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Observational Study
. 2021 Feb 24;22(1):67.
doi: 10.1186/s12931-021-01653-8.

Sputum sample positivity for Haemophilus influenzae or Moraxella catarrhalis in acute exacerbations of chronic obstructive pulmonary disease: evaluation of association with positivity at earlier stable disease timepoints

Affiliations
Observational Study

Sputum sample positivity for Haemophilus influenzae or Moraxella catarrhalis in acute exacerbations of chronic obstructive pulmonary disease: evaluation of association with positivity at earlier stable disease timepoints

Lucio Malvisi et al. Respir Res. .

Abstract

Background: 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.

Methods: 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.

Results: 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.

Conclusions: 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.

Keywords: Bacterial identification; COPD; Culture; Exacerbation; Haemophilus influenzae; Moraxella catarrhalis; PCR; Vaccination.

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Conflict of interest statement

LM, LT, and AKA are employees of the GSK group of companies. AY is a consultant of ICON for the GSK group of companies. LT and AKA hold shares in the GSK group of companies and AKA has a patent PCT/EP2018/071860 – Methods of boosting immune responses – pending to the GSK group of companies. TMAW has received grants from the GSK group of companies during the conduct of this study. TMAW has also received grants from AstraZeneca, Synairgen, and MyMHealth and fees, reimbursement for travel and meeting attendance from Boehringer Ingelheim, Chiesi, and AstraZeneca, outside of the submitted work. In addition, TMAW has a patent 2018 US Patent 62/479562 – Immunogenic Composition, Use and Methods of Treatment – A novel vaccine to prevent exacerbations of COPD pending to the GSK group of companies. TMAW is the Founder and Director of MyMHealth Ltd. All authors declare having no other non-financial relationships and activities.

Figures

Fig. 1
Fig. 1
Plain language summary
Fig. 2
Fig. 2
Positivity of first or second exacerbation by bacterial presence or absence at reference timepoint. Shown as percentage (95% CI) of samples that were positive for Haemophilus influenzae or Moraxella catarrhalis at first or second exacerbation given pathogen’s presence or absence at a the screening visit, b any stable visit within 90 days before the first exacerbation, or c any stable visit within 90 days before the second exacerbation (Full cohort, Year 1 and Year 2). 95% CI, 95% confidence interval; Culture +/− , H. influenzae- or M. catarrhalis-positive/negative by culture-based assay; PCR +/−, H. influenzae- or M. catarrhalis-positive/negative by PCR assay; p-value, p-value for difference between percentages, calculated by equality test between two independent proportions. Numbers in square brackets indicate the number of sputum samples positive at exacerbation/number positive or negative at reference timepoint
Fig. 3
Fig. 3
Risk ratio values for Haemophilus influenzae presence at exacerbation. Shown as risk ratio for H. influenzae presence at first exacerbation, given H. influenzae presence or absence at a the screening visit or b any stable visit within 90 days before the first exacerbation. c Risk ratio for H. influenzae presence at second exacerbation given H. influenzae presence or absence at any stable visit within 90 days before the second exacerbation (Full cohort, Year 1 and Year 2). a p-value < 0.001 for culture and PCR; b p-value < 0.0001 for culture and PCR; c p-value < 0.001 for PCR. Other p-values not statistically significant. 95% CI, 95% confidence interval
Fig. 4
Fig. 4
Risk ratio values for Moraxella catarrhalis presence at exacerbation. Shown as risk ratio for M. catarrhalis presence at first exacerbation, given M. catarrhalis presence or absence at a the screening visit or b any stable visit within 90 days before the first exacerbation. c Risk ratio for M. catarrhalis presence at second exacerbation, given M. catarrhalis presence or absence at any stable visit within 90 days before the second exacerbation (Full cohort, Year 1 and Year 2). a p-value = 0.03 for PCR; b p-value < 0.01 for PCR; c p-value = 0.03 for culture. Other p-values not statistically significant. 95% CI, 95% confidence interval

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