Recommendations on neurologic, cognitive, and psychiatric manifestations in patients with Sjögren's disease by the Brazilian Society of Rheumatology.

IF 2.1 4区 医学 Q3 RHEUMATOLOGY Advances in Rheumatology Pub Date : 2025-02-11 DOI:10.1186/s42358-025-00438-7
Fabiola Reis de Oliveira, Simone Appenzeller, Sandra Gofinet Pasoto, Marilena Leal Mesquita Silvestre Fernandes, Maria Lucia Lemos Lopes, Sonia Cristina de Magalhães Souza Fialho, Aysa Cesar Pinheiro, Laura Caldas Dos Santos, Valeria Valim, Erica Vieira Serrano, Sandra Lucia Euzébio Ribeiro, Tatiana Nayara Libório-Kimura, Danielle Christinne Soares do Egypto, Diego Ustárroz Cantali, Juliana D'Agostino Gennari, Samira Tatiyama Miyamoto, Karina Gatz Capobianco, Alisson Aliel Vigano Pugliesi, Vinicius Tassoni Civile, Ana Carolina Pereira Nunes Pinto, César Ramos Rocha-Filho, Aline Pereira da Rocha, Virginia Fernandes Moça Trevisani
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Abstract

Background: Neurological and psychiatric manifestations occur in patients with primary Sjogren's disease (SjD) with a wide-ranging clinical presentation, affecting quality of life, social participation, and prognosis. Despite this, neither central nor peripheral neurological symptoms are systematically evaluated in the context of autoimmunity or identified as manifestations of SjD. The EULAR Sjogren's Syndrome Disease Activity Index (ESSDAI) covers only part of them in the neurological domain.

Methods: We performed a systematic review of the diagnosis and prevalence of central, peripheral, and autonomic nervous system manifestations in primary SjD, following the recommendations proposed by the Cochrane Collaboration Handbook. Observational studies were included when their main issue was the diagnosis and the prevalence of the manifestations individually. We employed a generalized linear mixed model (GLMM) method with a random-effects model, and the results were computed using logit transformation, implemented through the 'meta' and 'metafor' packages in the R software (version 3.6.1). To present these recommendations, agreement among experts was investigated using the Delphi method in in-person meetings.

Results: We propose ten recommendations regarding the investigation and management of neurological involvement in SjD that had 100% agreement among participants.

Conclusion: These recommendations add to the literature on the clinical care of patients with SjD.

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巴西风湿病学会关于Sjögren病患者神经、认知和精神表现的建议。
背景:原发性干燥病(SjD)患者可出现神经和精神方面的表现,临床表现广泛,影响生活质量、社会参与和预后。尽管如此,在自身免疫的背景下,中枢和周围神经系统症状都没有被系统地评估,也没有被确定为SjD的表现。EULAR干燥综合征疾病活动指数(ESSDAI)仅涵盖神经学领域的一部分。方法:根据Cochrane协作手册提出的建议,我们对原发性SjD的中枢、外周和自主神经系统表现的诊断和患病率进行了系统回顾。当观察性研究的主要问题是诊断和个别表现的患病率时,观察性研究被纳入。采用随机效应模型的广义线性混合模型(GLMM)方法,通过R软件(版本3.6.1)中的“meta”和“metafor”包实现logit变换计算结果。为了提出这些建议,专家之间的协议进行了调查,使用德尔菲法在面对面的会议。结果:我们提出了十项关于SjD神经受累的调查和管理的建议,这些建议在参与者中得到了100%的同意。结论:这些建议增加了SjD患者临床护理的文献。
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来源期刊
Advances in Rheumatology
Advances in Rheumatology Medicine-Rheumatology
CiteScore
4.00
自引率
4.30%
发文量
41
审稿时长
53 weeks
期刊介绍: Formerly named Revista Brasileira de Reumatologia, the journal is celebrating its 60th year of publication. Advances in Rheumatology is an international, open access journal publishing pre-clinical, translational and clinical studies on all aspects of paediatric and adult rheumatic diseases, including degenerative, inflammatory and autoimmune conditions. The journal is the official publication of the Brazilian Society of Rheumatology and welcomes original research (including systematic reviews and meta-analyses), literature reviews, guidelines and letters arising from published material.
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