Evidence map›Paper›PMID 40241499›Full record

ArticleHuman brain mapping2025

Volumetric Changes in Cerebellar Transverse Zones: Age and Sex Effects in Health and Neurological Disorders.

Farshid Ghiyamihoor, Payam Peymani, Jarrad Perron, Azam Asemi-Rad, Mehdi Marzban, Aashka Mohite, Karen Ardila, Bara Aljada, Asghar Marzban, Mehnosh Toback and 12 more

Abstract read
In one paragraph

Article in Human brain mapping, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Observational
  5. 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

22 authors.

Farshid GhiyamihoorDepartment of Human Anatomy and Cell Science, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
Payam PeymaniCollege of Pharmacy, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
Jarrad PerronGraduate Program in Biomedical Engineering, Price Faculty of Engineering, University of Manitoba, Winnipeg, Manitoba, Canada.
Azam Asemi-RadDepartment of Human Anatomy and Cell Science, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
Mehdi MarzbanDepartment of Electrical & Software Engineering, Schulich School of Engineering, University of Calgary, Calgary, Alberta, Canada.
Aashka MohiteDepartment of Biomedical Engineering, Schulich School of Engineering, University of Calgary, Calgary, Alberta, Canada.
Karen ArdilaDepartment of Biomedical Engineering, Schulich School of Engineering, University of Calgary, Calgary, Alberta, Canada.
Bara AljadaDepartment of Human Anatomy and Cell Science, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
Asghar MarzbanDepartment of Pediatrics, School of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran.
Mehnosh TobackDepartment of Human Anatomy and Cell Science, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
Sherif EltonsyThe Children's Hospital Research Institute of Manitoba (CHRIM), Rady Faculty of Health Science, University of Manitoba, Winnipeg, Manitoba, Canada.
Ji Hyun KoDepartment of Human Anatomy and Cell Science, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.ORCID 0000-0002-9700-7692
Tabrez J SiddiquiThe Children's Hospital Research Institute of Manitoba (CHRIM), Rady Faculty of Health Science, University of Manitoba, Winnipeg, Manitoba, Canada.
Christopher J SteeleDepartment of Psychology and School of Health, Concordia University, Montreal, Quebec, Canada.
Jiming KongDepartment of Human Anatomy and Cell Science, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
Mario MantoService des Neurosciences, Université de Mons, Mons, Belgium.
M Ethan MacDonaldDepartment of Biomedical Engineering, Schulich School of Engineering, University of Calgary, Calgary, Alberta, Canada.
Jason S GillJan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston, Texas, USA.
Roy V SillitoeDepartment of Pathology & Immunology, Baylor College of Medicine, Houston, Texas, USA.
Fuat BalcıThe Children's Hospital Research Institute of Manitoba (CHRIM), Rady Faculty of Health Science, University of Manitoba, Winnipeg, Manitoba, Canada.
Iman BeheshtiDepartment of Human Anatomy and Cell Science, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.
Hassan MarzbanDepartment of Human Anatomy and Cell Science, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.ORCID 0000-0001-6885-2590

Funding

Steps towards a paternal gene activation therapy for Angelman syndromeU54HD083092 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI NELSON, DAVID LOREN, NEUL, JEFFREY L · 2014 to 2019
$7.8M
Cerebellar Deep Brain StimulationR01NS119301 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI SILLITOE, ROY VINCENT · 2020 to 2024
$2.0M
Spatial and temporal pathophysiology of developmental dystoniaR01NS127435 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI Roy Vincent Sillitoe · 2022 to 2026
$2.0M
Unraveling the Dynamic Role of Purkinje Cell Neurotransmission in Neurodevelopment.K08NS121600 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI GILL, JASON SINGH · 2021 to 2025
$956k
Alzheimer Society of Manitoba Graduate Student FellowshipAtaxie Canada-Ataxia Canada, Research Manitoba Bridge FundingCanadian Institutes of Health Research (CIHR) PJT-463249Early Career Researcher Supplement DGECR-00124Fonds de Recherche Santé Chercheurs-Boursier FRQS CB Junior 2 349443Heart and Stroke Foundation of Canada New Investigator Award and Catalyst from the Canadian Institutes of Health Research HNC 170723McCrorie-West Family Fellowship in Alzheimer's Research 44172National Institutes of Neurological Disorders and Stroke (NINDS) 1K08NS121600National Institutes of Neurological Disorders and Stroke (NINDS) R01NS119301National Institutes of Neurological Disorders and Stroke (NINDS) R01NS127435Natural Sciences and Engineering Research Council of Canada RGPIN-2023-04283NICHD NIH HHS U54 HD083092NINDS NIH HHS K08 NS121600NINDS NIH HHS R01 NS119301NINDS NIH HHS R01 NS127435NSERC Discovery DGECR-2020-00146NSERC Discovery RGPIN-03552NSERC Discovery RGPIN-2020-06812NSERC Discovery RGPIN-2021-03334NSERC Discovery Grant, and the Ricard Foundation's Baxter BursaryUniversity of Manitoba Graduate Fellowship (UMGF)URGP
6 · The paper itself

Abstract

Cerebellar volumetric changes are intricately linked to aging, with distinct patterns across its transverse zones, the functional subdivisions characterized by unique cytoarchitectural and connectivity profiles. Despite research efforts, the cerebellar aging process in health and neurological disorders remains poorly understood. In this study, we investigated the effects of age and sex on total cerebellum, transverse zone, and lobule volumes using MRI data from over 45,000 participants compiled from six neuroimaging datasets. We also propose a framework for estimating cerebellum age as an indicator of cerebellar health. Significant age-dependent volume reductions were observed across transverse zones, with the central zone (CZ; lobules VI and VII) exhibiting the steepest decline in both health and neurological disorders. This finding highlights the CZ's vulnerability to aging and its critical role in cognitive and emotional processing. We also found prominent sex differences in age-dependent volumetric changes. Males exhibited smaller total intracranial volume (TIV)-adjusted cerebellum volume and faster age-dependent volume reduction than females in both health and mild cognitive impairment (MCI), Alzheimer disease (AD), and Parkinson disease (PD). In contrast, females with schizophrenia (SZ) and cocaine use disorder (CUD) revealed faster age-dependent cerebellar volume reduction than males. Patients with MCI, AD, and PD experienced more pronounced atrophy in the posterior (PZ) and nodular (NZ) zones compared to age-matched healthy controls, while SZ patients were characterized by a more prominent reduction in CZ. In CUD, a non-significant volume decline was observed in all zones compared to the controls. Moreover, our framework for estimating cerebellum age revealed a notable difference in cerebellar aging between healthy individuals and neurological patients. Finally, we charted age-dependent changes in cerebellar volume in healthy individuals, focusing on transverse zones capturing the functional subdivisions. These findings underscore the potential of cerebellar volumetric analysis as a biomarker for early detection and monitoring of neurodegenerative and neuropsychiatric disorders. Our novel approach complements and enhances MRI-based analyses, providing essential insights into the pathogenesis of aging, neurodegeneration, and chronic neuropsychiatric conditions.

Indexed as

AgingAlzheimer DiseaseCerebellumCognitive DysfunctionParkinson DiseaseSchizophreniaSex CharacteristicsAdultAgedAged, 80 and overFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedNeuroimagingagingAlzheimer disease (AD)cerebellar transverse zonecerebellum‐PADcocaine use disorder (CUD)mild cognitive impairment (MCI)MRIneuroimaging datasetsParkinson disease (PD)schizophrenia (SZ)

Identifiers

PMID40241499
PMCPMC12003958

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.