{
"METABOLOMICS WORKBENCH":{"STUDY_ID":"ST000352","ANALYSIS_ID":"AN000573","VERSION":"1","CREATED_ON":"February 22, 2016, 5:00 pm"},

"PROJECT":{"PROJECT_TITLE":"Metabolic profiling reveals biochemical pathways and potential biomarkers associated with the pathogenesis of Krabbe disease","PROJECT_TYPE":"Disease Profiling","PROJECT_SUMMARY":"Krabbe disease (KD) is caused by mutations in the galactosylceramidase (GALC) gene, which encodes a lysosomal enzyme that degrades galactolipids, including galactosylceramide and galactosylsphingosine (psychosine). GALC deficiency results in progressive intracellular accumulation of psychosine, which is believed to be the main cause for the demyelinating neurodegeneration in KD pathology. Umbilical cord blood transplantation slows disease progression if performed presymptomatically, but carries a significant risk of morbidity and mortality. Accurate presymptomatic diagnosis is therefore critical to facilitate the efficacy of existing transplant approaches and avoid unnecessary treatment of children who will not develop KD. Unfortunately current diagnostic criteria, including GALC activity, genetic analysis, and psychosine measurement, are insufficient for secure presymptomatic diagnosis. Herein, we performed a global metabolomic analysis to identify pathogenetic metabolic pathways and novel biomarkers implicated in the authentic mouse model of KD, twitcher. At a time point before onset of signs of disease, twitcher hindbrains had metabolic profiles similar to wild type, with the exception of a decrease in metabolites related to glucose energy metabolism. Instead, many metabolic pathways were altered after early signs of disease in the twitcher, including decreased phospholipid turnover, restricted mitochondrial metabolism of branched-chain amino acids, increased inflammation, neurotransmitter metabolism and osmolytes. Hypoxanthine, a purine derivative, is increased before signs of disease appear, suggesting its potential as a biomarker for early diagnosis of KD. Additionally, given the early changes in glucose metabolism in the pathogenesis of KD, diagnostic modalities that report metabolic function, such as positron emission tomography, may be useful in KD.","INSTITUTE":"University at Buffalo","DEPARTMENT":"Hunter James Kelly Research Institute","LABORATORY":"Shin Laboratory","LAST_NAME":"Shin","FIRST_NAME":"Daesung","ADDRESS":"NYS Center of Excellence in Bioinformatics & Life Sciences, 701 Ellicott Street, Buffalo, NY 14203","EMAIL":"daesungs@buffalo.edu","PHONE":"716-881-8980"},

"STUDY":{"STUDY_TITLE":"Metabolic profiling reveals biochemical pathways and potential biomarkers associated with the pathogenesis of Krabbe disease","STUDY_TYPE":"Animal hindbrain comparison","STUDY_SUMMARY":"P15 wildtype mouse hindbrains, P15 twitcher mouse hindbrains, P22 wildtype mouse hindbrains, P22 twitcher mouse hindbrains","INSTITUTE":"University at Buffalo","DEPARTMENT":"Hunter James Kelly Research Institute","LABORATORY":"Shin Laboratory","LAST_NAME":"Shin","FIRST_NAME":"Daesung","ADDRESS":"NYS Center of Excellence in Bioinformatics & Life Sciences, 701 Ellicott Street, Buffalo, NY 14203","EMAIL":"daesungs@buffalo.edu","PHONE":"716-881-8980","NUM_GROUPS":"4","TOTAL_SUBJECTS":"32"},

