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深度学习和单细胞测序分析揭示颈动脉粥样硬化斑块进展中的关键分子特征。

Deep Learning and Single-Cell Sequencing Analyses Unveiling Key Molecular Features in the Progression of Carotid Atherosclerotic Plaque.

机构信息

Department of Vascular Surgery, The First Hospital of China Medical University, Shenyang, Liaoning, China.

出版信息

J Cell Mol Med. 2024 Nov;28(22):e70220. doi: 10.1111/jcmm.70220.

DOI:10.1111/jcmm.70220
PMID:39586797
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11588433/
Abstract

Rupture of advanced carotid atherosclerotic plaques increases the risk of ischaemic stroke, which has significant global morbidity and mortality rates. However, the specific characteristics of immune cells with dysregulated function and proven biomarkers for the diagnosis of atherosclerotic plaque progression remain poorly characterised. Our study elucidated the role of immune cells and explored diagnostic biomarkers in advanced plaque progression using single-cell RNA sequencing and high-dimensional weighted gene co-expression network analysis. We identified a subcluster of monocytes with significantly increased infiltration in the advanced plaques. Based on the monocyte signature and machine-learning approaches, we accurately distinguished advanced plaques from early plaques, with an area under the curve (AUC) of 0.899 in independent external testing. Using microenvironment cell populations (MCP) counter and non-negative matrix factorisation, we determined the association between monocyte signatures and immune cell infiltration as well as the heterogeneity of the patient. Finally, we constructed a convolutional neural network deep learning model based on gene-immune correlation, which achieved an AUC of 0.933, a sensitivity of 92.3%, and a specificity of 87.5% in independent external testing for diagnosing advanced plaques. Our findings on unique subpopulations of monocytes that contribute to carotid plaque progression are crucial for the development of diagnostic tools for clinical diseases.

摘要

颈动脉粥样硬化斑块的破裂增加了缺血性中风的风险,而缺血性中风在全球具有显著的发病率和死亡率。然而,功能失调的免疫细胞的具体特征以及已证实的动脉粥样硬化斑块进展的诊断生物标志物仍未得到很好的描述。我们的研究使用单细胞 RNA 测序和高维加权基因共表达网络分析,阐明了免疫细胞在动脉粥样硬化斑块进展中的作用,并探讨了诊断生物标志物。我们在高级斑块中发现了单核细胞浸润明显增加的亚群。基于单核细胞特征和机器学习方法,我们可以准确地区分高级斑块和早期斑块,在独立的外部测试中曲线下面积(AUC)为 0.899。使用微环境细胞群体(MCP)计数器和非负矩阵分解,我们确定了单核细胞特征与免疫细胞浸润之间的关联以及患者的异质性。最后,我们基于基因-免疫相关性构建了一个卷积神经网络深度学习模型,在独立的外部测试中,该模型对诊断高级斑块的 AUC 为 0.933,灵敏度为 92.3%,特异性为 87.5%。我们对促进颈动脉斑块进展的独特单核细胞亚群的研究结果对于开发临床疾病的诊断工具至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9c0/11588433/727ff06bc0c1/JCMM-28-e70220-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9c0/11588433/9ca47d9b97d3/JCMM-28-e70220-g009.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9c0/11588433/c82f2a22eebf/JCMM-28-e70220-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9c0/11588433/d54176283ded/JCMM-28-e70220-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9c0/11588433/727ff06bc0c1/JCMM-28-e70220-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9c0/11588433/9ca47d9b97d3/JCMM-28-e70220-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9c0/11588433/3ee7d3291646/JCMM-28-e70220-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9c0/11588433/99da843426ca/JCMM-28-e70220-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9c0/11588433/06d51cae480f/JCMM-28-e70220-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9c0/11588433/c0b60fec4fea/JCMM-28-e70220-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9c0/11588433/285bed4a5613/JCMM-28-e70220-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9c0/11588433/c82f2a22eebf/JCMM-28-e70220-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9c0/11588433/d54176283ded/JCMM-28-e70220-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9c0/11588433/727ff06bc0c1/JCMM-28-e70220-g006.jpg

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