Zhang Shujun, Shi Xiaoli, Zheng Shaolin, Liang Xiaoli, Wang Fen, Xu Weijie, Yu Xuefeng, Yang Yan
Division of Endocrinology, Department of Internal Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei Province, China.
Hubei Clinical Medical Research Center for Endocrinology and Metabolic Diseases, Wuhan, Hubei Province, China.
J Diabetes Res. 2025 Apr 16;2025:8029913. doi: 10.1155/jdr/8029913. eCollection 2025.
Diabetes has been associated with an excess risk of cognitive impairment. The hyperphosphorylation of tau protein leads to neurodegeneration and is closely related to Type 2 diabetes (T2D). This study aimed to characterize the association between P-tau181 and diabetic cognitive impairment and to develop a nomogram-based score to screen cognitive impairment in T2D patients. We used a cohort of 379 patients diagnosed with T2D as a training dataset to develop a predictive model. Risk factors associated with cognitive impairment were identified using stepwise multivariate logistic regressive analysis. A nomogram was established by incorporating these risk factors, and the diabetic cognitive impairment score (DCIS) was built and externally validated in another cohort. In the training cohort, patients with cognitive impairment had higher levels of P-tau181 (13.3 [10.5-18.7] vs. 10.0 [8.0-13.0], < 0.001). P-tau181 was negatively correlated with MOCA ( = -0.308, < 0.001) and MMSE ( = -0.289, < 0.001), and it was independently associated with cognitive impairment in T2D patients (OR, 1.137 [95% CI, 1.080-1.198]; < 0.001). Other independent risk factors of diabetic cognitive impairment included age, education level, and diabetic retinopathy. The DCIS was built by nomogram based on the four risk factors, which had an area under the receiver operating characteristic curve (AUC) of 0.795 (95% CI, 0.751-0.840). The optimal cut-off of DCIS for the diagnosis of cognitive impairment in T2D patients was 139.5, with a sensitivity of 72.9% and a specificity of 75.3%. In the validation cohort, the AUC of DCIS for screening diabetic cognitive impairment was 0.770 (95% CI, 0.716-0.824). P-tau181 was independently associated with diabetic cognitive impairment. The DCIS, based on P-tau181, age, education level, and diabetic retinopathy, is effective to identify cognitive impairment in T2D patients.
糖尿病与认知障碍风险增加有关。tau蛋白的过度磷酸化会导致神经退行性变,且与2型糖尿病(T2D)密切相关。本研究旨在描述磷酸化tau蛋白181(P-tau181)与糖尿病认知障碍之间的关联,并开发一种基于列线图的评分系统以筛查T2D患者的认知障碍。我们将379例确诊为T2D的患者作为训练数据集来建立预测模型。采用逐步多因素逻辑回归分析确定与认知障碍相关的危险因素。纳入这些危险因素建立列线图,并构建糖尿病认知障碍评分(DCIS),并在另一队列中进行外部验证。在训练队列中,认知障碍患者的P-tau181水平较高(13.3[10.5 - 18.7]对10.0[8.0 - 13.0],<0.001)。P-tau181与蒙特利尔认知评估量表(MOCA)呈负相关(=-0.308,<0.001),与简易精神状态检查表(MMSE)也呈负相关(=-0.289,<0.001),并且它与T2D患者的认知障碍独立相关(比值比[OR],1.137[95%置信区间(CI),1.080 - 1.198];<0.001)。糖尿病认知障碍的其他独立危险因素包括年龄、教育水平和糖尿病视网膜病变。基于这四个危险因素通过列线图构建DCIS,其受试者操作特征曲线(AUC)下面积为0.795(95%CI,0.751 - 0.840)。T2D患者诊断认知障碍的DCIS最佳截断值为139.5,灵敏度为72.9%,特异度为75.3%。在验证队列中,DCIS筛查糖尿病认知障碍的AUC为0.770(95%CI,0.716 - 0.824)。P-tau181与糖尿病认知障碍独立相关。基于P-tau181、年龄、教育水平和糖尿病视网膜病变的DCIS能够有效识别T2D患者的认知障碍。