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Profiles of circulating T follicular helper (cTfh) cell subpopulations in patients with asthma, COPD and asthma-COPD overlap (ACO). 哮喘、COPD和哮喘-COPD重叠(ACO)患者循环T滤泡辅助细胞(cTfh)亚群的特征
IF 3.1 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-30 DOI: 10.1016/j.rmed.2026.108672
Vanesa Cunill, Valero Andreu, Amanda Iglesias, María Berman, Núria Toledo-Pons, Elisabet Pol-Pol, Mireia Vicens, Miguel A Estévez, Jaume Sauleda, Javier Verdú, Joana M Ferrer, Borja G Cosío, Jaime Pons

Background: Asthma, chronic obstructive pulmonary disease (COPD) and asthma-COPD Overlap (ACO) are inflammatory diseases characterized by specific T helper (Th) phenotypes. CD4 T follicular helper (Tfh) cells constitute a heterogeneous subset of T cells (Tfh1, Tfh2, Tfh17, Tfh17.1 and Tfr) essential for B cell differentiation and immunoglobulin production. Although alterations in their distribution and/or function have been associated with several pathologies, little is known about their relevance in these airway diseases.

Methods: We sought to evaluate, by flow cytometry, the pattern of blood follicular and non-follicular Th cell subpopulations in patients with asthma, COPD and ACO.

Results: We found a distinct and characteristic T cell pattern in these three inflammatory conditions: a predominance of cTfh2 in asthma patients, a Th17.1 and cTfh17.1 inflammatory profile in COPD patients, and a Th1 pattern in ACO patients. Regarding tobacco smoke, COPD patients who were active smokers had a higher ratio Th1/Th17 compared to ex-smokers with COPD, a trend not observed in ACO patients.

Conclusions: These results suggest that the assessment of the characteristic inflammatory profile for each of these pathologies could help to understand the pathobiology and to identify the most appropriate therapeutic target.

背景:哮喘、慢性阻塞性肺疾病(COPD)和哮喘-COPD重叠(ACO)是炎症性疾病,其特征是特异性辅助性T (Th)表型。CD4 T滤泡辅助细胞(Tfh)是B细胞分化和免疫球蛋白产生所必需的T细胞(Tfh1、Tfh2、Tfh17、Tfh17.1和Tfr)的异质亚群。虽然它们的分布和/或功能的改变与几种病理有关,但对它们在这些气道疾病中的相关性知之甚少。方法:我们试图通过流式细胞术评估哮喘、COPD和ACO患者血液滤泡和非滤泡Th细胞亚群的模式。结果:我们在这三种炎症中发现了一种独特的特征性T细胞模式:哮喘患者以cTfh2为主,COPD患者以Th17.1和cTfh17.1为主,ACO患者以Th1为主。在吸烟方面,活跃吸烟者的COPD患者Th1/Th17比值高于已戒烟的COPD患者,但在ACO患者中未观察到这一趋势。结论:这些结果表明,评估每种病理的特征性炎症特征有助于了解病理生物学并确定最合适的治疗靶点。
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引用次数: 0
Association between Epworth Sleepiness Scores and CPAP compliance in patients with obstructive sleep apnea. 阻塞性睡眠呼吸暂停患者Epworth嗜睡评分与CPAP依从性的关系
IF 3.1 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-30 DOI: 10.1016/j.rmed.2026.108673
Ziad T Baki, Mustafa A Alameri, Sushil K Singhi

Purpose: Continuous positive airway pressure (CPAP) therapy is the gold standard treatment for obstructive sleep apnea, but adherence remains suboptimal. Subjective symptoms such as excessive daytime sleepiness may influence motivation to maintain therapy. This study examined whether baseline Epworth Sleepiness Scale (ESS) scores predict early CPAP adherence compared with objective measures such as the Apnea-Hypopnea Index (AHI).

Methods: We conducted a retrospective observational study of 400 adults with Obstructive Sleep Apnea prescribed CPAP between 2021 and 2023. Thirty days of CPAP adherence data was downloaded and categorized into five ordinal groups ranging from very low to very high adherence. Associations between ESS and adherence were assessed using chi-square tests, Goodman and Kruskal's gamma, and ordinal logistic regression adjusted for AHI, age, sex, and body mass index.

Results: Higher ESS scores were significantly associated with greater adherence (χ2 = 28.7, P = 0.026; gamma = 0.199). Ordinal regression showed each 1-point increase predicted 7.4% higher odds of being in a greater adherence category (OR 1.072, 95% CI 1.027-1.117, P < 0.001). Age modestly predicted adherence (OR 1.010, P = 0.019). AHI, body mass index, and sex were not significant predictors. Patients with severe daytime sleepiness had the highest rates of excellent adherence (>90%).

Conclusion: Although causality cannot be inferred from a retrospective design, higher subjective sleepiness, measured by ESS, was associated with higher early adherence. Incorporating ESS into routine evaluation may identify patients at risk for nonadherence and guide targeted interventions.

