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Expression of IL-1β, HMGB1, HO-1, and LDH in malignant and non-malignant pleural effusions
Kun-Ming Wu1, Wen-Kuei Chang2, Chih-Hao Chen3
1Institute of Physiology, School of Medicine, National Yang-Ming University, Taipei, Taiwan; Chest Division, Department of Internal Medicine, MacKay Memorial Hospital, Taipei, Taiwan; Department of Medicine, Mackay Medical College, New Taipei City, Taiwan; Department of Nursing, Mackay Junior College of Medicine, Nursing and Management, New Taipei City, Taiwan.
IL-1β, HMGB1, HO-1, and LDH in the pleural effusions (PE) of patients with transudative, infectious, and malignant etiologies were determined using ELISA and enzymatic assays. IL-1β, HMGB1, HO-1, and LDH showed significant differences between the three etiologies. Post-hoc analysis revealed higher levels of HO-1 and HMGB1 in infectious versus transudative effusion. Higher levels of IL-1β were found in infectious versus transudative or malignant effusion. The comparison of LDH levels showed significant differences. Positive correlations were found between IL-1β, HMGB1, and LDH in infectious effusions. The samples were then divided into cancerous and non-cancerous groups, and logistic regression revealed that increasing IL-1β levels were significantly associated with a decrease in cancer risk after adjusting for HMGB1, HO-1, and LDH. Our findings suggest that IL-1β, HMGB1, HO-1, and LDH are expressed differently, with positive correlations between HMGB1, IL-1β, and LDH in infectious effusions, and low IL-1β expression in malignant effusions.
IL-1β, HMGB1, HO-1, and LDH in the pleural effusions (PE) of patients with transudative, infectious, and malignant etiologies were determined using ELISA and enzymatic assays. IL-1β, HMGB1, HO-1, and LDH showed significant differences between the three etiologies. Post-hoc analysis revealed higher levels of HO-1 and HMGB1 in infectious versus transudative effusion. Higher levels of IL-1β were found in infectious versus transudative or malignant effusion. The comparison of LDH levels showed significant differences. Positive correlations were found between IL-1β, HMGB1, and LDH in infectious effusions. The samples were then divided into cancerous and non-cancerous groups, and logistic regression revealed that increasing IL-1β levels were significantly associated with a decrease in cancer risk after adjusting for HMGB1, HO-1, and LDH. Our findings suggest that IL-1β, HMGB1, HO-1, and LDH are expressed differently, with positive correlations between HMGB1, IL-1β, and LDH in infectious effusions, and low IL-1β expression in malignant effusions.
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