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Azithromycin and risk of COPD exacerbations in patients with and without Helicobacter pylori

机译:阿奇霉素和有无幽门螺杆菌患者的COPD病情加重

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Background Helicobacter pylori (HP) infection is associated with reduced lung function and systemic inflammation in chronic obstructive pulmonary disease (COPD) patients. Azithromycin (AZ) is active against HP and reduces the risk of COPD exacerbation. We determined whether HP infection status modifies the effects of AZ in COPD patients. MethodsPlasma samples from 1018 subjects with COPD who participated in the Macrolide Azithromycin (MACRO) in COPD Study were used to determine the HP infection status at baseline and 12?months of follow-up using a serologic assay. Based on HP infection status and randomization to either AZ or placebo (PL), the subjects were divided into 4 groups: HP+/AZ, HP-/AZ, HP+/PL, and HP-/PL. Time to first exacerbation was compared across the 4 groups using Kaplan-Meier survival analysis and a Cox proportional hazards model. The rates of exacerbation were compared using both the Kruskal-Wallis test and negative binomial analysis. Blood biomarkers at enrolment and at follow-up visits 3, 12, and 13 (1?month after treatment was stopped) months were measured. ResultsOne hundred eighty one (17.8%) patients were seropositive to HP. Non-Caucasian participants were nearly three times more likely to be HP seropositive than Caucasian participants (37.4% vs 13.6%; p p =?0.001) with the longest time in the HP+/AZ group (11.2?months, 95% CI; 8.4–12.5+) followed by the HP-/AZ group (8.0?months, 95% CI; 6.7–9.7). Hazard ratio (HR) for exacerbations was lowest in the HP+/AZ group after adjustment for age, sex, smoking status, ethnicity, history of peptic ulcer, dyspnea, previous hospital admission, GOLD grade of severity, and forced vital capacity (HR, 0.612; 95% CI, 0.442–0.846 vs HR, 0.789; 95% CI, 0.663–0.938 in the HP-/AZ group). Circulating levels of soluble tumor necrosis factor receptor-75 were reduced only in the HP+/AZ group after 3?months of AZ treatment (?0.87?±?0.31?μg/L; p =?0.002); levels returned to baseline after discontinuing AZ. ConclusionsAZ is effective in preventing COPD exacerbations in patients with HP seropositivity, possibly by modulating TNF pathways related to HP infection.
机译:背景幽门螺杆菌(HP)感染与慢性阻塞性肺疾病(COPD)患者的肺功能下降和全身炎症相关。阿奇霉素(AZ)具有抗HP活性,可降低COPD恶化的风险。我们确定了HP感染状态是否改变了COPD患者的AZ疗效。方法采用血清学分析方法,从参加COPD研究的大环内酯阿奇霉素(MACRO)的1018名COPD受试者的血浆样本中确定HP感染状况。根据HP感染状况和随机分组到AZ或安慰剂(PL),将受试者分为4组:HP + / AZ,HP- / AZ,HP + / PL和HP- / PL。使用Kaplan-Meier生存分析和Cox比例风险模型比较了4组首次发作的时间。使用Kruskal-Wallis检验和阴性二项式分析比较恶化率。在入组时和随访3、12和13月(停止治疗后1个月)测量血液生物标志物。结果一百八十一(17.8%)例患者血清阳性。非高加索人群HP血清阳性的可能性是高加索人群的3倍(37.4%比13.6%; pp = 0.001),是HP + / AZ组中时间最长的(11.2个月,95%CI; 8.4– 12.5+),其次是HP- / AZ组(8.0个月,95%CI; 6.7-9.7)。在校正了年龄,性别,吸烟状况,种族,消化性溃疡病史,呼吸困难,入院前的病史,严重程度为GOLD以及强迫肺活量之后,HP + / AZ组的急性加重危险比(HR)最低。在HP- / AZ组中为0.612; 95%CI为0.442-0.846,而HR为0.789; 95%CI为0.663-0.938)。 AZ治疗3个月后,HP + / AZ组中可溶性肿瘤坏死因子受体75的循环水平降低了(?0.87?±?0.31?μg/ L; p =?0.002)。停用AZ后血脂水平恢复到基线。结论AZ可能通过调节与HP感染相关的TNF途径来有效预防HP血清阳性患者的COPD恶化。

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