Investigation into the impact of vitamin D supplementation on the microbiota of patients with and without ulcerative colitis.
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The Effect of Vitamin D on Intestinal Inflammation and Faecal Microbiota in Patients with Ulcerative Colitis.
Abstract
<h4>Background and aims</h4>Vitamin D may be immunomodulatory and alter faecal microbiota, but results from clinical studies in humans to date have been inconclusive. This study aimed to assess the effect of vitamin D replacement in vitamin D-deficient patients with and without ulcerative colitis [UC] on inflammation and faecal microbiota.<h4>Methods</h4>Vitamin D was replaced over 8 weeks in patients with active UC [defined by faecal calprotectin ≥ 100 µg/g], inactive UC [faecal calprotectin < 100 µg/g] and non-inflammatory bowel disease [IBD] controls with baseline serum 25[OH] vitamin D <50 nmol/l, and markers of inflammation and faecal microbiota were analysed.<h4>Results</h4>Eight patients with active UC, nine with inactive UC and eight non-IBD controls received 40000 units cholecalciferol weekly for 8 weeks. Mean baseline 25[OH] vitamin D increased from 34 [range 12-49] to 111 [71-158] nmol/l [p < 0.001], with no difference across the groups [p = 0.32]. In patients with active UC, faecal calprotectin levels decreased from a median 275 to 111 µg/g [p = 0.02], platelet count decreased [mean 375 to 313 × 109/l, p = 0.03] and albumin increased [mean 43 to 45 g/l, p = 0.04]. These parameters did not change in patients with inactive UC or non-IBD controls. No changes in overall faecal bacterial diversity were noted although a significant increase in Enterobacteriaceae abundance was observed in patients with UC [p = 0.03].<h4>Conclusions</h4>Vitamin D supplementation was associated with reduced intestinal inflammation in patients with active UC, with a concomitant increase in Enterobacteriaceae but no change in overall faecal microbial diversity.
Study facts
- Organism
- —
- Platform
- —
- Age group
- adult
- Disease groups
- Non-IBD controls, Ulcerative colitis
- Anatomical sites
- —
Data availability
Specific data assets have not been resolved from the source yet — see the source repository below for the full file listing.
Strengths & limitations for reuse
Strengths
- Participant counts are documented
Limitations
- Not documented: raw reads are advertised
- Not documented: feature/otu tables are advertised
- Not documented: taxonomic tables are advertised
Extraction evidence & provenance
Each extracted field is shown with the source excerpt and location used to resolve it.
Cohort
| Field | Value | Evidence |
|---|---|---|
cohort.age_group |
adult |
{"descriptorName": "Adult"} Section |
cohort.disease_activity_metadata_available |
True |
patients with active UC (defined by faecal calprotectin ≥ 100 µg/g), inactive UC (faecal calprotectin < 100 µg/g) Section |
cohort.non_ibd_controls |
8 |
Eight patients with active UC, 9 with inactive UC and 8 non-IBD controls Section |
cohort.study_design |
longitudinal inferred |
Vitamin D was replaced over 8 weeks Section |
cohort.total_participants |
25 computed |
Eight patients with active UC, 9 with inactive UC and 8 non-IBD controls Section |
cohort.treatment_exposure_documented |
True |
Vitamin D was replaced over 8 weeks to patients with active UC Section |
cohort.treatment_response_metadata_available |
True |
Faecal calprotectin levels reduced from median 275 to 111 Section |
cohort.ulcerative_colitis_participants |
17 computed |
Eight patients with active UC, 9 with inactive UC and 8 non-IBD controls Section |
Specimens
| Field | Value | Evidence |
|---|---|---|
specimens.body_site |
faeces |
alter faecal microbiota Section |
specimens.inflamed_status_available |
True |
patients with active UC (defined by faecal calprotectin ≥ 100 µg/g), inactive UC (faecal calprotectin < 100 µg/g) Section |
specimens.longitudinal_sampling |
True inferred |
Vitamin D was replaced over 8 weeks Section |
specimens.sample_type |
stool |
markers of inflammation and stool microbiota analysed Section |