1981– Dr. Cornelis Jakobs identified a mentally retarded boy with minimal language development. Urine organic acid analysis of this child revealed an increased quantity of gamma hydroxybutyric acid (GHB), a compound that had not previously been identified in human urine. Dr. Jakobs postulated that this child had an inherited defect in the metabolism of GABA.
1982– Dr. K. Michael Gibson alters career path to pursue documenting the enzyme defect in Dr. Jakob’s patient. During this time, Dr. Gibson drew his own blood to look for SSADH activity in white-cell extracts which provided a method and a peripheral tissue source in which to document the enzyme defect in the first three SSADH patients, and began a long journey in the investigation of this rare disorder.
1987– Dr. Garry Brown identifies DHHA in the urine of SSADH-deficient patients using GCMS
1985 through 1990– Dr. Gibson focuses his time on identifying patients, developing improved assay methods for enzyme and metabolite quantitation, performing the infrequent prenatal diagnosis, and beginning to outline the cloning of mammalian SSADH.
1990– Dr. Gibson employs a fluorometric assay and isotope dilution method for GHB which facilitated prenatal diagnoses, using parallel investigations of metaboloites in amniotic fluid with enzyme measurement in amniocytes and chorionic villus tissue.
1992– Dr. Gibson began to purify mammalian SSADH with the goal of cloning the gene and determining whether patients harboured mutations. His laboratory developed a new purification scheme for isolation of rat brain SSADH, combining ion-exchange and affinity chromatography steps to purify the protein to apparent homogeneity.
1995– Composite clones encoding mature rat brain SSADH predicted a protein with 488 amino acids, consistent with Dr. Gibson’s purified protein data. The cDNA clones were confirmed by expression of enzyme activity in bacteria, and the human gene was mapped to chromosome 6p22, spanning some 38 kb of genomic DNA.
1999-2009-Dr. Mike Gibson and Dr. O. Carter Snead are funded continuously by the NIH for their R01 studies on the mouse model of 4-hydroxybutyric aciduria (project entitled “Pathophysiology and Treatment of Inherited Gamma-Hydroxybutyric Aciduria in the Mouse”.
2000– Dr. Gibson is awarded a $6,000 grant from the PND Association contributing towards his GHB Research Fund.
2001– Dr. Gibson developed a murine knockout model of SSADH deficiency.
2004– Dr. Phil Pearl is awarded a $30,000 grant from the PND Association to add a research fellowship towards developing an SSADH clinical profile and database.
2004-2005- Dr. Gibson asked to present the 10th Annual Komrower Commemorative
Lecture, the key invited talk, at the Annual Meeting of the Society for the Study of Inborn Errors of Metabolism (SSIEM) Annual Meeting in Amsterdam, with a talk entitled “Gamma-Hydroxybutyric Aciduria: A Biochemist’s Education from a Heritable Disorder of GABA Metabolism”
2005– NIH Clinical Research Study “Cortical Excitability in Succinic Semialdehyde Dehydrogenase Deficiency Patients”
2005– NIH Clinical Research Study “PET Imaging of GABA Receptors in Succinic Semialdehyde Dehydrogenase Deficiency”
2006– NIH Clinical Research Study “Taurine and its effect on SSADH patients”
2006– Dr. Phil Pearl is awarded a $30,000 grant from the PND Association towards SSADH deficiency entitled “need to look up“.
2007– Dr. Gibson is awarded a $50,000 grant from the PND Association towards SSADH deficiency entitled “need to look up“.
2007– Dr. Pearl is awarded a $40,000 grant from the PND Association towards SSADH deficiency entitled “need to look up“.
2010– Dr. Gibson is awarded a $50,000 grant from the PND Association towards SSADH deficiency entitled“Efficacy of Ornithine Alpha Ketoglutarate Intervention in Succinic Semialdehyde Dehydrogenase (SSADH) Deficiency“.
