       Date:  2007-09       Impact factor: 3.756

10.  Brain injury in glutaric aciduria type I: the value of functional techniques in magnetic resonance imaging.

Authors:  Belén Pérez-Dueñas; Alberto De La Osa; Antoni Capdevila; Aleix Navarro-Sastre; Andy Leist; Antonia Ribes; Angels García-Cazorla; Mercedes Serrano; Mercedes Pineda; Jaume Campistol
Journal:  Eur J Paediatr Neurol       Date:  2009-01-22       Impact factor: 3.140

View more
  13 in total

1.  Clinical, biochemical and molecular findings of 24 Brazilian patients with glutaric acidemia type 1: 4 novel mutations in the GCDH gene.

Authors:  Angela Sitta; Gilian Guerreiro; Daniella de Moura Coelho; Vitoria Volfart da Rocha; Bianca Gomes Dos Reis; Carmen Sousa; Laura Vilarinho; Moacir Wajner; Carmen Regla Vargas
Journal:  Metab Brain Dis       Date:  2020-10-16       Impact factor: 3.584

Review 2.  Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision.

Authors:  Nikolas Boy; Chris Mühlhausen; Esther M Maier; Jana Heringer; Birgit Assmann; Peter Burgard; Marjorie Dixon; Sandra Fleissner; Cheryl R Greenberg; Inga Harting; Georg F Hoffmann; Daniela Karall; David M Koeller; Michael B Krawinkel; Jürgen G Okun; Thomas Opladen; Roland Posset; Katja Sahm; Johannes Zschocke; Stefan Kölker
Journal:  J Inherit Metab Dis       Date:  2016-11-16       Impact factor: 4.982

3.  Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement.

Authors:  I Harting; S Karch; U Moog; A Seitz; P J W Pouwels; N I Wolf
Journal:  AJNR Am J Neuroradiol       Date:  2019-05-02       Impact factor: 3.825

Review 4.  Clinical 1H MRS in childhood neurometabolic diseases - part 2: MRS signatures.

Authors:  Matthew T Whitehead; Lillian M Lai; Stefan Blüml
Journal:  Neuroradiology       Date:  2022-02-28       Impact factor: 2.804

5.  Glutaric aciduria type 1: Diagnosis, clinical features and long-term outcome in a large cohort of 34 Irish patients.

Authors:  Lydia Healy; Meabh O'Shea; Jennifer McNulty; Graham King; Eilish Twomey; Eileen Treacy; Ellen Crushell; Joanne Hughes; Ina Knerr; Ahmad Ardeshir Monavari
Journal:  JIMD Rep       Date:  2022-06-14

6.  Does glutaric aciduria type 1 affect hearing function?

Authors:  Dilek Demiral Özgedi K; Suna Tokgöz Yılmaz; Berrak Bilginer Gürbüz; H Serap Si Vri; Gonca Sennaroğlu
Journal:  Metab Brain Dis       Date:  2022-04-30       Impact factor: 3.655

7.  Long Lasting High Lysine Diet Aggravates White Matter Injury in Glutaryl-CoA Dehydrogenase Deficient (Gcdh-/-) Mice.

Authors:  Silvia Olivera-Bravo; Bianca Seminotti; Eugenia Isasi; César A Ribeiro; Guilhian Leipnitz; Michael Woontner; Stephen I Goodman; Diogo Souza; Luis Barbeito; Moacir Wajner
Journal:  Mol Neurobiol       Date:  2018-05-19       Impact factor: 5.590

Review 8.  Organic acidurias in adults: late complications and management.

Authors:  Ali Tunç Tuncel; Nikolas Boy; Marina A Morath; Friederike Hörster; Ulrike Mütze; Stefan Kölker
Journal:  J Inherit Metab Dis       Date:  2018-01-15       Impact factor: 4.982

Review 9.  [Metabolic induced changes of the central nervous system].

Authors:  W Reith; U Yilmaz; R Mühl-Bennighaus; A Haußmann
Journal:  Radiologe       Date:  2018-12       Impact factor: 0.635

10.  A cross-sectional controlled developmental study of neuropsychological functions in patients with glutaric aciduria type I.

Authors:  Nikolas Boy; Jana Heringer; Gisela Haege; Esther M Glahn; Georg F Hoffmann; Sven F Garbade; Stefan Kölker; Peter Burgard
Journal:  Orphanet J Rare Dis       Date:  2015-12-22       Impact factor: 4.123

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.