生物质烟雾相关慢性阻塞性肺病患者的呼出一氧化氮(FeNO)分数。

Q1 Medicine
Juan Silva-Gallardo, Raúl H Sansores, Alejandra Ramírez-Venegas, Robinson E Robles Hernández, Gustavo I Centeno-Saenz, Rafael J Hernández-Zenteno
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引用次数: 0

摘要

慢性阻塞性肺病(COPD)是一种以局部和全身炎症为特征的疾病,与危险因素无关;在病情加重时,这种炎症会加剧和扩大。人们一直在寻找一种实用的炎症标记物,并且这种标记物在随访中具有适用的预测价值。在哮喘方面, FeNO 表现出了卓越的性能,在烟草烟雾慢性阻塞性肺疾病(COPD-TS)中也进行了研究。据我们所知,尚未对生物质烟雾慢性阻塞性肺病(COPD-BS)进行过评估:测量 COPD-BS 患者的 FeNO 水平,并将其与 COPD-TS 稳定期患者和健康对照组的 FeNO 水平进行比较:横向、观察性、描述性、比较性和分析性研究。共 57 名患者,包括 23 名 COPD-BS 患者、17 名 COPD-TS 患者和 17 名健康对照组受试者。研究采用在线化学发光技术对所有这些患者进行了氧化亚铁的测量,测量值以十亿分之一(ppb)为单位进行分析:结果发现,慢性阻塞性肺疾病-BS 组和慢性阻塞性肺疾病-TS 组的 FeNO 值相似,而健康组和慢性阻塞性肺疾病稳定组(两组)的 FeNO 值有显著差异。在所有组别中,肺功能和症状与 FeNO 之间均未发现相关性:结论:COPD-BS 和 COPD-TS 中稳定期 COPD 患者的 FeNO 水平以相似的方式升高,与健康受试者相比差异显著。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fractional Exhaled Nitric Oxide (FeNO) in Biomass Smoke-Associated Chronic Obstructive Pulmonary Disease.

Chronic Obstructive Pulmonary Disease (COPD) is a disease characterized by local and systemic inflammation independently of the risk factor; during the exacerbations, such inflammation is accentuated and amplified. A practical inflammatory marker and one with an applicable predictive value in the follow-up has been sought. FeNO has shown an excellent performance in that respect within the context of asthma and has also been studied in tobacco-smoke COPD (COPD-TS). In Biomass-smoke COPD (COPD-BS), this, to our knowledge, has not been evaluated.

Objective: To measure FeNO levels in patients with COPD-BS and to compare these with those of patients with stable COPD-TS and in healthy controls.

Methods: Transversal, observational, descriptive, comparative, and analytical study. A total of 57 patients, including 23 with COPD-BS, 17 with COPD-TS, and 17 healthy control subjects. The measurement of FeNO was carried out on all of these by means of the on-line chemiluminescence technique; the values were expressed in parts per billion (ppb) for their analysis.

Results: It was observed that the FeNO values were similar between COPD-BS and COPD-TS and were significantly different between the healthy and stable COPD (both groups). No correlation was found between pulmonary function and symptoms with FeNO in any of the groups.

Conclusions: The level of FeNO in stable COPD is found to be increased in a similar manner in COPD-BS and COPD-TS, with a significant difference on comparing it with that of the healthy subjects.

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