Vitamin D Deficiency Linked to Disease Severity, Mortality Risk in IPF Patients
Vitamin D deficiency in patients with idiopathic pulmonary fibrosis (IPF) is associated with functional and clinical predictors of disease severity and a higher risk of mortality, according to a new study.
The research, “Vitamin D prevents experimental lung fibrosis and predicts survival in patients with idiopathic pulmonary fibrosis,” was published in the journal Pulmonary Pharmacology & Therapeutics.
Besides the regulation of calcium and phosphate, vitamin D has shown anti-inflammatory, anti-bacterial, and cell protective activities. In addition, vitamin D deficiency has been associated with a risk of developing respiratory diseases, including chronic obstructive pulmonary disease. It has also been linked with indicators of disease severity in various types of organ fibrosis, or scarring, which suggest a potential prognostic value. Based on these observations, researchers in Greece investigated the role of vitamin D in experimental and human lung fibrosis.
They used the bleomycin mouse model of pulmonary fibrosis, in which fibrosis was experimentally induced by by the cancer drug bleomycin. From day 3 to day 13 after bleomycin treatment, the animals received vitamin D orally (at 2 ug/kg of body weight). Results showed that vitamin D lowered levels of hydroxyproline, an amino acid that is a major component of collagen. It also reduced levels of RNA, of col1a1 and col3a1 (the genes coding for type I and III collagen, respectively), as well as a-SMA (a gene also associated with fibrosis). The team also tested the effects of vitamin D administration in mouse lung fibroblasts — cells that produce collagen and are key players in fibrosis. Fibroblasts were pre-treated with vitamin D for 24 hours, and then stimulated with TGF-beta1, which is a protein known to promote fibrosis. Results indicated that pre-treatment with vitamin D lessened the responsiveness of lung fibroblasts to TGF-beta1, as reflected in significant RNA reductions of col1a1, col3a1, and a-SMA. Smad3 phosphorylation, or activation (a pro-fibrotic protein mediator), also was prevented.
Researchers collected serum samples from 93 patients with IPF (mean age 71.7 years) and 40 patients with other forms of interstitial lung disease (ILD, mean age 69.4 years) to measure vitamin D levels. These patients showed lower-than-normal mean vitamin D serum concentrations (18.76 in IPF and 18.54 ng/ml in ILD, both under the reference value of 20 ng/ml), which correlated with measures of lung function, namely percent predicted forced vital capacity, diffusing capacity of the lungs for carbon monoxide (the lungs’ capacity to transfer oxygen from the air sacs into the blood), and GAP score (a clinical prognostic tool). Viitamin D levels below a threshold of 17.9 ng/ml identified a group of IPF patients with greater likelihood of mortality.
Overall, “our study suggests that [vitamin D] may display protective effects on experimental lung fibrosis and reliably predict clinical outcomes in patients with IPF,” the researchers wrote. According to them, a median vitamin D serum threshold of 17.9 ng/ml is a “strong predictor of all-cause mortality.”
The findings also suggest that IPF patients are at high risk of developing vitamin D deficiency, “and thus should be screened accordingly, for early supplementation treatment and prediction of clinical outcomes,” the team wrote.
A clinical trial exploring the therapeutic potential of vitamin D as add-on therapy to standard of care in patients with IPF “is sorely needed,” the team concluded.
Adapted from pulmonaryfibrosisnews.com