| Literature DB >> 24964810 |
Brett Tortelli1, Hideji Fujiwara1, Jessica H Bagel2, Jessie Zhang1, Rohini Sidhu1, Xuntian Jiang1, Nicole M Yanjanin3, Roopa Kanakatti Shankar3, Nuria Carillo-Carasco4, John Heiss4, Elizabeth Ottinger5, Forbes D Porter3, Jean E Schaffer1, Charles H Vite2, Daniel S Ory6.
Abstract
Niemann-Pick C1 (NPC1) disease is a rare, neurodegenerative lysosomal cholesterol storage disorder, typified by progressive cognitive and motor function impairment. Affected individuals usually succumb to the disease in adolescence. 2-Hydroxypropyl-β-cyclodextrin (HP-β-CD) has emerged as a promising intervention that reduces lipid storage and prolongs survival in NPC1 disease animal models. A barrier to the development of HP-β-CD and other treatments for NPC disease has been the lack of validated biochemical measures to evaluate efficacy. Here we explored whether cholesterol homeostatic responses resulting from HP-β-CD-mediated redistribution of sequestered lysosomal cholesterol could provide biomarkers to monitor treatment. Upon direct CNS delivery of HP-β-CD, we found increases in plasma 24(S)-HC in two independent NPC1 disease animal models, findings that were confirmed in human NPC1 subjects receiving HP-β-CD. Since circulating 24(S)-HC is almost exclusively CNS-derived, the increase in plasma 24(S)-HC provides a peripheral, non-invasive measure of the CNS effect of HP-β-CD. Our findings suggest that plasma 24(S)-HC, along with the other cholesterol-derived markers examined in this study, can serve as biomarkers that will accelerate development of therapeutics for NPC1 disease.Entities:
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Year: 2014 PMID: 24964810 PMCID: PMC4204776 DOI: 10.1093/hmg/ddu331
Source DB: PubMed Journal: Hum Mol Genet ISSN: 0964-6906 Impact factor: 6.150