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Circulating Dickkof-1 as a potential biomarker associated with the prognosis of patients with rheumatoid arthritis-associated interstitial lung disease

机译:循环Dickkof-1作为与类风湿性关节炎相关的间质性肺病患者预后相关的潜在生物标志物

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摘要

To the Editor: Interstitial lung disease (ILD) is a common extra-articular manifestation in patients with connective tissue diseases (CTDs), including rheumatoid arthritis (RA), which contributes significantly to the disease burden and excess mortality.[1] It has been well-recognized that RA-associated ILD (RA-ILD) patients have a threefold higher risk of death than RA patients without ILD.[2] However, among approximately 30% of ILD patients, the specific diagnosis cannot be made from clinical findings and high-resolution computed tomography features, resulting in diagnostic and management uncertainty.[3] Noninvasive blood biomarkers with diagnostic and prognostic utility may, therefore, provide alternative information for identifying vulnerable patients,[4] especially in clinical settings with limited medical resources. Dickkof-1 (DKK1) protein level was found to increase in lung tissue specimens from donors and idiopathic pulmonary fibrosis (IPF) patients.[5] In this context, the DKK1 was able to alter Wnt-induced epithelial cell proliferation in a dose-dependent manner,[5] implying clinical relevance of DKK1 in both ILD and RA.
机译:向编辑:间质肺病(ILD)是结缔组织疾病(CTD)患者的常见关节表现,包括类风湿性关节炎(RA),这对疾病负担有显着贡献和过度的死亡率。[1]已经公认出现,RA相关的ILD(RA-ILD)患者的死亡风险高于RA患者,没有ILD。[2]然而,在大约30%的ILD患者中,不能从临床调查结果和高分辨率计算断层扫描特征进行具体诊断,导致诊断和管理不确定性。[3]因此,具有诊断和预测效用的非侵入性血液生物标志物可以为识别脆弱的患者提供替代信息[4],尤其是医疗资源有限的临床环境。发现Dickkof-1(DKK1)蛋白质水平来自供体和特发性肺纤维化(IPF)患者的肺组织标本增加。[5]在这种情况下,DKK1能够以剂量依赖性方式改变WNT诱导的上皮细胞增殖,[5]暗示DKK1在ILD和RA中的临床相关性。

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