Department of Internal Medicine, Division of Rheumatology, FacultyofMedicine, Cukurova University, Adana, Turkey.
Department of Chest Diseases, FacultyofMedicine, Cukurova University, Adana, Turkey.
Clin Rheumatol. 2024 Aug;43(8):2679-2687. doi: 10.1007/s10067-024-07049-5. Epub 2024 Jul 4.
Connective tissue-associated interstitial lung diseases (CTD-ILD) are believed to be caused by microvascular damage. The objective of this study was to assess the nailfold capillaroscopy (NFC) pattern in patients diagnosed with both CTD-ILD and non-CTD-ILD to identify microvascular changes and determine the relation between capillaroscopic parameters, clinical variables, and disease-related measurements.
This cross-sectional study included 95 patients with interstitial lung disease who applied to our Rheumatology and Chest Clinics between September 2021 and July 2023. The patients were divided into two groups based on their diagnosis: non-CTD-ILD (group 1) and CTD-ILD (group 2). Nailfold capillaroscopy was performed.
Ninety-five patients, 49 (51% female, mean age 62.31 ± 11.027 years) in group 1 and 46 (69.6% female, mean age 62.09 ± 10.887 years) in group 2, were included in the study. Abnormal capillary morphologies were both detected in the CTD-ILD group and the non-CTD-ILD groups. In patients with a usual interstitial pneumonia (UIP) pattern on chest computed tomography (CT), tortuosity was higher than in patients with non-specific interstitial pneumonia (NSIP) (P = 0.041), and the proportion of tortuosity increased significantly as the duration of the disease increased (P = 0.016).
Our study highlights capillaroscopic abnormalities alone may not be sufficient to differentiate CTD-ILD (other than systemic sclerosis) from non-CTD-ILD. The presence of NFC abnormalities in non-CTD-ILD may suggest that fibrotic lung disease could potentially play a role in the deterioration of the microvascular structure or abnormal angiogenesis. Our study demonstrated that a multidisciplinary approach, incorporating clinical, morphological, pathological, and serological evaluations, is necessary for interpreting ILD. Key Points • Capillaroscopic abnormalities can also be seen in non-CTD-ILD. • Capillaroscopy findings do not distinguish the non-Ssc etiology of ILD. • Nailfold capillaroscopy may have the potential to serve as a useful tool in predicting prognosis and monitoring the disease progression in patients with idiopathic pulmonary fibrosis (IPF).
结缔组织相关间质性肺病(CTD-ILD)被认为是由微血管损伤引起的。本研究的目的是评估同时患有 CTD-ILD 和非 CTD-ILD 的患者的甲襞毛细血管显微镜检查(NFC)模式,以识别微血管变化,并确定毛细血管参数、临床变量和与疾病相关的测量值之间的关系。
这项横断面研究纳入了 2021 年 9 月至 2023 年 7 月期间到我院风湿科和胸科诊所就诊的 95 名间质性肺病患者。根据诊断将患者分为两组:非 CTD-ILD(第 1 组)和 CTD-ILD(第 2 组)。对患者进行甲襞毛细血管显微镜检查。
本研究共纳入 95 名患者,其中第 1 组 49 名(51%为女性,平均年龄 62.31±11.027 岁),第 2 组 46 名(69.6%为女性,平均年龄 62.09±10.887 岁)。在 CTD-ILD 组和非 CTD-ILD 组均检测到异常毛细血管形态。在胸部计算机断层扫描(CT)显示寻常型间质性肺炎(UIP)模式的患者中,迂曲度高于非特异性间质性肺炎(NSIP)患者(P=0.041),且随着疾病持续时间的延长,迂曲度显著增加(P=0.016)。
我们的研究强调,单纯的毛细血管镜异常可能不足以区分 CTD-ILD(除系统性硬化症外)与非 CTD-ILD。非 CTD-ILD 中存在 NFC 异常可能表明纤维化性肺疾病可能在微血管结构恶化或异常血管生成中起作用。我们的研究表明,需要采用多学科方法,结合临床、形态学、病理学和血清学评估来解释ILD。关键点:
非 CTD-ILD 也可出现毛细血管镜异常。
毛细血管镜检查结果不能区分ILD 的非 SSc 病因。
甲襞毛细血管显微镜检查可能有潜力作为一种有用的工具,用于预测特发性肺纤维化(IPF)患者的预后并监测疾病进展。