Junbo Zeng

and 17 more

Background: Atelectasis and attic retraction pocket are two common tympanic membranes changes. However, general practitioners, pediatricians and otolaryngologists showed low diagnostic accuracy for these ear diseases. Therefore, there is a need to develop a deep learning model to detect atelectasis and attic retraction pocket automatically. Method: 6393 OME otoscopic images from 3 centers were used to develop and validate a deep learning model to detect atelectasis and attic retraction pocket. 3-fold random cross validation was adopted to divided dataset into training set and validation set. A team of otologists were assigned to diagnose and label. Receiver operating characteristic (ROC) curve, 3-fold average classification accuracy, sensitivity and specificity were used to assess the performance of deep learning model. Class Activation Mapping (CAM) was applied to show the discriminative region in the otoscopic images. Result: Among all the otoscopic images, 3564 (55.74%) images were identified with attic retraction pocket, and 2460 (38.48%) images were identified with atelectasis. The automatically diagnostic model of attic retraction pocket and atelectasis achieved 3-fold cross validation accuracy of 89% and 79%, AUC of 0.89 and 0.87, sensitivity of 0.93 and 0.71, and specificity of 0.62 and 0.84 respectively. Bigger and deeper atelectasis and attic retraction pocket showed more weight with red color in the heat map of CAM. Conclusion: Deep learning algorithm could be used to identify atelectasis and attic retraction pocket, which could be used as a tool to assist general practitioners, pediatricians and otolaryngologists. Key words: deep learning, otoscopic images, atelectasis, attic retraction pocket

Zhiyuan Tang

and 6 more

Objective: To assess whether secretory otitis media may be caused by immune imbalance of Treg/Th17 mediated by PI3K/Akt/mTOR signaling, so as to find new therapeutic target. Methods: IL-17, TGF- and IL-6, IL-10 and Th17 cytokines were detected in peripheral blood of OME patients (PC group) and healthy people (NC group) by ELISA. The expression of ROR t mRNA and Foxp3mRNA in PBMC was detected by RT-PCR. OME rat model was established and the changes of lymphocytes in middle ear mucosa and spleen and PI3K/Akt/mTOR signaling in middle ear mucosa were detected by HE staining, IHC, WB and flow cytometry. Results: The immune imbalance of Treg/Th17 in secretory otitis media (OME) was confirmed by the expression of cytokines in OME serum and analysis of ROR T and Foxp3 mRNA which was Th17 and Treg specific transcription respectively. OME rat model further confirmed that Treg/Th17 imbalance could lead to OME as demonstrated by staining of MIDDLE ear mucosa and expression of ROR T and Foxp3. PI3K, Akt, and mTOR proteins were expressed in the MIDDLE ear mucosa of OME group and CON group, respectively. Compared with CON group, the expression of P-MTOR and P-PI3K proteins in the middle ear mucosa of OME group was significantly increased. Conclusions: Treg/Th17 imbalances are found in OME patients and OME animal model and the pathogenic mechanism may be due to systemic abnormal immune response, activated PI3K/Akt/mTOR signaling, abnormal T cell differentiation, leading to middle ear mucosal hyperemia, edema and subsequent occurrence of OME.