Association between choroidal microvasculature in the eye and Alzheimer's disease risk in cognitively healthy mid-life adults: A pilot study.

IF 4.4 Q1 CLINICAL NEUROLOGY Alzheimer''s and Dementia: Diagnosis, Assessment and Disease Monitoring Pub Date : 2025-01-16 eCollection Date: 2025-01-01 DOI:10.1002/dad2.70075
Jamie Burke, Samuel Gibbon, Audrey Low, Charlene Hamid, Megan Reid-Schachter, Graciela Muniz-Terrera, Craig W Ritchie, Baljean Dhillon, John T O'Brien, Stuart King, Ian J C MacCormick, Thomas J MacGillivray
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Abstract

Introduction: We explored associations between measurements of the ocular choroid microvasculature and Alzheimer's disease (AD) risk.

Methods: We measured the choroidal vasculature appearing in optical coherence tomography (OCT) scans of 69 healthy, mid-life individuals in the PREVENT Dementia cohort. The cohort was prospectively split into low-, medium-, and high-risk groups based on the presence of known risk factors (apolipoprotein E [APOE] ε4 genotype and family history of dementia [FH]). We used ordinal logistic regression to test for cross-sectional associations between choroidal measurements and AD risk.

Results: Choroidal vasculature was progressively larger between ordinal risk groups, and significantly associated with risk group prediction. APOE ε4 carriers had thicker choroids and larger vascularity compared to non-carriers. Similar trends were observed for those with a FH.

Discussions: Our results suggest a potential link between the choroidal vasculature and AD risk. However, these exploratory findings should be replicated in a larger sample.

Highlights: Ocular choroidal microvasculature is of interest in relation to neurodegeneration due to its autonomic response to systemic, pathophysiological change.Choroidal changes in the prodromal stage of Alzheimer's disease (AD) are unexplored.The PREVENT Dementia cohort offers a unique, non-invasive study of the microvasculature in mid-life individuals at increased risk for developing AD.Significantly increased ocular choroidal vasculature was associated with increased risk (apolipoprotein E carrier and/or family history of dementia) for AD.These exploratory results suggest a potential association between the ocular choroidal vasculature and AD risk. However, findings should be replicated in a larger sample.

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认知健康的中年成人眼脉络膜微血管与阿尔茨海默病风险之间的关系:一项初步研究
简介:我们探讨了眼脉络膜微血管测量与阿尔茨海默病(AD)风险之间的关系。方法:我们测量了预防痴呆队列中69名健康中年个体的光学相干断层扫描(OCT)中出现的脉络膜血管。根据已知危险因素(载脂蛋白E [APOE] ε4基因型和痴呆家族史[FH])的存在,前瞻性地将该队列分为低、中、高风险组。我们使用有序逻辑回归来检验脉络膜测量与AD风险之间的横断面关联。结果:脉络膜血管在序贯危险组间逐渐变大,并与危险组预测显著相关。APOE ε4携带者与非携带者相比,其脉络膜更厚,血管更大。FH患者也有类似的趋势。讨论:我们的结果表明脉络膜血管和AD风险之间存在潜在的联系。然而,这些探索性的发现应该在更大的样本中得到重复。眼部脉络膜微血管因其对全身病理生理变化的自主反应而与神经变性有关。阿尔茨海默病(AD)前驱期脉络膜的变化尚不清楚。预防痴呆队列提供了一项独特的、非侵入性的研究,研究了患AD风险增加的中年个体的微血管。眼部脉络膜血管的明显增加与AD的风险增加(载脂蛋白E携带者和/或痴呆家族史)相关。这些探索性结果表明,眼脉络膜血管与AD风险之间存在潜在关联。然而,研究结果应该在更大的样本中得到重复。
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来源期刊
CiteScore
7.80
自引率
7.50%
发文量
101
审稿时长
8 weeks
期刊介绍: Alzheimer''s & Dementia: Diagnosis, Assessment & Disease Monitoring (DADM) is an open access, peer-reviewed, journal from the Alzheimer''s Association® that will publish new research that reports the discovery, development and validation of instruments, technologies, algorithms, and innovative processes. Papers will cover a range of topics interested in the early and accurate detection of individuals with memory complaints and/or among asymptomatic individuals at elevated risk for various forms of memory disorders. The expectation for published papers will be to translate fundamental knowledge about the neurobiology of the disease into practical reports that describe both the conceptual and methodological aspects of the submitted scientific inquiry. Published topics will explore the development of biomarkers, surrogate markers, and conceptual/methodological challenges. Publication priority will be given to papers that 1) describe putative surrogate markers that accurately track disease progression, 2) biomarkers that fulfill international regulatory requirements, 3) reports from large, well-characterized population-based cohorts that comprise the heterogeneity and diversity of asymptomatic individuals and 4) algorithmic development that considers multi-marker arrays (e.g., integrated-omics, genetics, biofluids, imaging, etc.) and advanced computational analytics and technologies.
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