Research Title: Evaluation of airway reactivity, allergy and inflammatory mediators in exhaled breath condensate in vitamin D resistant rickets. Aim: To assess the effect of absence of vitamin D receptors on airway reactivity, allergy and inflammatory mediators in exhaled breath condensate in a prospective study evaluating patients with vitamin D resistant rickets and in healthy controls. Sample size: 40 participants in the two groups. Primary end point: Airway reactivity as assessed by methacholine challenge test. Secondary outcome parameters: All other parameters are the secondary end points.
Research Title: Evaluation of airway reactivity, allergy and inflammatory mediators in exhaled breath condensate in vitamin D resistant rickets. Introduction: Vitamin D seems to play a role in allergic and asthmatic reactions. Vitamin D resistant rickets patients lack vitamin D receptors and cannot absorb vitamin D. Aim: To assess the effect of absence of vitamin D receptors on airway reactivity, allergy and inflammatory mediators in exhaled breath condensate. Design: Prospective study evaluating these parameters in patients with vitamin D resistant rickets and in healthy controls. Participant selection: The study group will consist of vitamin D resistant rickets patients followed and treated at the Pediatric Endocrinology Department at our hospital. The study group will be compared to an age- and sex-matched healthy control group that had a negative methacholine challenge test. Sample size: 40 participants in the two groups. Intervention: Each subject will undergo evaluation including a respiratory questionnaire, pulmonary function tests, methacholine challenge test with determination of PC20, exhaled nitric oxide (eNO), and exhaled breath condensate (EBC). Venous blood will be analyzed for complete blood count + eosinophils, IGE levels, and Vitamin D levels. Prick skin test for inhaled allergens will be performed. All measurements will be evaluated in a single 3 hour visit, with no follow up study visits. Primary end point: Airway reactivity as assessed by methacholine challenge test. Secondary outcome parameters: All other parameters are the secondary end points.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
SCREENING
Masking
NONE
Enrollment
26
Evaluation of airway hyperreactivity as assessed by doubling dose of methacholine with determination of PC20
RAMBAM Health Care Campus
Haifa, Israel, Israel
Metacholine Challenge Test
As assessed by methacholine challenge test with determination of PC20.
Time frame: participants will be followed for the duration of hospital visit, an average of 3 hours
IgE
in peripheral Blood count
Time frame: participants will be followed for the duration of hospital visit, an average of 3 hours
CBC
in peripheral Blood count
Time frame: participants will be followed for the duration of hospital visit, an average of 3 hours
Fractional Exhaled NO
determination of exhaled NO in Exhaled breath
Time frame: participants will be followed for the duration of hospital visit, an average of 3 hours
skin tests for inhaled allergens
Time frame: participants will be followed for the duration of hospital visit, an average of 3 hours
Inhaled breath condensate
Time frame: participants will be followed for the duration of hospital visit, an average of 3 hours
C reactive protein
in peripheral Blood count
Time frame: participants will be followed for the duration of hospital visit, an average of 3 hours
25 OH vitamin D3
in peripheral Blood count
Time frame: participants will be followed for the duration of hospital visit, an average of 3 hours
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