AI Article Synopsis

  • Functional PET (fPET) is a new technique for examining brain metabolism and neurotransmitter activity, typically requiring invasive blood sampling to measure arterial input function (AIF).
  • This study developed a non-invasive method using cardiac IDIF from twenty healthy individuals, validating its accuracy against traditional methods through blood sampling while participants engaged in a monetary incentive delay task.
  • Results showed a strong correlation between the new IDIF method and AIF, demonstrating that this non-invasive approach provides reliable quantification of brain activity changes, making fPET more accessible in clinical settings.

Article Abstract

Purpose: Functional PET (fPET) is a novel technique for studying dynamic changes in brain metabolism and neurotransmitter signaling. Accurate quantification of fPET relies on measuring the arterial input function (AIF), traditionally achieved through invasive arterial blood sampling. While non-invasive image-derived input functions (IDIF) offer an alternative, they suffer from limited spatial resolution and field of view. To overcome these issues, we developed and validated a scan protocol for brain fPET utilizing cardiac IDIF, aiming to mitigate known IDIF limitations.

Methods: Twenty healthy individuals underwent fPET/MR scans using [F]FDG or 6-[F]FDOPA, utilizing bed motion shuttling to capture cardiac IDIF and brain task-induced changes. Arterial and venous blood sampling was used to validate IDIFs. Participants performed a monetary incentive delay task. IDIFs from various blood pools and composites estimated from a linear fit over all IDIF blood pools (3VOI) and further supplemented with venous blood samples (3VOIVB) were compared to the AIF. Quantitative task-specific images from both tracers were compared to assess the performance of each input function to the gold standard.

Results: For both radiotracer cohorts, moderate to high agreement (r: 0.60-0.89) between IDIFs and AIF for both radiotracer cohorts was observed, with further improvement (r: 0.87-0.93) for composite IDIFs (3VOI and 3VOIVB). Both methods showed equivalent quantitative values and high agreement (r: 0.975-0.998) with AIF-derived measurements.

Conclusion: Our proposed protocol enables accurate non-invasive estimation of the input function with full quantification of task-specific changes, addressing the limitations of IDIF for brain imaging by sampling larger blood pools over the thorax. These advancements increase applicability to any PET scanner and clinical research setting by reducing experimental complexity and increasing patient comfort.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11224076PMC
http://dx.doi.org/10.1007/s00259-024-06716-8DOI Listing

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