Multi-threshold polygenic risk improves hippocampal-based cognitive decline prediction.

IF 10.8 1区 生物学 Q1 GENETICS & HEREDITY
Mohammed Janahi, Luigi Lorenzini, Neil P Oxtoby, Frederik Barkhof, Younes Mokrab, Jonathan M Schott, Andre Altmann, For The Alzheimer's Disease Neuroimaging Initiative
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引用次数: 0

Abstract

Background: Predicting cognitive decline from brain MRI is a central question in neuroscience. Hippocampal volume (HV) is a key cognitive biomarker, and normative models can be augmented with multimodal information. Here we augment normative models with genetic information and show improvements in cognitive decline prediction across multiple experimental setups.

Methods: We improve normative models for HV by integrating multi-threshold polygenic scores (PGS) with demographic and imaging data using Gaussian Process Regression (GPR). Models were trained on 23,997 participants from UK Biobank (UKBB) and validated on 3,000 out-of-sample participants from the Alzheimer's Disease Neuroimaging Initiative (ADNI) and the European Prevention of Alzheimer's Disease (EPAD) cohorts.

Results: Our genetically-informed models significantly strengthened associations across six experimental designs and 13 key neurocognitive measures, including Mini-Mental State Examination (MMSE), Clinical Dementia Rating (CDR), and Alzheimer's Disease Assessment Scale (ADAS), while enhancing prediction of future cognitive decline.

Conclusions: Together, these findings underscore the promise of integrating multi-threshold PGS with neuroimaging-based predictive models to improve prognostication and early intervention strategies for neurodegenerative diseases.

多阈值多基因风险改善基于海马的认知衰退预测。
背景:通过脑MRI预测认知能力下降是神经科学的一个核心问题。海马体积(HV)是一个关键的认知生物标志物,规范模型可以用多模态信息增强。在这里,我们用遗传信息增强了规范模型,并在多个实验设置中显示了认知衰退预测的改进。方法:利用高斯过程回归(GPR)将多阈值多基因评分(PGS)与人口统计学和影像学数据相结合,改进HV的规范模型。模型在来自英国生物银行(UKBB)的23,997名参与者上进行了训练,并在来自阿尔茨海默病神经影像学倡议(ADNI)和欧洲阿尔茨海默病预防(EPAD)队列的3,000名样本外参与者上进行了验证。结果:我们的遗传信息模型显著增强了六个实验设计和13个关键神经认知测量的关联,包括迷你精神状态检查(MMSE)、临床痴呆评分(CDR)和阿尔茨海默病评估量表(ADAS),同时增强了对未来认知能力下降的预测。总之,这些发现强调了将多阈值PGS与基于神经影像学的预测模型相结合,以改善神经退行性疾病的预后和早期干预策略的前景。
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来源期刊
Genome Medicine
Genome Medicine GENETICS & HEREDITY-
CiteScore
20.80
自引率
0.80%
发文量
128
审稿时长
6-12 weeks
期刊介绍: Genome Medicine is an open access journal that publishes outstanding research applying genetics, genomics, and multi-omics to understand, diagnose, and treat disease. Bridging basic science and clinical research, it covers areas such as cancer genomics, immuno-oncology, immunogenomics, infectious disease, microbiome, neurogenomics, systems medicine, clinical genomics, gene therapies, precision medicine, and clinical trials. The journal publishes original research, methods, software, and reviews to serve authors and promote broad interest and importance in the field.
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