Evidence map›Paper›PMID 41940508›Full record

ReviewPediatric pulmonology2026

Patient-Derived Intestinal Organoids in the Global Cystic Fibrosis Landscape.

Suzanne Kroes, Jennifer L Taylor-Cousar, Marco Zampoli, Bülent Karadag, Cornelis K van der Ent, Karin M de Winter-de Groot, Jeffrey M Beekman, Sacha Spelier

Abstract readReview
In one paragraph

Review in Pediatric pulmonology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Suzanne KroesDepartment of Paediatric Pulmonology, Wilhelmina Children's Hospital - University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.
Jennifer L Taylor-CousarDepartments of Internal Medicine and Pediatrics Denver, National Jewish Health, Denver, Colorado, USA.
Marco ZampoliDepartment of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital, University of Cape Town, Cape Town, South Africa.ORCID https://orcid.org/0000-0002-6899-6137
Bülent KaradagDivision of Pediatric Pulmonology, Faculty of Medicine, Marmara University, Istanbul, Turkey.ORCID https://orcid.org/0000-0003-0605-8871
Cornelis K van der EntDepartment of Paediatric Pulmonology, Wilhelmina Children's Hospital - University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.
Karin M de Winter-de GrootDepartment of Paediatric Pulmonology, Wilhelmina Children's Hospital - University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.
Jeffrey M BeekmanDepartment of Paediatric Pulmonology, Wilhelmina Children's Hospital - University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.
Sacha SpelierDepartment of Paediatric Pulmonology, Wilhelmina Children's Hospital - University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cystic fibrosis (CF) care has advanced rapidly, yet diagnosis and inclusion in patient registries remain severely limited in low- and middle-income countries (LMICs). Barriers include restricted newborn screening, limited availability of sweat chloride testing, and underrepresentation of non-European CFTR variants in standard panels. Sparse registries further impede epidemiological insight and resource planning. Also, access to comprehensive CF care remains a major challenge in LMICs, where limitations in basic therapies, including pancreatic enzyme replacement, airway clearance strategies, and infection control, continue to result in markedly reduced life expectancy. Within this context, access to CFTR modulators (CFTRm) represents an additional and critical barrier, constrained by prohibitive costs, restricted variant eligibility, and few tiered pricing mechanisms. Patient-derived intestinal organoids (PDIOs) offer a versatile platform to help address some of these gaps. PDIOs enable functional diagnosis, genotype-phenotype characterization, and renewable material for comprehensive CFTR sequencing and drug testing, including for rare variants. While implementation in LMICs is challenging, targeted mentorship, collaborative screening pipelines, and sustained funding could expand access. Integrating PDIOs into CF care could help bridge some global disparities, but success will require coordinated scientific, clinical, and policy efforts.

Indexed as

Cystic FibrosisIntestinesOrganoidsCystic Fibrosis Transmembrane Conductance RegulatorDeveloping CountriesHumansCystic Fibrosis Transmembrane Conductance Regulatorcystic fibrosisdiagnosticsindividualized treatmentintestinal organoidsLMIC

Identifiers

PMID41940508
PMCPMC13051416

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.