Pediatrics & Neonatology https://doi.org/10.1016/j.pedneo.2018.07.001
|Vitamin D level||Cystic Fibrosis periods|
|49 ng||routine follow-up|
- Cystic Fibrosis category listing has
41 items along with related searches
- If vitamin D levels are less than 40 ng some children get cystic fibrosis – March 2018
- Powder-based Vitamin D may be gut-friendly (Cystic Fibrosis) – RCT Aug 2017
- Cystic Fibrosis got some benefit from 50,000 IU of vitamin D weekly (need gut-friendly form) – Feb 2018
- Cystic fibrosis treatment by vitamin D improved quality of life and breathing (8200 IU daily)– RCT Dec 2016
- Cystic fibrosis problems cut in half by Omega-3 – RCT June 2015
Speculations by founder of Vitamin D Life
- CF patients should use a form of vitamin D which deals with associated poor gut function
- Gut friendly or perhaps inhaled
- Consider taking more Vitamin D when person feels that there might be a colonization or future exacerbation
- Consider taking Vitamin D AND Omega-3
- Consider aiding the gut with probiotics, etc
The prevalence of Vitamin D deficiency remains high in cystic fibrosis despite daily supplementation. Vitamin D as an immunomodulator has been related to lower respiratory tract infections in children.
The present study was undertaken to examine the association between vitamin D status and markers of cystic fibrosis-related pulmonary disease including exacerbations, bacterial colonization and pulmonary function.
The study includes review of records of 51 cystic fibrosis patients. Baseline patient variables and serum vitamin D levels were recorded. Based on vitamin D levels study patients were divided into three groups: vitamin-D sufficient (≥20 ng/mL), vitamin-D insufficient (12 to 20 ng/mL), and vitamin D-deficient (≤12 ng/ml).
The proportion of children with deficient, insufficient and sufficient vitamin D levels were 47.1%, 15.7%, and 37.2%, respectively. Female sex, bacterial colonization and a greater number of exacerbations were associated with highest odds of developing vitamin D deficiency in patients with CF with 1.77(0.22‒14.61)(p = 0.002), 2.9(0.57‒14.82)(p = 0.011), and 5.12(1.28‒20.50)(p = 0.021) respectively.
The comparison of vitamin-D levels taken during exacerbations, colonization and during routine follow-up were significant [16.04(7.42‒27.91), 24.3(15.5‒32.4) and 48.54(18.37‒78.7)ng/ml, p <0.001].
The FEV1 was determined in 24 patients; the comparison was significant between vitamin D-deficient and -sufficient groups [0.75(0.717‒0.777) vs. 0.82(0.74‒0.92) p <0.05].
We concluded that vitamin D deficiency was highly prevalent in children with CF, despite daily supplementation of the vitamin in diet. Further, vitamin D deficiency was associated with a higher rate of pulmonary exacerbations and higher incidence of pulmonary bacterial colonization. In addition, in younger patients, low vitamin D levels were associated with reduced pulmonary function.