目的:持续气道正压通气(CPAP)治疗是阻塞性睡眠呼吸暂停的金标准治疗,但依从性仍不理想。主观症状如白天过度嗜睡可能影响维持治疗的动机。本研究考察了基线Epworth嗜睡量表(ESS)评分与呼吸暂停低通气指数(AHI)等客观指标相比,是否能预测早期CPAP依从性。方法:我们对2021年至2023年间400名患有阻塞性睡眠呼吸暂停的成年人进行了回顾性观察研究。下载30天的CPAP依从性数据,并将其分为从非常低到非常高依从性的五个顺序组。采用卡方检验、Goodman和Kruskal伽玛,并根据AHI、年龄、性别和体重指数调整有序逻辑回归,评估ESS与依从性之间的关系。结果:ESS评分越高,依从性越高(χ2=28.7, P=0.026; gamma=0.199)。序数回归显示,每增加1点,进入更强依从性类别的几率将增加7.4% (OR 1.072, 95% CI 1.027-1.117, P90%)。结论:虽然不能从回顾性设计中推断出因果关系,但ESS测量的较高的主观困倦与较高的早期依从性相关。将ESS纳入常规评估可以识别有不依从风险的患者,并指导有针对性的干预措施。
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引用次数: 0
Comparative effectiveness and safety of novel antidiabetic agents in the management of obstructive sleep apnea: a systematic review, meta-analysis, and network meta-analysis. 新型降糖药治疗阻塞性睡眠呼吸暂停的有效性和安全性比较:系统综述、meta分析和网络meta分析
IF 3.1 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-29 DOI: 10.1016/j.rmed.2026.108671
Ying-Tian Yang, Xin-Zheng Hou, Xi-Rui Zhang, Zhen-Peng Zhang, Shi-Han Wang

Background: Obstructive sleep apnea (OSA) is a prevalent but frequently underdiagnosed type of sleep-disordered breathing. Excessive obesity is a primary reversible risk factor for OSA. A range of novel antidiabetic agents has recently demonstrated promising potential for improving OSA severity through weight loss and metabolic regulation.

Objective: This study aimed to examine the effectiveness and safety of novel antidiabetic agents for people with OSA.

Methods: We searched PubMed, Web of Science, Cochrane Library, and Embase database from inception to May 18, 2025. Pairwise meta-analysis and Bayesian network meta-analysis (NMA) were conducted to compare relative efficacy.

Results: A total of 8 RCTs and 2 non-RCTs involving 1280 OSA participants were enrolled. Compared with the control group, SGLT-2i (MD = -7.73 events/h, 95 % CI [-9.83, -5.64]), GLP-1 RAs (MD = -5.19 events/h, 95 % CI [-6.87, -3.51]), and tirzepatide (-21.89 events/h, 95 % CI [-26.01, -17.77]) could significantly decrease AHI. The NMA results suggested that tirzepatide ranking highest of producing the greatest AHI reduction (MD = -21.85 events/h, 95 % CI [-27.52, -16.34]), along with the most substantial decreases in body weight (MD = -19.41 kg, 95 % CI [-21.00, -17.82]) and blood pressure (MDSBP = -5.86 mmHg, 95 % CI [-7.97, -3.74]; MDDBP = -1.96 mmHg, 95 % CI [-3.45, -0.46]).

Conclusion: Based on indirect evidence, tirzepatide was associated with the largest estimated magnitude of AHI reduction, presumably mediated by its weight-loss effects. For obesity-related OSA patients intolerant to continuous positive airway pressure therapy, tirzepatide may represent a potential adjunctive or alternative pharmacological option. High-quality studies are still needed to validate these findings further.

Prospero registration number: CRD420251165267.

背景:阻塞性睡眠呼吸暂停(OSA)是一种普遍但常被误诊的睡眠呼吸障碍类型。过度肥胖是阻塞性睡眠呼吸暂停的主要可逆危险因素。一系列新型抗糖尿病药物最近显示出通过减轻体重和调节代谢来改善OSA严重程度的潜力。目的:探讨新型降糖药对OSA患者的有效性和安全性。方法:检索PubMed、Web of Science、Cochrane Library和Embase数据库,检索时间为成立至2025年5月18日。两两荟萃分析和贝叶斯网络荟萃分析(NMA)比较相对疗效。结果:共纳入8项随机对照试验和2项非随机对照试验,涉及1,280名OSA参与者。​NMA结果显示,替西帕肽在降低AHI (MD= -21.85事件/小时,95% CI[-27.52, -16.34])、降低体重(MD=-19.41 kg, 95% CI[-21.00, -17.82])和血压(MDSBP=-5.86 mmHg, 95% CI [-7.97, -3.74]; MDDBP=-1.96 mmHg, 95% CI[-3.45, -0.46])方面排名最高。结论:基于间接证据,替西帕肽与最大的AHI降低估计值相关,可能是由其减肥作用介导的。对于不耐受持续气道正压治疗的肥胖相关OSA患者,替西帕肽可能是一种潜在的辅助或替代药物选择。仍然需要高质量的研究来进一步验证这些发现。普洛斯彼罗注册号:CRD420251165267。
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引用次数: 0
Comorbidities in Pediatric Cystic Fibrosis: ABPA, Celiac Disease and Prediabetes in Georgia. 乔治亚州儿童囊性纤维化的合并症:ABPA、乳糜泻和前驱糖尿病
IF 3.1 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-29 DOI: 10.1016/j.rmed.2026.108674
Nino Vardosanidze, Dodo Agladze, Nani Kavlashvili

Background: Cystic fibrosis is a chronic autosomal-recessive disorder characterized by progressive lung disease, pancreatic insufficiency, and multiple systemic complications. Early identification and treatment of comorbidities such as allergic bronchopulmonary aspergillosis (ABPA), celiac disease (CD), and prediabetes/cystic fibrosis-related diabetes (CFRD) improves outcomes.

