Distinct Gastrointestinal Symptom Phenotypes in Adults with Cystic Fibrosis are linked to complications and medication use

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Authors: J. Holaman, D. Sills, Hisham A. Saumtally, Charlotte Johnson, A. Flores Recto, Ryan Marsh, Andrew Prayle, Tanya Marie Monaghan, Luca Marciani, Robin C. Spiller, Helen I Barr, Damian G. Downey
+4 more Christopher van der Gast, Daniel Edgar Peckham, Iain D. Stewart, Smyth R Alan
Cited by: 1
References: 42

Abstract

ABSTRACT Background and aims Gastrointestinal symptoms remain common in adults with cystic fibrosis (CF) despite cystic fibrosis transmembrane conductance regulator modulator use, suggesting persistent and heterogeneous gut dysfunction. This prospective observational study tests the hypothesis that distinct gut symptom phenotypes in CF can be observed and linked to underlying mechanisms. Methods Adults from three UK CF centres completed the Gastrointestinal Symptom Rating Scale, Patient Assessment of Constipation Symptoms and a bowel-habit questionnaire. Latent class analysis using an ordinal logistic model was applied to 36 symptom indicators. Associations between phenotypes and demographic, clinical, and treatment variables were examined using generalised linear models. Results Three hundred participants completed questionnaires (54% male; median 31 years). We identified four symptom phenotypes: mild; moderate-constipation predominant; moderate-diarrhoea predominant and severe. The severe phenotype was associated with gastroesophageal reflux (RRR 2.86; 95%CI: 1.30-6.31; p=0.009), distal intestinal obstruction syndrome (RRR 2.46; 95%CI: 1.04-5.81; p=0.04), proton pump inhibitor (RRR 3.29; 95%CI 1.39-7.74; p=0.007), and laxative use (RRR 6.13; 95%CI 2.54-14.84; p

Fields of Study & Subjects

Cystic Fibrosis Research Advances Gastrointestinal motility and disorders Gastroesophageal reflux and treatments

Publication details

Journal / source
medRxiv
Publisher
openRxiv
Publication date
21 January 2026
Document type
Preprint