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Genetic association of ABCA7 and PSEN1 polymorphisms with Alzheimer’s disease in the northeast Algerian population: Exploring risk factors
Rayene Achou, Ouarda Sariyah Ayachi, Yasmina Boukhenaf, Rania Laouar, Gharzouli Razika, M’zahem Abderrahim, Houda Boulala, Noureddine Abadi et al.. Archives of Biological Sciences, 2025-01-01
Topic: Amyloid, tau and blood-test diagnosis
Plain-language summary
Alzheimer?s disease (AD) is a neurodegenerative disorder with a strong genetic component. This research aims to identify the relationship between ABCA7 rs3764650, PSEN1 rs165932, and AD in the northeast Algerian population and investigate genetic risk factors contributing to disease susceptibility. A case-control study was performed with 98 patients and 156 controls. DNA was isolated from blood samples by salting out. Genotyping of ABCA7 and PSEN1 polymorphisms was conducted using PCR-RFLP. Significant associations were observed between ABCA7 rs3764650 and AD under dominant and additive models. Similarly, PSEN1 rs165932 was associated with a higher risk of AD under dominant, recessive, and additive models. The frequency of the ABCA7 G allele was significantly associated with PSEN1 T allele carriers (P=0.033), with no significant association observed in non-carriers. In contrast, the PSEN1 T allele frequency was significant in both ABCA7 G allele carriers (P=0.006) and non-carriers (P=0.001). Allelic frequencies for ABCA7 and PSEN1 were higher in late-onset cases (P=0.003; P< 0.001) and females (P=0.006; P< 0.001). This study highlights the association of the ABCA7 rs3764650 G and PSEN1 rs165932 T alleles with AD susceptibility, particularly in females and late-onset cases, suggesting their relevance as genetic markers of disease risk.
What this study adds
Evidence grade: Moderate
This is a case-control study of 98 participants. In a case-control study of 98 patients and 156 controls in northeast Algeria, the ABCA7 rs3764650 and PSEN1 rs165932 variants were associated with higher Alzheimer's disease risk, particularly in females and late-onset cases. These findings suggest these variants may serve as genetic markers of disease risk, but they do not demonstrate a treatment or cure.
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
Achou, R., Ayachi, O. S., Boukhenaf, Y., Laouar, R., Razika, G., Abderrahim, M., et al. (2025). Genetic association of ABCA7 and PSEN1 polymorphisms with Alzheimer’s disease in the northeast Algerian population: Exploring risk factors. Archives of Biological Sciences. https://doi.org/10.2298/abs250208005a
Vancouver
Achou R, Ayachi OS, Boukhenaf Y, Laouar R, Razika G, Abderrahim M, et al. Genetic association of ABCA7 and PSEN1 polymorphisms with Alzheimer’s disease in the northeast Algerian population: Exploring risk factors. Archives of Biological Sciences. 2025. doi:10.2298/abs250208005a.
BibTeX
@article{achou2025-0c99f57b,
author = {Achou, Rayene and Ayachi, Ouarda Sariyah and Boukhenaf, Yasmina and Laouar, Rania and Razika, Gharzouli and Abderrahim, M’zahem and Boulala, Houda and Abadi, Noureddine and others},
title = {{Genetic association of ABCA7 and PSEN1 polymorphisms with Alzheimer’s disease in the northeast Algerian population: Exploring risk factors}},
journal = {Archives of Biological Sciences},
year = {2025},
doi = {10.2298/abs250208005a},
url = {https://doi.org/10.2298/abs250208005a}
}
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Key findings
- Significant associations were observed between ABCA7 rs3764650 and AD under dominant and additive models.
- Similarly, PSEN1 rs165932 was associated with a higher risk of AD under dominant, recessive, and additive models.
- The frequency of the ABCA7 G allele was significantly associated with PSEN1 T allele carriers (P=0.033), with no significant association observed in non-carriers.
- In contrast, the PSEN1 T allele frequency was significant in both ABCA7 G allele carriers (P=0.006) and non-carriers (P=0.001).
Why it matters
In a case-control study of 98 patients and 156 controls in northeast Algeria, the ABCA7 rs3764650 and PSEN1 rs165932 variants were associated with higher Alzheimer's disease risk, particularly in females and late-onset cases. These findings suggest these variants may serve as genetic markers of disease risk, but they do not demonstrate a treatment or cure.
New to this subject? Start with our plain-English guide: Genetics →
Study details
- Study designcase-control study
- Participants98
- Evidence strengthModerate
How this study scored 38/100
Published in a peer-reviewed journal, and it is a case-control study. Scored zero for effect reported and randomized / blinded because the record does not state it.
| Component | Points | Why |
|---|---|---|
| Journal tier | 7 / 10 | Tier 3 — peer-reviewed journal (Archives of Biological Sciences) |
| Journal's citation record | 0 / 4 | Archives of Biological Sciences: journal h-index 42 (OpenAlex, 2026-10-29) |
| Study design | 6 / 12 | A case-control study |
| 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 | 1 / 4 | 98 participants |
| Effect reported | 0 / 3 | No effect size reported — scores zero (not stated in the record — scored 0) |
| Studied in people | 3 / 3 | Studied in people (participant count stated) |
| Randomized / blinded | 0 / 2 | No randomization or blinding stated — scores zero (not stated in the record — scored 0) |
| Times cited | 0 / 7 | Cited 0 times (OpenAlex, 2026-10-10) |
| Citations per year | 0 / 5 | 0.0 citations a year over 3 year(s) since 2025 |
| Impact for its field and year | 0 / 6 | Cited 0.0× the average for papers of its field and year (OpenAlex FWCI) |
| Cited by studies here | 0 / 6 | No other study in this library cites it |
| Still being cited | 0 / 4 | Cited 0 times in 2024–2026 (2026 still in progress; OpenAlex) |
| Senior author's track record | 1 / 4 | Last-listed author Dalila Satta: h-index 15 (OpenAlex, whole career) |
| Institution's track record | 0 / 3 | University Frères Mentouri Constantine 1: institution h-index 139 (OpenAlex) |
| Multicenter collaboration | 0 / 3 | OpenAlex lists 1 institution(s) in 1 country — scores zero (affiliation lists can be incomplete) |
| Indexed in PubMed | 1 / 2 | Not in PubMed, but has a DOI |
| Free to read | 2 / 2 | Free to read |
| Total | 38 / 100 | — |
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