Methods: This prospective observational study included 68 pediatric CF patients registered in the Georgian National Monitoring Program of Rare Diseases (2022-2025). All children had a confirmed diagnosis of CF based on national criteria, established either through newborn screening (elevated IRT followed by sweat chloride and fecal elastase testing) or direct clinical referral for sweat chloride testing. Sweat chloride <29 mmol/L was considered negative, 30-60 mmol/L borderline (requiring repeat testing), and ≥60 mmol/L abnormal and referred for CFTR gene testing [4]. All patients underwent three fasting plasma glucose tests, total IgE measurement, and Aspergillus-specific IgG testing. Anti-tissue transglutaminase IgA (anti-TTG IgA) was measured once for celiac disease screening. Age-specific reference ranges and established diagnostic criteria for ABPA, CD, and CFRD were applied.

Results: Three patients had elevated anti-TTG IgA; one was diagnosed with CD and treated with a gluten-free diet. Impaired fasting glucose was observed in 14 patients (22%). Two patients with persistently elevated HbA1c (≥6.0%) were referred to endocrinology for evaluation of prediabetes/CFRD. Aspergillus-specific IgG was elevated in two patients; one had markedly elevated total IgE (>1500 IU/mL) and was diagnosed with ABPA requiring systemic corticosteroids and antifungal therapy. Several patients had elevated IgE without ABPA but due to sensitization to multiple allergens, they were referred to an allergologist.

Conclusion: Comorbidities including CD, prediabetes/CFRD, and ABPA are present in Georgian children with CF and can negatively affect nutrition and lung function if untreated. Routine screening for glucose abnormalities, CD, and ABPA should be implemented into national CF care protocols for timely treatment and better outcomes.

背景:囊性纤维化是一种慢性常染色体隐性疾病,以进行性肺部疾病、胰腺功能不全和多种全身并发症为特征。早期识别和治疗合并症,如过敏性支气管肺曲霉病(ABPA)、乳糜泻(CD)和前驱糖尿病/囊性纤维化相关糖尿病(CFRD),可改善预后。方法:这项前瞻性观察性研究纳入了在格鲁吉亚国家罕见疾病监测计划(2022-2025)中登记的68例儿童CF患者。所有儿童均根据国家标准确诊CF,这些标准是通过新生儿筛查(IRT升高,随后进行汗液氯化物和粪便弹性酶检测)或直接临床转诊进行汗液氯化物检测确定的。结果:3例患者抗ttg IgA升高;其中一名被诊断患有乳糜泻,并接受无谷蛋白饮食治疗。14例(22%)患者空腹血糖受损。2例HbA1c持续升高(≥6.0%)的患者转介内分泌科评估糖尿病前期/CFRD。2例患者曲霉特异性IgG升高;1例总IgE明显升高(约1500 IU/mL),诊断为ABPA,需要全身皮质类固醇和抗真菌治疗。一些患者没有ABPA,但由于对多种过敏原的致敏,他们被转介到过敏症专家。结论:格鲁吉亚CF患儿存在CD、前驱糖尿病/CFRD和ABPA等合并症,如果不治疗,会对营养和肺功能产生负面影响。常规筛查葡萄糖异常、乳糜泻和ABPA应纳入国家CF护理方案,以便及时治疗并获得更好的结果。
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引用次数: 0
The match 2 study: Robotic assisted bronchoscopy with integrated imaging with assessment of digital tomosynthesis (DT) and augmented fluoroscopy (AF): Three-Dimensional accuracy as confirmed by cone beam computed tomography (CBCT). Match 2研究:机器人辅助支气管镜与数字断层合成(DT)和增强透视(AF)的综合成像评估:锥束计算机断层扫描(CBCT)证实的三维精度。
IF 3.1 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-29 DOI: 10.1016/j.rmed.2026.108693
Amit K Mahajan, Duy K Duong, Johanna Cortes, Krish Bhadra

Purpose: Robotic-assisted bronchoscopy (RAB) with embedded digital tomosynthesis (DT) provides real-time, intraoperative nodule localization. This study examines the performance of RAB with embedded DT and integrated AF to achieve tool-in-lesion (TIL) confirmation via cone beam computer tomography (CBCT).

Methods: This was a prospective, bicentric, single-arm, non-randomized observational trial. Thirty-one patients with peripheral pulmonary nodules underwent RAB with embedded DT. Navigation was guided by DT and augmented fluoroscopy (AF). Primary endpoints were successful navigation to target lesions and successful TIL as confirmed by CBCT. Secondary endpoints included diagnostic yield based on the strict Delphi consensus definition of diagnostic yield along with serious device or procedure-related adverse events.

Results: Thirty-one patients were enrolled across two sites. Thirty-one lung nodules were successfully biopsied. The mean lesion size measured by longest cross-sectional diameter was 16 mm (±6.7 mm). DT demonstrated TIL in 30 of 31 nodules (96.7 %), with one case resulting in tool-touching-lesion (TTL). Of the 30 nodules demonstrating TIL by DT, TIL was confirmed in 29 nodules by CBCT (concordance rate of 96.7 %). Overall TIL confirmed by CBCT was 29 of 31 nodules (93.5 %). A diagnosis was obtained in 30 of 31, resulting in a 96.7 % diagnostic yield by strict definition. Pneumothorax occurred in 1 of 31 cases (3 %).

Conclusions: RAB with embedded DT demonstrated a high rate of TIL confirmed by CBCT. The strong concordance between the DT with AF and CBCT demonstrates the reliability of DT and AF for real-time intraprocedural guidance.

