Why the study?
Comparison between IVPA-US and NIRS-IVUS was needed to understand the relative advantages of each hybrid modality in detecting arterial lipid.
Does IVPA-US imaging provide comparable lipid quantification and better depth resolution compared to NIRS-IVUS in detecting arterial lipid?
Does IVPA-US imaging provide comparable lipid quantification and better depth resolution compared to NIRS-IVUS in detecting arterial lipid?
IVPA-US imaging offers comparable sensitivity to NIRS-IVUS for detecting arterial lipid while providing superior depth resolution to localize lipid cores within plaques.
IVPA-US supports preclinical lipid localization in MetS models; leaves open clinical translation versus NIRS-IVUS.
Intravascular photoacoustic-ultrasound (IVPA-US) imaging and near-infrared spectroscopy-intravascular ultrasound (NIRS-IVUS) are two hybrid modalities that detect arterial lipid, with comparison necessary to understand the relative advantages of each. We performed in vivo and ex vivo IVPA-US imaging of the iliac arteries of Ossabaw swine with metabolic syndrome (MetS) and lean swine to investigate sensitivity for early-stage atherosclerosis. We repeated imaging ex vivo with NIRS-IVUS for comparison to IVPA-US and histology. Both modalities showed significantly greater lipid in MetS vs. lean swine, but only IVPA-US localized the lipid as perivascular. To investigate late-stage atherosclerosis, we performed ex vivo IVPA-US imaging of a human coronary artery with comparison to NIRS-IVUS and histology. Two advanced fibroatheromas were identified, with agreement between IVPA-measured lipid area and NIRS-derived lipid content. As confirmed histologically, IVPA-US has sensitivity to detect lipid content similar to NIRS-IVUS and provides additional depth resolution, enabling quantification and localization of lipid cores within plaques.
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Kole et al. (2018) studied this question.
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