GSK, Siena, Italy.
ICON, Chennai, India c/o GSK, Wavre, Belgium.
Respir Res. 2021 Feb 24;22(1):67. doi: 10.1186/s12931-021-01653-8.
Infection with Haemophilus influenzae (Hi) or Moraxella catarrhalis (Mcat) is a risk factor for exacerbation in chronic obstructive pulmonary disease (COPD). The ability to predict Hi- or Mcat-associated exacerbations may be useful for interventions developed to reduce exacerbation frequency.
In a COPD observational study, sputum samples were collected at monthly stable-state visits and at exacerbation during two years of follow-up. Bacterial species (Hi, Mcat) were identified by culture and quantitative PCR assay. Post-hoc analyses were conducted to assess: (1) first Hi- or Mcat-positive exacerbations given presence or absence of Hi or Mcat at the screening visit (stable-state timepoint); (2) first Hi- or Mcat-positive exacerbations given presence or absence of Hi or Mcat at stable timepoints within previous 90 days; (3) second Hi- or Mcat-positive exacerbations given presence or absence of Hi or Mcat at stable timepoints within previous 90 days. Percentages and risk ratios (RRs) with 95% confidence intervals were calculated.
PCR results for analyses 1, 2 and 3 (samples from 84, 88 and 83 subjects, respectively) showed that the risk of an Hi- or Mcat-positive exacerbation is significantly higher if sputum sample was Hi- or Mcat-positive than if Hi- or Mcat-negative at previous stable timepoints (apart from Mcat in analysis 3); RRs ranged from 2.1 to 3.2 for Hi and 1.9 to 2.6 for Mcat.For all analyses, the percentage of Hi- or Mcat-positive exacerbations given previous Hi- or Mcat-positive stable timepoints was higher than the percentage of Hi- or Mcat-positive exacerbations if Hi- or Mcat-negative at previous stable timepoints. Percentage of Hi- or Mcat-positive exacerbations given previous Hi- or Mcat-negative stable timepoints was 26.3%-37.0% for Hi and 17.6%-19.7% for Mcat.
Presence of Hi or Mcat at a stable timepoint was associated with a higher risk of a subsequent Hi- or Mcat-associated exacerbation compared with earlier absence. However, a large percentage of Hi- or Mcat-associated exacerbations was not associated with Hi/Mcat detection at an earlier timepoint. This suggests that administration of an intervention to reduce these exacerbations should be independent of bacterial presence at baseline. Trial Registration https://clinicaltrials.gov/ ; NCT01360398, registered May 25, 2011.
流感嗜血杆菌(Hi)或卡他莫拉菌(Mcat)感染是慢性阻塞性肺疾病(COPD)恶化的危险因素。预测 Hi 或 Mcat 相关恶化的能力可能有助于开发减少恶化频率的干预措施。
在 COPD 观察性研究中,每月在稳定状态就诊时采集痰标本,并在两年的随访期间采集恶化时的标本。通过培养和定量 PCR 检测鉴定细菌种类(Hi、Mcat)。进行了事后分析以评估:(1)在筛选就诊(稳定状态时间点)时存在或不存在 Hi 或 Mcat 的情况下,首次出现 Hi 或 Mcat 阳性恶化;(2)在之前 90 天内的稳定时间点存在或不存在 Hi 或 Mcat 的情况下,首次出现 Hi 或 Mcat 阳性恶化;(3)在之前 90 天内的稳定时间点存在或不存在 Hi 或 Mcat 的情况下,第二次出现 Hi 或 Mcat 阳性恶化。计算了百分比和风险比(RR)及其 95%置信区间。
分析 1、2 和 3 的 PCR 结果(分别来自 84、88 和 83 名受试者的样本)表明,如果痰样本为 Hi 或 Mcat 阳性,则 Hi 或 Mcat 阳性恶化的风险显著高于之前稳定时间点为 Hi 或 Mcat 阴性的情况(除了分析 3 中的 Mcat);RR 范围为 Hi 为 2.1 至 3.2,Mcat 为 1.9 至 2.6。对于所有分析,与之前稳定时间点为 Hi 或 Mcat 阴性的情况下相比,之前 Hi 或 Mcat 阳性稳定时间点的 Hi 或 Mcat 阳性恶化的百分比更高。之前 Hi 或 Mcat 阴性稳定时间点的 Hi 或 Mcat 阳性恶化的百分比为 Hi 为 26.3%-37.0%,Mcat 为 17.6%-19.7%。
与之前不存在相比,稳定时间点存在 Hi 或 Mcat 与随后的 Hi 或 Mcat 相关恶化的风险更高。然而,很大一部分 Hi 或 Mcat 相关恶化与更早时间点的 Hi/Mcat 检测无关。这表明,为减少这些恶化而给予干预措施不应依赖于基线时的细菌存在。
https://clinicaltrials.gov/;NCT01360398,于 2011 年 5 月 25 日注册。