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The Journal of Allergy and Clinical Immunology
Volume 126, Issue 1
, Pages
52-58.e5
, July 2010
Serum vitamin D levels and severe asthma exacerbations in the Childhood Asthma Management Program study
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Sensitivity analysis of risk of hospitalization or ED visit by vitamin D level. The probabilities of severe exacerbations were plotted for the range of vitamin D levels in the study, and a smoothing f
Sensitivity analysis of risk of hospitalization or ED visit by vitamin D level. The probabilities of severe exacerbations were plotted for the range of vitamin D levels in the study, and a smoothing function was used to draw a line through the values. Vertical lines represent quartiles of vitamin D levels. The risk of hospitalization starts to decrease around a vitamin D level of 30 ng/mL.
We acknowledge the Childhood Asthma Management Program (CAMP) investigators and research team, supported by the National Heart, Lung, and Blood Institute, for collection of CAMP Genetics Ancillary Study data. All work on data collected from the CAMP Genetics Ancillary Study was conducted at the Channing Laboratory of the Brigham and Women's Hospital under appropriate CAMP policies and human subject's protections. The CAMP Genetics Ancillary Study is supported by U01 HL075419, U01 HL65899, P01 HL083069, R01 HL086601, and T32 HL07427 from the National Heart, Lung, and Blood Institute(NHLBI)/National Institutes of Health. We also acknowledge the Asthma Clinical Research Network (ACRN) investigators and research teams supported by U01 HL51510, U01 HL51834, U01 HL51831, U01 HL51845, U01 HL 51843, M01 RR00079, and M01 RR03186 from the NHLBI. This work was also supported by National Institutes of Health grant R21HL089842.
Disclosure of potential conflict of interest: A. L. Fuhlbrigge is on an advisory board for and has given talks for Merck and has received continuing medical education from Advanced Health Media, funded through GlaxoSmithKline. B. W. Hollis has consulted for DiaSorin and has received research support from the National Institutes of Health. R. S. Zeiger has consulted for AstraZeneca, Aerocrine, Genentech, Novartis, Merck, Schering-Plough, and MedImmune and has received indirect research support from Aerocrine, Genentech, GlaxoSmithKline, Merck, AstraZeneca, and TEVA Pharmaceuticals. A. A. Litonjua has received research support from the National Institutes of Health. The rest of the authors have declared that they have no conflict of interest.
PII: S0091-6749(10)00657-3
doi: 10.1016/j.jaci.2010.03.043
© 2010 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.
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The Journal of Allergy and Clinical Immunology
Volume 126, Issue 1
, Pages
52-58.e5
, July 2010
