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  • Beneficial role for supplemental vitamin D3 treatment in chronic urticaria: a randomized study.

Beneficial role for supplemental vitamin D3 treatment in chronic urticaria: a randomized study.

Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology (2014-02-11)
Andy Rorie, Whitney S Goldner, Elizabeth Lyden, Jill A Poole
ABSTRACT

Observational reports have linked vitamin D with chronic urticaria, yet no randomized controlled trial has been conducted. To determine whether high-dose vitamin D supplementation would decrease Urticaria Symptom Severity (USS) scores and medication burden in patients with chronic urticaria. In a prospective, double-blinded, single-center study, 42 subjects with chronic urticaria were randomized to high (4,000 IU/d) or low (600 IU/d) vitamin D3 supplementation for 12 weeks. All subjects were provided with a standardized triple-drug therapy (cetirizine, ranitidine, and montelukast) and a written action plan. Data on USS scores, medication use, blood for 25-hydroxyvitamin D, and safety measurements were collected. Triple-drug therapy decreased total USS scores by 33% in the first week. There was a further significant decrease (40%) in total USS scores in the high, but not low, vitamin D3 treatment group by week 12. Compared with low treatment, the high treatment group demonstrated a trend (P = .052) toward lower total USS scores at week 12, which was driven by significant decreases in body distribution and number of days with hives. Beneficial trends for sleep quality and pruritus scores were observed with high vitamin D3. Serum 25-hydroxyvitamin D levels increased with high vitamin D3 supplementation, but there was no correlation between 25-hydroxyvitamin D levels and USS scores. There was no difference in allergy medication use between groups. No adverse events occurred. Add-on therapy with high-dose vitamin D3 (4,000 IU/d) could be considered a safe and potentially beneficial immunomodulator in patients with chronic urticaria. clinicaltrials.gov Identifier: NCT01371877.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Cholecalciferol, meets USP testing specifications
Sigma-Aldrich
Cholecalciferol, ≥98% (HPLC)
Cetirizine dihydrochloride, European Pharmacopoeia (EP) Reference Standard
Cetirizine for peak identification, European Pharmacopoeia (EP) Reference Standard
Cholecalciferol, European Pharmacopoeia (EP) Reference Standard
Montelukast sodium, European Pharmacopoeia (EP) Reference Standard
Sigma-Aldrich
Cholecalciferol, analytical standard
Supelco
Cholecalciferol (D3), analytical standard
USP
Cholecalciferol, United States Pharmacopeia (USP) Reference Standard
Sigma-Aldrich
Cetirizin dihydrochloride, ≥98.0% (HPLC)
Supelco
Cholecalciferol (Vitamin D3), Pharmaceutical Secondary Standard; Certified Reference Material
Ranitidine hydrochloride, European Pharmacopoeia (EP) Reference Standard
Supelco
Vitamin D3 solution, 1 mg/mL in ethanol, ampule of 1 mL, certified reference material, Cerilliant®
Supelco
Ranitidine hydrochloride, Pharmaceutical Secondary Standard; Certified Reference Material
Sigma-Aldrich
Ranitidine hydrochloride, solid
USP
Ranitidine hydrochloride, United States Pharmacopeia (USP) Reference Standard