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Impact of CPAP in Patients With Central, Neuromuscular and Chest Wall Causes of Chronic Respiratory Failure and Comorbid OSA: A Retrospective Study CPAP对中枢、神经肌肉和胸壁原因的慢性呼吸衰竭和共病性OSA患者的影响:一项回顾性研究。
IF 9.2 3区 医学 Q1 RESPIRATORY SYSTEM Pub Date : 2026-02-01 DOI: 10.1016/j.arbres.2025.07.025
Antoine Léotard , Maxime Patout , Vincent Delord , Marie-Christine Blandin , Hélène Prigent , Pierre Tankéré
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引用次数: 0
Spontaneous Tracheal Fistulization of a Progressive Bronchogenic Cyst: A Four-Year Conservative Follow-Up Case Report 进行性支气管源性囊肿自发性气管瘘:保守随访4年病例报告。
IF 9.2 3区 医学 Q1 RESPIRATORY SYSTEM Pub Date : 2026-02-01 DOI: 10.1016/j.arbres.2025.07.019
Elvan Senturk Topaloglu , Omer Topaloglu
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引用次数: 0
CC16 Expression Restoration in Sputum of People With Cystic Fibrosis After Initiation of Elexacaftor/Tezacaftor/Ivacaftor 囊性纤维化患者服用elexaftor /Tezacaftor/Ivacaftor后痰中CC16表达的恢复
IF 9.2 3区 医学 Q1 RESPIRATORY SYSTEM Pub Date : 2026-02-01 DOI: 10.1016/j.arbres.2025.07.022
Angélique Mottais , Bruno Detry , Ziyu Alessia Qiu , Amandine M. Collin , Marylène Lecocq , Caroline Bouzin , Clara Chamlou , Chloé Bruart , Charlotte de Fays , Bart Vanaudenaerde , Lieven Dupont , Astrid Vermaut , Marianne Schulte , Mieke Boon , Christophe Goubau , Silvia Berardis , Valérie Hox , Antoine Froidure , Charles Pilette , Sophie Gohy
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引用次数: 0
Wheelchair-assisted Ventilation in Neuromuscular Disease: The Abdominal Press-and-release Technique 神经肌肉疾病的轮椅辅助通气:腹部按压和释放技术。
IF 9.2 3区 医学 Q1 RESPIRATORY SYSTEM Pub Date : 2026-02-01 DOI: 10.1016/j.arbres.2025.09.020
Andrea Vianello, Gabriella Guarnieri, Federico Lionello
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引用次数: 0
The Role of miR-320d in Regulation of Cigarette Smoke-Induced Pro-Inflammatory Responses in COPD miR-320d在COPD患者吸烟诱导的促炎反应中的调控作用
IF 9.2 3区 医学 Q1 RESPIRATORY SYSTEM Pub Date : 2026-02-01 DOI: 10.1016/j.arbres.2025.06.015
Mirjam P. Roffel , Corry-Anke Brandsma , Alen Faiz , Marnix R. Jonker , Wim Timens , Guy F. Joos , Guy G. Brusselle , Tania Maes , Ken R. Bracke , Maarten van den Berge , Irene H. Heijink

Introduction

The mechanisms driving abnormal pro-inflammatory responses to cigarette smoke in COPD remain unclear. MicroRNA (miR)-320d was previously shown to have anti-inflammatory effects, being upregulated by inhaled corticosteroids. Therefore, our objective was to study whether miR-320d suppresses smoke-induced airway epithelial pro-inflammatory responses and if this is compromised in COPD.

Methods

We investigated the anti-inflammatory mechanisms of miR-320d in cigarette smoke extract (CSE)-exposed primary bronchial epithelial cells (PBECs), comparing COPD and control cells using a miR-320d mimic. Additionally, we assessed whether miR-320d expression is altered with COPD and its severity, investigating lung tissue from two independent cohorts of non-COPD controls (non/current/ex-smokers) and COPD patients (current/ex-smokers) with mild/moderate and severe disease.

