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PET [C]acetate is also a perfusion tracer for kidney evaluation purposes. | LitMetric

PET [C]acetate is also a perfusion tracer for kidney evaluation purposes.

Nucl Med Biol

Department of Nephrology and Renal Functional Explorations, Hôpital Edouard Herriot, Hospices Civils de Lyon, Lyon, France; CarMeN: Cardiovasculaire, Métabolisme, Diabétologie & Nutrition-INSERM U1060/INRA U1397/Université Lyon1, France; CERMEP, MR-PET Center, Lyon, France; Université Claude Bernard Lyon 1, Lyon, France.

Published: July 2020

Rationale: Renal positron emission tomography (PET) functional imaging allows non-invasive and dynamic measurements of functional and metabolic parameters. [O]HO is used as a perfusion tracer, and [C]acetate as an oxidative metabolism in this purpose, requiring two injections to assess those fundamental parameters. Yet, in cardiac physiology study, the high first-pass myocardial extraction fraction of [C]acetate allowed to use its influx rate as a blood flow marker too. Since [C]acetate has been characterized by a 20-25% single pass renal extraction in dogs, it could be used as a potential tracer for renal perfusion. The aim of this study was to determine whether [C]acetate influx rate can be used as quantitative in vivo marker of kidney perfusion in human.

Methods: In 10 healthy subjects, dynamic PET acquisitions were performed after [O]HO and [C]acetate injections spaced by a 15-minute interval. As previously validated, with compartmental modeling of kinetics, renal perfusion and oxidative metabolism were estimated respectively with influx rate of [O]HO and efflux rate of [C]acetate. Additionally, influx rate of [C]acetate was regressed to influx rate of [O]HO.

Results: Renal time activity curves of [C]-acetate was best fitted with a mono compartmental model compared to a bi-compartmental model (p < 0.0001). [C]acetate influx rate was significantly correlated with perfusion quantified with [O]HO (r = 0.37, p < 0.001) at baseline. This regression allowed the computation of a renal [C]acetate extraction fraction (EF), and further the computation of renal blood flow from its influx rate.

Conclusion: In healthy subjects, over a wide range of renal perfusion, direct estimates of renal oxygen consumption as well as tissue perfusion can be obtained by PET with a single tracer [C]acetate. This approach needs to be validated in CKD patients, and would be of great interest to design clinical protocol aiming at evaluating ischemic nephropathies candidate to revascularization.

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Source
http://dx.doi.org/10.1016/j.nucmedbio.2019.08.004DOI Listing

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