Literature DB >> 31428412

A high prevalence of chronic gastrointestinal symptoms in adults with cystic fibrosis is detected using tools already validated in other GI disorders.

Bu'Hussain Hayee1, Kerry-Lee Watson2, Sanchika Campbell3, Anna Simpson3, Emma Farrell2, Penelope Hutchings2, Patricia Macedo2, Felicity Perrin2, Kevin Whelan4, Caroline Elston2.   

Abstract

Background: People with cystic fibrosis (CF) report a variety of gastrointestinal (GI) symptoms, independent of pancreatic enzyme insufficiency (PEI), reminiscent of other chronic GI disorders. There are currently no accepted or validated assessment tools and neither the range, frequency nor severity of GI symptoms has been systematically described in CF. We present results of a cross-sectional study using established tools and compare them to current measures of quality of life (QOL).
Methods: Consecutive patients attending specialist CF appointments were asked to complete questionnaires including the GI Symptom Rating Scale (GSRS); Irritable Bowel Syndrome Symptom Severity Score (IBS-SSS) and Cystic Fibrosis Questionnaire (CFQ-R). Questionnaire terminology was altered to replace references to 'IBS' with 'GI symptoms'.
Results: In total, 107 patients were recruited (mean age, 27.8 ± 9.6 years; 60 female), and 94 (88%) had PEI. Body mass index was 22.1 ± 3.6 kg/m2, forced expiratory volume in one second was 59 + 27.7% predicted. Fifty-three (49.5%) were p.Phe508del homozygous. Overall 69/107 (65%) reported significant GI symptoms independent of PEI or adherence to pancreatic enzyme replacement therapy (PERT), with the four most frequent being attributable to the lower GI tract: bloating/distension, flatulence, abdominal pain and borborygmi (gurgling). There was no numerical correlation between any CFQ-R domain (particularly Digestion domain) and GSRS or SSS.
Conclusion: This is the first systematic study measuring GI symptoms in CF using validated GI tools. Symptoms are not related to PERT or genotype and appear to be captured well by the GSRS. Further research will study longitudinal changes with treatment, and therapeutic trials in CF may use these tools to demonstrate a positive impact on 'non-respiratory' symptoms and QOL.

Entities:  

Keywords:  Cystic fibrosis; gastrointestinal; symptom score; validated

Mesh:

Year:  2019        PMID: 31428412      PMCID: PMC6683632          DOI: 10.1177/2050640619841545

Source DB:  PubMed          Journal:  United European Gastroenterol J        ISSN: 2050-6406            Impact factor:   4.623


  34 in total

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Review 2.  Irritable bowel syndrome.

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Journal:  Nat Rev Dis Primers       Date:  2016-03-24       Impact factor: 52.329

3.  Small intestine bacterial overgrowth does not correspond to intestinal inflammation in cystic fibrosis.

Authors:  Aleksandra Lisowska; Edyta Madry; Andrzej Pogorzelski; Jarosław Szydłowski; Andrzej Radzikowski; Jarosław Walkowiak
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4.  Development and validation of the Patient Assessment of Constipation Quality of Life questionnaire.

Authors:  Patrick Marquis; Christine De La Loge; Dominique Dubois; Anne McDermott; Olivier Chassany
Journal:  Scand J Gastroenterol       Date:  2005-05       Impact factor: 2.423

5.  Intestinal inflammation is a frequent feature of cystic fibrosis and is reduced by probiotic administration.

Authors:  E Bruzzese; V Raia; G Gaudiello; G Polito; V Buccigrossi; V Formicola; A Guarino
Journal:  Aliment Pharmacol Ther       Date:  2004-10-01       Impact factor: 8.171

6.  Outcome measures in irritable bowel syndrome: comparison of psychometric and methodological characteristics.

Authors:  C J Bijkerk; N J de Wit; J W M Muris; R H Jones; J A Knottnerus; A W Hoes
Journal:  Am J Gastroenterol       Date:  2003-01       Impact factor: 10.864

7.  Normal mouse intestinal mucus release requires cystic fibrosis transmembrane regulator-dependent bicarbonate secretion.

