| Literature DB >> 29701803 |
Yuta Murakami1, Yuka Matsumoto1, Kyoka Hoshi2, Hiromi Ito2, Takashi J Fuwa2, Yoshiki Yamaguchi3, Madoka Nakajima4, Masakazu Miyajima4, Hajime Arai4, Kenneth Nollet5, Naho Kato6, Rie Nishikata6, Naohito Kuroda6, Takashi Honda7, Jun Sakuma1, Kiyoshi Saito1, Yasuhiro Hashimoto2.
Abstract
Idiopathic normal pressure hydrocephalus (iNPH) is a dementia-inducing disorder. Primary cause of iNPH is speculated to be a reduction of cerebrospinal fluid (CSF) absorption, which secondarily induces hydrocephalus, compression of brain, and reduction of CSF production. Patients are treated by surgically inserting a shunt to deliver excess CSF to the abdominal cavity. The prognosis for cognitive improvement after shunt surgery has been difficult to predict. We therefore investigated various CSF proteins, hoping to find a biomarker predictive of cognitive performance one to two years after shunt surgery. CSF proteins of 34 iNPH and 15 non-iNPH patients were analysed by Western blotting, revealing two glycan isoforms of transferrin (Tf); 'brain-type' Tf with N-acetylglucosaminylated glycans and 'serum-type' Tf with α2, 6-sialylated glycans. Brain-type Tf levels decreased in iNPH but rapidly returned to normal levels within 1-3 months after shunt surgery. This change was positively correlated with recovery from dementia, per Mini-Mental State Examination and Frontal Assessment Battery scores at 11.8 ± 7.7 months post-operation, suggesting that brain-type Tf is a prognostic marker for recovery from dementia after shunt surgery for iNPH. Histochemical staining with anti-Tf antibody and an N-acetylglucosamine-binding lectin suggests that brain-type Tf is secreted from choroid plexus, CSF-producing tissue.Entities:
Mesh:
Substances:
Year: 2018 PMID: 29701803 DOI: 10.1093/jb/mvy043
Source DB: PubMed Journal: J Biochem ISSN: 0021-924X Impact factor: 3.387