目的:机器人辅助支气管镜(RAB)与嵌入式数字断层合成(DT)提供实时,术中结节定位。本研究考察了带有嵌入式DT和集成AF的RAB通过锥形束计算机断层扫描(CBCT)实现病灶内工具(TIL)确认的性能。方法:这是一项前瞻性、双中心、单组、非随机观察性试验。31例周围性肺结节患者行包埋DT的RAB。导航由DT和增强透视(AF)引导。主要终点是CBCT证实的成功导航到目标病变和成功TIL。次要终点包括基于严格的德尔菲诊断率共识定义的诊断率以及与设备或手术相关的严重不良事件。结果:来自两个地点的31名患者入组。31个肺结节成功活检。最长横截直径测量的平均病变大小为16 mm(±6.7 mm)。DT显示31个结节中有30个(96.7%)为TIL,其中1例导致工具接触病变(TTL)。30例经DT诊断为TIL的结节中,29例经CBCT证实为TIL(符合率为96.7%)。31个结节中有29个经CBCT证实为TIL(93.5%)。31例中有30例获得诊断,严格定义诊断率为96.7%。31例中有1例(3%)发生气胸。结论:CBCT证实RAB伴嵌入DT的TIL发生率高。DT与AF与CBCT之间的强一致性证明了DT和AF对实时术中指导的可靠性。
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引用次数: 0
Severity and phenotype of sleep-disordered breathing in Prader-Willi syndrome compared to obstructive sleep apnea syndrome in children 与儿童阻塞性睡眠呼吸暂停综合征相比,Prader-Willi综合征睡眠呼吸障碍的严重程度和表型
IF 3.1 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-29 DOI: 10.1016/j.rmed.2026.108694
Xueyun Xu , Yanyu He , Meng Lv , Jiapeng Ji , Bolin Chen , Zhiqing Liu , Jun Han , Qianqian Tong , Rongrong Xie , Yuqing Wang

Background

Sleep disordered breathing (SDB) is prevalent in individuals with Prader-Willi syndrome (PWS). However, its clinical characteristics, risk factors, and impact on sleep architecture remain incompletely understood. This retrospective case-control study aims to characterize respiratory events in PWS; asses body mass index (BMI)-SDB severity association; and quantify sleep architectural changes to inform PWS screening and management.

Methods

Children with PWS who underwent PSG in the Department of Respiratory Medicine, Children's Hospital of Soochow University from December 2020 to January 2025 were enrolled in this study. Age- and gender-matched control subjects of children diagnosed with obstructive sleep apnea-hypopnea syndrome (OSAS) without underlying comorbidities, evaluated using identical PSG equipment. SPSS30.0 was used to perform 1:2 matching according to age and gender. The clinical characteristics and PSG results were compared between groups. Correlations between BMI, adenoid/tonsil hypertrophy and the severity of SDB were analyzed.

Results

19 children with PWS underwent sleep monitoring, of whom 16 completed PSG. The PWS cohort (n = 16) included 9 males (56.3 %) and 7 females (43.8 %), ranging in age from 3.4 to 14.7 years (mean age: 8.4 ± 3.5 years), with a median BMI of 24.5 kg/m2 (IQR: 21.6–35.1). All 16 PWS children were diagnosed with OSAS, 75 % presenting moderate-to-severe OSAS (P < 0.001). Compared with the OSAS control group, the PWS group exhibited significantly higher BMI values (P < 0.001),fewer awakenings (P = 0.007) and a reduced proportion of NREM3 sleep (P = 0.040). While OSA predominates in the SDB spectrum of PWS, central sleep apnea (CSA), mixed apnea, and hypoventilation events were also observed, with all respiratory event indices significantly higher in PWS than controls (all P < 0.05). PWS children demonstrated significantly lower mean oxygen saturation and lowest oxygen saturation (LSaO2) (all P < 0.001), as well as higher oxygen desaturation index (ODI) and obstructive apnea-hypopnea index (OAHI) (all P < 0.005). BMI was positively correlated with obstructive apnea‐hypopnea index (OAHI) (r = 0.558, P = 0.025) and Hypopnea index (HI) (r = 0.639, P = 0.008), and negatively correlated with LSaO2 (r = −0.551, P = 0.027).

Conclusion

PWS children exhibit a diverse spectrum of SDB, with OSA as the dominant respiratory event type with abnormal arousal responses to respiratory events. The severity of SDB in PWS is strongly related to BMI. These findings highlight the critical role of obesity in exacerbating respiratory compromise and emphasize the necessity of routine PSG screening and targeted BMI management in PWS care.
睡眠呼吸障碍(SDB)在普瑞德-威利综合征(PWS)患者中很普遍。然而,其临床特征、危险因素和对睡眠结构的影响仍不完全清楚。本回顾性病例对照研究旨在描述PWS患者的呼吸事件特征;评估体重指数(BMI)与sdb严重程度的关联;量化睡眠结构变化,为PWS筛查和管理提供信息。方法选取2020年12月至2025年1月在苏州大学儿童医院呼吸内科接受PSG治疗的PWS患儿为研究对象。年龄和性别匹配的无潜在合并症的诊断为阻塞性睡眠呼吸暂停低通气综合征(OSAS)的儿童作为对照,使用相同的PSG设备进行评估。采用SPSS30.0按年龄、性别进行1:2匹配。比较两组患者的临床特征和PSG结果。分析BMI、腺样体/扁桃体肥大与SDB严重程度的相关性。结果19例PWS患儿接受睡眠监测,其中16例完成PSG。PWS队列(n = 16)包括9名男性(56.3%)和7名女性(43.8%),年龄3.4 ~ 14.7岁(平均年龄8.4±3.5岁),中位BMI为24.5 kg/m2 (IQR: 21.6 ~ 35.1)。所有16名PWS儿童均被诊断为OSAS,其中75%表现为中度至重度OSAS (P < 0.001)。与OSAS对照组相比,PWS组BMI值显著升高(P < 0.001),觉醒次数显著减少(P = 0.007), NREM3睡眠比例显著降低(P = 0.040)。PWS患者SDB谱中以OSA为主,还存在中枢性睡眠呼吸暂停(CSA)、混合性呼吸暂停和低通气事件,PWS患者所有呼吸事件指标均显著高于对照组(P < 0.05)。PWS患儿平均血氧饱和度和最低血氧饱和度(LSaO2)均显著降低(P < 0.001),血氧去饱和指数(ODI)和阻塞性呼吸暂停低通气指数(OAHI)均较高(P < 0.005)。BMI与阻塞性呼吸暂停低通气指数(OAHI) (r = 0.558, P = 0.025)、低通气指数(HI) (r = 0.639, P = 0.008)呈正相关,与LSaO2 (r = - 0.551, P = 0.027)呈负相关。结论pws患儿SDB表现多样,呼吸事件类型以OSA为主,呼吸事件唤醒反应异常。PWS患者SDB的严重程度与BMI密切相关。这些发现强调了肥胖在加剧呼吸系统损害中的关键作用,并强调了在PWS护理中进行常规PSG筛查和有针对性的BMI管理的必要性。
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引用次数: 0
Association between urinary metabolites of volatile organic compounds and lung function: A cross-sectional study. 尿中挥发性有机化合物代谢物与肺功能的关系:一项横断面研究。
IF 3.1 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-28 DOI: 10.1016/j.rmed.2026.108683
Jian Chen, Yan Li, Zhenzong Han, Jixiang Liu, Lin Hou