"SUBJECT":{"SUBJECT_TYPE":"Animal","SUBJECT_SPECIES":"Mus musculus","TAXONOMY_ID":"10090","GENOTYPE_STRAIN":"C57BL/6N|C57BL/6N Twitcher","AGE_OR_AGE_RANGE":"P15-P22 days"},
"SUBJECT_SAMPLE_FACTORS":[
{
"Subject ID":"-",
"Sample ID":"UBUF-00091",
"Factors":{"age":"P15","genotype":"Wild Type"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00092",
"Factors":{"age":"P15","genotype":"Wild Type"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00093",
"Factors":{"age":"P15","genotype":"Wild Type"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00094",
"Factors":{"age":"P15","genotype":"Wild Type"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00095",
"Factors":{"age":"P15","genotype":"Wild Type"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00096",
"Factors":{"age":"P15","genotype":"Wild Type"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00097",
"Factors":{"age":"P15","genotype":"Wild Type"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00098",
"Factors":{"age":"P15","genotype":"Wild Type"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00099",
"Factors":{"age":"P15","genotype":"Twitcher"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00100",
"Factors":{"age":"P15","genotype":"Twitcher"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00101",
"Factors":{"age":"P15","genotype":"Twitcher"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00102",
"Factors":{"age":"P15","genotype":"Twitcher"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00103",
"Factors":{"age":"P15","genotype":"Twitcher"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00104",
"Factors":{"age":"P15","genotype":"Twitcher"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00105",
"Factors":{"age":"P15","genotype":"Twitcher"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00106",
"Factors":{"age":"P15","genotype":"Twitcher"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00107",
"Factors":{"age":"P22","genotype":"Wild Type"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00108",
"Factors":{"age":"P22","genotype":"Wild Type"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00109",
"Factors":{"age":"P22","genotype":"Wild Type"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00110",
"Factors":{"age":"P22","genotype":"Wild Type"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00111",
"Factors":{"age":"P22","genotype":"Wild Type"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00112",
"Factors":{"age":"P22","genotype":"Wild Type"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00113",
"Factors":{"age":"P22","genotype":"Wild Type"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00114",
"Factors":{"age":"P22","genotype":"Wild Type"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00115",
"Factors":{"age":"P22","genotype":"Twitcher"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00116",
"Factors":{"age":"P22","genotype":"Twitcher"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00117",
"Factors":{"age":"P22","genotype":"Twitcher"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00118",
"Factors":{"age":"P22","genotype":"Twitcher"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00119",
"Factors":{"age":"P22","genotype":"Twitcher"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00120",
"Factors":{"age":"P22","genotype":"Twitcher"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00121",
"Factors":{"age":"P22","genotype":"Twitcher"}
},
{
"Subject ID":"-",
"Sample ID":"UBUF-00122",
"Factors":{"age":"P22","genotype":"Twitcher"}
}
],
"COLLECTION":{"COLLECTION_SUMMARY":"None","COLLECTION_PROTOCOL_ID":"COL_PROT","COLLECTION_PROTOCOL_FILENAME":"COL_PROT.pdf","SAMPLE_TYPE":"Hindbrain (pons, medulla, brainstem, cerebellum)","VOLUMEORAMOUNT_COLLECTED":"entire hindbrain"},

"TREATMENT":{"TREATMENT_SUMMARY":"none"},

"SAMPLEPREP":{"SAMPLEPREP_SUMMARY":"None","PROCESSING_METHOD":"Homogenization","PROCESSING_STORAGE_CONDITIONS":"On Ice","ORGAN":"Brain","ORGAN_SPECIFICATION":"Hindbrain"},

"CHROMATOGRAPHY":{"CHROMATOGRAPHY_SUMMARY":"Experiments were conducted according to the protocols approved by the Institutional Animal Care and Use Committee of University at Buffalo and Roswell Park Cancer Institute. Twitcher mice were maintained on the background of C57BL/6N. Breeder C57BL/6N mice were purchased from Charles River. Freshly collected hindbrain regions from twitcher and WT littermate mice at P8, P15, P22, and P34 days were transferred into polypropylene cryovials, and then frozen in liquid nitrogen and stored at - 80°C until the analysis.","CHROMATOGRAPHY_TYPE":"UPLC","INSTRUMENT_NAME":"Waters ACQUITY UPLC","COLUMN_NAME":"See doc","METHODS_FILENAME":"Protocol.pdf"},

"ANALYSIS":{"ANALYSIS_TYPE":"MS","ANALYSIS_PROTOCOL_FILE":"Protocol.pdf"},

"MS":{"MS_COMMENTS":"-","INSTRUMENT_NAME":"Thermo LTQ","INSTRUMENT_TYPE":"Single quadrupole","MS_TYPE":"ESI","ION_MODE":"NEGATIVE"},

"MS_METABOLITE_DATA":{
"Units":"Peak height",

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}

}