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Assessing the impact of circulating inflammatory cytokines and proteins as drivers and therapeutic targets in epilepsy: A Mendelian randomization study.
Wang, Wencai; Ma, Luyao; Liu, Menghao; Zhao, Yongqiang; Ye, Wei; Li, Xianfeng.
  • Wang W; The Second Affiliated Hospital of Harbin Medical University, Harbin 150086, China. Electronic address: wangwencai0912@163.com.
  • Ma L; The Second Affiliated Hospital of Harbin Medical University, Harbin 150086, China. Electronic address: maluyao19971219@163.com.
  • Liu M; The Second Affiliated Hospital of Harbin Medical University, Harbin 150086, China. Electronic address: lmh15837415296@163.com.
  • Zhao Y; The Second Affiliated Hospital of Harbin Medical University, Harbin 150086, China. Electronic address: 786397754@qq.com.
  • Ye W; The Second Affiliated Hospital of Harbin Medical University, Harbin 150086, China. Electronic address: yewei9999@aliyun.com.
  • Li X; The Second Affiliated Hospital of Harbin Medical University, Harbin 150086, China. Electronic address: lixianfeng2000@163.com.
Epilepsy Behav ; 157: 109868, 2024 Aug.
Article en En | MEDLINE | ID: mdl-38823075
ABSTRACT

BACKGROUND:

Previous research has demonstrated that neuroinflammation is a key element in the progress of epilepsy. Nevertheless, it is currently unidentified which inflammatory factors and proteins increase or decrease the risk of epilepsy.

METHODS:

We adopted Mendelian randomization techniques to explore the causal relationship between circulating inflammatory factors and proteins and various epilepsy. Our principal approach was inverse variance weighting, supplemented by several sensitivity analyses to guarantee the robustness of our findings.

RESULTS:

Studies have identified associations between epilepsy and specific inflammatory factors and proteins three inflammatory factors and six proteins are linked to epilepsy in general; one inflammatory factor and four proteins are associated with focal epilepsy with no documented lesions; two inflammatory factors and three proteins are related to focal epilepsy, excluding cases with hippocampal sclerosis; two inflammatory factors and two proteins are connected to juvenile myoclonic epilepsy; two inflammatory factors and five proteins are linked to juvenile absence epilepsy; four inflammatory proteins are associated with childhood absence epilepsy; two inflammatory factors are related to focal epilepsy overall; two inflammatory factors and two proteins are connected to generalized epilepsy; and two inflammatory proteins are linked to generalized epilepsy with tonic-clonic seizures. Additionally, six inflammatory factors may play a downstream role in focal epilepsy.

CONCLUSION:

Our study uncovers various inflammatory factors and proteins that influence the risk of epilepsy, offering instructive insights to the diagnosis and therapy of the condition.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Citocinas / Epilepsia / Análisis de la Aleatorización Mendeliana Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Citocinas / Epilepsia / Análisis de la Aleatorización Mendeliana Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article