Subclinical pleuro-pulmonary disease in patients with SLE: functional and radiological methods

Hanaa S. Hamed, Mohammed M. N. Abozaid, Enas Mekawy
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Abstract

Systemic lupus erythematosus (SLE) is a multisystem autoimmune disease with highest prevalence of chest involvement; however, early detection of subclinical pleuropulmonary diseases may improve the quality of life and prognosis of patients. This study aimed to identify the subclinical pleuro-pulmonary involvement in SLE patients without respiratory symptoms. A total of 228 patients diagnosed with SLE were recruited and subjected to high-resolution computed tomography (HRCT) chest, ultrasound (US) chest, and spirometry for further evaluation and finding of sub-clinical signs. Around 52.63% of patients had pulmonary involvement in HRCT, while in US, it was 73.68%. Ground glass opacity was observed in 31.58% of HRCT cases, and > 1/3 of patients had pleural thickness in US. Spirometry showed that 26.32% of patients had small airway disease. SLE patients with subclinical lung involvement were significantly female and younger and had shorter disease duration, p < 0.05 for all. SLE severity showed a significant negative correlation with lung function, and was positively correlated with pleural thickness and effusion, and pleural nodules in US finding. However, diaphragmatic excursion showed a negative correlation. Moreover, ground glass opacities, honey combing opacities, interlobular septal thickening, pleural thickness, and effusion in HRCT showed positive correlation with disease severity, p < 0.001 for all, yet, the mosaic pattern showed a negative relationship. The radiological assessments of SLE patients via HRCT and ultrasound unveiled prevalent findings such as ground glass opacities and pleural abnormalities. The severity of SLE correlated significantly with pulmonary function tests in a negative way, plus the positive correlation with lung opacities and pleural abnormalities.
系统性红斑狼疮患者的亚临床胸肺疾病:功能和放射学方法
系统性红斑狼疮(SLE)是一种多系统自身免疫性疾病,其中胸部受累的发病率最高;然而,早期发现亚临床胸肺疾病可改善患者的生活质量和预后。本研究旨在确定无呼吸道症状的系统性红斑狼疮患者的亚临床胸肺受累情况。研究共招募了 228 名确诊为系统性红斑狼疮的患者,并对他们进行了高分辨率计算机断层扫描(HRCT)胸部检查、胸部超声波检查和肺活量测定,以进一步评估和发现亚临床症状。约 52.63% 的患者在高分辨率计算机断层扫描中发现肺部受累,而在胸部超声检查中,这一比例为 73.68%。在 31.58% 的 HRCT 病例中观察到磨玻璃不透明,而在 US 检查中,超过 1/3 的患者有胸膜厚度。肺活量测定显示,26.32%的患者有小气道疾病。亚临床肺部受累的系统性红斑狼疮患者中,女性明显多于男性,年龄明显小于男性,病程明显短于男性。系统性红斑狼疮的严重程度与肺功能呈显著负相关,与胸膜厚度、积液和胸膜结节呈正相关。然而,膈肌外展呈负相关。此外,HRCT 中的磨玻璃不透光、蜜蜂梳状不透光、小叶间隔增厚、胸膜厚度和渗出与疾病严重程度呈正相关(P < 0.001),但马赛克模式与疾病严重程度呈负相关。通过 HRCT 和超声波对系统性红斑狼疮患者进行的放射学评估发现,患者普遍存在磨玻璃不透明和胸膜异常。系统性红斑狼疮的严重程度与肺功能测试呈显著负相关,与肺不张和胸膜异常呈正相关。
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