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ArticleHealth science reports2025

Growth-Associated Protein 43 Levels in the Cerebrospinal Fluid Correspond to the Cerebral Blood Flow Alterations in Alzheimer's Dementia Continuum: An Original Study.

Neda Songhori, Maryam Shamsi Goushky, Mohammad Mehdi Khaleghi, Marzieh Mojerloo, Mohammad Sadeghi, Mehrdad Mozafar, Zahra Babaie Aghdam, Maryam Ghajar, Yalda Kianifar, Farough Karimzadeh and 2 more

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Article in Health science reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

12 authors.

Neda SonghoriAmirkabir University of Technology Tehran Iran.ORCID 0009-0002-3991-7994
Maryam Shamsi GoushkyMedical Research Center of Shahid Beheshti University of Medical Science Tehran Iran.
Mohammad Mehdi KhaleghiStudents Research Committee, School of Pharmacy and Pharmaceutical Science Isfahan University of Medical Sciences Isfahan Iran.
Marzieh MojerlooIslamic Azad University of Khalkhal Ardebil Iran.
Mohammad SadeghiSchool of Medicine Tehran University of Medical Science Tehran Iran.
Mehrdad MozafarSchool of Medicine Tehran University of Medical Science Tehran Iran.
Zahra Babaie AghdamDepartment of Radiology Tabriz University of Medical Science Tabriz Iran.
Maryam GhajarMaster of Psychology Azad University of Tehran Tehran Iran.
Yalda KianifarMaster of Children and Adolescent Clinical Psychology of Tabriz University Tabriz Iran.
Farough KarimzadehDepartment of Occupational Therapy, School of Rehabilitation Sciences Shiraz University of Medical Sciences, Rehabilitation Science of Research Center Shiraz Iran.
Farbod KhosraviShahid Beheshti University of Medical Science Tehran Iran.
Mahsa MayeliSchool of Medicine Tehran University of Medical Science Tehran Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aims: Alzheimer's disease (AD) is a widespread neurodegenerative condition that has a growing impact on a global scale. This study aims to examine the relationship between cerebral blood flow (CBF) and the synaptic biomarker growth-associated protein 43 (GAP-43) through the utilization of arterial spin labeling (ASL). The research identified noteworthy correlations between cerebrospinal fluid (CSF) GAP-43 levels, CBF, and cognitive composite scores, especially among participants with mild cognitive impairment (MCI) who possess the APOE-ε4 gene. Methods: The study examined 92 participants from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database, including 36 cognitively normal (CN) and 56 MCI. The cognitive status of 42 participants was evaluated using ADNI composite scores. Independent t-tests and Mann-Whitney tests were used for the comparison of continuous variables between groups, and multiple linear regression analysis with adjustments for confounding factors was used to assess the relationship between GAP-43 and CBF values. Results: Significant positive correlations were observed between GAP-43 levels and (A) the executive function composite score (ADNI_EF) in CN individuals, as well as (B) the language composite score (ADNI_LAN) in individuals with MCI. CSF biomarkers and ASL regions did not show statistical significance between diagnostic groups after correction for multiple comparisons. No significant differences in baseline characteristics were found between diagnostic groups. However, associations were observed between ROI CBF and Mini Mental State Examination in various subgroups. Conclusion: The findings indicate a potential function for ASL perfusion in identifying early AD-related alterations and gaining insight into the pathophysiology of AD and mild cognitive impairment.The study revealed associations between CBF, cognitive scores, and APOE-ε4 gene status. This study contributes to the comprehension of the correlation between CSF biomarkers, regional brain perfusion, and cognitive function in individuals with AD using ASL as a noninvasive approach.

Indexed as

alzheimer's diseasearterial spin labelingbiomarkergrowth‐associated protein 43

Identifiers

PMID40078900
PMCPMC11896815

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