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Automated Data Quality Control in FDOPA brain PET Imaging using Deep Learning.

Antonella D Pontoriero1, Giovanna Nordio1, Rubaida Easmin1

  • 1Department of Neuroimaging, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, United Kingdom.

Computer Methods and Programs in Biomedicine
|July 21, 2021
PubMed
Summary
This summary is machine-generated.

This study demonstrates that artificial intelligence (AI), specifically Convolutional Neural Networks (CNNs), can effectively automate quality control (QC) for brain [18F]-FDOPA PET imaging. The developed AI pipeline achieved 100% accuracy on validation datasets, showing promise for broader applications.

Keywords:
FDOPAPETQCconvolutional neural networksquality control

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Area of Science:

  • Biomedical Imaging
  • Artificial Intelligence
  • Neuroscience

Background:

  • Biomedical imaging research increasingly relies on large datasets, necessitating automated quality control (QC) methods.
  • Existing AI-based QC approaches for neuroimaging (EEG, MRI) have limited replication across different domains.
  • Automated QC is crucial for ensuring data integrity and reliability in multi-site and large-scale studies.

Purpose of the Study:

  • To assess the feasibility of an automated QC pipeline for brain [18F]-FDOPA Positron Emission Tomography (PET) imaging.
  • To evaluate the performance of Convolutional Neural Networks (CNNs) in identifying spatial misalignment and signal-to-noise ratio (SNR) issues in [18F]-FDOPA PET scans.
  • To determine the potential of AI for operator-free QC in dopamine system biomarker imaging.

Main Methods:

  • Two CNNs were developed and combined to analyze spatial misalignment and SNR in 200 manually QC'd [18F]-FDOPA PET scans.
  • An additional 400 scans were created with simulated misalignment (200) and low SNR (200).
  • A cross-validation approach (80% training, 20% validation) and out-of-sample validation with two independent datasets were employed.

Main Results:

  • CNNs achieved high accuracy in the training dataset (motion: 0.86 ± 0.01, SNR: 0.69 ± 0.01).
  • The automated QC pipeline demonstrated 100% accuracy when applied to two independent out-of-sample datasets.
  • Data dimensionality reduction negatively impacted CNN generalizability, particularly when transitioning from 3D to 1D datasets.

Conclusions:

  • Automated quality control of [18F]-FDOPA PET imaging using CNNs is feasible.
  • This AI-driven approach shows potential for extension to other PET tracers and applications (brain and non-brain).
  • Successful implementation is contingent upon the availability of large, diverse datasets for robust algorithm training.