Academic Journal
Visual evoked potentials in succinate semialdehyde dehydrogenase (SSADH) deficiency
| العنوان: | Visual evoked potentials in succinate semialdehyde dehydrogenase (SSADH) deficiency |
|---|---|
| المؤلفون: | Di Rosa, G, Dionisi Vici, C, Rizzo, C, Tortorella, G, Crutchfield, SR, Gibson, KM, MALASPINA, PATRIZIA, BLASI, PAOLA |
| المساهمون: | Di Rosa, G, Malaspina, P, Blasi, P, Dionisi Vici, C, Rizzo, C, Tortorella, G, Crutchfield, S, Gibson, K |
| سنة النشر: | 2009 |
| المجموعة: | Universitá degli Studi di Roma "Tor Vergata": ART - Archivio Istituzionale della Ricerca |
| مصطلحات موضوعية: | SSADH deficiency, GABA metabolism, Settore BIO/18 - GENETICA |
| الوصف: | In mammals, increased GABA in the central nervous system has been associated with abnormalities of visual evoked potentials (VEPs), predominantly manifested as increased latency of the major positive component P100. Accordingly, we hypothesized that patients with a defect in GABA metabolism, succinate semialdehyde dehydrogenase (SSADH) deficiency (in whom supraphysiological levels of GABA accumulate), would manifest VEP anomalies. We evaluated VEPs on two patients with confirmed SSADH deficiency. Whereas the P100 latencies and amplitudes for binocular VEP analyses were within normal ranges for both patients, the P100 latencies were markedly delayed for left eye (OS) (and right eye (OD), patient 1) and monocular OS (patient 2): 134-147 ms; normal <118 ms. We hypothesize that elevated GABA in ocular tissue of SSADH patients leads to a use-dependent downregulation of the major GABAergic receptor in eye, GABA(C), and that the VEP recordings' abnormalities, as evidenced by P100 latency and/or amplitude measurements, may be reflective of abnormalities within visual systems. This is a preliminary finding that may suggest the utility of performing VEP analysis in a larger sample of SSADH-deficient patients, and encourage a neurophysiological assessment of GABA(C) receptor function in Aldh5a1(-/-) mice to reveal new pathophysiological mechanisms of this rare disorder of GABA degradation. |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| Relation: | journal:JOURNAL OF INHERITED METABOLIC DISEASE; http://hdl.handle.net/2108/8757; info:eu-repo/semantics/altIdentifier/scopus/http://www.scopus.com/inward/record.url?eid=2-s2.0-66149124455&partnerID=40&md5=817cb046b2737fac0f5e2043509b6de0 |
| DOI: | 10.1007/s10545-009-1154-4 |
| الاتاحة: | http://hdl.handle.net/2108/8757 https://doi.org/10.1007/s10545-009-1154-4 |
| Rights: | info:eu-repo/semantics/openAccess |
| رقم الانضمام: | edsbas.B024503 |
| قاعدة البيانات: | BASE |
| DOI: | 10.1007/s10545-009-1154-4 |
|---|