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用于诊断和预后结节病的临床有用的血清生物标志物。

Clinically-useful serum biomarkers for diagnosis and prognosis of sarcoidosis.

机构信息

a Laboratory of Autoimmune Diseases Josep Font, IDIBAPS-CELLEX, Department of Autoimmune Diseases , ICMiD, Hospital Clínic , Barcelona , Spain.

b SarcoGEAS-SEMI Study Group, Study Group of Autoimmune Diseases (GEAS) , Spanish Society of Internal Medicine (SEMI) , Spain.

出版信息

Expert Rev Clin Immunol. 2019 Apr;15(4):391-405. doi: 10.1080/1744666X.2019.1568240. Epub 2019 Jan 26.

Abstract

Sarcoidosis is a complex systemic disease with a silent, long-term evolution, and a heterogeneous clinical presentation. The diagnostic approach is complex with no single diagnostic test that may confirm the disease. Areas covered: A large list of serum biomarkers has been tested during the last 40 years. In this review, we analyse the potential usefulness in the diagnosis and prognosis of sarcoidosis of serum biomarkers classified according to their corresponding cellular source. Expert commentary: Diagnosis of sarcoidosis must always be approached as a multistep process based on a case-by-case integration of clinical, radiological, histological and serological data, none of which being pathognomonic. We found sIL-2R, CRP, SAA and chitotriosidase to be the best markers to confirm sarcoidosis (highest sensitivity), while ACE, gammaglobulins and lysozyme may be more useful for discarding sarcoidosis (highest specificity), taking into account that with the use of a higher cut-off we can increase specificity and with a lower cut-off we can increase sensitivity. Other biomarkers (TNF-a and CCL18) could help to identify patients with an enhanced risk of developing pulmonary fibrosis or progressive disease. The future scenario of the serological diagnostic approach of sarcoidosis will be the use of multi-assays including biomarkers from different cellular sources.

摘要

结节病是一种复杂的系统性疾病,具有隐匿性、长期性和异质性的临床特征。其诊断方法复杂,没有单一的诊断测试可以确诊该病。

涵盖领域

在过去的 40 年中,已经测试了大量的血清生物标志物。在这篇综述中,我们根据其相应的细胞来源,分析了这些血清生物标志物在结节病诊断和预后中的潜在作用。

专家评论

结节病的诊断必须始终作为一个多步骤的过程,根据临床、放射学、组织学和血清学数据的个体化综合来进行,这些数据都没有特异性。我们发现 sIL-2R、CRP、SAA 和几丁质酶是确诊结节病的最佳标志物(最高灵敏度),而 ACE、γ球蛋白和溶菌酶可能更有助于排除结节病(最高特异性),考虑到使用更高的截止值可以提高特异性,使用更低的截止值可以提高灵敏度。其他生物标志物(TNF-a 和 CCL18)可能有助于识别出发生肺纤维化或疾病进展风险较高的患者。结节病血清学诊断方法的未来前景将是使用包括来自不同细胞来源的生物标志物的多分析方法。

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