| Literature DB >> 33459505 |
Hong Wei Yang1,2,3, Semin Lee2,3, Dejun Yang1, Huijun Dai1, Yan Zhang1, Lei Han2,3, Sijun Zhao1, Shuo Zhang1, Yan Ma1, Marciana F Johnson2,3, Anna K Rattray2,3, Tatyana A Johnson2,3, George Wang1,2,3, Shaokuan Zheng1, Rona S Carroll1,2,3, Peter J Park2,3, Mark D Johnson1,2,3,4.
Abstract
Idiopathic normal pressure hydrocephalus (iNPH) is a neurological disorder that occurs in about 1% of individuals over age 60 and is characterized by enlarged cerebral ventricles, gait difficulty, incontinence, and cognitive decline. The cause and pathophysiology of iNPH are largely unknown. We performed whole exome sequencing of DNA obtained from 53 unrelated iNPH patients. Two recurrent heterozygous loss of function deletions in CWH43 were observed in 15% of iNPH patients and were significantly enriched 6.6-fold and 2.7-fold, respectively, when compared to the general population. Cwh43 modifies the lipid anchor of glycosylphosphatidylinositol-anchored proteins. Mice heterozygous for CWH43 deletion appeared grossly normal but displayed hydrocephalus, gait and balance abnormalities, decreased numbers of ependymal cilia, and decreased localization of glycosylphosphatidylinositol-anchored proteins to the apical surfaces of choroid plexus and ependymal cells. Our findings provide novel mechanistic insights into the origins of iNPH and demonstrate that it represents a distinct disease entity.Entities:
Keywords: CWH43; GPI-anchored protein; hydrocephalus; normal pressure hydrocephalus
Year: 2021 PMID: 33459505 PMCID: PMC7933959 DOI: 10.15252/emmm.202013249
Source DB: PubMed Journal: EMBO Mol Med ISSN: 1757-4676 Impact factor: 12.137