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心血管疾病大分子标志物的高级生物分子光谱分析:SIL-6、IL-9、LpA、ApoB、PCSK9和NT-ProBNP用于快速原位检测和监测。

Advanced biomolecular spectroscopic profiling of cardiovascular disease macromolecular markers: SIL-6, IL-9, LpA, ApoB, PCSK9 and NT-ProBNP for rapid in-situ detection and monitoring.

作者信息

Buchan Emma, Harbi Maan H, Rickard Jonathan J S, Thomas Mark, Goldberg Oppenheimer Pola

机构信息

School of Chemical Engineering, College of Engineering and Physical Science, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.

Pharmacology and Toxicology Department, College of Pharmacy, Umm Al-Qura University, Makkah, Saudi Arabia.

出版信息

Int J Biol Macromol. 2025 Jan;284(Pt 1):138115. doi: 10.1016/j.ijbiomac.2024.138115. Epub 2024 Nov 26.

DOI:10.1016/j.ijbiomac.2024.138115
PMID:39608533
Abstract

Cardiovascular disease (CVD) remains a major global health concern and a leading cause of morbidity and mortality worldwide. Early-diagnosis and prompt medical attention are crucial in managing and reducing overall impact on health-and-wellbeing, necessitating the development of innovative diagnostics, which transcend traditional methodologies. Raman spectroscopy uniquely provides molecular fingerprinting and structural information, offering insights into biochemical composition. Integration of Raman spectroscopy with advanced machine learning is established as a powerful clinical adjunct for point-of-care detection of CVDs. A non-invasive, label-free spectroscopic platform coupled with neural network algorithm, 'SKiNET' has been developed to accurately detect the biomolecular changes within plasma of CVD versus healthy cohorts, enabling rapid diagnosis and longer-term monitoring, where the real-time capabilities provide dynamic assessment of progression, aligning treatment strategies with evolving states. CVD has been detected and classified via SKiNET with 88.6 %-accuracy, 92.9 %-specificity and 85.1 %-sensitivity and with 83.8 %-accuracy. The hybrid RS-SKiNET bio-molecularly specific detection signposted a comprehensive panel of CVD-indicative biomarkers, including SIL-6, IL-9, LpA, ApoB, PCSK9 and NT-ProBNP, offering important insights into disease mechanisms and risk-stratification. This multidimensional technique holds potential for improved patient-and-healthcare management for CVDs, laying the platform toward high-throughput biomolecular profiling of CVD-indicative macromolecular biomarkers, particularly vital for widespread point-of-care diagnostics and monitoring.

摘要

心血管疾病(CVD)仍然是全球主要的健康问题,也是全球发病和死亡的主要原因。早期诊断和及时的医疗护理对于控制和减少对健康和幸福的总体影响至关重要,因此需要开发超越传统方法的创新诊断方法。拉曼光谱独特地提供分子指纹和结构信息,有助于深入了解生化组成。拉曼光谱与先进的机器学习相结合,已成为用于心血管疾病即时检测的强大临床辅助手段。一种结合神经网络算法的非侵入性、无标记光谱平台“SKiNET”已被开发出来,用于准确检测心血管疾病患者与健康人群血浆中的生物分子变化,实现快速诊断和长期监测,其实时功能可对病情进展进行动态评估,使治疗策略与病情发展相匹配。通过SKiNET检测和分类心血管疾病的准确率为88.6%,特异性为92.9%,灵敏度为85.1%,另一次检测准确率为83.8%。RS-SKiNET这种混合生物分子特异性检测方法明确了一组全面的心血管疾病指示生物标志物,包括SIL-6、IL-9、LpA、ApoB、PCSK9和NT-ProBNP,为疾病机制和风险分层提供了重要见解。这种多维技术有望改善心血管疾病患者的管理和医疗保健,为心血管疾病指示大分子生物标志物的高通量生物分子分析奠定基础,这对于广泛的即时诊断和监测尤为重要。

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