Paper Details 
Original Abstract of the Article :
Lumacaftor-ivacaftor is a cystic fibrosis transmembrane conductance regulator (CFTR) modulator combination approved for patients with cystic fibrosis (CF) who are homozygous for the F508del allele. This treatment showed significant clinical improvement; however, few studies have addressed the evolut...See full text at original site
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引用元:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10100832/

データ提供:米国国立医学図書館(NLM)

The Impact of Lumacaftor-Ivacaftor on Airway Microbiota and Inflammation in Cystic Fibrosis Patients

Lumacaftor-ivacaftor, a combination therapy for cystic fibrosis (CF), has shown promise in improving lung function and reducing symptoms. This study investigates the impact of this treatment on the airway microbiota-mycobiota and inflammation in CF patients.

Lumacaftor-Ivacaftor: A Complex Impact on Airway Microbiota

The researchers found that lumacaftor-ivacaftor treatment resulted in significant improvements in body mass index and reduced intravenous antibiotic courses. However, the study also revealed a complex impact on the airway microbiota-mycobiota, with the evolution of the airway ecosystem depending on the patient's characteristics at treatment initiation, particularly the presence of chronic colonization with Pseudomonas aeruginosa.

Early Intervention: A Key to Success

This study emphasizes the importance of early initiation of CFTR modulator therapy, ideally before chronic colonization with P. aeruginosa. The researchers suggest that early intervention with lumacaftor-ivacaftor may help to maintain a more balanced airway microbiota and reduce the risk of persistent inflammation and lung damage.

Dr. Camel's Conclusion

Just as a camel adapts to the ever-changing desert landscape, CF patients require a personalized approach to treatment. This study provides valuable insights into the impact of lumacaftor-ivacaftor on the airway ecosystem, highlighting the importance of early intervention for optimizing patient outcomes.
Date :
  1. Date Completed n.d.
  2. Date Revised 2023-04-15
Further Info :

Pubmed ID

36971560

DOI: Digital Object Identifier

PMC10100832

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Languages

English

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