Primary CNS vasculitis (PCNSV): a cohort study

医学 血管炎 队列 儿科 头痛 内科学 外科 放射科 疾病
作者
Ayush Agarwal,Jyoti Sharma,M. V. Padma Srivastava,Mehar Chand Sharma,Rohit Bhatia,Deepa Dash,Vinay Goyal,Achal Kumar Srivastava,Manjari Tripathi,Vaishali Suri,Mamta Bhushan Singh,Sushant Agarwal,Chitra Sarkar,Leve Joseph,Manmohan Singh,Ashish Suri,Rajesh Singh,Deepti Vibha,Awadh Kishor Pandit,Roopa Rajan,Anu Gupta,Arunmozhimaran Elavarasi,Divya M. Radhakrishnan,Animesh Das,Shailesh Gaikwad,Vivek Tandon,Ramesh Doddamani,Ashish Datt Upadhyay,Ajay Garg,Venugopalan Y Vishnu
出处
期刊:Scientific Reports [Nature Portfolio]
卷期号:12 (1) 被引量:9
标识
DOI:10.1038/s41598-022-17869-7
摘要

Abstract Primary CNS Vasculitis (PCNSV) is a rare inflammatory disorder affecting the blood vessels of the central nervous system. Patients present with a combination of headaches, seizures, and focal neurological deficits. There is usually a diagnostic delay. Treatment is based on observational studies and expert opinion. Our objective was to identify clinical, laboratory, neuroimaging, pathologic or management-related associations with 2 year outcome in patients with primary CNS vasculitis. We conducted a cohort study at a single tertiary care referral centre of prospectively (2018-2019) and retrospectively (2010-2018) identified individuals with primary CNS vasculitis (diagnosis was proven by either brain biopsy or cerebral digital subtraction angiography). Clinical, imaging and histopathologic findings, treatment, and functional outcomes were recorded. Univariate and stepwise multiple logistic regression were applied. P-value<0.05 was considered statistically significant. The main outcome measures were documentation of clinical improvement or worsening (defined by mRS scores) and identification of independent predictors of good functional outcome (mRS 0-2) at 2 years. We enrolled eighty-two biopsy and/or angiographically proven PCNSV cases. The median age at presentation was 34 years with a male predilection and a median diagnostic delay of 23 months. Most patients presented with seizures (70.7%). All patients had haemorrhages on MRI. Histologically lymphocytic subtype was the commonest. Corticosteroids with cyclophosphamide was the commonest medication used. The median mRS at follow-up of 2 years was 2 (0-3), and 65.2% of patients achieved a good functional outcome. Myelitis and longer duration of illness before diagnosis were associated with poorer outcomes. The presence of hemorrhages on SWI sequence of MRI might be a sensitive imaging marker. Treatment with steroids and another immunosuppressant probably reduced relapse rates in our cohort. We have described the third largest PCNSV cohort and multi-centre randomised controlled trials are required to study the relative efficacy of various immunosuppressants. Study registration: CTRI/2018/03/012721.

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