Neuropsychiatric involvement in juvenile-onset systemic lupus erythematosus: A multicenter study
Tarih
2023Yazar
Sözeri, Betül
Şahin, Nihal
Demir, Ferhat
Bağlan, Esra
Kara, Mehtap Akbalık
Selçuk, Şenay Zırhlı
Özdel, Semanur
Çomak, Elif
Akkoyunlu, Betül
Yener, Gülçin Otar
Yıldırım, Deniz Gezgin
Öztürk, Kübra
Yıldız, Mehmet
Haşlak, Fatih
Şener, Seher
Kısaoğlu, Hakan
Baba, Özge
Kızıldağ, Zehra
İşgüder, Rana
Çağlayan, Şengül
Bilgin, Raziye B. Güven
Aytaç, Gülçin
Yücel, Burcu Bozkaya
Tanatar, Ayşe
Sönmez, Hafize E.
Çakan, Mustafa
Kara, Aslıhan
Elmas, Ahmet T.
Kılıç, Beltinge Demircioğlu
Ayaz, Nuray Aktay
Kasap, Belde
Kısaarslan, Ayşenur Paç
Çiçek, Sümeyra Özdemir
BATU AKAL, EZGİ DENİZ
Şahin, Sezgin
Gürgöze, Metin K.
BARUT, KENAN
Acar, Banu Çelikel
Ozkaya, Ozan
Yüksel, Selçuk
Bakkaloğlu, Sevcan
Aydoğ, Özlem
Aksu, Güzide
Akman, Sema
Dönmez, Osman
Bülbül, Mehmet
Büyükçelik, Mithat
Tabel, Yılmaz
Kalyoncu, Mukaddes
Bilginer, Yelda
Poyrazoğlu, Muammer H.
Ünsal, Erbil
Kasapçopur, Özgür
Özen, Seza
Düşünsel, Ruhan
Çetinkaya, Sibel Balcı
Ekinci, Miray Kışla
ATMIŞ, BAHRİYE
Adrovic, Amra
Ağar, Buket Esen
Üst veri
Tüm öğe kaydını gösterÖzet
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 Collaborating 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, activity 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.
Bağlantı
http://hdl.handle.net/20.500.12627/189112https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85150809280&origin=inward
https://doi.org/10.1016/j.jbspin.2023.105559
Koleksiyonlar
- Makale [92796]