Developing multifactorial dementia prediction models using clinical variables from cohorts in the US and Australia.

IF 5.8 1区 医学 Q1 PSYCHIATRY Translational Psychiatry Pub Date : 2025-01-21 DOI:10.1038/s41398-025-03247-0
Caitlin A Finney, David A Brown, Artur Shvetcov
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Abstract

Existing dementia prediction models using non-neuroimaging clinical measures have been limited in their ability to identify disease. This study used machine learning to re-examine the diagnostic potential of clinical measures for dementia. Data was sourced from the Australian Imaging, Biomarkers, and Lifestyle Flagship Study of Ageing (AIBL) and the Alzheimer's Disease Neuroimaging Initiative (ADNI). Clinical variables included 21 measures across medical history, hematological and other blood tests, and APOE genotype. Tree-based machine learning algorithms and artificial neural networks were used. APOE genotype was the best predictor of dementia cases and healthy controls. Our results, however, demonstrated that there are limitations when using publicly accessible cohort data that may limit the generalizability and interpretability of such predictive models. Future research should examine the use of routine APOE genetic testing for dementia diagnostics. It should also focus on clearly unifying data across clinical cohorts.

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利用来自美国和澳大利亚队列的临床变量开发多因素痴呆预测模型。
使用非神经影像学临床措施的现有痴呆预测模型在识别疾病的能力方面受到限制。这项研究使用机器学习来重新检查痴呆症临床措施的诊断潜力。数据来自澳大利亚老龄化成像、生物标志物和生活方式旗舰研究(AIBL)和阿尔茨海默病神经成像倡议(ADNI)。临床变量包括21项措施,包括病史、血液学和其他血液检查以及APOE基因型。使用基于树的机器学习算法和人工神经网络。APOE基因型是痴呆病例和健康对照的最佳预测因子。然而,我们的结果表明,在使用可公开访问的队列数据时存在局限性,这可能会限制此类预测模型的通用性和可解释性。未来的研究应该检查常规APOE基因检测在痴呆诊断中的应用。它还应该专注于明确统一临床队列的数据。
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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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