1 / 17

Background & Objective

High doses of vitamin d to reduce exacerbation in chronic obstructive pulmonary disease: a randomized trial.

kerry
Download Presentation

Background & Objective

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. High doses of vitamin d to reduce exacerbation in chronic obstructive pulmonary disease: a randomized trial An Lehouck, PhD; Chantal Mathieu, MD, PhD; Claudia Carremans, MS; FemkeBaeke, PhD; Jan Verhaegen, MD, PhD; Johan Van Eldere, MD, PhD; Brigitte Decallonne, MD, PhD; Roger Bouillon, MD, PhD; Marc Decramer, PhD; and WimJanssens, MD, PhD

  2. Background & Objective • COPD is defined as an abnormal inflammatory response of the airways that block airflow and make breathing difficult. • Vitamin D deficiency is present in 60-75% of patients with COPD.

  3. Background & Objective • Background: Low serum Vitamin D (25-hydroxyvitamin D, or 25-[OH]D) levels associated with lower FEV1 and increased airway inflammation. • Objective: To investigate whether high doses of Vitamin D supplementation could reduce occurrence of COPD exacerbations/flare-ups.

  4. Methods: Study design and participants • Single-center, double-blind, randomized, placebo-controlled trial in Belgium over 1.5 year period • 182 patients with moderate to severe COPD recruited

  5. Methods: Study design and participants • Inclusion Criteria: • Have COPD diagnosis • 50+ years of age • Current/former smokers • Had less than 80% predicted FEV1 • Exclusion Criteria: • Hx of hypercalcemia, sarcoidosis, or active cancer • Those being treated with Vitamin D supplements for newly diagnosed osteoporosis • Those on long-term antibiotics with anti-inflammatory functions

  6. Methods: Randomization and Masking • First, 1 group received low dose Vitamin D (400-880 IU/day) at baseline for osteoporosis; one group not receiving low dose Vitamin D • Then, participants randomly assigned to blocks of 20 in which they would either receive monthly oral dose of 100,000 IU Vitamin D or a placebo • (those on low dose Vitamin D at starting point were divided evenly among groups)

  7. Methods: Procedures • Patients screened during hospitalization for an exacerbation of COPD • Randomization occurred 5-6 weeks after screening • Baseline characteristics • BMI • Airflow obstruction • Shortness of breath • Exercise Capacity Index • CharlsonComorbidity Index

  8. Methods: Procedures • Primary endpoint: time to first exacerbation • Secondary endpoints: exacerbation rate, time to 1st hospitalization, time to 2nd exacerbation, FEV1, QOL, death

  9. Methods: Procedures • Follow-up visits every 4 months • Patients asked to keep diary every 2 weeks of: • Respiratory tract symptoms • Hospitalizations • Visits to healthcare providers • Changes in meds

  10. Methods: Statistical Analysis • Study designed to demonstrate at least 25% delay in time to 1st flare-up • 20% receiving low dose Vitamin D at baseline for osteoporosis • Of 182 participants, at least 120 needed who were not receiving any Vitamin D treatment at baseline • P values <0.05 statistically significant

  11. Results • 419 patients screened-> 340 eligible-> 182 included • 150 participants completed the study, 15 died, 17 dropped out • Overall, collected info on flare-ups for 175 participants, information on survival for all 182

  12. Results • Total of 468 exacerbations • 229 in Vitamin D group • 239 in placebo group

  13. Results • No significant difference in median time to 1st or 2nd exacerbation, exacerbations per year, or median time to hospitalization for flare-up • No significant difference in survival • 30 participants were Vitamin D deficient at baseline- 15 randomly chosen to receive Vitamin D supplement • Significant increase in serum 25-(OH)D levels

  14. Discussion • Main finding: monthly dose of 100,000 IU Vitamin D in addition to regular therapy does not reduce time to 1st exacerbation or amount of exacerbations in patients with moderate to severe COPD

  15. Discussion: Advantages • Study sample prone to exacerbations • Most participants chosen during hospitalization were admitted for acute exacerbation

  16. Discussion: Disadvantages • Small sample size • Most were already receiving treatment to control/decrease exacerbations • Difficult to obtain additional information on effect of Vitamin D alone

  17. Discussion • Lack of overall Vitamin D effect could be explained by local insensitivity due to smoking or chronic inflammation • Supports idea that Vitamin D deficiency in COPD patients could increase risk of flare-ups • More studies needed to explore need and safety for recommending higher doses of Vitamin D to see beneficial effects in areas other than bone health

More Related