Autism spectrum disorder and GABA levels in children with succinic semialdehyde dehydrogenase deficiency

被引:13
|
作者
Latzer, Itay Tokatly [1 ,2 ]
Hanson, Ellen [3 ,4 ]
Bertoldi, Mariarita [5 ]
Garcia-Cazorla, Angeles [6 ]
Tsuboyama, Melissa [1 ]
MacMullin, Paul [1 ]
Rotenberg, Alexander [1 ,7 ]
Roullet, Jean-Baptiste L. [8 ]
Pearl, Phillip [1 ]
机构
[1] Harvard Med Sch, Boston Childrens Hosp, Dept Neurol, Boston, MA USA
[2] Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel
[3] Boston Childrens Hosp, Human Neurobehav Core Serv, Div Neurol, Boston, MA USA
[4] Boston Childrens Hosp, Rosamund Stone Zander Translat Neurosci Ctr, Boston, MA USA
[5] Univ Verona, Dept Neurosci Biomed & Movement Sci, Verona, Italy
[6] Hosp St Joan Deu, Inst Recerca, Neurol Dept, Neurometab Unit, Barcelona, Spain
[7] Boston Childrens Hosp, FM Kirby Neurobiol Ctr, Boston, MA USA
[8] Washington State Univ, Coll Pharm & Pharmaceut Sci, Dept Pharmacotherapy, Spokane, WA USA
来源
关键词
EPILEPSY;
D O I
10.1111/dmcn.15659
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
AimTo elucidate the etiological aspects of autism spectrum disorder (ASD) in succinic semialdehyde dehydrogenase deficiency (SSADHD), related to dysregulation of gamma-aminobutyric acid (GABA) and the imbalance of excitatory and inhibitory neurotransmission. MethodIn this prospective, international study, individuals with SSADHD underwent neuropsychological assessments, as well as biochemical, neurophysiological, and neuroimaging evaluations. ResultsOf the 29 individuals (17 females) enrolled (median age [IQR] 10 years 5 months [5 years 11 months-18 years 1 month]), 16 were diagnosed with ASD. ASD severity significantly increased with age (r = 0.67, p < 0.001) but was inversely correlated with plasma GABA (r = -0.67, p < 0.001) and gamma-hydroxybutyrate levels (r = -0.538, p = 0.004), and resting motor threshold as measured by transcranial magnetic stimulation (r = -0.44, p = 0.03). A discriminative analysis indicated that an age older than 7 years 2 months (p = 0.004) and plasma GABA levels less than 2.47 mu M (p = 0.01) are the threshold values beyond which the likelihood of ASD presenting in individuals with SSADHD is increased. InterpretationASD is prevalent but not universal in SSADHD, and it can be predicted by lower levels of plasma GABA and GABA-related metabolites. ASD severity in SSADHD increases with age and the loss of cortical inhibition. These findings add insight into the pathophysiology of ASD and may facilitate its early diagnosis and intervention in individuals with SSADHD.
引用
收藏
页码:1596 / 1606
页数:11
相关论文
共 50 条
  • [21] Succinic semialdehyde dehydrogenase deficiency in two siblings
    Opp, J
    Raab, K
    Jakobs, C
    Lehnert, W
    Gibson, KM
    MONATSSCHRIFT KINDERHEILKUNDE, 1996, 144 (07) : 695 - 698
  • [22] Succinic Semialdehyde Dehydrogenase Deficiency: Case Reports
    Gulgun, Mustafa
    Vurucu, Sebahattin
    Kocaoglu, Murat
    Unay, Bulent
    Akin, Ridvan
    ERCIYES MEDICAL JOURNAL, 2008, 30 (03) : 180 - 183
  • [23] Succinic semialdehyde dehydrogenase deficiency (SSADHD): Pathophysiological complexity and multifactorial trait associations in a rare monogenic disorder of GABA metabolism
    Malaspina, P.
    Roullet, J. -B.
    Pearl, P. L.
    Ainslie, G. R.
    Vogel, K. R.
    Gibson, K. M.
    NEUROCHEMISTRY INTERNATIONAL, 2016, 99 : 72 - 84
  • [24] Functional Characterization of a Spectrum of Genetic Variants in a Family with Succinic Semialdehyde Dehydrogenase Deficiency
    Didiasova, Miroslava
    Cesaro, Samuele
    Feldhoff, Simon
    Bettin, Ilaria
    Tiegel, Nana
    Fuessgen, Vera
    Bertoldi, Mariarita
    Tikkanen, Ritva
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2024, 25 (10)
  • [25] Seizures in a boy with succinic semialdehyde dehydrogenase deficiency treated with vigabatrin (gamma-vinyl-GABA)
    Matern, D
    Lehnert, W
    Gibson, KM
    Korinthenberg, R
    JOURNAL OF INHERITED METABOLIC DISEASE, 1996, 19 (03) : 313 - 318
  • [26] Circadian distribution of generalized tonic-clonic seizures associated with murine succinic semialdehyde dehydrogenase deficiency, a disorder of GABA metabolism
    Stewart, Lee S.
    Nylen, Kirk J.
    Persinger, Michael A.
    Cortez, Miguel A.
    Gibson, K. Michael
    Snead, O. Carter, III
    EPILEPSY & BEHAVIOR, 2008, 13 (02) : 290 - 294
  • [27] The continuously evolving phenotype of succinic semialdehyde dehydrogenase deficiency
    Julia-Palacios, Natalia Alexandra
    Huebschmann, Oya Kuseyri
    Olivella, Mireia
    Pons, Roser
    Horvath, Gabriella
    Luecke, Thomas
    Fung, Cheuk-Wing
    Wong, Suet-Na
    Cortes-Saladelafont, Elisenda
    Rovira-Remisa, M. Mar
    Yildiz, Yilmaz
    Mercimek-Andrews, Saadet
    Assmann, Birgit
    Stevanovic, Galina
    Manti, Filippo
    Brennenstuhl, Heiko
    Jung-Klawitter, Sabine
    Jeltsch, Kathrin
    Sivri, H. Serap
    Garbade, Sven F.
    Garcia-Cazorla, Angels
    Opladen, Thomas
    JOURNAL OF INHERITED METABOLIC DISEASE, 2024, 47 (03) : 447 - 462
  • [28] SUCCINIC SEMIALDEHYDE DEHYDROGENASE-DEFICIENCY - A FURTHER CASE
    HAAN, EA
    BROWN, GK
    MITCHELL, D
    DANKS, DM
    JOURNAL OF INHERITED METABOLIC DISEASE, 1985, 8 (03) : 99 - 99
  • [29] Succinic Semialdehyde Dehydrogenase Deficiency: An Inheritable Neurometabolic Disease
    Gahr, M.
    Connemann, B. J.
    Schoenfeldt-Lecuona, C. J.
    Freudenmann, R. W.
    FORTSCHRITTE DER NEUROLOGIE PSYCHIATRIE, 2013, 81 (03) : 154 - 161
  • [30] Polysomnographic Abnormalities in Succinic Semialdehyde Dehydrogenase (SSADH) Deficiency
    Pearl, Phillip L.
    Shamim, Sadat
    Theodore, William H.
    Gibson, K. Michael
    Forester, Katherine
    Combs, Susan E.
    Lewin, Daniel
    Dustin, Irene
    Reeves-Tyer, Patricia
    Jakobs, Cornelis
    Sato, Susumu
    SLEEP, 2009, 32 (12) : 1645 - 1648