Results

MiR-320d overexpression attenuated baseline and CSE-induced pro-inflammatory CXCL8, IL-1α and GM-CSF secretion in non-COPD-derived PBECs. This effect was not observed for CXCL8 and IL-1α in COPD-derived PBECs. RNA-sequencing showed that miR-320d significantly regulates the expression of 137 genes in CSE-exposed epithelium, the upregulated genes being enriched in “interleukin-33-mediated signaling” and the downregulated genes in “response to cytokine” (including IRAK1) pathways. Higher miR-320d levels were associated with lower IRAK1 expression in control but not COPD-derived PBECs. Finally, miR-320d levels were lower in lung tissue of COPD patients vs non-smoking controls and in severe vs mild/moderate COPD patients.

Conclusions

miR-320d's suppressive effect on bronchial epithelial pro-inflammatory responses cells may be compromised in COPD. Additionally, miR-320d expression in lung tissue was lower with COPD severity. Thus, lower miR-320d anti-inflammatory action may contribute to persisting inflammation in COPD.
慢性阻塞性肺病患者吸烟引起异常促炎反应的机制尚不清楚。MicroRNA (miR)-320d先前被证明具有抗炎作用,被吸入皮质类固醇上调。因此,我们的目的是研究miR-320d是否抑制烟雾诱导的气道上皮促炎反应,以及这种作用是否在COPD中受到损害。方法:我们研究了miR-320d在香烟烟雾提取物(CSE)暴露的原代支气管上皮细胞(PBECs)中的抗炎机制,使用miR-320d模拟物比较COPD和对照细胞。此外,我们评估了miR-320d表达是否随COPD及其严重程度而改变,研究了两个独立队列的肺组织,分别是轻度/中度和重度疾病的非COPD对照组(非/当前/戒烟者)和COPD患者(当前/戒烟者)。结果:在非copd源性PBECs中,MiR-320d过表达减弱了基线和cse诱导的促炎CXCL8、IL-1α和GM-CSF分泌。在copd衍生的PBECs中,CXCL8和IL-1α未观察到这种作用。rna测序结果显示,miR-320d显著调控cse暴露上皮中137个基因的表达,上调的基因富集于“白细胞介素-33介导的信号通路”,下调的基因富集于“细胞因子应答”(包括IRAK1)通路。在对照组中,较高的miR-320d水平与较低的IRAK1表达相关,但与copd衍生的PBECs无关。最后,COPD患者肺组织中miR-320d水平低于非吸烟对照组,重度COPD患者肺组织中miR-320d水平低于轻度/中度COPD患者肺组织中miR-320d水平。结论:miR-320d对支气管上皮促炎反应细胞的抑制作用可能在COPD中受损。此外,miR-320d在肺组织中的表达随COPD严重程度的降低而降低。因此,较低的miR-320d抗炎作用可能有助于COPD的持续炎症。
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引用次数: 0
Inclusion of the Intermediate Respiratory Care Unit as a Detection Area for Controlled Donation After Circulatory Death: Results of a Pilot Project 将中级呼吸护理病房作为循环性死亡后控制捐献的检测区域:一个试点项目的结果。
IF 9.2 3区 医学 Q1 RESPIRATORY SYSTEM Pub Date : 2026-02-01 DOI: 10.1016/j.arbres.2025.07.004
Alejandro Romero-Linares , Antonio Cárdenas-Cruz , Jose M. Pérez-Villares , Jose A. Sánchez-Martínez , Patricia Fuentes-García , Bernardino Alcázar-Navarrete
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引用次数: 0
Splenic Silicosis 脾矽肺病。
IF 9.2 3区 医学 Q1 RESPIRATORY SYSTEM Pub Date : 2026-02-01 DOI: 10.1016/j.arbres.2025.08.006
Eric Andrey Rodríguez-Vega, Karen Pamela Martínez-Espinosa, Ana Linet Bravo-Gutiérrez
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引用次数: 0
Unusual Case of Multiple and Delayed Recurrence of a Solitary Fibrous Tumor of the Pleura After Complete Resection 胸膜单发纤维性肿瘤完全切除后多发迟发的罕见病例。
IF 9.2 3区 医学 Q1 RESPIRATORY SYSTEM Pub Date : 2026-02-01 DOI: 10.1016/j.arbres.2025.08.007
Génesis Isabel Victoriano Soriano , Begoña Gregorio Crespo , José Soro García
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引用次数: 0
Inhaled Corticosteroid Reduction Effects on Asthma Outcomes After Three Years of Benralizumab Treatment in Severe Asthma Patients 吸入皮质类固醇减少对严重哮喘患者贝那利珠单抗治疗3年后哮喘结局的影响。
IF 9.2 3区 医学 Q1 RESPIRATORY SYSTEM Pub Date : 2026-02-01 DOI: 10.1016/j.arbres.2025.08.001
Marta Arteaga , Laura López-Duque , Daniel Laorden , Inés Torrado , David Romero-Ribate , Elena Villamañán , Santiago Quirce , Rodolfo Álvarez-Sala , Javier Domínguez-Ortega
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引用次数: 0
Telemonitoring in Respiratory Diseases: Current Evidence, Clinical Experience, and Future Challenges. 呼吸系统疾病的远程监测:目前的证据、临床经验和未来的挑战。
IF 9.2 3区 医学 Q1 RESPIRATORY SYSTEM Pub Date : 2026-01-15 DOI: 10.1016/j.arbres.2026.01.001
Daniel López-Padilla, Vitalii Poberezhets, Nicolas Roche, Catharina C Moor, Marie Bruyneel, Carla Ribeiro, Hilary Pinnock

