Effects of vitamin D supplementation on intestinal permeability, cathelicidin and disease markers in Crohn's disease: Results from a randomised double-blind placebo-controlled study.
Raftery. Tara T; Martineau. Adrian R AR; Greiller. Claire L CL; Ghosh. Subrata S; McNamara. Deirdre D; Bennett. Kathleen K; Meddings. Jon J; O'Sullivan. Maria M
Key Findings
- Vitamin D supplementation (2000 IU/day) significantly raised serum 25(OH)D levels.
- Higher vitamin D status (≥75 nmol/L) was linked to increased circulating LL‑37 levels.
- Maintaining adequate vitamin D prevented increases in intestinal permeability seen in the placebo group.
- Participants with higher vitamin D had lower CRP (inflammation) and better quality‑of‑life scores.
Practical Outcomes
- For self‑directed health optimizers, a daily dose of about 2000 IU vitamin D for at least three months can help raise LL‑37, a natural antimicrobial peptide, and support gut barrier integrity. Aim for a serum 25(OH)D of 75 nmol/L or higher to maximize anti‑inflammatory and wellbeing benefits. Regular testing of vitamin D levels is advisable to adjust dosing.
Summary
In a small study of Crohn's patients in remission, taking 2000 IU of vitamin D each day for three months boosted blood levels of the antimicrobial peptide LL‑37, kept the gut lining from getting leakier, lowered inflammation markers, and improved quality of life, especially when vitamin D levels reached at least 75 nmol/L.
Abstract
Vitamin D (vitD) supplementation may prolong remission in Crohn's disease (CD); however, the clinical efficacy and mechanisms are unclear. To determine changes in intestinal permeability (IP), antimicrobial peptide (AMP) concentrations and disease markers in CD, in response to vitD supplementation. In a double-blind randomised placebo-controlled study, we assigned 27 CD patients in remission to 2000 IU/day vitD or placebo for 3 mos. We determined IP, plasma cathelicidin (LL-37 in ng/mL), human-beta-defensin-2 (hBD2 in pg/mL), disease activity (Crohn's Disease Activity Index (CDAI)), C-reactive protein (CRP in mg/L), fecal calprotectin (µg/g), Quality of Life (QoL) and serum 25-hydroxyvitamin D (25(OH)D in nmol/L) at 0 and 3 mos. At 3 mos., 25(OH)D concentrations were significantly higher in those whom were treated (p < 0.001). Intra-group analysis showed increased LL-37 concentrations (p = 0.050) and maintenance of IP measures in the treated group. In contrast, in the placebo group, the small bowel (p = 0.018) and gastro-duodenal permeability (p = 0.030) increased from baseline. At 3 mos., patients with 25(OH)D ≥ 75 nmol/L had significantly lower CRP (p = 0.019), higher QoL (p = 0.037), higher LL-37 concentrations (p < 0.001) and non-significantly lower CDAI scores (p = 0.082), compared to those with levels <75 nmol/L. Short-term treatment with 2000 IU/day vitD significantly increased 25(OH)D levels in CD patients in remission and it was associated with increased LL-37 concentrations and maintenance of IP. Achieving 25(OH)D ≥ 75 nmol/l was accompanied by higher circulating LL-37, higher QoL scores and reduced CRP. Registered at ClinicalTrials.gov (NCT01792388).
Study Information
pubmed
2015
2015-02-11T00:00:00.000Z
10.1177/2050640615572176
154
48