Background: Volatile organic compounds (VOCs), play a major role in exacerbating air pollution and present a threat to human health. However, the association between specific VOCs and lung function in the general population has not been extensively explored.

Objectives: Our study aimed to examine the correlation between urinary VOC metabolites (mVOCs) concentrations and lung function, among a typical sample of the adult population.

Methods: The correlation between urinary mVOCs and lung function was analyzed using logistic regression models, QG-C, WQS, and BKMR models were employed.

Results: Our study revealed that higher concentrations of certain urinary mVOCs significantly correlated with an increased risk of abnormal lung function, especially URXAMC and URXDHB. A significant nonlinear correlation was observed between URXDHB and FEV1 % pred <80 % (P for overall <0.001, P for nonlinear <0.001), and a nonlinear correlation was noted between URXAMC and the incidence of FEV1 % pred <80 % (P for overall, P for nonlinear = 0.012).

Conclusion: VOCs exposure is associated with compromised lung health, and particularly strong correlations exist between URXAMC/URXDHB and abnormal lung function; These findings provide new insights for respiratory disease prevention and control.

背景:挥发性有机化合物(VOCs)在加剧空气污染方面发挥着重要作用,并对人类健康构成威胁。然而,在普通人群中,特定挥发性有机化合物与肺功能之间的关系尚未得到广泛探讨。目的:我们的研究旨在研究尿中挥发性有机化合物代谢物(mVOCs)浓度与肺功能之间的关系,在一个典型的成年人样本中。方法:采用logistic回归模型,采用QG-C、WQS、BKMR模型分析尿VOC代谢物与肺功能的相关性。结果:我们的研究表明,尿中某些mVOCs浓度较高与肺功能异常风险增加显著相关,尤其是URXAMC和URXDHB。URXDHB与FEV1% pred < 80%之间存在显著的非线性相关(总体P < 0.001,非线性P < 0.001), URXAMC与FEV1% pred < 80%发生率之间存在非线性相关(总体P,非线性P = 0.012)。结论:VOC暴露与肺部健康受损相关,尤其是URXAMC/URXDHB与肺功能异常之间存在很强的相关性;这些发现为呼吸系统疾病的预防和控制提供了新的见解。
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引用次数: 0
The impact of stepping up treatment from LABA/LAMA to extrafine single inhaler triple therapy on exacerbations of Greek patients with Chronic Obstructive Pulmonary Disease: The IMPROVE study. 从LABA/LAMA到体外单吸入器三联治疗对希腊慢性阻塞性肺疾病患者加重的影响:改进研究
IF 3.1 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-28 DOI: 10.1016/j.rmed.2026.108682
Epaminondas Kosmas, Konstantinos Bartziokas, Stylianos Loukides, Petros Bakakos, Nikoletta Rovina, Niki Georgatou, Dimosthenis Papapetrou, Panos Katerelos, Evangelia Papapostolou, Petros Efstathopoulos, Paschalis Steiropoulos, Konstantinos Kostikas

Objective: Extrafine single inhaler triple therapy (efSITT) with beclometasone dipropionate, formoterol fumarate, and glycopyrronium (BDP/FF/G 87/5/9 μg) has shown clinical benefits in Chronic Obstructive Pulmonary Disease (COPD) patients, including fewer exacerbations in randomized controlled trials. The IMPROVE study evaluated its real-world effectiveness in Greece in COPD patients previously treated with dual bronchodilation, focusing on exacerbations and other clinical outcomes.

Methods: This prospective, multicenter, observational study was conducted over 52 weeks. The 1103 eligible patients had moderate-to-severe COPD, an indication for treatment with efSITT, and were symptomatic despite receiving dual bronchodilation. The number of exacerbations, COPD Assessment Test (CAT) score, lung function parameters, use of rescue medication and adherence were recorded at baseline (visit 1), 6 months (visit 2), and 12 months (visit 3) after treatment.

