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Autoimmune Diseases and Sjoegren's Syndrome: An Autoimmune Exocrinopathy

机译:自身免疫性疾病和Sjogren综合征:一种自身免疫外分疗法

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Autoimmune diseases include a diverse group of over 80 conditions. Sjoegren's syndrome is the second most common autoimmune rheumatic disease, with an estimated prevalence in the United States of 2-4 million persons. There are prominent and consistent oral and dental findings in Sjoegren's syndrome related to the autoimmune-mediated loss of normal salivary function. Additionally, nonoral clinical manifestations of Sjoegren's syndrome include: dry eyes (with specific ocular surface changes termed keratoconjunctivitis sicca); other xeroses, such as dryness of the nose, throat, skin, and vagina; peripheral (and less frequently central) neuropathies; myalgias and arthralgias; thyroid disorders (particularly autoimmune thyroiditis); pulmonary disorders; renal disorders; and lymphoma. There is a significant (20- to 40-fold) increase in the incidence of malignant lymphoma, particularly in primary Sjoegren's syndrome. Establishing the diagnosis of Sjoegren's syndrome has been difficult in the light of its nonspecific symptoms (dry eyes and mouth), disagreement on diagnostic criteria, and a lack of both sensitive and specific laboratory markers. Many serum and salivary biomark-ers for Sjoegren's syndrome have been proposed although, to date, none has proven to be sufficiently specific for diagnostic purposes or has been well correlated with disease activity measures. Investigators have recently begun to apply modern genomic and proteomic approaches to identify candidate biomarkers in Sjoegren's syndrome. The results of these investigations promise to provide a wealth of information on candidate biomarkers and possible etiopathological mechanisms underlying this disorder. Further, this information will improve clinical outcomes by fostering the design of new rational therapeutics and assisting in the monitoring of clinical disease.
机译:自身免疫疾病包括超过80个条件的多种组。 Sjoegren的综合征是第二种最常见的自身免疫性疾病,估计在美国2-400万人的普遍存在。在Sjoegren的综合征有与自身免疫介导的正常唾液功能损失有关的突出和一致的口腔和牙科发现。另外,Sjoegren综合征的非临床表现包括:干眼(具有特异性眼表面变化,称为角膜炎咽炎SICCA);其他Xerose,如鼻子,喉咙,皮肤和阴道的干燥;外周(和较不经常中央)神经病;肌肉和关节痛;甲状腺障碍(特别是自身免疫甲状腺炎);肺病;肾病;和淋巴瘤。恶性淋巴瘤发生率显着(20至40倍)增加,特别是在原发性Sjoegren的综合征中。根据其非特异性症状(干眼症和口腔),在诊断症状(干眼症),诊断标准中的分歧,以及缺乏敏感和特定的实验室标记,建立了Sjoegren综合征的诊断。许多血清和唾液生物科学为Sjoegren的综合症患者已经提出,但迄今为止,无需证明诊断目的足够特异或与疾病活动措施完全相关。调查人员最近开始应用现代基因组和蛋白质组学方法来识别Sjoegren综合征中的候选生物标志物。这些调查的结果承诺提供有关候选生物标志物的大量信息,以及潜在这种疾病的可能性机制。此外,该信息将通过培养新的理性治疗方法的设计和协助监测临床疾病来改善临床结果。

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