| Literature DB >> 28806407 |
Péter Varjú1,2, Nelli Farkas3, Péter Hegyi1,4,5, András Garami1, Imre Szabó4, Anita Illés4, Margit Solymár1, Áron Vincze4, Márta Balaskó1, Gabriella Pár4, Judit Bajor4, Ákos Szűcs6, Orsolya Huszár6, Dániel Pécsi1, József Czimmer4.
Abstract
BACKGROUND: Irritable bowel syndrome (IBS) and functional digestive tract disorders, e.g. functional bloating, carbohydrate maldigestion and intolerances, are very common disorders frequently causing significant symptoms that challenge health care systems. A low Fermentable Oligosaccharides, Disaccharides, Monosaccharides and Polyols (FODMAP) diet is one of the possible therapeutic approaches for decreasing abdominal symptoms and improving quality of life.Entities:
Mesh:
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Year: 2017 PMID: 28806407 PMCID: PMC5555627 DOI: 10.1371/journal.pone.0182942
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.240
Fig 1Flow chart for the systematic literature search.
Baseline characteristics of the studies involved in the meta-analysis.
| References | Country | Study design | Study duration | total or low-FODMAP/control cohort size | IBS diagnostic criteria | Age (years) | Percentage of females (%) |
|---|---|---|---|---|---|---|---|
| Böhn et al. [ | Sweden | multi-centre, parallel, randomized, controlled, single-blind, comparative trial | 4 weeks | 33/34 | Rome III | low-FODMAP: mean: 44 (18–69); | total: 81; |
| McIntosh et al. [ | Canada | prospective, randomized, single-blind, parallel study | 3 weeks | 18/19 | Rome III | low- FODMAP: mean: 50.28 (26–77); | total: 86; |
| Pedersen et al. (B) [ | Denmark | randomized, non-blind, controlled trial | 6 weeks | 42/40 started, 34/37 finished | Rome III | low-FODMAP: median: 37 (18–71); | total: 77; |
| Laatikainen et al. [ | Finland | randomized, double-blind, 2x2 cross-over study | 13 weeks (1- week run-in, 2x4- week intervention, 4 -week wash-out period) | 80 started, 73 finished | Rome III | mean: 42.9 (21–64) | 91 |
| Schultz et al. (Suppl.) [ | New -Zealand | randomized controlled trial | 12 weeks | 23/27 | Rome III | no data | no data |
| Pedersen et al. (A) [ | Denmark | single-blind, cross-over intervention | 12 weeks (0–6 and 7–12 weeks) | 19 | Rome III | median 35 (18–74) | 74 |
| Piacentino et al. (Suppl.) [ | Italy | prospective controlled trial | 4 weeks | 28/28 | no data | 21–68 | 68 |
| Ones et al. (Suppl.) [ | Norway | non-controlled prospective study | 6 weeks | 23 | Rome III | mean: 35±11 | 87 |
| Rossi et al. (Suppl.) [ | Italy | non-controlled prospective study | 8 weeks | 12 | Rome III | mean: 44.2±15.5 | 92 |
| Valeur et al. [ | Norway | non-controlled prospective study | 4 weeks | 63 | Rome III | mean: 38.4 (19–67) | 89 |
FODMAP = Fermentable Oligosaccharides, Disaccharides, Monosaccharides and Polyols; IBS = Irritable Bowel Syndrome; Suppl. = Supplementary material
The proportion of each IBS subtype in the studies included in the meta-analysis.
| References | IBS subtype | |
|---|---|---|
| Low-FODMAP group (%) | Control diet group (%) | |
| IBS-D: 26; IBS-C: 24; IBS-M/U: 50 | IBS-D: 22; IBS-C: 35; IBS-M/U: 43 | |
| IBS-D: 22; IBS-C: 6; IBS-M: 67; IBS-U: 5 | IBS-D: 32; IBS-C: 5; IBS-M: 58; IBS-U: 5 | |
| IBS-D: 45; IBS-C: 12; IBS-M: 33; IBS-U: 10 | IBS-D: 45; IBS-C: 17.5; IBS-M: 35; IBS-U: 2.5 | |
| IBS-D: 32.5; IBS-M: 62.5; IBS-U: 5 | ||
| no data | no data | |
| IBS-D: 42; IBS-C: 21; IBS-A: 37 | ||
| no data | no data | |
| no data | - | |
| IBS-D: 25; IBS-C: 17; IBS-M: 58 | - | |
| IBS-D: 54; IBS-C: 16; IBS-M: 30 | - | |
FODMAP = Fermentable Oligosaccharides, Disaccharides, Monosaccharides and Polyols; IBS = Irritable Bowel Syndrome; IBS-D = IBS-Diarrhoeal subtype; IBS-C = IBS-Constipation subtype; IBS-M/A = IBS-Mixed/Alternation subtype; IBS-U = IBS-Unsubtyped; Suppl. = Supplementary material. The number of patients in each IBS subtype groups is expressed in S1 Table.
Quality assessment of the studies included in the meta-analysis.
| Study design | Jadad score | MINORS | |
|---|---|---|---|
| multi-centre, parallel, randomized, controlled, single-blind, comparative trial | |||
| prospective, randomized, single-blind, parallel study | |||
| Randomized, non-blind, controlled trial | |||
| randomized, double-blind, 2x2 cross-over study | |||
| randomized controlled trial | |||
| single-blind cross-over intervention | |||
| prospective controlled trial | |||
| non-controlled prospective study | |||
| non-controlled prospective study | |||
| non-controlled prospective study |
Randomized controlled trials were evaluated with the Jadad score (0 = very poor, 5 = rigorous) [40]. Non-randomized studies were evaluated with the MINORS (Methodological Index for Non-Randomized Studies) [41], in which 12 items are scored (0: not reported; 1: reported, but inadequate; 2: reported and adequate). The global ideal score is 16 for non-comparative studies and 24 for comparative studies. Suppl. = Supplementary material.
Fig 2Forest plot of IBS-SSS DIMs, comparing pre- vs. post-intervention values within groups (low-FODMAP and control).
IBS-SSS = Irritable Bowel Syndrome Symptom Severity Score (0–500); DIM = Difference in Means; FODMAP = Fermentable Oligosaccharides, Disaccharides, Monosaccharides and Polyols.
Fig 3Forest plot of IBS-SSS DIMs, comparing pre- and post-intervention values between groups (low-FODMAP vs. control).
IBS-SSS = Irritable Bowel Syndrome Symptom Severity Score (0–500); DIM = Difference in Means; FODMAP = Fermentable Oligosaccharides, Disaccharides, Monosaccharides and Polyols.