Results: The percentage of patients with ≥1 exacerbation decreased from 100 % at visit 1 to 23.1% at visit 3 (p < 0.001). The mean CAT score decreased from 22.5 points at visit 1, to 16.6 at visit 2 and 14.2 at visit 3 (p < 0.001 for all pair comparisons). The mean TAI score increased from 44.6 points at visit 1, to 47.1 at visit 2 and 47.6 at visit 3. (p < 0.001 for V1/2 and V1/3 pairs, p = 0.024 for V2/3). Between visit 1 and visit 3, mean FEV1 increased from 1.6 L to 1.7 L (p < 0.001, n = 396).

Conclusions: The IMPROVE findings indicate that extrafine BDP/FF/G improves clinical outcomes in symptomatic COPD patients previously treated with dual bronchodilation in a real-world setting in Greece.

目的:在随机对照试验中,双丙酸倍氯米松、富马酸福莫特罗和甘溴铵(BDP/FF/G 87/5/9 μg)的体外单吸入三联疗法(efSITT)在慢性阻塞性肺疾病(COPD)患者中显示出临床益处,包括更少的加重。改善研究评估了其在希腊对先前接受双重支气管扩张治疗的COPD患者的实际疗效,重点关注恶化和其他临床结果。方法:这项前瞻性、多中心、观察性研究进行了52周。1103例符合条件的患者患有中度至重度COPD,这是efSITT治疗的指征,尽管接受了双支气管扩张,但仍有症状。在治疗后的基线(访问1)、6个月(访问2)和12个月(访问3)记录加重次数、COPD评估测试(CAT)评分、肺功能参数、抢救药物的使用和依从性。结果:≥1次急性加重的患者百分比从第一次就诊时的100%下降到第3次就诊时的23.1% (p)。结论:改进研究结果表明,在希腊的现实世界环境中,体外BDP/FF/G改善了先前接受双重支气管扩张治疗的症状性COPD患者的临床结果。
{"title":"The impact of stepping up treatment from LABA/LAMA to extrafine single inhaler triple therapy on exacerbations of Greek patients with Chronic Obstructive Pulmonary Disease: The IMPROVE study.","authors":"Epaminondas Kosmas, Konstantinos Bartziokas, Stylianos Loukides, Petros Bakakos, Nikoletta Rovina, Niki Georgatou, Dimosthenis Papapetrou, Panos Katerelos, Evangelia Papapostolou, Petros Efstathopoulos, Paschalis Steiropoulos, Konstantinos Kostikas","doi":"10.1016/j.rmed.2026.108682","DOIUrl":"10.1016/j.rmed.2026.108682","url":null,"abstract":"<p><strong>Objective: </strong>Extrafine single inhaler triple therapy (efSITT) with beclometasone dipropionate, formoterol fumarate, and glycopyrronium (BDP/FF/G 87/5/9 μg) has shown clinical benefits in Chronic Obstructive Pulmonary Disease (COPD) patients, including fewer exacerbations in randomized controlled trials. The IMPROVE study evaluated its real-world effectiveness in Greece in COPD patients previously treated with dual bronchodilation, focusing on exacerbations and other clinical outcomes.</p><p><strong>Methods: </strong>This prospective, multicenter, observational study was conducted over 52 weeks. The 1103 eligible patients had moderate-to-severe COPD, an indication for treatment with efSITT, and were symptomatic despite receiving dual bronchodilation. The number of exacerbations, COPD Assessment Test (CAT) score, lung function parameters, use of rescue medication and adherence were recorded at baseline (visit 1), 6 months (visit 2), and 12 months (visit 3) after treatment.</p><p><strong>Results: </strong>The percentage of patients with ≥1 exacerbation decreased from 100 % at visit 1 to 23.1% at visit 3 (p < 0.001). The mean CAT score decreased from 22.5 points at visit 1, to 16.6 at visit 2 and 14.2 at visit 3 (p < 0.001 for all pair comparisons). The mean TAI score increased from 44.6 points at visit 1, to 47.1 at visit 2 and 47.6 at visit 3. (p < 0.001 for V1/2 and V1/3 pairs, p = 0.024 for V2/3). Between visit 1 and visit 3, mean FEV1 increased from 1.6 L to 1.7 L (p < 0.001, n = 396).</p><p><strong>Conclusions: </strong>The IMPROVE findings indicate that extrafine BDP/FF/G improves clinical outcomes in symptomatic COPD patients previously treated with dual bronchodilation in a real-world setting in Greece.</p>","PeriodicalId":21057,"journal":{"name":"Respiratory medicine","volume":" ","pages":"108682"},"PeriodicalIF":3.1,"publicationDate":"2026-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146093852","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Eligibility for biological treatments in COPD patients experiencing a severe COPD exacerbation 重度COPD加重期COPD患者接受生物治疗的资格
IF 3.1 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-28 DOI: 10.1016/j.rmed.2026.108681
Stavroula Zaneli , Agamemnon Bakakos , Konstantinos Bartziokas , Anastasia Papaporfyriou , Kyriaki Cholidou , Nektarios Anagnostopoulos , Georgios Zakynthinos , Evangelos Oikonomou , Angelos Vontetsianos , Nikolaos Chynkiamis , Christina Anagnostopoulou , Nikoletta Rovina , Petros Bakakos , Andriana I. Papaioannou

Introduction

Chronic obstructive pulmonary disease (COPD) exacerbations are important events in the natural history of the disease with debilitating consequences which include more rapid lung function decline, quality of life deterioration and increased risk of cardiovascular events and mortality. Inflammation in COPD is complex and is intrinsically less responsive to corticosteroids compared to asthma. Biologics could possibly reduce the burden of inflammation in selected patients.

