Literature DB >> 26268900

Natural history of succinic semialdehyde dehydrogenase deficiency through adulthood.

Samuel Lapalme-Remis1, Evan Cole Lewis2, Christine De Meulemeester2, Pranesh Chakraborty2, K Michael Gibson2, Carlos Torres2, Alan Guberman2, Gajja S Salomons2, Cornelis Jakobs2, Andre Ali-Ridha2, Mahsa Parviz2, Phillip L Pearl2.   

Abstract

OBJECTIVE: The natural history of succinic semialdehyde dehydrogenase (SSADH) deficiency in adulthood is unknown; we elucidate the clinical manifestations of the disease later in life.
METHODS: A 63-year-old man with long-standing intellectual disability was diagnosed with SSADH deficiency following hospitalization for progressive decline, escalating seizures, and prolonged periods of altered consciousness. We present a detailed review of his clinical course and reviewed our SSADH deficiency database adult cohort to derive natural history information.
RESULTS: Of 95 patients in the database for whom age at diagnosis is recorded, there are 40 individuals currently aged 18 years or older. Only 3 patients were diagnosed after age 18 years. Of 25 adults for whom data are available after age 18, 60% have a history of epilepsy. Predominant seizure types are generalized tonic-clonic, absence, and myoclonic. EEGs showed background slowing or generalized epileptiform discharges in two-thirds of adults for whom EEG data were collected. History of psychiatric symptoms was prominent, with frequent anxiety, sleep disturbances, and obsessive-compulsive disorder.
CONCLUSIONS: We identified patients older than 18 years with SSADH deficiency in our database following identification and review of a patient diagnosed in the seventh decade of life. The illness had a progressive course with escalating seizures in the index case, with fatality at age 63. Diagnosis in adulthood is rare. Epilepsy is more common in the adult than the pediatric SSADH deficiency cohort; neuropsychiatric morbidity remains prominent.
© 2015 American Academy of Neurology.

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Year:  2015        PMID: 26268900      PMCID: PMC4560056          DOI: 10.1212/WNL.0000000000001906

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  10 in total

Review 1.  Evidence report: Genetic and metabolic testing on children with global developmental delay: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society.

Authors:  D J Michelson; M I Shevell; E H Sherr; J B Moeschler; A L Gropman; S Ashwal
Journal:  Neurology       Date:  2011-09-28       Impact factor: 9.910

2.  A boy with a severe phenotype of succinic semialdehyde dehydrogenase deficiency.

Authors:  Yoko Yamakawa; Tomoyuki Nakazawa; Asuka Ishida; Nobutomo Saito; Mitsutaka Komatsu; Tomoyo Matsubara; Kaoru Obinata; Shinichi Hirose; Akihisa Okumura; Toshiaki Shimizu
Journal:  Brain Dev       Date:  2011-05-25       Impact factor: 1.961

3.  Epilepsy in succinic semialdehyde dehydrogenase deficiency, a disorder of GABA metabolism.

Authors:  Phillip L Pearl; Lovy Shukla; William H Theodore; Cornelis Jakobs; K Michael Gibson
Journal:  Brain Dev       Date:  2011-06-12       Impact factor: 1.961

4.  The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria): case reports of 23 new patients.

Authors:  K M Gibson; E Christensen; C Jakobs; B Fowler; M A Clarke; G Hammersen; K Raab; J Kobori; A Moosa; B Vollmer; E Rossier; A K Iafolla; D Matern; O F Brouwer; J Finkelstein; F Aksu; H P Weber; J A Bakkeren; F J Gabreels; D Bluestone; T F Barron; P Beauvais; D Rabier; C Santos; W Lehnert
Journal:  Pediatrics       Date:  1997-04       Impact factor: 7.124

5.  Neuropathology in succinic semialdehyde dehydrogenase deficiency.

Authors:  Ina Knerr; K Michael Gibson; Geoffrey Murdoch; Gajja S Salomons; Cornelis Jakobs; Susan Combs; Phillip L Pearl
Journal:  Pediatr Neurol       Date:  2010-04       Impact factor: 3.372

Review 6.  Epilepsy and inborn errors of metabolism in adults: a diagnostic approach.

Authors:  F Sedel; I Gourfinkel-An; O Lyon-Caen; M Baulac; J-M Saudubray; V Navarro
Journal:  J Inherit Metab Dis       Date:  2007-10-22       Impact factor: 4.982

Review 7.  Succinic semialdehyde dehydrogenase deficiency in children and adults.

