Application of Forced Oscillation Technique in Assessing Pulmonary Fibrosis in Hermansky-Pudlak Syndrome.

IF 1.8 Q3 RESPIRATORY SYSTEM Advances in respiratory medicine Pub Date : 2024-10-24 DOI:10.3390/arm92060040
Wilfredo De Jesús-Rojas, Luis Reyes-Peña, José Muñiz-Hernandez, Rolando Mena-Ventura, Gabriel Camareno-Soto, Gabriel Rosario-Ortiz, Marcos J Ramos-Benitez, Monica Egozcue-Dionisi, Enid Rivera-Jimenez, Rosa Román-Carlo
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Abstract

Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder characterized by defects in lysosome-related organelles. Given the high mortality rate associated with HPS pulmonary fibrosis (PF) and the significant risks tied to lung transplantation, it is essential to explore new tools for the early surveillance of PF to monitor its progression before clinical symptoms become apparent. This study evaluates the forced oscillation technique (FOT) for assessing PF in five adult patients with HPS, all homozygous for the HPS-1 (c.1472_1487dup p.His497Glnfs*90) founder mutation. Using the Resmon™ Pro V3 device, the FOT measured resistance (Rrs) and reactance (Xrs) at 5, 11, and 19 Hertz (Hz). High-resolution computed tomography (HRCT) scans of the chest were reviewed for radiographic findings. The cohort (n = 5) had a median age of 43 years. All patients exhibited HPS clinical features, including oculocutaneous albinism and respiratory symptoms such as dry cough and dyspnea. Radiographic analysis revealed PF in four patients (80%), with traction bronchiectasis, reticular patterns, honeycombing, and ground-glass opacities. The FOT detected progressive changes in pulmonary resistance and reactance correlating with fibrosis severity. These findings suggest that the FOT is a valuable non-invasive tool for monitoring PF in patients with HPS-1, potentially improving early diagnosis and management.

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强迫振荡技术在评估赫尔曼斯基-普德拉克综合征肺纤维化中的应用
赫尔曼斯基-普德拉克综合征(HPS)是一种罕见的常染色体隐性遗传疾病,其特征是溶酶体相关细胞器的缺陷。鉴于HPS肺纤维化(PF)的高死亡率和肺移植的巨大风险,有必要探索早期监测PF的新工具,以便在临床症状明显之前监测其进展。本研究评估了强迫振荡技术(FOT)对五名成年 HPS 患者肺纤维化的评估效果,这些患者均为 HPS-1 基因突变(c.1472_1487dup p.His497Glnfs*90)的同基因患者。FOT 使用 Resmon™ Pro V3 设备测量了 5、11 和 19 赫兹 (Hz) 的电阻 (Rrs) 和电抗 (Xrs)。对胸部的高分辨率计算机断层扫描 (HRCT) 进行了放射学检查。组群(n = 5)的中位年龄为 43 岁。所有患者均具有 HPS 临床特征,包括眼部白化病和呼吸道症状,如干咳和呼吸困难。影像学分析显示,4 名患者(80%)出现了 PF,伴有牵引性支气管扩张、网状结构、蜂窝状和磨玻璃不透明。FOT 检测出肺部阻力和反应的进行性变化与纤维化的严重程度相关。这些研究结果表明,FOT 是监测 HPS-1 患者 PF 的一种有价值的非侵入性工具,有可能改善早期诊断和管理。
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来源期刊
Advances in respiratory medicine
Advances in respiratory medicine RESPIRATORY SYSTEM-
CiteScore
2.60
自引率
0.00%
发文量
90
期刊介绍: "Advances in Respiratory Medicine" is a new international title for "Pneumonologia i Alergologia Polska", edited bimonthly and addressed to respiratory professionals. The Journal contains peer-reviewed original research papers, short communications, case-reports, recommendations of the Polish Respiratory Society concerning the diagnosis and treatment of lung diseases, editorials, postgraduate education articles, letters and book reviews in the field of pneumonology, allergology, oncology, immunology and infectious diseases. "Advances in Respiratory Medicine" is an open access, official journal of Polish Society of Lung Diseases, Polish Society of Allergology and National Research Institute of Tuberculosis and Lung Diseases.
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