2011– The NIH receives a $45,000 grant from the PND Association towards the encapsulation of SGS-742, a medication that will be studied in a NIH Clinical Research Study.
2012- The NIH Authorizes a Taurine Trial to combat the impact of SSADH.
2013– Testing of an experimental drug’s effectiveness on SSADH has been funded by a $743,974 grant from the National Institutes of Health to Dr. Gibson Washington State University professor.
2013- SSADH Association awards $79,500 Fellowship Research Grant to Ronak Lakhani, PhD at the University of California, San Diego to understand the use of rapamycin and other autophagy-inducing drugs for treating SSADH deficiency.
2014- NIH Phase 2 Clinical Trial of SGS-742 Therapy in Succinic Semialdehyde Dehydrogenase Deficiency is Recruiting Patients: 2/14/14.
2014- SSADH Association awards an additional One Year Research Grant to Ronak Lakhani, PhD at the University of California, San Diego to determine if the induction of autophagy by Rapamycin would remove surplus organelles, thus reducing oxidative stress and restoring cellular homeostasis which may lead to potential treatments for SSADH Deficiency.
2015 - SSADH Association awarded $158,950
to the University of California, San Diego to determine if the induction of
autophagy by rapamycin would remove surplus organelles, thus reducing oxidative
stress and restoring cellular homeostasis which may lead to potential
treatments for SSADH deficiency.
2015 - SSADH Association awarded $100,000 to K. Michael Gibson, PhD, FACMG at
Washington State University to garner efficacy data in the SSADH deficient
animal model to form the framework for the Investigational New Drug Application
with the NIH for the use of compounds NCS-382 and HOCPCA.
2015 - SSADH Association awarded $5,000
was awarded to Kestutis G. Bendinskas, PhD at SUNY-Oswego to develop an easy to
use field colorimetric assay screen to detect the biomarker for SSADH
deficiency gamma hydroxybutyric acid (GHB), in either urine or saliva to screen
2015 - Evaluation of Metabolites
in SSADH Urine is being studied by Dr. Kara Vogel at Washington State University to explore
possibilities for SSADH patients.
2015 - Investigation of the
immunological response in SSADH cells by Karen Newell-Rogers, PhD at Texas A&M to
understand the alterations in metabolism and immunity using the SSADH mouse
2016 – SSADH Awarded $100,000 to Phil Pearl, MD & Robin
Kleiman, PhD, to fund a one year
research grant in conjunction with Boston Children’s Hospital. The objective of
this project is to develop an in vitro disease model of SSADH Deficiency from
patient iPSC lines differentiated into GABAergic neurons that will support
phenotypic drug screening.
2016 – SSADH committed $10,000 to kick off a Natural History Study with
the US medical team of Phil Pearl, MD, (Boston Children's Hospital),
Jean-Baptiste Roullet, PhD, and Mike Gibson, PhD, FACMG, (both from WSU),
together with Evangeline Wassmer, PhD (UK), Thomas Opladen, MD, (Germany) and Garcia-Cazorla, PhD, (Spain) will work with the SSADH Association on
a grant proposal to support a multi-year (5+) and multi-site natural history
study of SSADH patients.
2017 – SSADH
Awarded $305,616 to K. Michael Gibson, PhD, FACMG at Washington State
University for the SSADH Biorepository project which aims at creating a biobank
where biospecimens and matching clinical data are collected longitudinally from
all interested: patients, siblings and family members, unaffected, age-matched
control individuals. The Biorepository will be created over the next five years
with the following team: Drs. Gibson and
Roullet, (WSU), Dr. Pearl (BCH), Dr. Opladen (iNTD, Heidelberg, Germany) and
the SSADH Association.
2017 – SSADH committed
$10,000 to establish a Backup SSADH Mice Colony at JEX Services to ensure the
availability of SSADH Mice should something happen to the existing colony at
Washington State University, preventing any lapse in research due to the lack
of SSADH mice.