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特发性肺纤维化患者血清 S100 钙结合蛋白 A4 的临床意义。

Clinical significance of serum S100 calcium-binding protein A4 in idiopathic pulmonary fibrosis.

机构信息

Second Division, Department of Internal Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan.

Medical & Biological Laboratories Co., Ltd., Nagoya, Japan.

出版信息

Respirology. 2020 Jul;25(7):743-749. doi: 10.1111/resp.13707. Epub 2019 Oct 9.

Abstract

BACKGROUND AND OBJECTIVE

Idiopathic pulmonary fibrosis (IPF) is a progressive interstitial lung disease with a poor prognosis. There are no established serum biomarkers for predicting the outcomes of IPF. S100 calcium-binding protein A4 (S100A4) is considered as a marker of fibroblasts; however, its clinical application remains to be investigated. We evaluated the clinical relevance of S100A4 in IPF patients.

METHODS

Serum S100A4 levels in 95 consecutive IPF patients and 50 healthy controls (HC) were measured using enzyme-linked immunosorbent assay. S100A4 expression in lung tissues was determined using immunohistochemistry/immunofluorescence and its association with disease progression (defined as deterioration in lung function or death) and mortality was assessed using Kaplan-Meier method and Cox hazards analysis.

RESULTS

Serum S100A4 levels were undetectable in all HC but were detectable in 26 (27.3%) of the 95 IPF patients (P < 0.01). Immunostaining of lung tissues from IPF patients showed aggregation of numerous S100A4-expressing cells around the fibroblastic foci and mature fibrotic regions. IPF patients with higher serum S100A4 levels had a significantly worse prognosis than those with low serum levels (2-year cumulative survival rate: 41.7% vs 77.0%, respectively, P < 0.01). On multivariate analyses, baseline serum S100A4 levels (per 10 ng/mL increase) were independently associated with higher disease progression rate (odds ratio: 1.06, P = 0.01) and higher mortality (hazard ratio: 1.18, P = 0.03).

CONCLUSION

S100A4 is a promising serum biomarker that may help predict disease progression/mortality. Our findings may help establish treatment strategies for IPF.

摘要

背景和目的

特发性肺纤维化(IPF)是一种预后不良的进行性间质性肺疾病。目前尚无确定的血清生物标志物可预测 IPF 的结局。S100 钙结合蛋白 A4(S100A4)被认为是成纤维细胞的标志物;然而,其临床应用仍有待研究。我们评估了 S100A4 在 IPF 患者中的临床相关性。

方法

采用酶联免疫吸附试验检测 95 例连续 IPF 患者和 50 例健康对照者(HC)的血清 S100A4 水平。采用免疫组化/免疫荧光法检测肺组织中 S100A4 的表达,并采用 Kaplan-Meier 法和 Cox 风险分析评估其与疾病进展(定义为肺功能恶化或死亡)和死亡率的关系。

结果

所有 HC 的血清 S100A4 水平均无法检测到,但在 95 例 IPF 患者中的 26 例(27.3%)中可检测到(P<0.01)。IPF 患者的肺组织免疫染色显示,大量表达 S100A4 的细胞聚集在成纤维细胞灶和成熟纤维化区域周围。血清 S100A4 水平较高的 IPF 患者的预后明显差于血清水平较低的患者(2 年累积生存率分别为 41.7%和 77.0%,P<0.01)。多因素分析显示,基线血清 S100A4 水平(每增加 10ng/ml)与更高的疾病进展率(优势比:1.06,P=0.01)和更高的死亡率(风险比:1.18,P=0.03)独立相关。

结论

S100A4 是一种有前途的血清生物标志物,可能有助于预测疾病进展/死亡率。我们的研究结果可能有助于为 IPF 制定治疗策略。

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