Lu Jingjing, Liang Weiwei, Cui Lijun, Mou Shaoqi, Pei Xuedan, Shen Xinhua, Shen Zhongxia, Shen Ping
Sleep Medical Center of Huzhou Third Municipal Hospital, The Affiliated Hospital of Huzhou University, Huzhou, China.
Hangzhou Seventh People's Hospital, Hangzhou, China.
Neuropsychobiology. 2025;84(2):74-85. doi: 10.1159/000543646. Epub 2025 Jan 22.
Activation of the inflammatory response system is involved in the pathogenesis of generalized anxiety disorder (GAD). The purpose of this study was to identify and characterize inflammatory biomarkers in the diagnosis of GAD based on machine learning algorithms.
The evaluation of peripheral immune parameters and lymphocyte subsets was performed on patients with GAD. Multivariable linear regression was used to explore the association between lymphocyte subsets and the severity of GAD. Receiver operating characteristic (ROC) analysis was used to determine the predictive value of these immunological parameters for GAD. Machine learning technology was applied to classify the collected data from patients in the GAD and healthy control groups.
Of the 340 patients enrolled, 171 were GAD patients, and 169 were non-GAD patients as healthy control. The levels of neutrophil, monocytes, and systemic immune-inflammation index (SII) were significantly elevated in GAD patients (p < 0.01), and the count and proportion of immune cells, including CD3+CD4+ T cells, CD3+CD8+ T cells, CD19+ B cells, and CD3-CD16+CD56+ NK cells (p < 0.001), have undergone large changes. The classification analysis conducted by machine learning using a weighted ensemble-L2 algorithm demonstrated an accuracy of 95.00 ± 2.04% in assessing the predictive value of these lymphocyte subsets in GAD. In addition, the feature importance analysis score is 0.255, which was much more predictive of GAD severity than for other lymphocyte subsets.
In the presented work, we show the level of lymphocyte subsets altered in GAD. Lymphocyte subsets, specifically CD3+CD4+ T %, can serve as neuroinflammatory biomarkers for GAD diagnostics. Furthermore, the application of machine learning offers a highly efficient approach for investigating neuroinflammatory biomarkers and predicting GAD. Our research has provided novel insights into the involvement of cellular immunity in GAD and highlighted the potential predictive value and therapeutic targets of lymphocyte subsets in this disorder.
炎症反应系统的激活参与了广泛性焦虑症(GAD)的发病机制。本研究的目的是基于机器学习算法识别和表征用于GAD诊断的炎症生物标志物。
对GAD患者进行外周免疫参数和淋巴细胞亚群评估。采用多变量线性回归探讨淋巴细胞亚群与GAD严重程度之间的关联。采用受试者工作特征(ROC)分析来确定这些免疫参数对GAD的预测价值。应用机器学习技术对GAD组和健康对照组患者收集的数据进行分类。
在纳入的340例患者中,171例为GAD患者,169例非GAD患者作为健康对照。GAD患者的中性粒细胞、单核细胞和全身免疫炎症指数(SII)水平显著升高(p<0.01),包括CD3 + CD4 + T细胞、CD3 + CD8 + T细胞、CD19 + B细胞和CD3 - CD16 + CD56 + NK细胞在内的免疫细胞计数和比例发生了很大变化(p<0.001)。使用加权集成-L2算法的机器学习进行的分类分析在评估这些淋巴细胞亚群对GAD的预测价值时显示准确率为95.00±2.04%。此外,特征重要性分析得分是0.255,其对GAD严重程度的预测性远高于其他淋巴细胞亚群。
在本研究中,我们展示了GAD中淋巴细胞亚群水平的改变。淋巴细胞亚群,特别是CD3 + CD4 + T%,可作为GAD诊断的神经炎症生物标志物。此外,机器学习的应用为研究神经炎症生物标志物和预测GAD提供了一种高效方法。我们的研究为细胞免疫参与GAD提供了新的见解,并突出了淋巴细胞亚群在该疾病中的潜在预测价值和治疗靶点。