التفاصيل البيبلوغرافية
| العنوان: |
Clinical characteristics and outcome of IgG4-related disease with hypocomplementemia: a prospective cohort study |
| المؤلفون: |
Linyi Peng, Hui Lu, Jiaxin Zhou, Panpan Zhang, Jieqiong Li, Zheng Liu, Di Wu, Shangzhu Zhang, Yunjiao Yang, Wei Bai, Li Wang, Yunyun Fei, Wen Zhang, Yan Zhao, Xiaofeng Zeng, Fengchun Zhang |
| المصدر: |
Arthritis Research & Therapy, Vol 23, Iss 1, Pp 1-10 (2021) |
| بيانات النشر: |
BMC, 2021. |
| سنة النشر: |
2021 |
| المجموعة: |
LCC:Diseases of the musculoskeletal system |
| مصطلحات موضوعية: |
IgG4-related disease, Hypocomplementemia, Complement, Immunoglobulin G4, Relapse, Diseases of the musculoskeletal system, RC925-935 |
| الوصف: |
Abstract Background Immunoglobulin G4-related disease (IgG4-RD) is a newly recognized systemic, immune-mediated, and fibro-inflammatory disease. Hypocomplementemia was found in part of IgG4-RD patients especially in the setting of active disease. Objectives This study aimed to clarify the clinical features, treatment efficacy, and outcome in IgG4-RD patients with hypocomplementemia. Methods 312 IgG4-RD patients were recruited in our prospective cohort conducted in Peking Union Medical College Hospital. Patients were divided into hypocomplementemia group and normal complement group according to serum C3 and C4 levels measured at baseline before treatment. Low serum C3 levels ( |
| نوع الوثيقة: |
article |
| وصف الملف: |
electronic resource |
| اللغة: |
English |
| تدمد: |
1478-6362 |
| Relation: |
https://doaj.org/toc/1478-6362 |
| DOI: |
10.1186/s13075-021-02481-3 |
| URL الوصول: |
https://doaj.org/article/b0c285cb03204a7681fe17a5caa29da7 |
| رقم الانضمام: |
edsdoj.b0c285cb03204a7681fe17a5caa29da7 |
| قاعدة البيانات: |
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