Evidence map›Paper›PMID 42687944›Full record

ArticleResearch square2026

A Distinct Second Spectral Peak in White Matter BOLD Signals: Mathematical Modeling, Spatial Distribution and Age-Related Evolution.

Sijing Wu, Muwei Li, Yurui Gao, Lyuan Xu, Yu Zhao, John C Gore, Zhaohua Ding

Abstract readPreprint
In one paragraph

Article in Research square, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Sijing WuVanderbilt University Medical Center.
Muwei LiVanderbilt University Medical Center.ORCID https://orcid.org/0000-0003-3596-9287
Yurui GaoVanderbilt University.ORCID https://orcid.org/0000-0002-4339-5351
Lyuan XuOregon Institute of Technology.ORCID https://orcid.org/0000-0002-9791-0806
Yu ZhaoWest China Hospital of Sichuan University.ORCID https://orcid.org/0000-0002-7076-9486
John C GoreVanderbilt University Medical Center.ORCID https://orcid.org/0000-0002-9480-0900
Zhaohua DingVanderbilt University Medical Center.ORCID https://orcid.org/0000-0002-1805-2955

Funding

Biophysical basis of functional MRI of white matterR01NS113832 · NINDS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI GORE, JOHN C · 2020 to 2024
$2.4M
Functional Connectome of Brain White MatterR01NS129855 · NINDS · VANDERBILT UNIVERSITY · PI ZHAOHUA DING · 2023 to 2026
$1.9M
NINDS NIH HHS R01 NS113832NINDS NIH HHS R01 NS129855
6 · The paper itself

Abstract

White matter blood-oxygenation-level-dependent (BOLD) signals in resting-state functional magnetic resonance imaging (rs-fMRI) are increasingly recognized for their physiological significance, yet their intrinsic spectral architecture remains largely uncharted. In this work, using high quality data from the Human Connectome Project (HCP), we mathematically model and quantitatively characterize a robustly detectable "second peak" superimposed on the canonical exponentially decaying white matter BOLD spectrum. The spectral signature, with a peak frequency around ~ 0.06 Hz, emerges as a stable individual-level phenotype with broad spatial penetrance across white matter. Cross-tissue analyses reveal that while BOLD signals in cerebrospinal fluid (CSF) exhibit similar low frequency dynamics, white matter provides the most prominent and organized manifestation of this spectral feature. Spatially, the peak follows distinct gradients that mirror macroscopic white matter anatomy. Exploratory analyses in the HCP-Aging cohort further suggest that this band-specific spectral signature undergoes systematic evolution with age. Synthesizing the frequency profile, spatial distribution, and aging trajectory, we propose that the white matter second peak may serve as an organized, tissue-modulated readout of ubiquitous low-frequency physiological dynamics, potentially linked to glymphatic or perivascular clearance mechanisms in the brain. Together, these findings point to a robust spectral phenotype that may open a new noninvasive dimension for investigating white matter functional integrity, brain aging, and relevant physiological mechanisms.

Identifiers

PMID42687944
PMCPMC13533017

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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.