Fujii Takayuki, Murata Koichi, Kohjitani Hirohiko, Onishi Akira, Murakami Kosaku, Tanaka Masao, Yamamoto Wataru, Nagai Koji, Yoshikawa Ayaka, Etani Yuki, Okita Yasutaka, Yoshida Naofumi, Amuro Hideki, Okano Tadashi, Ueda Yo, Okano Takaichi, Hara Ryota, Hashimoto Motomu, Morinobu Akio, Matsuda Shuichi
Department of Advanced Medicine for Rheumatic Diseases, Graduate School of Medicine, Kyoto University, 54 Shogoin Kawaharacho, Sakyo, Kyoto, Japan.
Department of Orthopaedic Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Arthritis Res Ther. 2025 Mar 26;27(1):65. doi: 10.1186/s13075-025-03541-8.
Undifferentiated arthritis (UA) often develops into rheumatoid arthritis (RA), but predicting disease progression from seronegative UA remains challenging because seronegative RA often does not meet the classification criteria. This study aims to build a machine learning (ML) model to predict the progression from seronegative UA to RA using clinical and laboratory parameters.
KURAMA cohort (training dataset) and ANSWER cohort (validation dataset) were utilized. Patients with seronegative UA were selected based on specific inclusion and exclusion criteria. Clinical and laboratory parameters, including demographic data, acute phase reactants, autoantibodies, and physical examination findings, were collected. Various ML models, including a Feedforward Neural Network (FNN), were developed and compared. Model performance was evaluated using the area under the receiver operating characteristic curve (AUC), sensitivity, and other metrics. SHapley Additive exPlanations (SHAP) values were computed to interpret the importance of variables.
KURAMA cohort included 210 patients with seronegative UA, of whom 57 (27.1%) progressed to RA. The FNN model demonstrated the highest predictive performance with an AUC of 0.924 and a sensitivity of 80.7% in the training dataset. Validation with ANSWER cohort (140 patients; 32.1% progressed to RA) showed an AUC of 0.777, sensitivity of 77.8%. MMP-3 had the highest impact on the model.
The FNN model exhibited robust performance in predicting the progression of RA from seronegative UA and maintained substantial sensitivity in an independent validation cohort. This model using only clinical and laboratory parameters has potential for predicting RA progression in patients with seronegative UA.
未分化关节炎(UA)常发展为类风湿关节炎(RA),但由于血清阴性RA往往不符合分类标准,预测血清阴性UA的疾病进展仍具有挑战性。本研究旨在构建一个机器学习(ML)模型,使用临床和实验室参数预测血清阴性UA向RA的进展。
使用了KURAMA队列(训练数据集)和ANSWER队列(验证数据集)。根据特定的纳入和排除标准选择血清阴性UA患者。收集了临床和实验室参数,包括人口统计学数据、急性期反应物、自身抗体和体格检查结果。开发并比较了各种ML模型,包括前馈神经网络(FNN)。使用受试者操作特征曲线下面积(AUC)、敏感性和其他指标评估模型性能。计算SHapley加性解释(SHAP)值以解释变量的重要性。
KURAMA队列包括210例血清阴性UA患者,其中57例(27.1%)进展为RA。FNN模型在训练数据集中表现出最高的预测性能,AUC为0.924,敏感性为80.7%。用ANSWER队列(140例患者;32.1%进展为RA)进行验证,AUC为0.777,敏感性为77.8%。基质金属蛋白酶-3(MMP-3)对模型的影响最大。
FNN模型在预测血清阴性UA向RA的进展方面表现出强大的性能,并且在独立验证队列中保持了较高的敏感性。这个仅使用临床和实验室参数的模型具有预测血清阴性UA患者RA进展的潜力。