IL-8 correlates with reduced baseline femoral neck bone mineral density in adults with cystic fibrosis: a single center retrospective study

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Grace Y. Lam
Sameer Desai
Joey Fu
Xun Yang Hu
Jiah Jang
Azita Goshtasebi
Shirin Kalyan
Bradley S. Quon
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[1] University of Alberta,Division of Pulmonary Medicine
[2] University of British Columbia,School of Population and Public Health
[3] St. Paul’s Hospital,Division of Respiratory Medicine
[4] St. Paul’s Hospital,Centre for Heart Lung Innovation
[5] University of British Columbia,Centre for Menstrual Cycle and Ovulation Research (CeMCOR)
[6] University of British Columbia,Division of Endocrinology and Metabolism, Department of Medicine
[7] University of British Columbia,undefined
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Cystic fibrosis (CF) is a multi-system disease that is characterized by lung disease due to recurrent airway infection and inflammation. Endocrine complications, such as CF bone disease (CFBD), are increasingly identified as patients are living longer. The cause of CFBD is multifactorial with chronic systemic inflammation theorized to be a contributing factor. Thus, we attempted to identify inflammatory biomarkers that are associated with CFBD. We conducted a retrospective observational study of 56 adult patients with CF with an average percentage predictive forced expiratory volume in one second (ppFEV1) of 73.7% (standard deviation: 30.0) who underwent baseline serum analysis for osteoprotegerin (OPG) and pro-inflammatory biomarkers (IL-1β, IL-6, IL-8 and TNF-α), and had repeated dual-energy x-ray absorptiometry (DXA) scans separated by at least 2 years to examine correlations between serum biomarkers and bone mineral density (BMD) measurements. Univariate linear regression model analysis demonstrated that serum IL-1β and IL-8, but not other pro-inflammatory markers, were negatively correlated with baseline BMD results. However, after accounting for confounding variables, only the relationship between IL-8 and left femoral neck BMD remained statistically significant. Additionally, IL-8 level was associated with BMD decline over time. These results suggest that IL-8 might play a unique role in the pathophysiology of CFBD relative to other pro-inflammatory cytokines but further study is warranted before firm conclusions can be made.
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