Methods

In this single center retrospective study, we evaluated the eligibility of COPD patients hospitalized during the last 6 years in the respiratory department of a tertiary hospital for a severe COPD exacerbation, to receive either dupilumab or mepolizumab according to the inclusion criteria of their respective randomized controlled trials and GOLD 2026 recommendations.

Results

496 patients were included in the study, 83 (16.7 %) patients were eligible for treatment with mepolizumab and 29 (5.8 %) for treatment with dupilumab, while 413 (83.3 %) were not eligible for any of the biologics currently approved for COPD treatment. Patients who were eligible for biologics had lower FEV1/FVC ratio and had experienced more COPD exacerbations and more hospitalizations for COPD exacerbations in the previous year compared to those characterized as non-eligible. The main factor missing from non-eligible patients was treatment with triple inhaled medication, prior to hospitalization.

Conclusion

Only a minority of patients hospitalized due to severe COPD exacerbation would have been eligible to receive biologic therapy. Optimization of medical treatment including inhaled medication in addition to disease phenotyping are pivotal for the recognition of the patients which will benefit from the use of biologics.
慢性阻塞性肺疾病(COPD)恶化是该疾病自然史上的重要事件,其衰弱后果包括肺功能更快下降、生活质量恶化、心血管事件和死亡率风险增加。慢性阻塞性肺病的炎症是复杂的,与哮喘相比,其本质上对皮质类固醇的反应较弱。生物制剂可能会减轻某些患者的炎症负担。方法在这项单中心回顾性研究中,我们根据随机对照试验的纳入标准和GOLD 2026推荐,评估了过去6年在某三级医院呼吸科因严重COPD加重住院的COPD患者接受dupilumab或mepolizumab治疗的资格。结果496例患者纳入研究,83例(16.7%)患者适合mepolizumab治疗,29例(5.8%)患者适合dupilumab治疗,而413例(83.3%)患者不适合目前批准用于COPD治疗的任何生物制剂。与不符合条件的患者相比,符合生物制剂条件的患者FEV1/FVC比较低,并且在过去一年中经历了更多的COPD加重和更多的COPD加重住院治疗。不符合条件的患者缺少的主要因素是住院前三次吸入药物治疗。结论只有少数因严重COPD加重而住院的患者有资格接受生物治疗。除了疾病表型外,包括吸入药物在内的医疗治疗优化对于识别将从生物制剂使用中受益的患者至关重要。
{"title":"Eligibility for biological treatments in COPD patients experiencing a severe COPD exacerbation","authors":"Stavroula Zaneli ,&nbsp;Agamemnon Bakakos ,&nbsp;Konstantinos Bartziokas ,&nbsp;Anastasia Papaporfyriou ,&nbsp;Kyriaki Cholidou ,&nbsp;Nektarios Anagnostopoulos ,&nbsp;Georgios Zakynthinos ,&nbsp;Evangelos Oikonomou ,&nbsp;Angelos Vontetsianos ,&nbsp;Nikolaos Chynkiamis ,&nbsp;Christina Anagnostopoulou ,&nbsp;Nikoletta Rovina ,&nbsp;Petros Bakakos ,&nbsp;Andriana I. Papaioannou","doi":"10.1016/j.rmed.2026.108681","DOIUrl":"10.1016/j.rmed.2026.108681","url":null,"abstract":"<div><h3>Introduction</h3><div>Chronic obstructive pulmonary disease (COPD) exacerbations are important events in the natural history of the disease with debilitating consequences which include more rapid lung function decline, quality of life deterioration and increased risk of cardiovascular events and mortality. Inflammation in COPD is complex and is intrinsically less responsive to corticosteroids compared to asthma. Biologics could possibly reduce the burden of inflammation in selected patients.</div></div><div><h3>Methods</h3><div>In this single center retrospective study, we evaluated the eligibility of COPD patients hospitalized during the last 6 years in the respiratory department of a tertiary hospital for a severe COPD exacerbation, to receive either dupilumab or mepolizumab according to the inclusion criteria of their respective randomized controlled trials and GOLD 2026 recommendations.</div></div><div><h3>Results</h3><div>496 patients were included in the study, 83 (16.7 %) patients were eligible for treatment with mepolizumab and 29 (5.8 %) for treatment with dupilumab, while 413 (83.3 %) were not eligible for any of the biologics currently approved for COPD treatment. Patients who were eligible for biologics had lower FEV<sub>1</sub>/FVC ratio and had experienced more COPD exacerbations and more hospitalizations for COPD exacerbations in the previous year compared to those characterized as non-eligible. The main factor missing from non-eligible patients was treatment with triple inhaled medication, prior to hospitalization.</div></div><div><h3>Conclusion</h3><div>Only a minority of patients hospitalized due to severe COPD exacerbation would have been eligible to receive biologic therapy. Optimization of medical treatment including inhaled medication in addition to disease phenotyping are pivotal for the recognition of the patients which will benefit from the use of biologics.</div></div>","PeriodicalId":21057,"journal":{"name":"Respiratory medicine","volume":"253 ","pages":"Article 108681"},"PeriodicalIF":3.1,"publicationDate":"2026-01-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146090295","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
One-year lung function change and variability post allogeneic hematopoietic stem cell transplantation 同种异体造血干细胞移植后一年肺功能的变化和变异性
IF 3.1 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Pub Date : 2026-01-24 DOI: 10.1016/j.rmed.2026.108670
Kaj E.C. Blokland , Troy J. Cross , Fei Ni Hau , David Touma , David G. Chapman , G Kim Prisk , Sandra Rutting , Mark Barrios , Matthew Greenwood , Gregory G. King

Background and objective

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a well-established treatment for various haematologic and oncologic disorders, yet its clinical success is frequently compromised by complications such as pulmonary graft-versus-host disease (GvHD). Spirometry is the gold standard for monitoring and diagnosis, but it is insensitive to small airway changes. Oscillometry may complement spirometry as a way of detecting change in small airway function. This study assessed the longitudinal change and variability in spirometry and oscillometry following allo-HSCT and predictors of this change.

