Label-Free Multiphoton Microscopy for the Detection and Monitoring of Calcific Aortic Valve Disease

被引:5
作者
Tandon, Ishita [1 ]
Quinn, Kyle P. [1 ]
Balachandran, Kartik [1 ]
机构
[1] Univ Arkansas, Dept Biomed Engn, Fayetteville, AR 72701 USA
基金
美国国家科学基金会;
关键词
calcific aortic valve disease; multiphoton microscopy; valve interstitial cell metabolism; aortic stenosis; early diagnosis; IN-VIVO MULTIPHOTON; VALVULAR HEART-DISEASE; 2-PHOTON MICROSCOPY; RAPID QUANTIFICATION; INTERSTITIAL-CELLS; CARDIAC METABOLISM; PROTEOMIC ANALYSIS; FLUORESCENCE; MITOCHONDRIAL; INFLAMMATION;
D O I
10.3389/fcvm.2021.688513
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Calcific aortic valve disease (CAVD) is the most common valvular heart disease. CAVD results in a considerable socio-economic burden, especially considering the aging population in Europe and North America. The only treatment standard is surgical valve replacement as early diagnostic, mitigation, and drug strategies remain underdeveloped. Novel diagnostic techniques and biomarkers for early detection and monitoring of CAVD progression are thus a pressing need. Additionally, non-destructive tools are required for longitudinal in vitro and in vivo assessment of CAVD initiation and progression that can be translated into clinical practice in the future. Multiphoton microscopy (MPM) facilitates label-free and non-destructive imaging to obtain quantitative, optical biomarkers that have been shown to correlate with key events during CAVD progression. MPM can also be used to obtain spatiotemporal readouts of metabolic changes that occur in the cells. While cellular metabolism has been extensively explored for various cardiovascular disorders like atherosclerosis, hypertension, and heart failure, and has shown potential in elucidating key pathophysiological processes in heart valve diseases, it has yet to gain traction in the study of CAVD. Furthermore, MPM also provides structural, functional, and metabolic readouts that have the potential to correlate with key pathophysiological events in CAVD progression. This review outlines the applicability of MPM and its derived quantitative metrics for the detection and monitoring of early CAVD progression. The review will further focus on the MPM-detectable metabolic biomarkers that correlate with key biological events during valve pathogenesis and their potential role in assessing CAVD pathophysiology.
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页数:10
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