• Chest · Mar 2014

    25-hydroxyvitamin d in malignant and nonmalignant pleural effusions.

    • Konstantinos Kostikas, Marios Panagiotou, Filia Diamantea, Anna Takou, Styliani Giannakaki, Elvira Markela Antonogiannaki, Sofia Pouriki, Alexandros Kalkanis, George Maropoulos, Emmanuel Kastanakis, Vlasis Polychronopoulos, and Napoleon Karagianidis.
    • Chest. 2014 Mar 1;145(3 Suppl):270A.

    Session TitlePleural Disease/Pleural Effusion PostersSESSION TYPE: Poster PresentationsPRESENTED ON: Saturday, March 22, 2014 at 01:15 PM - 02:15 PMPURPOSE: Serum vitamin D has been associated with the risk of developing lung cancer, degree of histological differentiation, tumor metastatic growth in lung cancer cells, response to chemotherapy and survival. Similar evidence exists for other types of cancer. However, the potential role of vitamin D in malignant pleural disease has not been studied to date. The purpose of this study is to evaluate the diagnostic and prognostic role of Vitamin D in pleural effusions of various etiologies.MethodsProspective study of consecutive patients with a new diagnosis of pleural effusion admitted to a General Hospital, Athens, Greece. Patients were followed-up for 6 months. Exclusion criteria included previous diagnostic or therapeutic attempts or no definite diagnosis within the follow-up period. Pleural fluid and serum samples were collected, protected from light exposure and immediately stored in -80°C until testing for 25-Hydroxyvitamin D (VitD) with electro-chemiluminescence immunoassay (ECLIA).ResultsFifty patients were studied. Pleural VitD was higher than serum VitD (p<0.001). Pleural VitD did not differ between exudates and transudates (p=0.492) but it was significantly higher in malignant compared to benign effusions (p=0.033). Pleural VitD ≥11.6 ng/ml was diagnostic for malignant effusions (Sensitivity=67%,Specificity=73%,PPV=76%,NPV=63%). Pleural VitD did not differ between malignant effusions caused by lung cancer versus non-lung cancer (p=0.086). Although pleural VitD above the upper quartile (i.e.24.5ng/ml) was not related to survival, serum VitD above the upper quartile (i.e.17.6ng/ml) was related to better survival (p=0.114,p=0.022 respectively, log rank test). Reproducibility of the measurement of pleural VitD was acceptable.ConclusionsMalignant pleural effusions present increased levels of VitD compared to non-malignant effusions. Pleural VitD cutoff 11.6 ng/ml was diagnostic for malignant effusions with moderate sensitivity and specificity and good PPV. Increased levels of serum VitD were associated with better survival in this small population. Higher levels of pleural VitD may reflect a greater local immune response or a sequestration of a systemic response in the pleural space.Clinical ImplicationsPleural and serum VitD might have a diagnostic and prognostic role in malignant pleural effusions.DisclosureThe following authors have nothing to disclose: Marios Panagiotou, Andriana Papaioannou, Filia Diamantea, Anna Takou, Styliani Giannakaki, Elvira Markela Antonogiannaki, Sofia Pouriki, Alexandros Kalkanis, George Maropoulos, Emmanuel Kastanakis, Vlasis Polychronopoulos, Konstantinos Kostikas, Napoleon KaragianidisNo Product/Research Disclosure Information.

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