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Vitamin D Deficiency in Cystic Fibrosis
Joint Authors
Sparks, Amy A.
Aris, Robert M.
Hall, William B.
Source
International Journal of Endocrinology
Issue
Vol. 2010, Issue 2010 (31 Dec. 2010), pp.1-9, 9 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2010-01-28
Country of Publication
Egypt
No. of Pages
9
Main Subjects
Abstract EN
Cystic Fibrosis is the most common inherited genetic respiratory disorder in the Western World.
Hypovitaminosis D is almost universal in CF patients, likely due to a combination of inadequate absorption, impaired metabolism, and lack of sun exposure.
Inadequate levels are associated with the high prevalence of bone disease or osteoporosis in CF patients, which is associated with increased morbidity including fractures, kyphosis, and worsening pulmonary status.
Treatment goals include regular monitoring 25 hydroxyvitamin D (25OHD) levels with aggressive treatment for those with levels <75 nmol/L (<30 ng/mL).
More research is needed to determine optimal supplementation goals and strategies.
American Psychological Association (APA)
Hall, William B.& Sparks, Amy A.& Aris, Robert M.. 2010. Vitamin D Deficiency in Cystic Fibrosis. International Journal of Endocrinology،Vol. 2010, no. 2010, pp.1-9.
https://search.emarefa.net/detail/BIM-455529
Modern Language Association (MLA)
Hall, William B.…[et al.]. Vitamin D Deficiency in Cystic Fibrosis. International Journal of Endocrinology No. 2010 (2010), pp.1-9.
https://search.emarefa.net/detail/BIM-455529
American Medical Association (AMA)
Hall, William B.& Sparks, Amy A.& Aris, Robert M.. Vitamin D Deficiency in Cystic Fibrosis. International Journal of Endocrinology. 2010. Vol. 2010, no. 2010, pp.1-9.
https://search.emarefa.net/detail/BIM-455529
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-455529