首页> 外文期刊>Open Journal of Rheumatology and Autoimmune Diseases >The Differences of Interstitial Lung Diseases in High-Resolution Computerized Tomography and Pulmonary Function Test among Different Connective Tissue Diseases, and the Correlated Factors
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The Differences of Interstitial Lung Diseases in High-Resolution Computerized Tomography and Pulmonary Function Test among Different Connective Tissue Diseases, and the Correlated Factors

机译:不同结缔组织病之间高分辨率CT和肺功能检查中间质性肺疾病的差异及相关因素

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Objective. To study the difference of interstitial lung diseases (ILDs) in high-resolution computerized tomography and pulmonary function test among different connective tissue diseases (CTDs). Methods. 209 patients with different CTDs were recruited and underwent lung HRCT and PFT. Eerythrocyte sedimentation rate (ESR), C-reactive protein (CRP), serum ferritin (SF), anti-SSA, and so on were tested. Based on HRCT, a patient was classified into ILD group (CTD+ILD) or non-ILD group (CTD-ILD). HRCT, PFT, and laboratory markers were compared according to CTDs and CTD-associated ILDs. Results. The incidences of ILD were 79.6%, 82.0%, 89.7%, and 97.1% respectively for Rheumatoid arthritis (RA), primary Sjogren’s symptom (pSS), dermatomyositis/polymyositis (DM/PM), and systemic sclerosis (SSc) groups. RA and pSS patients exhibited more nodules, patching, ground-glass opacity, and cord shadow foci in HRCT, DM/PM and SSc patients exhibited more reticular opacity and honeycombing foci. RA and pSS patients exhibited more obstructive ventilatory disorder, small airway dysfunction and emphysema in PFT, and DM/PM and SSc patients exhibited more restrictive ventilatory disorder, mixed ventilatory disorder. ESR, CRP and SF were significantly higher in total CTD+ILD group than in total CTD-ILD group (P = 0.047, 0.006, 0.004, respectively), and higher in different CTD+ ILD groups than in comparable CTD-ILD groups (P = 0.049, 0.048, and 0.023, pSS+ILD, SSc+ILD and RA+ILD compared to pSS-ILD, SSc-ILD and RA-ILD, respectively for ESR, CRP, SF). The positive rate of anti-SSA was significantly higher in DM/PM+ILD group than in DM/PM-ILD group (P = 0.025). Conclusions. The manifestations and incidences of ILDs differ among different CTDs in HRCT and PFT, and inflammation and anti-SSA are positively correlated with ILDs in different CTDs, which provide important evidences for judging disease condition and prognosis.
机译:目的。研究不同结缔组织疾病(CTD)在高分辨率计算机断层扫描和肺功能测试中的间质性肺疾病(ILD)的差异。方法。招募了209名具有不同CTD的患者并进行了肺HRCT和PFT。测试了红细胞沉降率(ESR),C反应蛋白(CRP),血清铁蛋白(SF),抗SSA等。根据HRCT,将患者分为ILD组(CTD + ILD)或非ILD组(CTD-ILD)。根据CTD和与CTD相关的ILD对HRCT,PFT和实验室标记进行了比较。结果。类风湿性关节炎(RA),原发性干燥综合征(pSS),皮肌炎/多发性肌炎(DM / PM)和系统性硬化症(SSc)组的ILD发生率分别为79.6%,82.0%,89.7%和97.1%。 RA和pSS患者在HRCT,DM / PM和SSc患者中表现出更多的结节,斑块,毛玻璃样浑浊和脐带阴影病灶,而网状浑浊和蜂窝状灶更为明显。 RA和pSS患者在PFT中表现出更多的阻塞性通气障碍,小气道功能障碍和肺气肿,而DM / PM和SSc患者则表现出更多的限制性通气障碍,混合通气障碍。总CTD + ILD组的ESR,CRP和SF显着高于总CTD-ILD组(分别为P = 0.047、0.006、0.004),不同CTD + ILD组的ESR,CRP和SF均高于同类CTD-ILD组(P =对于ESR,CRP,SF,pSS + ILD,SSc + ILD和RA-ILD分别为0.049、0.048和0.023)。 DM / PM + ILD组的抗SSA阳性率显着高于DM / PM-ILD组(P = 0.025)。结论。 HRCT和PFT中不同CTD之间ILD的表现和发生率不同,炎症和抗SSA与不同CTD中ILD呈正相关,为判断疾病状况和预后提供重要依据。

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