Soluble α-klotho is a potential biomarker associated with neuropsychiatric systemic lupus erythematosus

Copyright © 2016 Elsevier Inc. All rights reserved.

Détails bibliographiques
Publié dans:Clinical immunology (Orlando, Fla.). - 1999. - 165(2016) vom: 05. Apr., Seite 29-34
Auteur principal: Ushigusa, Takeshi (Auteur)
Autres auteurs: Ichinose, Kunihiro, Sato, Shuntaro, Michitsuji, Toru, Shimizu, Toshimasa, Umeda, Masataka, Fukui, Shoichi, Nishino, Ayako, Nakashima, Yoshikazu, Koga, Tomohiro, Kawashiri, Shin-ya, Iwamoto, Naoki, Hirai, Yasuko, Tamai, Mami, Nakamura, Hideki, Origuchi, Tomoki, Kawakami, Atsushi
Format: Article en ligne
Langue:English
Publié: 2016
Accès à la collection:Clinical immunology (Orlando, Fla.)
Sujets:Journal Article Research Support, Non-U.S. Gov't Systemic lupus erythematosus biomarker cerebrospinal fluid neuropsychiatric systemic lupus erythematosus serum α-Klotho Biomarkers Glucuronidase plus... EC 3.2.1.31 Klotho Proteins
Description
Résumé:Copyright © 2016 Elsevier Inc. All rights reserved.
A reduced level of the single-pass transmembrane protein α-Klotho is known to be associated with neuronal damage. We investigated whether α-Klotho in cerebrospinal fluid (CSF) could be a candidate marker for the diagnosis of neuropsychiatric systemic lupus erythematosus (NPSLE). We analyzed the laboratory data, symptoms and radiological image findings of 34 NPSLE patients. Patients with SLE without neuropsychiatric manifestations (SLE) (n=25), and patients with viral meningitis (VM) (n=19), multiple sclerosis (MS) (n=20) or neuromyelitis optica (NMO) (n=20) were included as controls. The multivariable analyses revealed that lower CSF α-Klotho level, lower serum anti-Smith antibodies (U/mL) and higher serum C3 (mg/dL) were significant factors for predicting NPSLE. The CSF α-Klotho levels of the NPSLE patients were inversely correlated with the level of granulocyte/macrophage-colony stimulating factor. Our data suggested that the determination of CSF α-Klotho levels will contribute to the diagnosis of NPSLE and help elucidate the mechanisms underlying this disease
Description:Date Completed 31.08.2016
Date Revised 03.12.2021
published: Print-Electronic
Citation Status MEDLINE
ISSN:1521-7035
DOI:10.1016/j.clim.2016.03.001