Nutritional safety and status following a 12‐week strict low FODMAP diet in patients with irritable bowel syndrome

Author:

Hillestad Eline Margrete Randulff12ORCID,Steinsvik Elisabeth Kjelsvik2,Teige Erica Sande12,Rasmussen Stella Hellgren1,Brønstad Ingeborg2,Lundervold Arvid34,Hausken Trygve25,Hanevik Kurt6,Lied Gülen Arslan12,Berentsen Birgitte25

Affiliation:

1. Department of Clinical Medicine, Faculty of Medicine, Center for Nutrition University of Bergen Bergen Norway

2. Department of Medicine, Division of Gastroenterology, National Center for Functional Gastrointestinal Disorders Haukeland University Hospital Bergen Norway

3. Department of Biomedicine University of Bergen Bergen Norway

4. Department of Radiology, Mohn Medical Imaging and Visualization Center Haukeland University Hospital Bergen Norway

5. Department of Clinical Medicine Faculty of Medicine, University of Bergen Bergen Norway

6. Department of Clinical Science Faculty of Medicine, University of Bergen Bergen Norway

Abstract

AbstractBackgroundA low FODMAP diet (LFD) is an established dietary treatment for patients with irritable bowel syndrome (IBS). However, knowledge on the extended effects of the restriction phase regarding nutrient intake, symptom severity, and quality of life (QoL) is sparse. Therefore, our objectives were to evaluate the safety of a dietitian‐led 12‐week strict LFD on measures of blood biochemistry, nutritional status, symptom severity, and QoL.MethodsIn this open‐label dietitian‐led 12‐week strict LFD intervention for IBS patients with predominantly diarrhea or mixed stool pattern (IBS‐D/−M), we collected data on diet intake (3‐day dietary record), overnight fasting routine blood samples, body weight, IBS symptoms (IBS Severity Scoring System (IBS‐SSS)), and IBS‐related QoL (IBS‐QoL) at baseline and after 12 weeks.Key ResultsThirty‐six participants completed the 12‐week follow‐up (mean age: 37 years, 67% women, IBS‐SSS: 242 (101)). All blood parameters measured were within established reference values at both time points. We found no change in intake of macro‐ or micronutrients, but several micronutrients were below the recommendations both before and after 12 weeks. BMI slightly decreased, primarily driven by participants with BMI >25 (p < 0.005). QoL improved among most subdomains (p ≤ 0.002), except food avoidance and social reaction.ConclusionAn extended dietitian‐guided LFD (12 weeks) is not inferior to the participants' baseline diet, since no clinically meaningful changes in nutritionally related blood samples and no changes in macro‐ or micronutrient intake were observed. However, the intake of several nutrients was below the recommendations at both time points indicating low diet quality.

Funder

Norges Forskningsråd

Helse Vest

Publisher

Wiley

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