This narrative review summarizes current evidence and clinical experience regarding telemonitoring across major respiratory diseases and care settings, including chronic obstructive pulmonary disease (COPD), asthma, interstitial lung diseases, obstructive sleep apnea, as well as non-invasive ventilation and pulmonary rehabilitation programmes. Advances in connectivity, artificial intelligence (AI), and wearable devices are facilitating the early detection of clinical deterioration, personalized interventions, and improved self-management, thereby optimizing the use of healthcare resources. Strong evidence supports the benefits of telemonitoring in COPD, particularly in reducing exacerbations and hospital admissions, whereas results are more heterogeneous in asthma and emerging conditions such as interstitial lung diseases. Telemonitoring systems leverage AI-driven analytical frameworks and interoperable digital platforms to process and interpret large volumes of patient data, enabling both automated responses and targeted human interventions. Key challenges include ensuring patient engagement, addressing digital literacy and inequities in access, safeguarding data privacy, and integrating digital solutions into standard care and reimbursement frameworks. The COVID-19 pandemic accelerated the adoption of telemonitoring, confirming its feasibility and acceptability, but also revealed persistent gaps in long-term cost-effectiveness and implementation strategies. Future directions should focus on integrating telemonitoring with AI-supported, coordinated clinical decision-making, enhancing system interoperability, and above all, prioritizing equitable access to digital care. Telemonitoring is poised to become a central component of respiratory patient management, although its large-scale implementation will require overcoming existing technical, ethical, and organizational barriers to fully realize its clinical potential.

这篇叙述性综述总结了目前关于主要呼吸系统疾病和护理机构远程监测的证据和临床经验,包括慢性阻塞性肺疾病(COPD)、哮喘、间质性肺疾病、阻塞性睡眠呼吸暂停以及无创通气和肺康复规划。互联互通、人工智能(AI)和可穿戴设备的进步促进了临床恶化的早期发现、个性化干预和改进的自我管理,从而优化了医疗资源的利用。强有力的证据支持远程监测在慢性阻塞性肺病中的益处,特别是在减少病情恶化和住院方面,而在哮喘和肺间质性疾病等新发疾病中,结果则更加不一致。远程监控系统利用人工智能驱动的分析框架和可互操作的数字平台来处理和解释大量患者数据,从而实现自动化响应和有针对性的人工干预。主要挑战包括确保患者参与,解决数字素养和访问不公平问题,保护数据隐私,以及将数字解决方案整合到标准护理和报销框架中。2019冠状病毒病大流行加速了远程监测的采用,证实了其可行性和可接受性,但也暴露了长期成本效益和实施战略方面的持续差距。未来的方向应侧重于将远程监测与人工智能支持的协调临床决策相结合,增强系统互操作性,最重要的是,优先考虑公平获得数字医疗。远程监护有望成为呼吸系统患者管理的核心组成部分,尽管其大规模实施将需要克服现有的技术、伦理和组织障碍,以充分发挥其临床潜力。
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引用次数: 0
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Archivos De Bronconeumologia
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