State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Centre, Sun Yat-sen University, Guangzhou, China.
Department of Hepatobiliary Surgery, Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Lancet Digit Health. 2021 Feb;3(2):e88-e97. doi: 10.1016/S2589-7500(20)30288-0.
Ocular changes are traditionally associated with only a few hepatobiliary diseases. These changes are non-specific and have a low detection rate, limiting their potential use as clinically independent diagnostic features. Therefore, we aimed to engineer deep learning models to establish associations between ocular features and major hepatobiliary diseases and to advance automated screening and identification of hepatobiliary diseases from ocular images.
We did a multicentre, prospective study to develop models using slit-lamp or retinal fundus images from participants in three hepatobiliary departments and two medical examination centres. Included participants were older than 18 years and had complete clinical information; participants diagnosed with acute hepatobiliary diseases were excluded. We trained seven slit-lamp models and seven fundus models (with or without hepatobiliary disease [screening model] or one specific disease type within six categories [identifying model]) using a development dataset, and we tested the models with an external test dataset. Additionally, we did a visual explanation and occlusion test. Model performances were evaluated using the area under the receiver operating characteristic curve (AUROC), sensitivity, specificity, and F1* score.
Between Dec 16, 2018, and July 31, 2019, we collected data from 1252 participants (from the Department of Hepatobiliary Surgery of the Third Affiliated Hospital of Sun Yat-sen University, the Department of Infectious Diseases of the Affiliated Huadu Hospital of Southern Medical University, and the Nantian Medical Centre of Aikang Health Care [Guangzhou, China]) for the development dataset; between Aug 14, 2019, and Jan 31, 2020, we collected data from 537 participants (from the Department of Infectious Diseases of the Third Affiliated Hospital of Sun Yat-sen University and the Huanshidong Medical Centre of Aikang Health Care [Guangzhou, China]) for the test dataset. The AUROC for screening for hepatobiliary diseases of the slit-lamp model was 0·74 (95% CI 0·71-0·76), whereas that of the fundus model was 0·68 (0·65-0·71). For the identification of hepatobiliary diseases, the AUROCs were 0·93 (0·91-0·94; slit-lamp) and 0·84 (0·81-0·86; fundus) for liver cancer, 0·90 (0·88-0·91; slit-lamp) and 0·83 (0·81-0·86; fundus) for liver cirrhosis, and ranged 0·58-0·69 (0·55-0·71; slit-lamp) and 0·62-0·70 (0·58-0·73; fundus) for other hepatobiliary diseases, including chronic viral hepatitis, non-alcoholic fatty liver disease, cholelithiasis, and hepatic cyst. In addition to the conjunctiva and sclera, our deep learning model revealed that the structures of the iris and fundus also contributed to the classification.
Our study established qualitative associations between ocular features and major hepatobiliary diseases, providing a non-invasive, convenient, and complementary method for hepatobiliary disease screening and identification, which could be applied as an opportunistic screening tool.
Science and Technology Planning Projects of Guangdong Province; National Key R&D Program of China; Guangzhou Key Laboratory Project; National Natural Science Foundation of China.
传统上,眼部变化仅与少数肝胆疾病有关。这些变化是非特异性的,检测率较低,限制了它们作为临床独立诊断特征的潜在用途。因此,我们旨在利用深度学习模型建立眼部特征与主要肝胆疾病之间的关联,并推进从眼部图像自动筛查和识别肝胆疾病。
我们进行了一项多中心前瞻性研究,使用来自三个肝胆科和两个体检中心的参与者的裂隙灯或视网膜眼底图像来开发模型。纳入的参与者年龄大于 18 岁,且具有完整的临床信息;排除了诊断为急性肝胆疾病的参与者。我们使用开发数据集训练了 7 个裂隙灯模型和 7 个眼底模型(有或无肝胆疾病[筛查模型]或 6 个类别中的一种特定疾病类型[识别模型]),并使用外部测试数据集对模型进行了测试。此外,我们还进行了视觉解释和遮挡测试。使用受试者工作特征曲线下的面积(AUROC)、敏感性、特异性和 F1*评分评估模型性能。
在 2018 年 12 月 16 日至 2019 年 7 月 31 日期间,我们从中山大学附属第三医院肝胆外科、南方医科大学附属花都医院传染病科和爱康华南区南天医疗中心(中国广州)收集了 1252 名参与者的数据,用于开发数据集;在 2019 年 8 月 14 日至 2020 年 1 月 31 日期间,我们从中山大学附属第三医院传染病科和爱康华南区环市东医疗中心(中国广州)收集了 537 名参与者的数据,用于测试数据集。裂隙灯模型筛查肝胆疾病的 AUROC 为 0.74(95%CI 0.71-0.76),眼底模型为 0.68(0.65-0.71)。对于肝胆疾病的识别,肝癌的 AUROCs 分别为 0.93(0.91-0.94;裂隙灯)和 0.84(0.81-0.86;眼底),肝硬化为 0.90(0.88-0.91;裂隙灯)和 0.83(0.81-0.86;眼底),其他肝胆疾病包括慢性病毒性肝炎、非酒精性脂肪性肝病、胆石症和肝囊肿的 AUROCs 范围为 0.58-0.69(0.55-0.71;裂隙灯)和 0.62-0.70(0.58-0.73;眼底)。除了结膜和巩膜外,我们的深度学习模型还揭示了虹膜和眼底的结构也有助于分类。
我们的研究建立了眼部特征与主要肝胆疾病之间的定性关联,为肝胆疾病的筛查和识别提供了一种非侵入性、方便、互补的方法,可作为一种机会性筛查工具。
广东省科技计划项目;国家重点研发计划;广州市重点实验室项目;国家自然科学基金。