Treatable traits in children with bronchiectasis

Bronchiectasis in children is a heterogeneous, chronic respiratory condition for which standardised, evidence-based management is essential. While international guidelines have improved diagnostic and therapeutic consistency, the treatable traits (TT) approach offers a complementary precision-medicine framework aimed at identifying all clinically relevant, measurable, and modifiable factors in individual patients. Through a comprehensive literature review, we identified 40 potential TT in paediatric bronchiectasis, spanning aetiological, pulmonary, extrapulmonary, and behavioural/environmental domains. However, the level of evidence supporting many TT remains limited in children, with most data extrapolated from adults or other respiratory diseases. This framework should therefore be considered dynamic, guiding systematic assessment while emphasising the urgent need for paediatric-specific clinical trials.

Authors

Institutions

Publication Details

Journal
Paediatric Respiratory Reviews
Published
2026-02-01
DOI
https://doi.org/10.1016/j.prrv.2026.02.002
Primary Topic
Cystic Fibrosis Research Advances
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Treatable traits in children with bronchiectasis

Apolline Gonsard, Rola Abou Taam, David Drummond, Joséphine Annereau et al.
Paediatric Respiratory Reviews
Cystic Fibrosis Research Advances
article

Treatable traits in children with bronchiectasis

Apolline Gonsard, Rola Abou Taam, David Drummond, Joséphine Annereau, Isabelle Sermet-Gaudelus, Anaïs Le, Charlotte Roy, Christophe Delacourt, Alice Hadchouel
article en

Abstract

Bronchiectasis in children is a heterogeneous, chronic respiratory condition for which standardised, evidence-based management is essential. While international guidelines have improved diagnostic and therapeutic consistency, the treatable traits (TT) approach offers a complementary precision-medicine framework aimed at identifying all clinically relevant, measurable, and modifiable factors in individual patients. Through a comprehensive literature review, we identified 40 potential TT in paediatric bronchiectasis, spanning aetiological, pulmonary, extrapulmonary, and behavioural/environmental domains. However, the level of evidence supporting many TT remains limited in children, with most data extrapolated from adults or other respiratory diseases. This framework should therefore be considered dynamic, guiding systematic assessment while emphasising the urgent need for paediatric-specific clinical trials.

Paediatric Respiratory Reviews
Délégation Paris 5 (FR), Hôpital Necker-Enfants Malades (FR), Inserm (FR), Université Paris Cité (FR), Institut Necker Enfants Malades (FR), Assistance Publique – Hôpitaux de Paris (FR)
Openalex Percentile: Top 64%
Cystic Fibrosis Research Advances
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Treatable traits in children with bronchiectasis — Apolline Gonsard, Rola Abou Taam, et al. · Paediatric Respiratory Reviews (2026) | TGRS Research Map | TGRS