Double stranded RNA activated EIF2 α kinase (EIF2AK2; PKR) is associated with Alzheimer's disease
Abstract
Sporadic Alzheimer's disease (AD) appears to be the consequence of the interaction between combinations of genes and environmental factors (for example virus infections). To test this hypothesis, we are examining human genes relevant to herpes simplex virus type 1 (HSV-1) infection via genetic association studies in AD case-control samples. Recently, we found that a variant in TAP2, a major target used by HSV-1 to evade immune surveillance, is associated with AD. The present work analyses another gene involved in the host cell response to HSV-1, EIF2AK2 (eukaryotic translation initiation factor 2-alpha kinase 2; coding for PKR); PKR mediates the virus-induced shut-off of translation, and levels of activated PKR are high in the brains of AD patients. An EIF2AK2 SNP (rs2254958) located in the 5'-UTR region within an exonic splicing enhancer was found to be associated with AD. More specifically: the C allele was more commonly found in the patients and, compared to non-CC genotypes, the CC homozygotes showed earlier (around 3.3 years) onset of AD, especially in the absence of the APOE4 allele. These results further support the hypothesis that variants of human genes participating in HSV-1 infection modulate the susceptibility and/or clinical manifestations of AD.
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Polymorphisms within eIF2AK2 have been genetically associated with AD.
“polymorphisms within eIF2AK2 havebeengenetically associated with AD (32)”
From An Unbiased Approach to Identifying Tau Kinases That Phosphorylate Tau at Sites Associated with Alzheimer Disease (2013) · cites this paper as [32]
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Role of p38/MAPKs in Alzheimer's Disease: Implications for Amyloid Beta Toxicity Targeted Therapy
Kheiri, G., Dolatshahi, M., Rahmani, F., & Rezaei, N. (2018) · Reviews in the Neurosciences · doi:10.1515/revneuro-2018-0008 · Cited by 211 · see citing works
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- Authors
- Bullido, M. J., Martínez-García, A., Tenorio, R., Sastre, I., Muñoz, D. G., Frank, A., & Valdivieso, F.
- Affiliations
- Centro de Biología Molecular Severo Ochoa (ES)
- St. Michael's Hospital (CA)
- Hospital Universitario La Paz (ES)
- Corresponding author
- Valdivieso, Fernando
- Venue
- Neurobiology of Aging
- Publisher
- Elsevier BV
- Published
- 2008-08
- Volume
- 29
- Issue
- 8
- Pages
- 1160-1166
- ISSN
- 0197-4580 (ISSN-L)
- OpenAlex
- W1971278860
- Cited by
- 51
- References
- 2
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 1 · 2023: 3 · 2022: 7 · 2021: 2 · 2020: 5 · 2019: 1 · 2018: 4 · 2017: 1 · 2016: 2 · 2015: 3 · 2014: 3 · 2013: 5
- FWCI
- 1.56
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neurobiology of Aging (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Fundación Ramón Areces
- Centro de Biología Molecular Severo Ochoa
- Instituto de Salud Carlos III
- Topics
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Keywords
- Alzheimer's disease, PKR, herpes simplex virus type 1, genetic susceptibility, single nucleotide polymorphisms, exonic splicing enhancers, TAP2, APOE ε4, viral infection hypothesis, age of onset
- MeSH terms
- Aged, Alzheimer Disease, Female, Humans, Male, Risk Factors, RNA, Double-Stranded, Sensitivity and Specificity, Spain, Reproducibility of Results, Prevalence, Case-Control Studies, Risk Assessment, eIF-2 Kinase, Genetic Predisposition to Disease
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