Association Between Serum 25-hydroxyvitamin D Level and Pulmonary Exacerbations in Cystic Fibrosis
Overview
Pulmonary Medicine
Affiliations
Objective: To identify effects of vitamin D status, as defined by circulating 25-hydroxyvitamin D (25-OHD) levels on the annual frequency of pulmonary exacerbations (Pex) and hospitalizations, on standard measures of pulmonary function, and to identify determinants of 25-OHD levels in pediatric patients with cystic fibrosis (CF).
Hypothesis: Higher levels of serum 25-OHD would be associated with fewer Pex and hospitalizations, and improved lung function based on pulmonary function tests (PFTs).
Study Design: Retrospective chart review of 53 pediatric patients from January 2011 to December 2011. Significant relationships were examined using linear and logistic regression analyses.
Patient Selection: Patients ages 5 through 22 years followed at the CF Care Center and Clinic at Yale-New Haven Hospital, New Haven, CT., who had at least four clinic visits and at least one 25-OHD measurement between January 1, 2011 and December 31, 2011.
Results: Serum 25-OHD level and gender were strong independent determinants of the annual number of Pex (P < 0.01, with lower 25-OHD level and female gender associated with Pex). There was a significant influence of gender (P < 0.05) and a near-significant influence of serum 25-OHD (P < 0.08) on hospitalization rate. There was no effect of 25-OHD levels on PFTs. Other candidate factors (age, season, gender, pancreatic sufficiency, or severity of genetic mutation) did not significantly effect 25-OHD level.
Conclusions: The annual number of Pex in pediatric CF patients is significantly associated with 25-OHD levels and gender, raising the consideration that maintaining vitamin D sufficiency may lead to decreased incidence of Pex and hospitalizations requiring antibiotic therapy.
Braun A, Lai H, Laxova A, Biller J, Hubertz E, Zhao Z J Cyst Fibros. 2024; 23(4):754-757.
PMID: 38383231 PMC: 11624284. DOI: 10.1016/j.jcf.2024.02.005.
Vitamin D deficiency in patients with cystic fibrosis: a systematic review and meta-analysis.
Farahbakhsh N, Fatahi S, Shirvani A, Motaharifard M, Mohkam M, Tabatabaii S J Health Popul Nutr. 2024; 43(1):11.
PMID: 38233891 PMC: 10795301. DOI: 10.1186/s41043-024-00499-2.
Hope in Every Breath: Navigating the Therapeutic Landscape of Cystic Fibrosis.
Sreenivasulu H, Muppalla S, Vuppalapati S, Shokrolahi M, Reddy Pulliahgaru A Cureus. 2023; 15(8):e43603.
PMID: 37719614 PMC: 10504422. DOI: 10.7759/cureus.43603.
Nutritional Care in Children with Cystic Fibrosis.
Mariotti Zani E, Grandinetti R, Cunico D, Torelli L, Fainardi V, Pisi G Nutrients. 2023; 15(3).
PMID: 36771186 PMC: 9921127. DOI: 10.3390/nu15030479.
Lai H, Song J, Lu Q, Murali S, Gajapathy M, Wilk B Clin Nutr ESPEN. 2022; 51:367-376.
PMID: 36184229 PMC: 11648032. DOI: 10.1016/j.clnesp.2022.07.018.