Cystic Fibrosis in Children
Conditions
Keywords
Cystic Fibrosis, Children, Microbiota, Quality of life, Probiotic supplement, CFTR modulators, elexacaftor-tezacaftor-ivacaftor
Brief summary
The aim of the present study is to investigate the effect of probiotic supplementation on GI related quality of life, through a randomised placebo-controlled clinical trial. Moreover, the invetigators wish to study CF microbiota and intestinal inflammation in the setting of probiotic supplementation and newly started treatment with a highly effective CF-specific treatment, elexacaftor-tezacaftor-ivacaftor (ETI). The proposed project has the potential to increase QoL and decrease GI morbidity in children with CF. If successful, the results of this study can contribute to alter the care of CF patients by including supplementation of probiotics in routine CF care. Morever, the study can provide much needed insights to GI microbiota and inflammation in pediatric CF patients.
Detailed description
The project targets pediatric patients with cystic fibrosis (CF), and has to work packages (WP). WP1 is an observational study, and WP2 is a randomised placebo-controlled clinical trial. The goal of the study is to investigate the effect of probiotics on pediatric CF patients' quality of life (QoL). Moreover the investigators wish to explore effects of both a highly effective CFTR modulator and probiotics on gut microbiota and intestinal inflammation. The primary question it aims to answer are: • Can probiotics improve GI related QoL in children with CF? Secondary aims are to: * Investigate GI microbiota and GI inflammation before and after commencement of the highly effective triple-combination elexacaftor-tezacaftor-ivacaftor (ETI) * Explore GI microbiota before and after treatment with probiotics vs. placebo * Study intestinal inflammation before and after treatment with probiotics vs. placebo * Examine body composition and its relation to lung function In WP1 participants will during routine examination before starting treatment with ETI be asked to deliver stool samples, and fill in QoL questionnaires. In WP2 participants will be randomized to intervention with probiotics or placebo, and the same parameters as in WP1 will also be collected.
Interventions
DIETARY_SUPPLEMENTMultistrain Probiotic
Participants will recieve a multi-strain probiotic daily for 6 months
DIETARY_SUPPLEMENTPlacebo - maltodextrin
Participants will recieve placebo/ maltodextri daily for 6 months
Sponsors
Norwegian National Advisory Unit on Rare Disorders, Oslo University Hospital
Oslo University Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)
Eligibility
Sex/Gender
ALL
Age
2 Years to 18 Years
Healthy volunteers
No
Inclusion criteria
for WP1: * CFTR mutations eligible for treatment with ETI * Age 2-18 years. Majority of patients will be 2-6 years of age as ETI was approved from 6 years of age in 2022, and will be available for children above 2 years from 2024. * Included in the Norwegian CF Register and consented to participation in CF general research biobank
Exclusion criteria
for WP1: * Other CFTR modulators commenced the last 6 months before inclusion * Use of probiotics or prebiotics last 2 months * Current pulmonary exacerbation Inclusion criteria for WP2: * Age 3-18 years * CFTR modulator treatment naïve or treated with CFTR modulator for at least 6 months * Included in the Norwegian CF Register and consented to participation in CF general research biobank
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Changes in GI related QoL using the questionnaire PedsQL GI | 0-6 months | PEDsQL GI has been validated for use in the CF population. Participants will be scored before and 6 months after treatment start with ETI (WP2), and before and after 6 months treatment with probiotics vs placebo (WP2). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Changes in microbiota | 0-6 months | Stool samples for microbiota will be collected using a collection kit provided to the participants at recruitment, and then after 6 month of ETI treamtment (WP1), or probiotic/placebo (WP2). Microbiota analysis will be done using 16s rRNA amplicon sequencing and reduced metagenome sequencing. |
| Changes in intestinal inflammation | 0-6 months | Stool samples for gut inflammation markers will be collected using a collection kit provided to the participants at recruitment and after 6 months of ETI treamtment (WP1), or probiotic/placebo (WP2. Levels of calprotectin, neopterin and myeloperoxidase will be measured. |
Countries
Norway
Outcome results
None listed