Blood-based bioenergetics: An emerging translational and clinical tool

Accumulating studies demonstrate that mitochondrial genetics and function are central to determining the susceptibility to, and prognosis of numerous diseases across all organ systems. Despite this recognition, mitochondrial function remains poorly characterized in humans primarily due to the invasi...

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Veröffentlicht in:Molecular aspects of medicine 2020-02, Vol.71, p.100835-100835, Article 100835
Hauptverfasser: Braganza, Andrea, Annarapu, Gowtham K., Shiva, Sruti
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Sprache:eng
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Zusammenfassung:Accumulating studies demonstrate that mitochondrial genetics and function are central to determining the susceptibility to, and prognosis of numerous diseases across all organ systems. Despite this recognition, mitochondrial function remains poorly characterized in humans primarily due to the invasiveness of obtaining viable tissue for mitochondrial studies. Recent studies have begun to test the hypothesis that circulating blood cells, which can be obtained by minimally invasive methodology, can be utilized as a biomarker of systemic bioenergetic function in human populations. Here we present the available methodologies for assessing blood cell bioenergetics and review studies that have applied these techniques to healthy and disease populations. We focus on the validation of this methodology in healthy subjects, as well as studies testing whether blood cell bioenergetics are altered in disease, correlate with clinical parameters, and compare with other methodology for assessing human mitochondrial function. Finally, we present the challenges and goals for the development of this emerging approach into a tool for translational research and personalized medicine. •Platelets and PBMCs have fully functional and metabolically active mitochondria.•Blood cell bioenergetics change in disease and correlate with tissue bioenergetics.•Circulating blood cells can serve as a minimally invasive biomarker for systemic bioenergetics.
ISSN:0098-2997
1872-9452
DOI:10.1016/j.mam.2019.100835