Authors:  Mary Abigail S Garcia; Ning Yang; Paul M Quinton
Journal:  J Clin Invest       Date:  2009-08-24       Impact factor: 14.808

8.  Linaclotide activates guanylate cyclase-C/cGMP/protein kinase-II-dependent trafficking of CFTR in the intestine.

Authors:  Md Kaimul Ahsan; Boris Tchernychev; Marco M Kessler; Robert M Solinga; David Arthur; Cristina I Linde; Inmaculada Silos-Santiago; Gerhard Hannig; Nadia A Ameen
Journal:  Physiol Rep       Date:  2017-06

9.  Colon Hypersensitivity to Distension, Rather Than Excessive Gas Production, Produces Carbohydrate-Related Symptoms in Individuals With Irritable Bowel Syndrome.

Authors:  Giles Major; Sue Pritchard; Kathryn Murray; Jan Paul Alappadan; Caroline L Hoad; Luca Marciani; Penny Gowland; Robin Spiller
Journal:  Gastroenterology       Date:  2016-10-14       Impact factor: 22.682

10.  Distinct Abnormalities of Small Bowel and Regional Colonic Volumes in Subtypes of Irritable Bowel Syndrome Revealed by MRI.

Authors:  Ching Lam; Gemma Chaddock; Luca Marciani Laurea; Carolyn Costigan; Eleanor Cox; Caroline Hoad; Susan Pritchard; Penny Gowland; Robin Spiller
Journal:  Am J Gastroenterol       Date:  2016-12-13       Impact factor: 10.864

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  7 in total

1.  To establish a treatment for GI symptoms of cystic fibrosis, it is necessary to develop a symptom evaluation tool.

Authors:  Hidekazu Suzuki
Journal:  United European Gastroenterol J       Date:  2019-06-02       Impact factor: 4.623

Review 2.  Luminal Gastrointestinal Manifestations of Cystic Fibrosis.

Authors:  Samuel J Burton; Christine Hachem; James M Abraham
Journal:  Curr Gastroenterol Rep       Date:  2021-03-23

3.  Designing the GALAXY study: Partnering with the cystic fibrosis community to optimize assessment of gastrointestinal symptoms.

Authors:  A Jay Freeman; Meghana Sathe; Enid Aliaj; Drucy Borowitz; Barbra Fogarty; Christopher H Goss; Steven Freedman; Sonya L Heltshe; Umer Khan; Dara Riva; Christina Roman; Melita Romasco; Sarah Jane Schwarzenberg; Carmen A Ufret-Vincenty; Baha Moshiree
Journal:  J Cyst Fibros       Date:  2021-01-13       Impact factor: 5.527

4.  High Prevalence and Gender-Related Differences of Gastrointestinal Manifestations in a Cohort of DM1 Patients: A Perspective, Cross-Sectional Study.

Authors:  Alessia Perna; Daria Maccora; Salvatore Rossi; Tommaso Filippo Nicoletti; Maria Assunta Zocco; Vittorio Riso; Anna Modoni; Antonio Petrucci; Venanzio Valenza; Antonio Grieco; Luca Miele; Gabriella Silvestri
Journal:  Front Neurol       Date:  2020-06-12       Impact factor: 4.003

5.  How can we relieve gastrointestinal symptoms in people with cystic fibrosis? An international qualitative survey.

Authors:  Sherie Smith; Nicola Rowbotham; Gwyneth Davies; Katie Gathercole; Sarah J Collins; Zoe Elliott; Sophie Herbert; Lorna Allen; Christabella Ng; Alan Smyth
Journal:  BMJ Open Respir Res       Date:  2020-09

6.  Correlates of Pancreatic Enzyme Replacement Therapy Intake in Adults with Cystic Fibrosis: Results of a Cross-Sectional Study.

Authors:  Mette F Olsen; Maria S Kjøller-Svarre; Grith Møller; Terese L Katzenstein; Bibi U Nielsen; Tacjana Pressler; Jack I Lewis; Inger H Mathiesen; Christian Mølgaard; Daniel Faurholt-Jepsen
Journal:  Nutrients       Date:  2022-03-22       Impact factor: 5.717

7.  The NHE3 Inhibitor Tenapanor Prevents Intestinal Obstructions in CFTR-Deleted Mice.

Authors:  Xinjie Tan; Archana Kini; Dorothee Römermann; Ursula Seidler
Journal:  Int J Mol Sci       Date:  2022-09-01       Impact factor: 6.208

  7 in total

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