Authors:  Phillip L Pearl; Edward J Novotny; Maria T Acosta; Cornelis Jakobs; K Michael Gibson
Journal:  Ann Neurol       Date:  2003       Impact factor: 10.422

8.  Succinic semialdehyde dehydrogenase deficiency: an inborn error of gamma-aminobutyric acid metabolism.

Authors:  K M Gibson; L Sweetman; W L Nyhan; C Jakobs; D Rating; H Siemes; F Hanefeld
Journal:  Clin Chim Acta       Date:  1983-09-15       Impact factor: 3.786

9.  Evidence for oxidative stress in tissues derived from succinate semialdehyde dehydrogenase-deficient mice.

Authors:  A Latini; K Scussiato; G Leipnitz; K M Gibson; M Wajner
Journal:  J Inherit Metab Dis       Date:  2007-09-21       Impact factor: 4.982

Review 10.  The pediatric neurotransmitter disorders.

Authors:  Phillip L Pearl; Jacob L Taylor; Stacey Trzcinski; Alex Sokohl
Journal:  J Child Neurol       Date:  2007-05       Impact factor: 1.987

  10 in total
  17 in total

1.  Gamma-Hydroxybutyrate content in dried bloodspots facilitates newborn detection of succinic semialdehyde dehydrogenase deficiency.

Authors:  Madalyn Brown; Paula Ashcraft; Erland Arning; Teodoro Bottiglieri; Jean-Baptiste Roullet; K Michael Gibson
Journal:  Mol Genet Metab       Date:  2019-07-18       Impact factor: 4.797

2.  Incidence and Geographic Distribution of Succinic Semialdehyde Dehydrogenase (SSADH) Deficiency.

Authors:  Savita Verma Attri; Pratibha Singhi; Natrujee Wiwattanadittakul; Jyotindra N Goswami; Naveen Sankhyan; Gajja S Salomons; Jean-Baptiste Roullett; Ryan Hodgeman; Mahsa Parviz; K Michael Gibson; Phillip L Pearl
Journal:  JIMD Rep       Date:  2016-11-05

3.  Therapeutic relevance of mTOR inhibition in murine succinate semialdehyde dehydrogenase deficiency (SSADHD), a disorder of GABA metabolism.

Authors:  K R Vogel; G R Ainslie; E E W Jansen; G S Salomons; K M Gibson
Journal:  Biochim Biophys Acta Mol Basis Dis       Date:  2016-10-17       Impact factor: 5.187

4.  Novel mutations in two unrelated Italian patients with SSADH deficiency.

Authors:  Marta Balzarini; Valentina Rovelli; Sabrina Paci; Miriam Rigoldi; Giuseppina Sanna; Sara Pillai; Marilisa Asunis; Rossella Parini; Bianca Maria Ciminelli; Patrizia Malaspina
Journal:  Metab Brain Dis       Date:  2019-07-02       Impact factor: 3.584

Review 5.  Epilepsy in inherited neurotransmitter disorders: Spotlights on pathophysiology and clinical management.

Authors:  Mario Mastrangelo
Journal:  Metab Brain Dis       Date:  2020-10-23       Impact factor: 3.584

6.  Correlation of blood biomarkers with age informs pathomechanisms in succinic semialdehyde dehydrogenase deficiency (SSADHD), a disorder of GABA metabolism.

Authors:  E E Jansen; K R Vogel; G S Salomons; P L Pearl; J-B Roullet; K M Gibson
Journal:  J Inherit Metab Dis       Date:  2016-09-29       Impact factor: 4.982

7.  mTOR inhibitors rescue premature lethality and attenuate dysregulation of GABAergic/glutamatergic transcription in murine succinate semialdehyde dehydrogenase deficiency (SSADHD), a disorder of GABA metabolism.

Authors:  Kara R Vogel; Garrett R Ainslie; K Michael Gibson
Journal:  J Inherit Metab Dis       Date:  2016-08-12       Impact factor: 4.982

Review 8.  Succinic semialdehyde dehydrogenase deficiency (SSADHD): Pathophysiological complexity and multifactorial trait associations in a rare monogenic disorder of GABA metabolism.

Authors:  P Malaspina; J-B Roullet; P L Pearl; G R Ainslie; K R Vogel; K M Gibson
Journal:  Neurochem Int       Date:  2016-06-14       Impact factor: 3.921

9.  Enzyme Replacement Therapy for Succinic Semialdehyde Dehydrogenase Deficiency: Relevance in γ-Aminobutyric Acid Plasticity.

Authors:  Henry Hing Cheong Lee; Phillip L Pearl; Alexander Rotenberg
Journal:  J Child Neurol       Date:  2021-02-24       Impact factor: 1.987

10.  Succinic Semialdehyde Dehydrogenase Deficiency: Review of the Natural History Study.

Authors:  Phillip L Pearl; Melissa L DiBacco; Christos Papadelis; Thomas Opladen; Ellen Hanson; Jean-Baptiste Roullet; K Michael Gibson
Journal:  J Child Neurol       Date:  2021-01-04       Impact factor: 1.987

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