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Completed

NCT Number: NCT02464059

Cathelicidin and Vitamin D: Impact on Populations At-Risk and With COPD

This proposal will evaluate a potential mechanism of increased risk of lung function impairment, cathelicidin levels, as well as determine if vitamin D replacement can alter this pathway. This study will improve the understanding of factors which can lead to chronic lung disease. If effective, this application would also provide the justification to study vitamin D as a therapy to improve lung health.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Johns Hopkins Clinical Research Unit, Baltimore, Maryland, United States

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About this study

Understanding mechanisms leading to decrements in lung function, the physiologic hallmark of obstructive lung diseases including chronic obstructive pulmonary disease (COPD), are necessary to inform interventions to improve lung health. The antimicrobial peptide cathelicidin, and its primary regulator vitamin D, has been implicated in development and progression of chronic lung disease. In this study, the investigators will evaluate the effect of oral vitamin D supplementation on lung cathelicidin levels in humans. Cathelicidin has bactericidal and inflammatory activities in the lung and is regulated by vitamin D levels. The investigators hypothesize that oral vitamin D supplementation will raise cathelicidin levels in the pulmonary compartment, thereby restoring lung cathelicidin deficiency. To test this hypothesis, the investigators will recruit from two ongoing cohort studies: 1) At Johns Hopkins, the Subpopulations and Intermediate Outcome Measures in COPD Study study and 2)at University of North Carolina at Chapel Hill pulmonary and general medicine clinic. The investigators will measure blood and lung lavage cathelicidin levels in 40 vitamin D insufficient individuals (20 from each cohort) before and after eight weeks of oral vitamin D supplementation to determine the effect of vitamin D supplementation on cathelicidin levels.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Men and women age 18-65 who are current or former smokers
  • Serum calcium<10.5mg/dL
  • 25-Hydroxy Vitamin D (OHD)<20 ng/mL
  • Creatinine Clearance ≥60 mL/min as estimated by the Cockcroft-Gault equation
  • Women of reproductive potential with negative serum or urine pregnancy test and subjects must refrain from participating in a conception process and subject/partner must use at least 2 reliable forms of contraceptives for the duration of the study
  • For participants with COPD, Forced Expiratory Volume in 1 second (FEV1) greater than 50% predicted.
  • For smokers, current cigarette use (defined as regularly smoking 5 cigarettes per day)

Exclusion criteria

  • Current use of vitamin D supplements
  • Known allergy/sensitivity or any hypersensitivity to components of study drugs or their formulations
  • Pregnancy or currently breast-feeding
  • History of nephrolithiasis
  • HIV positive serostatus
  • Continuous oxygen use >2 liters/min via nasal cannula
  • Any condition that, in the opinion of the site investigator, would compromise the subject's ability to participate in the study.

Treatment and study plan

Vitamin D3

Drug

Oral supplementation with 50,000 IU vitamin D3 weekly for eight weeks in individuals with reduced vitamin D levels.

Other names: cholecalciferol

Primary outcomes

  1. Change From Baseline in Lung Cathelicidin Level at 8 Weeks

    Time frame: Baseline and 8 weeks

    Change from baseline to 8 weeks in bronchoscopic lavage lung cathelicidin levels after vitamin D supplementation (comparison between pre- and post-supplementation cathelicidin levels using paired t-tests for repeated measures)

Secondary outcomes

  1. Change From Baseline in Blood Cathelicidin at 8 Weeks

    Time frame: Baseline and 8 weeks

    Change from baseline to 8 weeks in blood cathelicidin levels after vitamin D supplementation (comparison between pre- and post-supplementation cathelicidin levels using paired t-tests for repeated measures)

  2. Change From Baseline in Blood Vitamin D Binding Protein at 8 Weeks

    Time frame: Baseline and 8 weeks

    Change from baseline to 8 weeks in blood vitamin D binding protein after vitamin D supplementation (comparison between pre- and post-supplementation cathelicidin levels using paired t-tests for repeated measures)

Sponsors and collaborators

Lead sponsor

University of North Carolina, Chapel Hill

Other

Collaborators

  • Johns Hopkins University

Registry information

Important dates

Study start
2015
Primary completion
2020
Study completion
2020
First posted
Jun 8, 2015
Registry last updated
Jul 24, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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