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Vitamin D Metabolism Is Dysregulated in Asthma and Chronic Obstructive Pulmonary Disease.
Jolliffe, David A; Stefanidis, Christos; Wang, Zhican; Kermani, Nazanin Z; Dimitrov, Vassil; White, John H; McDonough, John E; Janssens, Wim; Pfeffer, Paul; Griffiths, Christopher J; Bush, Andrew; Guo, Yike; Christenson, Stephanie; Adcock, Ian M; Chung, Kian Fan; Thummel, Kenneth E; Martineau, Adrian R.
  • Jolliffe DA; Asthma UK Centre for Applied Research, Institute of Population Health Sciences, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
  • Stefanidis C; Asthma UK Centre for Applied Research, Institute of Population Health Sciences, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
  • Wang Z; Department of Pharmaceutics, University of Washington, Seattle, Washington.
  • Kermani NZ; Data Science Institute, William Penney Laboratory and.
  • Dimitrov V; Department of Physiology, McGill University, Montreal, Quebec, Canada.
  • White JH; Department of Physiology, McGill University, Montreal, Quebec, Canada.
  • McDonough JE; Yale School of Medicine, New Haven, Connecticut.
  • Janssens W; Laboratory of Respiratory Diseases and Thoracic Surgery, Department of Chronic Diseases, Metabolism and Ageing, Katholieke Universiteit Leuven, Leuven, Belgium; and.
  • Pfeffer P; Asthma UK Centre for Applied Research, Institute of Population Health Sciences, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
  • Griffiths CJ; Asthma UK Centre for Applied Research, Institute of Population Health Sciences, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
  • Bush A; National Heart and Lung Institute, Faculty of Medicine, Imperial College London, London, United Kingdom.
  • Guo Y; Data Science Institute, William Penney Laboratory and.
  • Christenson S; Division of Pulmonary, Critical Care, Allergy, & Sleep Medicine, Department of Medicine, University of California, San Francisco, California.
  • Adcock IM; National Heart and Lung Institute, Faculty of Medicine, Imperial College London, London, United Kingdom.
  • Chung KF; National Heart and Lung Institute, Faculty of Medicine, Imperial College London, London, United Kingdom.
  • Thummel KE; Department of Pharmaceutics, University of Washington, Seattle, Washington.
  • Martineau AR; Asthma UK Centre for Applied Research, Institute of Population Health Sciences, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
Am J Respir Crit Care Med ; 202(3): 371-382, 2020 08 01.
Article en En | MEDLINE | ID: mdl-32186892
ABSTRACT
Rationale Vitamin D deficiency is common in patients with asthma and chronic obstructive pulmonary disease (COPD). Low 25-hydroxyvitamin D (25[OH]D) levels may represent a cause or a consequence of these conditions.

Objectives:

To determine whether vitamin D metabolism is altered in asthma or COPD.

Methods:

We conducted a longitudinal study in 186 adults to determine whether the 25(OH)D response to six oral doses of 3 mg vitamin D3, administered over 1 year, differed between those with asthma or COPD versus control subjects. Serum concentrations of vitamin D3, 25(OH)D3, and 1α,25-dihydroxyvitamin D3 (1α,25[OH]2D3) were determined presupplementation and postsupplementation in 93 adults with asthma, COPD, or neither condition, and metabolite-to-parent compound molar ratios were compared between groups to estimate hydroxylase activity. Additionally, we analyzed 14 datasets to compare expression of 1α,25(OH)2D3-inducible gene expression signatures in clinical samples taken from adults with asthma or COPD versus control subjects.Measurements and Main

Results:

The mean postsupplementation 25(OH)D increase in participants with asthma (20.9 nmol/L) and COPD (21.5 nmol/L) was lower than in control subjects (39.8 nmol/L; P = 0.001). Compared with control subjects, patients with asthma and COPD had lower molar ratios of 25(OH)D3-to-vitamin D3 and higher molar ratios of 1α,25(OH)2D3-to-25(OH)D3 both presupplementation and postsupplementation (P ≤ 0.005). Intergroup differences in 1α,25(OH)2D3-inducible gene expression signatures were modest and variable if statistically significant.

Conclusions:

Attenuation of the 25(OH)D response to vitamin D supplementation in asthma and COPD associated with reduced molar ratios of 25(OH)D3-to-vitamin D3 and increased molar ratios of 1α,25(OH)2D3-to-25(OH)D3 in serum, suggesting that vitamin D metabolism is dysregulated in these conditions.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Asma / Vitaminas / Calcifediol / Calcitriol / Colecalciferol / Enfermedad Pulmonar Obstructiva Crónica Tipo de estudio: Clinical_trials / Observational_studies / Risk_factors_studies Límite: Female / Humans / Male / Middle aged Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Asma / Vitaminas / Calcifediol / Calcitriol / Colecalciferol / Enfermedad Pulmonar Obstructiva Crónica Tipo de estudio: Clinical_trials / Observational_studies / Risk_factors_studies Límite: Female / Humans / Male / Middle aged Idioma: En Año: 2020 Tipo del documento: Article