Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/51062
Title: Neuropsychiatric involvement in juvenile-onset systemic lupus erythematosus: A multicenter study
Authors: Kışaarslan, Ayşenur Pac
Özdemir Çicek, Sümeyra
Batu, Ezgi D.
Şahin, Sezgin
Gürgöze, Metin K.
Balcı Çetinkaya, Sibel
Ekinci, Miray Kışla
Atmis, Bahriye
Barut, Kenan
Adrovic, Amra
Agar, Buket Esen
Sahin, Nihal
Demir, Ferhat
Baglan, Esra
Kara, Mehtap Akbalik
Selcuk, Senay Zirhli
Ozdel, Semanur
Comak, Elif
Akkoyunlu, Betul
Yener, Gulcin Otar
Yildirim, Deniz Gezgin
Ozturk, Kubra
Yildiz, Mehmet
Haslak, Fatih
Sener, Seher
Kisaoglu, Hakan
Baba, Ozge
Kizildag, Zehra
Isguder, Rana
Caglayan, Sengul
Bilgin, Raziye B. Güven
Aytac, Gulcin
Yucel, Burcu Bozkaya
Tanatar, Ayse
Sonmez, Hafize E.
Cakan, Mustafa
Kara, Aslihan
Elmas, Ahmet T.
Ayaz, Nuray Aktay
Kasap, Belde
Acar, Banu Celikel
Ozkaya, Ozan
Bakkaloglu, Sevcan
Aydog, Ozlem
Aksu, Guzide
Akman, Sema
Donmez, Osman
Bulbul, Mehmet
Buyukcelik, Mithat
Tabel, Yilmaz
Sozeri, Betul
Kalyoncu, Mukaddes
Bilginer, Yelda
Poyrazoglu, Muammer H.
Unsal, Erbil
Kasapcopur, Ozgur
Ozen, Seza
Dusunsel, Ruhan
Yüksel, Selçuk
Keywords: Cluster
Juvenile
Systemic lupus erythematosus
Neurologic manifestations
Manifestations
Validation
Publisher: Elsevier France-Editions Scientifiques Medicales Elsevier
Abstract: Introduction: Neuropsychiatric (NP) involvement is a restricted area in juvenile-onset systemic lupus erythematosus (jSLE). Aim: To investigate the prevalence, demographic and clinical features, and outcomes of the neurological involvement in the Turkish jSLE population. Methods: This study was based upon 24 referral centers' SLE cohorts, multicenter and multidisciplinary network in Turkey. Patient data were collected by a case report form which was standardized for NP definitions according to American Collage of Rheumatology (ACR). Systemic Lupus International Collab-orating Clinics/American College of Rheumatology Damage Index (SDI) neuropsychiatric part was used to determine NP damage. Variables were evaluated Ward's hierarchical clustering analyses, univariate, and multivariate logistic regression analyses. Results: A hundred forty-nine of 1107 jSLE patients had NP involvement (13.5%). The most common NPSLE findings were headache (50.3%), seizure (38.3%), and acute confusional state (33.6%). Five clusters were identified with all clinical and laboratory findings. The first two clusters involved neuropathies, demyelinating diseases, aseptic meningitis, and movement disorder. Cluster 3 involved headache, activ-ity markers and other SLE involvements. Idiopathic intracranial hypertension, cerebrovascular disease, cognitive dysfunction, psychiatric disorders and SLE antibodies were in the fourth, and acute confusional state was in the fifth cluster. In multivariate analysis, APA positivity; OR: 2.820, (%95CI: 1.002-7.939), P: 0,050, plasmapheresis; OR: 13.804 (%95CI: 2.785-68.432), P: 0,001, SLEDAI scores; OR: 1.115 (%95CI: (1.049-1.186), P: 0,001 were associated with increased risk for neurologic sequelae. Conclusion: We detected the prevalence of juvenile NPSLE manifestations in Turkey. We have identified five clusters that may shed light pathogenesis, treatment and prognosis of NP involvements. We also determined risk factors of neurological sequelae. Our study showed that new definitions NP involvements and sequelae for childhood period are needed. (c) 2023 Socie ' te ' franc,aise de rhumatologie. Published by Elsevier Masson SAS. All rights reserved.
URI: https://doi.org/10.1016/j.jbspin.2023.105559
https://hdl.handle.net/11499/51062
ISSN: 1297-319X
1778-7254
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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