结合血浆 pTau181 和结构成像特征的轻度认知障碍痴呆转换预测模型

IF 4.8 1区 医学 Q1 NEUROSCIENCES CNS Neuroscience & Therapeutics Pub Date : 2024-09-18 DOI:10.1111/cns.70051
Tao-Ran Li, Bai-Le Li, Jin Zhong, Xin-Ran Xu, Tai-Shan Wang, Feng-Qi Liu, for the Alzheimer's Disease Neuroimaging Initiative
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引用次数: 0

摘要

目的 老年痴呆症(AD)的早期阶段已不再是不可逾越的障碍。因此,识别高危人群对于精确治疗具有重要意义。我们建立了一个模型来预测轻度认知障碍(MCI)患者的认知功能退化。 方法 我们以阿尔茨海默病神经影像倡议(ADNI)数据库为基础,在 761 名 MCI 患者(其中 138 人在第 36 个月时患上痴呆症)组成的衍生队列中构建了模型,并在 353 名认知正常的对照组(其中 54 人在第 36 个月时患上 MCI,19 人患上痴呆症)组成的验证队列中对模型进行了验证。此外,我们还挑选了1303名具有AD脑脊液核心生物标志物的参与者,以明确该模型预测AD核心特征的能力。我们评估了32个候选预测参数,包括临床信息、血液生物标志物和结构影像特征,并使用多变量逻辑回归分析建立了预测模型。 结果 发现了MCI恶化的六个独立变量:载脂蛋白E ε4等位基因状态、较低的迷你精神状态检查评分、较高的血浆pTau181水平、较小的左侧海马和右侧杏仁核体积以及较薄的右侧下颞皮层。我们根据这些风险因素建立了一个易于使用的风险热图和风险评分。内部和外部验证的曲线下面积(AUC)均接近 0.850。此外,在识别脑淀粉样蛋白-β负荷高的参与者方面,AUC也超过了0.800。校准图显示,在内部和外部验证中,预测概率与实际观察结果之间的一致性很好。 结论 我们开发并验证了 MCI 患者痴呆转化的准确预测模型。同时,该模型还能预测 AD 特异性病理变化。我们希望该模型能有助于更精确的临床治疗和更好的医疗资源分配。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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A prediction model of dementia conversion for mild cognitive impairment by combining plasma pTau181 and structural imaging features

Aims

The early stages of Alzheimer's disease (AD) are no longer insurmountable. Therefore, identifying at-risk individuals is of great importance for precise treatment. We developed a model to predict cognitive deterioration in patients with mild cognitive impairment (MCI).

Methods

Based on the Alzheimer's Disease Neuroimaging Initiative (ADNI) database, we constructed models in a derivation cohort of 761 participants with MCI (138 of whom developed dementia at the 36th month) and verified them in a validation cohort of 353 cognitively normal controls (54 developed MCI and 19 developed dementia at the 36th month). In addition, 1303 participants with available AD cerebrospinal fluid core biomarkers were selected to clarify the ability of the model to predict AD core features. We assessed 32 parameters as candidate predictors, including clinical information, blood biomarkers, and structural imaging features, and used multivariable logistic regression analysis to develop our prediction model.

Results

Six independent variables of MCI deterioration were identified: apolipoprotein E ε4 allele status, lower Mini-Mental State Examination scores, higher levels of plasma pTau181, smaller volumes of the left hippocampus and right amygdala, and a thinner right inferior temporal cortex. We established an easy-to-use risk heat map and risk score based on these risk factors. The area under the curve (AUC) for both internal and external validations was close to 0.850. Furthermore, the AUC was above 0.800 in identifying participants with high brain amyloid-β loads. Calibration plots demonstrated good agreement between the predicted probability and actual observations in the internal and external validations.

Conclusion

We developed and validated an accurate prediction model for dementia conversion in patients with MCI. Simultaneously, the model predicts AD-specific pathological changes. We hope that this model will contribute to more precise clinical treatment and better healthcare resource allocation.

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来源期刊
CNS Neuroscience & Therapeutics
CNS Neuroscience & Therapeutics 医学-神经科学
CiteScore
7.30
自引率
12.70%
发文量
240
审稿时长
2 months
期刊介绍: CNS Neuroscience & Therapeutics provides a medium for rapid publication of original clinical, experimental, and translational research papers, timely reviews and reports of novel findings of therapeutic relevance to the central nervous system, as well as papers related to clinical pharmacology, drug development and novel methodologies for drug evaluation. The journal focuses on neurological and psychiatric diseases such as stroke, Parkinson’s disease, Alzheimer’s disease, depression, schizophrenia, epilepsy, and drug abuse.
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