# Dietary recommendations for people with cystic fibrosis, a relevantly changing field

**Authors:** Jochen G. Mainz, Carlos Zagoya

PMC · DOI: 10.1016/j.jped.2026.101500 · Jornal de Pediatria · 2026-01-30

## Full-text entities

- **Genes:** CFTR (CF transmembrane conductance regulator) [NCBI Gene 1080] {aka ABC35, ABCC7, CF, CFTR/MRP, MRP7, TNR-CFTR}
- **Diseases:** obesity (MESH:D009765), diabetes (MESH:D003920), cardiovascular pathologies (MESH:D002318), infection (MESH:D007239), death (MESH:D003643), meconium-ileus (MESH:D000074270), constipation (MESH:D003248), Malnutrition (MESH:D044342), DIOS (MESH:D007415), CF (MESH:D003550), intussusception (MESH:D007443), diarrhea (MESH:D003967), metabolic (MESH:D008659), Overweight (MESH:D050177), underweight (MESH:D013851), gastric hyperacidity (MESH:D013272), loss of pulmonary function (OMIM:608852), metabolic syndrome (MESH:D024821), EPI (MESH:D010188), respiratory failure (MESH:D012131), failure to thrive (MESH:D005183), weight gain (MESH:D015430), chronic (MESH:D002908), inflammation (MESH:D007249), inherited disease (MESH:D030342), lung function loss (MESH:D055370), prolapses (MESH:D011391)
- **Chemicals:** elexacaftor (MESH:C000629074), carbohydrate (MESH:D002241), ivacaftor (MESH:C545203), AEDK (-), tezacaftor (MESH:C000625213), fat (MESH:D005223)
- **Species:** Pseudomonas aeruginosa (species) [taxon 287], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** F508del, G551D

## Full text

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## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC12881749/full.md

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Source: https://tomesphere.com/paper/PMC12881749