Methods

Longitudinal spirometry and oscillometry were retrospectively obtained from all patients (n = 374) who underwent allo-HSCT at Royal North Shore Hospital in Sydney, Australia, between January 2015 and December 2023.

Results

Baseline post allo-HSCT assessments showed significantly lower FEV1 and FVC in the allo-HSCT group compared to controls. Over the follow-up period, oscillometric indices displayed significant worsening of Rrs5 and Xrs5, whereas FEV1 did not significantly change. Severe cGvHD was associated with a modest decline in FEV1/FVC and Xrs5 trajectory. Notably, a subset of patients demonstrated discordant changes between spirometry and oscillometry, suggesting that oscillometry may capture early small airway dysfunction not evident on traditional spirometric measures.

Conclusion

These findings underscore the potential of oscillometry as a complementary tool in the routine monitoring of lung function post-allo-HSCT. By detecting subtle changes in small airway mechanics, oscillometry could facilitate earlier identification and intervention in patients at risk for developing pulmonary cGvHD, thereby improving long-term clinical outcomes.
背景和目的同种异体造血干细胞移植(allogeneic hematopoietic stem cell transplantation, alloo - hsct)是治疗多种血液学和肿瘤学疾病的一种行之有效的方法,但其临床成功常常受到诸如肺移植物抗宿主病(GvHD)等并发症的影响。肺活量测定法是监测和诊断的金标准,但它对微小的气道变化不敏感。振荡测量法可以作为肺活量测定法的补充,作为检测小气道功能变化的一种方法。本研究评估了同种异体造血干细胞移植后肺活量测定和振荡测量的纵向变化和可变性,以及这种变化的预测因素。方法回顾性分析2015年1月至2023年12月在澳大利亚悉尼皇家北岸医院接受同种异体造血干细胞移植的所有患者(n = 374)的纵向肺活量测定和振荡测量。结果:同种异体造血干细胞移植后基线评估显示,与对照组相比,同种异体造血干细胞移植组FEV1和FVC显著降低。在随访期间,振荡指标显示Rrs5和Xrs5显著恶化,而FEV1无显著变化。严重cGvHD与FEV1/FVC和Xrs5轨迹的适度下降相关。值得注意的是,一部分患者表现出肺活量测定法和振荡测量法之间的不一致变化,这表明振荡测量法可能捕捉到传统肺活量测量法不明显的早期小气道功能障碍。结论:这些发现强调了振荡测量法作为常规监测同种异体造血干细胞移植后肺功能的补充工具的潜力。通过检测小气道力学的细微变化,振荡测量法可以帮助早期识别和干预有发生肺部cGvHD风险的患者,从而改善长期临床结果。
{"title":"One-year lung function change and variability post allogeneic hematopoietic stem cell transplantation","authors":"Kaj E.C. Blokland ,&nbsp;Troy J. Cross ,&nbsp;Fei Ni Hau ,&nbsp;David Touma ,&nbsp;David G. Chapman ,&nbsp;G Kim Prisk ,&nbsp;Sandra Rutting ,&nbsp;Mark Barrios ,&nbsp;Matthew Greenwood ,&nbsp;Gregory G. King","doi":"10.1016/j.rmed.2026.108670","DOIUrl":"10.1016/j.rmed.2026.108670","url":null,"abstract":"<div><h3>Background and objective</h3><div>Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a well-established treatment for various haematologic and oncologic disorders, yet its clinical success is frequently compromised by complications such as pulmonary graft-versus-host disease (GvHD). Spirometry is the gold standard for monitoring and diagnosis, but it is insensitive to small airway changes. Oscillometry may complement spirometry as a way of detecting change in small airway function. This study assessed the longitudinal change and variability in spirometry and oscillometry following allo-HSCT and predictors of this change.</div></div><div><h3>Methods</h3><div>Longitudinal spirometry and oscillometry were retrospectively obtained from all patients (n = 374) who underwent allo-HSCT at Royal North Shore Hospital in Sydney, Australia, between January 2015 and December 2023.</div></div><div><h3>Results</h3><div>Baseline post allo-HSCT assessments showed significantly lower FEV<sub>1</sub> and FVC in the allo-HSCT group compared to controls. Over the follow-up period, oscillometric indices displayed significant worsening of Rrs<sub>5</sub> and Xrs<sub>5</sub>, whereas FEV<sub>1</sub> did not significantly change. Severe cGvHD was associated with a modest decline in FEV<sub>1</sub>/FVC and Xrs<sub>5</sub> trajectory. Notably, a subset of patients demonstrated discordant changes between spirometry and oscillometry, suggesting that oscillometry may capture early small airway dysfunction not evident on traditional spirometric measures.</div></div><div><h3>Conclusion</h3><div>These findings underscore the potential of oscillometry as a complementary tool in the routine monitoring of lung function post-allo-HSCT. By detecting subtle changes in small airway mechanics, oscillometry could facilitate earlier identification and intervention in patients at risk for developing pulmonary cGvHD, thereby improving long-term clinical outcomes.</div></div>","PeriodicalId":21057,"journal":{"name":"Respiratory medicine","volume":"252 ","pages":"Article 108670"},"PeriodicalIF":3.1,"publicationDate":"2026-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146023127","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Respiratory medicine
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