Evidence map›Paper›PMID 40355774›Full record

ArticleAging clinical and experimental research2025

The associations between cerebral microhemorrhages and cognitive decline across Alzheimer's continuum.

Homayoon Khaledian, Ali Julaee Rad, Pardis Barjisi, Parsa Saberian, Mehrdad Mozafar, Sahar Ghahramani, Mohammad Sadeghi, Mahsa Mayeli, Seyed Mohammad Amin Alavi, Soorin Berenjian and 2 more

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Article in Aging clinical and experimental research, 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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4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Homayoon KhaledianBorderless Research, Advancement and Innovation in Neuroscience Network (BRAINet), Tehran, Iran.
Ali Julaee RadMaster's Student, Department of Psychology, Tehran University, Tehran, Iran.
Pardis BarjisiDepartment of Biomedical Engineering, Islamic Azad University of Urmia, Urmia, Iran.
Parsa SaberianFaculty of Medicine, Hormozgan University of Medical Sciences, Bandar Abbas, Iran. parsasaberian@gmail.com.
Mehrdad MozafarSchool of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Sahar GhahramaniHealth Policy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Mohammad SadeghiSchool of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Mahsa MayeliSchool of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Seyed Mohammad Amin AlaviFaculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Soorin BerenjianDepartment of Psychology, Islamic Azad University of Isfahan (Khorasgan) Branch, Isfahan, Iran.
Shaghayegh KaramiSchool of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Mohadeseh AndalibianDepartment of psychology, Hakim Toos Institute of Higher Education, Mashhad, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the associations between cerebral microhemorrhages (CMH) and cognitive decline across the Alzheimer's dementia continuum.

methodsUsing the Alzheimer's Disease Neuroimaging Initiative (ADNI) database, we studied 619 participants, categorized into 221 cognitively normal (CN) participants, 281 patients with mild cognitive impairment (MCI), and 117 patients with Alzheimer's disease (AD). CMH prevalence and distribution were determined using T2-weighted magnetic resonance imaging (MRI), focusing on the frontal, occipital, and parietal subcortical regions of interest (ROIs).Clinical dementia rating scale sum of boxes (CDR-SB) and mini-mental state examination (MMSE) were used for diagnosis and composite cognitive scores regarding visuospatial abilities, language, memory, and executive functions were used as outcome variables. Age, gender, and APOE ε4 positivity status were used as covariates.

resultsThe AD group displayed significantly elevated tau and P-tau levels compared to MCI and CN groups (p < 0.001). APOE ε4 positivity was 67.5% in the AD group, surpassing the 50.2% in MCI and 29% in CN individuals (p < 0.001). Cognitive assessments revealed that the AD group's CDR-SB score and MMSE both significantly differed from these scores in the MCI and CN groups (p < 0.001). Overall, CMH prevalence was 27.7%, with a predominant distribution in the frontal subcortical ROIs. MCI subjects with CMH showed notably diminished ADNI Visuospatial Composite Scores compared to those without CMH. Age significantly predicted CMH in CN and MCI (p < 0.05). In AD participants, APOE ε4 heterozygotes (p = 0.02) and homozygotes (p = 0.01) hadincreased CMH likelihood.

conclusionCMHs are significantly associated with cognitive decline in patients with MCI. This association is more prominent in regard to the decline in visuospatial abilities.

Indexed as

Alzheimer DiseaseCerebral HemorrhageCognitive DysfunctionAgedAged, 80 and overApolipoprotein E4FemaleHumansMagnetic Resonance ImagingMaleNeuropsychological Teststau ProteinsApolipoprotein E4tau ProteinsAlzheimer's diseaseCerebral microhemorrhagesCognitive declineMild cognitive impairmentT2-weighted MRI

Identifiers

PMID40355774
PMCPMC12069497

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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.