Skip to main navigation Skip to search Skip to main content

Direct machine learning reconstruction of respiratory variation waveforms from resting state fMRI data in a pediatric population

Abdoljalil Addeh, Fernando Vega, Prathistith Raj Medi, Rebecca J Williams, G Bruce Pike, M Ethan MacDonald

Research output: Contribution to journalArticlepeer-review

11 Citations (Scopus)

Abstract

In many functional magnetic resonance imaging (fMRI) studies, respiratory signals are unavailable or do not have acceptable quality due to issues with subject compliance, equipment failure or signal error. In large databases, such as the Human Connectome Projects, over half of the respiratory recordings may be unusable. As a result, the direct removal of low frequency respiratory variations from the blood oxygen level-dependent (BOLD) signal time series is not possible. This study proposes a deep learning-based method for reconstruction of respiratory variation (RV) waveforms directly from BOLD fMRI data in pediatric participants (aged 5 to 21 years old), and does not require any respiratory measurement device. To do this, the Lifespan Human Connectome Project in Development (HCP-D) dataset, which includes respiratory measurements, was used to both train a convolutional neural network (CNN) and evaluate its performance. Results show that a CNN can capture informative features from the BOLD signal time course and reconstruct accurate RV time series, especially when the subject has a prominent respiratory event. This work advances the use of direct estimation of physiological parameters from fMRI, which will eventually lead to reduced complexity and decrease the burden on participants because they may not be required to wear a respiratory bellows.

Original languageEnglish
Article number119904
Pages (from-to)1-15
JournalNeuroImage
Volume269
DOIs
Publication statusPublished - 1 Apr 2023

Fingerprint

Dive into the research topics of 'Direct machine learning reconstruction of respiratory variation waveforms from resting state fMRI data in a pediatric population'. Together they form a unique fingerprint.

Cite this