Dipartimento di Scienze Cliniche, Internistiche, Anestesiologiche e Cardiovascolari- Reumatologia, Sapienza University of Rome, 00161 Roma, Lazio, Italy.
Dipartimento di Sanità Pubblica e Malattie Infettive, Sapienza University of Rome, 00161 Roma, Lazio, Italy.
Int J Mol Sci. 2020 Jul 21;21(14):5162. doi: 10.3390/ijms21145162.
Lung involvement is related to the natural history of anti-citrullinated proteins antibodies (ACPA)-positive rheumatoid arthritis (RA), both during the pathogenesis of the disease and as a site of disease-related injury. Increasing evidence suggests that there is a subclinical, early lung involvement during the course of the disease, even before the onset of articular manifestations, which can potentially progress to a symptomatic interstitial lung disease. To date, reliable, non-invasive markers of subclinical lung involvement are still lacking in clinical practice. The aim of this study is to evaluate the diagnostic potential of functional assessment and serum biomarkers in the identification of subclinical lung involvement in ACPA-positive subjects. Fifty ACPA-positive subjects with or without confirmed diagnosis of RA (2010 ARC-EULAR criteria) were consecutively enrolled. Each subject underwent clinical evaluation, pulmonary function testing (PFT) with assessment of diffusion lung capacity for carbon monoxide (DL), cardiopulmonary exercise testing (CPET), surfactant protein D (SPD) serum levels dosage and high-resolution computed tomography (HRCT) of the chest. The cohort was composed of 21 ACPA-positive subjects without arthritis (ND), 10 early (disease duration < 6 months, treatment-naïve) RA (ERA) and 17 long-standing (disease duration < 36 months, on treatment) RA (LSRA). LSRA patients had a significantly higher frequency of overall HRCT abnormalities compared to the other groups ( = 0.001). SPD serum levels were significantly higher in ACPA-positive subjects compared with healthy controls (158.5 ± 132.3 ng/mL vs 61.27 ± 34.11 ng/mL; 0.0001) and showed an increasing trend from ND subjects to LSRD patients ( = 0.004). Patients with HRCT abnormalities showed significantly lower values of DL (74.19 ± 13.2% pred. vs 131.7 ± 93% pred.; 0.009), evidence of ventilatory inefficiency at CPET and significantly higher SPD serum levels compared with subjects with no HRCT abnormalities (213.5 ± 157.2 ng/mL vs 117.7 ± 157.3 ng/mL; 0.018). Abnormal CPET responses and higher SPD levels were also associated with specific radiological findings. Impaired DL and increased SPD serum levels were independently associated with the presence of HRCT abnormalities. Subclinical lung abnormalities occur early in RA-associated autoimmunity. The presence of subclinical HRCT abnormalities is associated with several functional abnormalities and increased SPD serum levels of SPD. Functional evaluation through PFT and CPET, together with SPD assessment, may have a diagnostic potential in ACPA-positive subjects, contributing to the identification of those patients to be referred to HRCT scan.
肺受累与抗瓜氨酸蛋白抗体(ACPA)阳性类风湿关节炎(RA)的自然病史有关,既发生在疾病发病机制期间,也发生在与疾病相关的损伤部位。越来越多的证据表明,在疾病过程中存在亚临床、早期肺受累,甚至在关节表现出现之前,这可能进展为有症状的间质性肺病。迄今为止,在临床实践中仍然缺乏可靠的、非侵入性的亚临床肺受累标志物。本研究旨在评估功能评估和血清生物标志物在识别 ACPA 阳性患者亚临床肺受累方面的诊断潜力。
连续纳入 50 名 ACPA 阳性患者,无论是否确诊为 RA(2010 年 ACR-EULAR 标准)。每位患者均接受临床评估、肺功能测试(PFT),包括一氧化碳扩散能力评估、心肺运动测试(CPET)、表面活性剂蛋白 D(SPD)血清水平检测和胸部高分辨率计算机断层扫描(HRCT)。
该队列由 21 名无关节炎的 ACPA 阳性患者(ND)、10 名早期(病程<6 个月,未治疗)RA(ERA)和 17 名长期(病程<36 个月,治疗)RA(LSRA)患者组成。LSRA 患者的整体 HRCT 异常频率明显高于其他组( = 0.001)。与健康对照组相比,ACPA 阳性患者的 SPD 血清水平明显升高(158.5±132.3ng/mL 比 61.27±34.11ng/mL; 0.0001),且从 ND 患者到 LSRA 患者呈升高趋势( = 0.004)。
HRCT 异常患者的 DL 值明显降低(74.19±13.2%pred. 比 131.7±93%pred.; 0.009),CPET 显示通气效率降低,与 HRCT 无异常患者相比,SPD 血清水平明显升高(213.5±157.2ng/mL 比 117.7±157.3ng/mL; 0.018)。异常 CPET 反应和更高的 SPD 水平也与特定的放射学发现有关。
受损的 DL 和升高的 SPD 血清水平与 HRCT 异常的存在独立相关。
亚临床肺部异常在 RA 相关自身免疫中早期发生。亚临床 HRCT 异常的存在与多种功能异常和 SPD 血清水平升高有关。通过 PFT 和 CPET 进行功能评估,以及 SPD 评估,可能在 ACPA 阳性患者中有诊断潜力,有助于识别需要进行 HRCT 扫描的患者。