原发性干燥综合征的临床特征和预后:一个大型亚洲印度队列。

Q4 Medicine
Open Rheumatology Journal Pub Date : 2015-06-26 eCollection Date: 2015-01-01 DOI:10.2174/1874312901409010036
Pulukool Sandhya, Lakshmanan Jeyaseelan, Robert Hal Scofield, Debashish Danda
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引用次数: 44

摘要

目的:研究亚洲印度原发性Sjögren综合征(SS)患者的临床特征、免疫学特征和预后。方法:对印度南部一家三级医疗教学医院2004 - 2011年的电子病历进行SS筛查。纳入符合美国欧洲共识组(AECG) 2002或美国风湿病学会(ACR) 2012分类标准的患者。进行了聚类分析,以确定临床和免疫特征之间的关联模式。进行多变量逻辑回归以确定主要系统性介入的预测因子。治疗和结果的数据从电子记录中检索。结果:423例疑似SS患者中,332例符合纳入标准。只有8.3%的患者在初次就诊时自诉有sicca症状。发病年龄较年轻,男女比例较高,低温球蛋白血症、雷诺现象和高球蛋白血症的发生率较低,是该队列所特有的。聚类分析揭示了两个亚群:第一个聚类由具有高抗体滴度的主要全身性疾病的患者组成,第二个聚类由具有轻度疾病的血清阴性患者组成。超过三分之一的SS病例有严重的全身表现,需要免疫抑制剂治疗。在多因素logistic回归分析中,抗ro和抗la抗体阳性与系统性疾病特征的较高几率相关(分别为OR=2.67, P=0.03和OR=3.25, P=0.003),而慢性疼痛与较低的几率相关(OR=0.4, P= 0.032)。临床改善包括sicca和肌肉骨骼特征的症状性获益,免疫调节剂在大多数情况下被注意到。结论:本组SS患者具有特征性的临床特征;其中一些与先前在欧洲患者中报道的观察结果相反。该队列由两个不同的患者组组成。第一组与主要全身性疾病和高抗体滴度相关,而第二组由血清阴性的轻度疾病患者组成。logistic回归分析进一步证实了抗体阳性与全身特征的相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clinical Characteristics and Outcome of Primary Sjogren's Syndrome: A Large Asian Indian Cohort.

Clinical Characteristics and Outcome of Primary Sjogren's Syndrome: A Large Asian Indian Cohort.

Clinical Characteristics and Outcome of Primary Sjogren's Syndrome: A Large Asian Indian Cohort.

Objective: To characterise the clinical features, immunological profile and outcome in a cohort of Asian Indian patients with primary Sjögren's syndrome (SS).

Methods: Electronic medical records from a tertiary care teaching hospital in south India were screened for SS between 2004 and 2011. Patients fulfilling American European Consensus group (AECG) 2002 or American College of Rheumatology (ACR) 2012 classification criteria were included. Agglomerative hierarchical cluster analysis to identify patterns of associations between clinical and immunological features was done. Multivariate logistic regression to identify predictors of major systemic involvement was performed. Data on treatment and outcome were retrieved from electronic records.

Results: Of 423 patients suspected to have SS, 332 fulfilled inclusion criteria. Only 8.3% of patients complained of sicca symptoms on their own at initial presentation. Younger age of onset, higher female to male ratio, paucity of cryoglobulinemia, Raynaud's phenomenon and hyperglobulinemia were unique to this cohort. Cluster analysis revealed two subsets: The first cluster comprised of patients having a major systemic illness with high antibody titers and the second comprised of seronegative patients with mild disease. Over a third of SS cases had severe systemic manifestations necessitating treatment with immunosuppressants. In multivariate logistic regression analysis, anti-Ro and anti-La antibody positivity was associated with higher odds for systemic disease features (OR=2.67, P=0.03 and OR=3.25, P=0.003, respectively) whereas chronic pain was associated with lower odds (OR=0.4, p=0.032). Clinical improvement including symptomatic benefit in sicca and musculoskeletal features was noted with immunomodulators in the majority.

Conclusion: Our cohort of patients with SS has characteristic clinical features; some of them are in contrast with previous observations reported in European patients. This cohort consisted of two distinct patient clusters. The first cluster was associated with major systemic illness and high antibody titers, where as the second cluster comprised of seronegative patients with mild disease. Association of antibody positivity with systemic features was further confirmed on logistic regression analysis.

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来源期刊
Open Rheumatology Journal
Open Rheumatology Journal Medicine-Rheumatology
CiteScore
0.80
自引率
0.00%
发文量
2
期刊介绍: ENTHAM Open publishes a number of peer-reviewed, open access journals. These free-to-view online journals cover all major disciplines of science, medicine, technology and social sciences. BENTHAM Open provides researchers a platform to rapidly publish their research in a good-quality peer-reviewed journal. All peer-reviewed accepted submissions meeting high research and ethical standards are published with free access to all.
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