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胸腔内结节病的高分辨率计算机断层扫描模式与血清 SAA、CA 15.3、SP-D 及其他间质性肺疾病生物标志物的相关性。

Correlation of the High-Resolution Computed Tomography Patterns of Intrathoracic Sarcoidosis with Serum Levels of SAA, CA 15.3, SP-D, and Other Biomarkers of Interstitial Lung Disease.

机构信息

Department of Pulmonary Diseases, University Medical Centre Ljubljana, Zaloška 7, 1000 Ljubljana, Slovenia.

Faculty of Mathematics, Natural Sciences and Information Technologies (FAMNIT), University of Primorska, 6000 Koper, Slovenia.

出版信息

Int J Mol Sci. 2023 Jun 28;24(13):10794. doi: 10.3390/ijms241310794.

Abstract

Studies on the serum biomarkers of granulomatous inflammation and pulmonary interstitial disease in intrathoracic sarcoidosis have shown conflicting results. We postulated that differences in the concentrations of serum biomarkers can be explained by the heterogenous patterns of sarcoidosis seen on thoracic HRCT. Serum biomarker levels in 79 consecutive patients, newly diagnosed with intrathoracic sarcoidosis, were compared to our control group of 56 healthy blood donors. An analysis was performed with respect to HRCT characteristics (the presence of lymph node enlargement, perilymphatic or peribronchovascular infiltrates, ground-glass lesions, or fibrosis), CXR, and disease extent. Serum levels of CXCL9, CXCL10, CTO, and CCL18 were statistically significantly increased in all patients compared to controls. Serum levels of CA15.3 were statistically significantly increased in all patients with parenchymal involvement. SAA was increased in patients with ground-glass lesions while SP-D levels were statistically significantly increased in patients with lung fibrosis. Only SP-D and CA15.3 showed a significant correlation to interstitial disease extent. In conclusion, we found that sarcoidosis patients with different HRCT patterns of intrathoracic sarcoidosis have underlying biochemical differences in their serum biomarkers transcending Scadding stages. The stratification of patients based on both radiologic and biochemical characteristics could enable more homogenous patient selection for further prognostic studies.

摘要

对胸内结节病的肉芽肿性炎症和肺间质疾病的血清生物标志物的研究结果相互矛盾。我们推测,在 HRCT 上观察到的结节病的异质性模式可以解释血清生物标志物浓度的差异。将 79 例新诊断为胸内结节病的连续患者的血清生物标志物水平与我们的 56 名健康献血者对照组进行比较。对 HRCT 特征(淋巴结肿大、支气管血管周围或淋巴管周围浸润、磨玻璃影或纤维化的存在)、CXR 和疾病范围进行了分析。与对照组相比,所有患者的血清 CXCL9、CXCL10、CTO 和 CCL18 水平均显著升高。所有实质受累患者的 CA15.3 血清水平均显著升高。SAA 在有磨玻璃病变的患者中增加,而 SP-D 水平在有肺纤维化的患者中显著增加。只有 SP-D 和 CA15.3 与间质性疾病程度有显著相关性。总之,我们发现,胸内结节病 HRCT 模式不同的结节病患者,其血清生物标志物存在潜在的生化差异,超越了 Scadding 分期。基于放射学和生化特征对患者进行分层,可以使进一步的预后研究更能选择同质的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad63/10341825/59a78ce12f27/ijms-24-10794-g001.jpg

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