牙周炎
二、侵袭性牙周炎
医学
免疫组织化学
病理
补体系统
接收机工作特性
免疫学
内科学
抗体
作者
Ren‐Yeong Huang,Fang-Yi Tseng,Chia-Dan Cheng,Thomas E. Van Dyke,Cheng‐En Sung,Jhong-Jhe You,Pei-Wei Weng,Yi‐Shing Shieh,Wan‐Chien Cheng
摘要
Abstract Objective This study aimed to investigate the correlation between the expression levels of C3b and C4b in human gingival tissue (GT) and gingival crevicular fluid (GCF) and disease severity in human periodontitis and to determine whether C3b and C4b are significant site‐specific complementary diagnostic markers for periodontitis. Background A variety of biomarkers that have potential for informing diagnoses of periodontitis have been proposed. The complement components C3b and C4b were found to be positively correlated with disease severity. The therapeutic effect of targeting C3b and C4b on inflammatory bone loss in experimental periodontitis models has been studied. However, studies on the diagnostic potential of the gingival C3b and C4b expression levels for periodontitis are scarce. Methods The expression levels of C3b and C4b in the GT and GCF were investigated via immunohistochemistry and enzyme‐linked immunosorbent assay, respectively. The correlation between the expression levels of C3b and C4b and disease severity with probing depth as well as the clinical attachment level were determined. To evaluate the diagnostic accuracy of the C3b and C4b expression levels at the periodontitis sites, the receiver operating characteristic (ROC) curve, cut‐off point, area under the ROC curve, sensitivity, and specificity were analyzed. Results The expression levels of C3b and C4b in human GT and GCF were significantly positively correlated with periodontitis severity. The expression levels of combined C3b + C4b in the GT can significantly differentiate the disease status at the tissue level ( p < .0001). Similarly, the expression levels of C3b + C4b in GCF can statistically distinguish periodontitis sites from healthy ones ( p < .0001). Conclusions Locally deposited C3b and C4b were positively correlated with periodontitis severity and recognized as site‐specific diagnostic biomarkers for clinicopathological features in periodontitis. The association between the C3b and C4b network and periodontitis may be further understood and provide a basis for the development of novel screening as well as diagnostic and therapeutic strategies for periodontitis.
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