4.1 Review

Succinic Semialdehyde Dehydrogenase Deficiency: Review of the Natural History Study

Journal

JOURNAL OF CHILD NEUROLOGY
Volume 36, Issue 13-14, Pages 1153-1161

Publisher

SAGE PUBLICATIONS INC
DOI: 10.1177/0883073820981262

Keywords

epilepsy; genetics; inborn errors of metabolism; intellectual disability; metabolism; neuroimaging

Funding

  1. Eunice Kennedy Shriver National Institute of Child Health & Human Development [5R01HD091142]
  2. BCH Intellectual and Developmental Disabilities Research Center (BCH IDDRC) [U54HD090255]

Ask authors/readers for more resources

The SSADHD Natural History Study aims to define the natural course of the disorder and identify biomarkers correlating with severity. At the halfway point, 28 subjects have been recruited, showing increasing incidence and severity of epilepsy and psychiatric symptoms in adolescence and adulthood. The study also found abnormal brain waves, with reduced gamma frequency band consistent with GABAergic dysfunction.
Objective: The SSADHD Natural History Study was initiated in 2019 to define the natural course and identify biomarkers correlating with severity. Methods: The study is conducted by 4 institutions: BCH (US clinical), WSU (bioanalytical core), USF (biostatistical core), and Heidelberg (iNTD), with support from the family advocacy group (SSADH Association). Recruitment goals were to study 20 patients on-site at BCH, 10 with iNTD, and 25 as a standard-of care cohort. Results: At this half-way point of this longitudinal study, 28 subjects have been recruited (57% female, mean 9 years, range 18 months-40 years). Epilepsy is present in half and increases in incidence and severity, as do psychiatric symptoms, in adolescence and adulthood. The average Full Scale IQ (FSIQ) was 53 (Verbal score of 56, Non Verbal score of 49), and half scored as having ASD. Although there was no correlation between gene variant and phenotypic severity, there were extreme cases of lowest functioning in one individual and highest in another that may have genotype-phenotype correlation. The most common EEG finding was mild background slowing with rare epileptiform activity, whereas high-density EEG and magnetoencephalography showed reduction in the gamma frequency band consistent with GABAergic dysfunction. MR spectroscopy showed elevations in the GABA/NAA ratio in all regions studied with no crossover between subjects and controls. Conclusions: The SSADH Natural History Study is providing a unique opportunity to study the complex pathophysiology longitudinally and derive electrophysiologic, neuroimaging, and laboratory data for correlation and to serve as biomarkers for clinical trials and prognostic assessments in this ultra-rare inherited disorder of GABA metabolism.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.1
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available