Role of apolipoprotein E (ApoE) ε4 in cognitive impairment after a stroke: a prospective cohort study
Jia‐Hung Chen, Lung Chan, Chien‐Tai Hong, Chaur Jong Hu, Yi‐Chen Hsieh. Aging, 2025-05-08
Topic: Brain proteins, microglia and lab models
Plain-language summary
Although apolipoprotein E (ApoE) ε4 is a well-established risk factor for Alzheimer disease, its role in the development of post-stroke cognitive impairment (PSCI) remains uncertain. In this prospective cohort study, we recruited patients aged ≥20 years who had ischemic stroke within the past 7 days and measured their ApoE genotype. Baseline characteristics, including age, sex, education level, medical history, stroke severity, stroke etiology, and neuroimaging findings were recorded. Cognitive function was evaluated using the Montreal Cognitive Assessment (MoCA) and Clinical Dementia Rating (CDR) at 3 and 12 months post-stroke, with PSCI defined as a MoCA score < 26. After adjusting for confounding factors, the ApoE ε4 allele was not associated with the risk of PSCI at 3 or 12 months post-stroke. Other factors, including age, body mass index, education level, and initial stroke severity, were found to be associated with the risk of PSCI at 3 months. In patients who developed PSCI at 12 months, only education level and the MoCA score at 3 months were significantly associated with the risk of PSCI. Our findings suggest that, aside from traditional risk factors, the ApoE ε4 allele does not contribute to the risk of PSCI at 3 or 12 months post-stroke. Further studies with a larger sample size and longer follow-up are warranted.
What this study adds
Evidence grade: Moderate
This is a follow-up (cohort) study. In this prospective cohort, the ApoE ε4 allele was not associated with the risk of post-stroke cognitive impairment at 3 or 12 months after stroke. Other factors such as age, body mass index, education level, and initial stroke severity were associated with risk at 3 months.
Taken from this record’s own fields, not from reading the paper. The grade is assigned from the abstract’s wording; what that means.
Cite this study APA, Vancouver, BibTeX · download .bib or .ris
APA 7th
Chen, J., Chan, L., Hong, C., Hu, C. J., & Hsieh, Y. (2025). Role of apolipoprotein E (ApoE) ε4 in cognitive impairment after a stroke: a prospective cohort study. Aging. https://doi.org/10.18632/aging.206248
Vancouver
Chen J, Chan L, Hong C, Hu CJ, Hsieh Y. Role of apolipoprotein E (ApoE) ε4 in cognitive impairment after a stroke: a prospective cohort study. Aging. 2025. doi:10.18632/aging.206248. PMID: 40349252.
BibTeX
@article{chen2025-40349252,
author = {Chen, Jia‐Hung and Chan, Lung and Hong, Chien‐Tai and Hu, Chaur Jong and Hsieh, Yi‐Chen},
title = {{Role of apolipoprotein E (ApoE) ε4 in cognitive impairment after a stroke: a prospective cohort study}},
journal = {Aging},
year = {2025},
doi = {10.18632/aging.206248},
pmid = {40349252},
url = {https://doi.org/10.18632/aging.206248}
}
Built from the record alzhub holds for this paper, not looked up. Volume, issue and page numbers are not held in the record. Check the citation against the original before you use it.
Key findings
- After adjusting for confounding factors, the ApoE ε4 allele was not associated with the risk of PSCI at 3 or 12 months post-stroke.
- Other factors, including age, body mass index, education level, and initial stroke severity, were found to be associated with the risk of PSCI at 3 months.
- In patients who developed PSCI at 12 months, only education level and the MoCA score at 3 months were significantly associated with the risk of PSCI.
- Our findings suggest that, aside from traditional risk factors, the ApoE ε4 allele does not contribute to the risk of PSCI at 3 or 12 months post-stroke.
Why it matters
In this prospective cohort, the ApoE ε4 allele was not associated with the risk of post-stroke cognitive impairment at 3 or 12 months after stroke. Other factors such as age, body mass index, education level, and initial stroke severity were associated with risk at 3 months.
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Study details
- Study designcohort study
- Evidence strengthModerate
How this study scored 44/100
Published in a peer-reviewed journal, and it is a cohort study following people over time. Scored zero for sample size, effect reported, studied in people and randomized / blinded because the record does not state it.
| Component | Points | Why |
|---|---|---|
| Journal tier | 7 / 10 | Tier 3 — peer-reviewed journal (Aging) |
| Journal's citation record | 2 / 4 | Aging: journal h-index 162 (OpenAlex, 2026-10-29) |
| Study design | 7 / 12 | A cohort study following people over time |
| Strength of evidence | 3 / 5 | Rated “moderate” in our summary |
| Peer-review validation | 10 / 10 | Peer-reviewed. Published as an article in a named peer-reviewed journal. |
| How recent | 4 / 5 | 2025 — within 3 year(s) of the newest study here |
| Sample size | 0 / 4 | Participant count not stated — scores zero (not stated in the record — scored 0) |
| Effect reported | 0 / 3 | No effect size reported — scores zero (not stated in the record — scored 0) |
| Studied in people | 0 / 3 | Not stated whether this was studied in people — scores zero (not stated in the record — scored 0) |
| Randomized / blinded | 0 / 2 | No randomization or blinding stated — scores zero (not stated in the record — scored 0) |
| Times cited | 1 / 7 | Cited 2 times (OpenAlex, 2026-10-10) |
| Citations per year | 0 / 5 | 0.7 citations a year over 3 year(s) since 2025 |
| Impact for its field and year | 2 / 6 | Cited 1.3× the average for papers of its field and year (OpenAlex FWCI) |
| Cited by studies here | 1 / 6 | Cited by 1 other studies in this library |
| Still being cited | 0 / 4 | Cited 2 times in 2024–2026 (2026 still in progress; OpenAlex) |
| Senior author's track record | 2 / 4 | Last-listed author Yi‐Chen Hsieh: h-index 27 (OpenAlex, whole career) |
| Institution's track record | 0 / 3 | Taipei Medical University: institution h-index 345 (OpenAlex) |
| Multicenter collaboration | 1 / 3 | OpenAlex lists 2 institution(s) in 1 country |
| Indexed in PubMed | 2 / 2 | Indexed in PubMed (PMID 40349252) |
| Free to read | 2 / 2 | Free to read |
| Total | 44 / 100 | — |
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