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Methylation of Interleukin-1 receptor-associated kinase-3 and the risk of multiple sclerosis relapse/activity.
Watany, Mona M; Elhosary, Marwa M; El-Horany, Hemat E; El-Horany, Mahmoud E.
Affiliation
  • Watany MM; Clinical pathology department, Faculty of Medicine, Tanta University, Tanta 31527, Egypt. Electronic address: mona.watany@med.tanta.edu.eg.
  • Elhosary MM; Msc Immunology from Tanta university, Faculty of Science, Tanta 31527, Egypt.
  • El-Horany HE; Medical biochemistry department, Faculty of Medicine. Tanta University, Tanta 31527, Egypt; Biochemistry Department, College of Medicine, Ha'il University, Ha'il 55211, Saudi Arabia.
  • El-Horany ME; Neurology department, Faculty of Medicine. Tanta University, Tanta 31527, Egypt.
Clin Immunol ; 266: 110327, 2024 Jul 23.
Article de En | MEDLINE | ID: mdl-39053866
ABSTRACT
This study retrospectively investigated the impact of interleukin-1 receptor-associated kinase-3 (IRAK-3/IRAK-M) silencing by methylation on the likelihood of multiple sclerosis (MS) activity. This cross-sectional study included 90 patients with MS 45 with active disease (Group 1), 45 in remission (Group 2), and 45 healthy controls. The study included quantitation of IRAK-3 methylation index (MI%), IRAK-3 mRNA, and myeloid differentiation factor88 (MyD88) and assessment of NF-κB activity. IRAK-3 MI% was significantly higher in group 1 compared to group 2, accompanied by lower IRAK-3 mRNA expression, elevated circulating MyD88, and increased NF-κB activity. IRAK-3 MI% correlated negatively with its transcript and positively with MyD88 and NF-κB activity. A logistic regression model was created to predict active demyelination. The C-index was 0.924, which indicates a very strong prediction model. Within the limitations of current work, IRAK-3 methylation level seems to be a promising candidate biomarker for identifying MS patients at risk of relapse.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Clin Immunol Sujet du journal: ALERGIA E IMUNOLOGIA Année: 2024 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Clin Immunol Sujet du journal: ALERGIA E IMUNOLOGIA Année: 2024 Type de document: Article