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Contributions of Gray Matter Microstructure to Differences in Fluid Cognition and Episodic Memory Across the Healthy Adult Lifespan.

Overview

  1. Department of Psychology, University of Utah, Salt Lake City, Utah, USA
  2. Department of Psychology, University of California, Riverside, California, USA
  3. Brain Imaging and Analysis Center, Duke University Medical Center, Durham, North Carolina, USA
  4. Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, North Carolina, USA
Institutions: University of Utah (United States); University of California, Riverside (United States); Duke Medical Center (United States)
Journal: Human brain mapping, volume 47, issue 5, article e70511
Dates: received 18 November 2025; accepted 11 March 2026; published online 23 March 2026; in print April 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1002/hbm.70511 · PMID 41873035 · PMCID PMC13081687 · OpenAlex W7140236695
Open access: gold, a free copy (OpenAlex)
Status: code on request
Categories: structural MRI / diffusion (modality), human (organism), cognitive (subfield)
Methods: Statistics, fMRI & imaging
Keywords: adult lifespan, cognitive performance, diffusion‐weighted imaging (DWI), moderation analyses, neurite orientation density and dispersion index (NODDI)
MeSH: Aging*, Cognition*, Gray Matter*, Memory, Episodic*, Nerve Net*, Adolescent, Adult, Aged, Aged, 80 and over, Diffusion Magnetic Resonance Imaging, Female, Humans, Male, Middle Aged, Young Adult (* major topic)
Topic: Advanced Neuroimaging Techniques and Applications (Radiology, Nuclear Medicine and Imaging, Medicine), according to OpenAlex
Funding: NIA NIH HHS (R01 AG039684); National Institute on Aging (R01 AG039684)
Citations: not cited yet (Europe PMC); 90 references in the paper

Abstract

Cognitive decline, in healthy older adults without cognitive impairment or dementia, has been associated with numerous microstructural alterations in brain tissue using magnetic resonance imaging (MRI). Prior studies have primarily linked age‐related cognitive decline to alterations in white matter tissue, but methodological advances in diffusion‐weighted imaging (dMRI) data acquisition and modeling now allow for these analyses to be extended to gray matter tissue. Here, using a sample of 152 healthy adults (18–88 years of age), we used a multicompartment dMRI model to assess (1) age‐related differences in gray matter microstructure of functionally defined networks and (2) whether microstructural alterations accounted for age‐related differences in episodic memory and speed‐dependent fluid cognition. We observed significant age‐related alterations in gray matter tissue in the form of nonlinear, age‐related increases and decreases in intracellular and dispersed diffusion, respectively, and linear increases in free diffusion. Free diffusion exhibited the most pronounced age‐related effects, especially for frontoparietal relative to occipital regions. Dispersed diffusion in the dorsal attention network statistically mediated age‐related differences in episodic memory performance. Moreover, higher intracellular diffusion in the default mode and ventral attention networks was related to worse fluid cognition performance, but only for adults > 51 years of age. These results suggest that healthy aging is accompanied by distinct profiles of gray matter microstructural alterations that negatively affect memory and speed‐dependent cognition, the latter of which is more pronounced after midlife.

Reproduced under the paper's license (CC BY), from the paper cited above.

Code

The paper says that its authors' code is available on request: it was not published with the paper, so there is nothing to verify.

The paper's code and data availability statement is in the Data section.

Tracing map

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Data

No dataset and no data link were found in the paper.

Data Availability Statement

The deidentified behavioral and preprocessed neuroimaging data from are available upon reasonable request to the corresponding author and a data sharing agreement will be required. The code that was used for data analyses will be made available on the GitHub profile of the corresponding author upon manuscript acceptance.

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

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Version 1, 28 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 3 authors, 5 keywords, 15 MeSH terms, 2 funders, 87 references.

Cite

This paper

Merenstein, J. L., Bennett, I. J., & Madden, D. J. (2026). Contributions of Gray Matter Microstructure to Differences in Fluid Cognition and Episodic Memory Across the Healthy Adult Lifespan. Human brain mapping, 47(5), e70511. https://doi.org/10.1002/hbm.70511

BibTeX

@article{merenstein2026contributions,
author = {Merenstein, Jenna L and Bennett, Ilana J and Madden, David J},
title = {{Contributions of Gray Matter Microstructure to Differences in Fluid Cognition and Episodic Memory Across the Healthy Adult Lifespan}},
journal = {Human brain mapping},
year = {2026},
month = apr,
volume = {47},
number = {5},
pages = {e70511},
publisher = {Wiley},
issn = {1065-9471},
doi = {10.1002/hbm.70511},
url = {https://doi.org/10.1002/hbm.70511},
pmid = {41873035},
pmcid = {PMC13081687}
}

RIS

TY - JOUR
AU - Merenstein, Jenna L
AU - Bennett, Ilana J
AU - Madden, David J
TI - Contributions of Gray Matter Microstructure to Differences in Fluid Cognition and Episodic Memory Across the Healthy Adult Lifespan
T2 - Human brain mapping
J2 - Hum Brain Mapp
PY - 2026
DA - 2026/04/01
VL - 47
IS - 5
SP - e70511
SN - 1065-9471
PB - Wiley
DO - 10.1002/hbm.70511
UR - https://doi.org/10.1002/hbm.70511
LA - en
ER -

CSL-JSON

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