Evidence map›Paper›PMID 40663267›Full record

ArticleMolecular neurobiology2025

Exploring the Link Between IL-6 rs1800795 G > C SNP and the Severity of Epstein-Barr Virus-Associated Multiple Sclerosis: Potential Impact on Cognitive Impairment.

Tokka M Hassan, Azza M El Amir, Nahla Elsayed Nagy, Nashwa El-Khazragy

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Article in Molecular neurobiology, 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

4 authors.

Tokka M HassanEgypt Center for Research and Regenerative Medicine (ECRRM), Cairo, 11599, Egypt.
Azza M El AmirDepartment of Biotechnology, Faculty of Science, Cairo University, Giza, 12613, Egypt.
Nahla Elsayed NagyDepartment of Neuropsychiatry, Faculty of Medicine, Ain Shams University, Cairo, 11566, Egypt.
Nashwa El-KhazragyDepartment of Clinical Pathology-Hematology and AinShams Medical Research Institute (MASRI), Faculty of Medicine, Ain Shams University, Cairo, 11566, Egypt. nashwaelkhazragy@med.asu.edu.eg.ORCID https://orcid.org/0000-0001-6646-4674

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple Sclerosis (MS) is a chronic immune-mediated neurological disorder frequently accompanied by cognitive impairment, which affects up to 60% of patients and is associated with faster disease progression and greater disability. Interleukin-6 (IL-6), a key proinflammatory cytokine involved in neuroinflammation, has been implicated in MS pathogenesis, and the rs1800795 (-174 G>C) single nucleotide polymorphism (SNP) in the IL6 gene may influence disease susceptibility and clinical severity. This study investigated the association between the IL6 rs1800795 polymorphism and clinical outcomes in Epstein-Barr virus (EBV)-positive MS patients, with a particular focus on cognitive dysfunction. A case-control design was employed, including 300 participants: 150 EBV-positive MS patients and 150 matched healthy controls. Genotyping was performed using TaqMan-based PCR, and clinical data such as disability status, disease progression, and cognitive performance were analyzed. The CC genotype was significantly more frequent in MS patients and was associated with a higher risk of severe disability (OR = 6.11, p = 0.0004), faster disease progression, and increased likelihood of cognitive impairment. These findings suggest that the IL6 rs1800795 polymorphism, particularly the CC genotype, contributes to MS susceptibility and adverse clinical outcomes. IL6 genotyping may hold promise as a predictive tool for disease progression and cognitive decline in EBV-associated MS, offering insights for more personalized therapeutic strategies.

Indexed as

Cognition DisordersCognitive DysfunctionEpstein-Barr Virus InfectionsGenetic Predisposition to DiseaseHerpesvirus 4, HumanInterleukin-6Multiple SclerosisPolymorphism, Single NucleotideSeverity of Illness IndexAdultCase-Control StudiesDisease ProgressionFemaleGene FrequencyHumansMaleIL6 protein, humanInterleukin-6Cognitive disabilityEBVIL-6 rs1800795 G > CMultiple sclerosis

Identifiers

PMID40663267
PMCPMC12511238

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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.