Evidence map›Paper›PMID 41033231›Full record

ArticlePediatric neurology2025

Biological Sex and Body Mass Index Influence the Longitudinal Evolution of Adolescent and Young Adult Magnetic Resonance Imaging-Visible Perivascular Spaces.

Erin A Yamamoto, Seiji Koike, Caitlyn Wong, Laura E Dennis, Madison N Luther, Avery Scatena, Seva Khambadkone, Jeffrey J Iliff, Miranda M Lim, Swati R Levendovszky and 7 more

Abstract readMulticenter Study
In one paragraph

Article in Pediatric neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors.

Erin A YamamotoDepartment of Neurological Surgery, Oregon Health & Science University, Portland, Oregon.
Seiji KoikeBiostatistics and Design Program, Oregon Health & Science University, Portland, Oregon.
Caitlyn WongDivision of Child Neurology, Department of Pediatrics, Doernbecher Children's Hospital, Oregon Health and Science University, Portland, Oregon.
Laura E DennisDivision of Child Neurology, Department of Pediatrics, Doernbecher Children's Hospital, Oregon Health and Science University, Portland, Oregon; Veterans Affairs (V.A.) Portland Health Care System, Portland, Oregon.
Madison N LutherDivision of Child Neurology, Department of Pediatrics, Doernbecher Children's Hospital, Oregon Health and Science University, Portland, Oregon.
Avery ScatenaDivision of Child Neurology, Department of Pediatrics, Doernbecher Children's Hospital, Oregon Health and Science University, Portland, Oregon.
Seva KhambadkoneDivision of Child Neurology, Department of Pediatrics, Doernbecher Children's Hospital, Oregon Health and Science University, Portland, Oregon.
Jeffrey J IliffDepartment of Psychiatry and Behavioral Sciences, University of Washington School of Medicine, Seattle, Washington; Department of Neurology, University of Washington School of Medicine, Seattle, Washington; VISN 20 Northwest Mental Illness, Research, Education, and Clinical Center (MIRECC), Veterans Affairs Puget Sound Health Care System, Seattle, Washington.
Miranda M LimVeterans Affairs (V.A.) Portland Health Care System, Portland, Oregon; VISN 20 Northwest Mental Illness, Research, Education, and Clinical Center (MIRECC), Veterans Affairs Puget Sound Health Care System, Seattle, Washington; Oregon Alzheimer's Disease Research Center, Department of Neurology, Oregon Health and Science University, Portland, Oregon.
Swati R LevendovszkyDepartment of Radiology, University of Washington School of Medicine, Seattle, Washington.
Jonathan E ElliottVeterans Affairs (V.A.) Portland Health Care System, Portland, Oregon; Department of Neurology, Oregon Health & Science University, Portland, Oregon.
Giuseppe BarisanoDepartment of Neurological Surgery, Stanford University, Stanford, California.
Eva M Müller-OehringCenter for Health Sciences, SRI International, Menlo Park, California; Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, California.
Angelica M MoralesDepartment of Psychiatry, Oregon Health & Science University, Portland, Oregon.
Fiona C BakerCenter for Health Sciences, SRI International, Menlo Park, California.
Bonnie J NagelDepartment of Psychiatry, Oregon Health & Science University, Portland, Oregon.
Juan PiantinoDivision of Child Neurology, Department of Pediatrics, Doernbecher Children's Hospital, Oregon Health and Science University, Portland, Oregon. Electronic address: piantino@ohsu.edu.

Funding

Research Education ComponentP30AG066518 · NIA · OREGON HEALTH & SCIENCE UNIVERSITY · PI Zachary Beattie · 2020 to 2026
$28.6M
Role of Sleep Disruption after mTBI as a Driver of Chronic Post-traumatic HeadacheR01NS129573 · NINDS · SEATTLE INST FOR BIOMEDICAL/CLINICAL RES · PI Jeffrey J Iliff, Andrew F Russo · 2023 to 2026
$2.4M
Understanding the effect of post-concussive sleep disruption on glymphatic function in collegiate athletesR01HL173372 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Juan Andres Piantino · 2025 to 2026
$1.5M
A link between sleep-wake disturbances and enlarged perivascular spaces in youth with traumatic brain injuryK23HL150217 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI PIANTINO, JUAN ANDRES · 2020 to 2024
$826k
The perivascular space: A structural link between inadequate sleep, glymphatic dysfunction, and neurocognitive outcomes in adolescentsR21HL167077 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI PIANTINO, JUAN ANDRES · 2023 to 2024
$231k
NHLBI NIH HHS K23 HL150217NHLBI NIH HHS R01 HL173372NHLBI NIH HHS R21 HL167077NIA NIH HHS P30 AG066518NINDS NIH HHS R01 NS129573
6 · The paper itself

Abstract

backgroundAn association recently emerged between magnetic resonance imaging (MRI)-visible perivascular spaces (MV-PVS) with intracerebral solute clearance and neuroinflammation, in adults. However, it is unknown how MV-PVS change throughout adolescence and what factors influence MV-PVS volume and morphology. This study assesses the temporal evolution of MV-PVS volume in adolescents and young adults, and secondarily evaluates the relationship between MV-PVS, age, sex, and body mass index (BMI).

methodsThis analysis included a 783 participant cohort from the longitudinal multicenter National Consortium on Alcohol and Neurodevelopment in Adolescence study that involved up to 6 imaging visits spanning 5 years. Healthy adolescents aged 12-21 years at study entry with at least two MRI scans were included. The primary outcome was mean MV-PVS volume (mm

resultsOn average, males had greater MV-PVS volume at all ages compared to females. A linear mixed-effect model for MV-PVS volume was performed. Mean BMI and increases in a person's BMI were associated with increases in MV-PVS volume over time. In females only, changes in BMI correlated with MV-PVS volume. One unit increase in BMI above a person's average BMI was associated with a 0.021 mm

conclusionsThis longitudinal study showed sex differences in MV-PVS features during adolescence and young adulthood. Importantly, we report that increases in BMI from a person's mean BMI are associated with increases in MV-PVS volume in females only. These findings suggest a potential link between MV-PVS, sex, and BMI that warrants future study.

Indexed as

Body Mass IndexGlymphatic SystemSex CharacteristicsWhite MatterAdolescentChildFemaleHumansLongitudinal StudiesMagnetic Resonance ImagingMaleSex FactorsYoung AdultAdolescenceBMIMRIPediatricPerivascular spaceSex

Identifiers

PMID41033231
PMCPMC12591043

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Registered trials

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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.