Evidence map›Paper›PMID 42328105›Full record

ArticleProceedings of SPIE--the International Society for Optical Engineering2025

Reconstructing physiological signals from fMRI across the adult lifespan.

Shiyu Wang, Ziyuan Xu, Laurent M Lochard, Yamin Li, Jiawen Fan, Jingyuan E Chen, Yuankai Huo, Mara Mather, Roza G Bayrak, Catie Chang

Abstract read
In one paragraph

Article in Proceedings of SPIE--the International Society for Optical Engineering, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Shiyu WangDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN, USA.
Ziyuan XuDepartment of Computer Science, Vanderbilt University, Nashville, TN, USA.
Laurent M LochardDepartment of Electrical and Computer Engineering, Vanderbilt University, Nashville, TN, USA.
Yamin LiDepartment of Computer Science, Vanderbilt University, Nashville, TN, USA.
Jiawen FanAthinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Boston, MA, USA.
Jingyuan E ChenAthinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Boston, MA, USA.
Yuankai HuoDepartment of Computer Science, Vanderbilt University, Nashville, TN, USA.
Mara MatherLeonard Davis School of Gerontology, Department of Psychology, Department of Biomedical Engineering, University of Southern California, Los Angeles, CA, USA.
Roza G BayrakDepartment of Computer Science, Vanderbilt University, Nashville, TN, USA.
Catie ChangDepartment of Biomedical Engineering, Vanderbilt University, Nashville, TN, USA.

Funding

Project 5: ComputationalP50MH109429 · NIMH · NATHAN S. KLINE INSTITUTE FOR PSYCH RES · PI Michael Peter Milham · 2017 to 2026
$25.3M
MAPPING THE HUMAN CONNECTOME DURING TYPICAL AGINGU01AG052564 · NIA · WASHINGTON UNIVERSITY · PI SALAT, DAVID H, TERPSTRA, MELISSA J · 2016 to 2020
$18.9M
fMRI physiological signatures of aging and Alzheimer's DiseaseRF1MH125931 · NIMH · VANDERBILT UNIVERSITY · PI CHANG, CATHERINE ELIZABETH · 2021 to 2021
$1.1M
NIA NIH HHS U01 AG052564NIMH NIH HHS P50 MH109429NIMH NIH HHS RF1 MH125931
6 · The paper itself

Abstract

Interactions between the brain and body are of fundamental importance for human behavior and health. Functional magnetic resonance imaging (fMRI) captures whole-brain activity noninvasively, and modeling how fMRI signals interact with physiological dynamics of the body can provide new insight into brain function and offer potential biomarkers of disease. However, physiological recordings are not always possible to acquire since they require extra equipment and setup, and even when they are, the recorded physiological signals may contain substantial artifacts. To overcome this limitation, machine learning models have been proposed to directly extract features of respiratory and cardiac activity from resting-state fMRI signals. To date, such work has been carried out only in healthy young adults and in a pediatric population, leaving open questions about the efficacy of these approaches on older adults. Here, we propose a novel framework that leverages Transformer-based architectures for reconstructing two key physiological signals - low-frequency respiratory volume (RV) and heart rate (HR) fluctuations - from fMRI data, and test these models on a dataset of individuals aged 36-89 years old. Our framework outperforms previously proposed approaches (attaining median correlations between predicted and measured signals of r ~ .698 for RV and r ~ .618 for HR), indicating the potential of leveraging attention mechanisms to model fMRI-physiological signal relationships. We also evaluate several model training and fine-tuning strategies, and find that incorporating young-adult data during training improves the performance when predicting physiological signals in the aging cohort. Overall, our approach successfully infers key physiological variables directly from fMRI data from individuals across a wide range of the adult lifespan.

Indexed as

agingcardiac activitydeep learningphysiologyrespirationResting-state fMRI

Identifiers

PMID42328105
PMCPMC13277321

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.