不应将SCN9A视为基因; 驳斥基因与疾病的关联
Ismael Ghanty1,2,3,4, Eduardo Perez-Palma5, Camilo Villaman5
1School of Health and Wellbeing, University of Glasgow, Glasgow, UK.
Epilepsia
|June 10, 2025
概括
遗传分析显示,没有强有力的证据表明SCN9A变异与有关. 由于缺乏令人信服的SCN9A基因与疾病的关联,建议在性遗传测试小组中重新评估SCN9A.
科学领域:
- 神经遗传学 神经遗传学
- 人类遗传学 人类遗传学
- 的研究研究.
背景情况:
- SCN9A基因主要存在于外周感知通路中,与疼痛障碍有关.
- 最近的研究表明,SCN9A是的潜在单一原因.
- 需要对SCN9A-基因与疾病的关系进行批判性评估.
研究的目的:
- 批判性地评估支持SCN9A作为的致病基因的证据.
- 评估与相关报道的SCN9A变异的可靠性.
- 为了确定SCN9A是否应该留在性遗传测试小组中.
主要方法:
- 从文献,患者推,HGMD和ClinVar中对SCN9A变异进行系统审查.
- 使用ACMG/AMP指南进行变异致病性评估.
- 将SCN9A变种频率与gnomAD V4种群数据进行比较.
主要成果:
- 只有三个SCN9A变异被归类为"可能致病".
- 在gnomAD.中,在健康个体中发现了两个"可能致病"的变体.
- 大多数ClinVar相关的SCN9A变异也与其他神经病变有关,通常具有有限的临床数据.
结论:
- 目前的遗传证据并不令人信服地支持SCN9A作为引起的基因.
- 将SCN9A纳入性遗传测试小组需要重新评估.
- 研究中心和实验室提交的数据库变体的一致性和严格性至关重要.
更多相关视频
08:22A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
Published on: December 1, 2017
9.0K
08:26Behavioral And Physiological Analysis In A Zebrafish Model Of Epilepsy
Published on: October 19, 2021
6.2K
相关概念视频
Epilepsy and Seizures: Overview
1.2K
Epilepsy is a chronic neurological disease marked by recurrent, unpredictable seizures. These seizures are caused by abnormal electrical discharges in the brain, leading to behavior, sensation, or consciousness alterations. They can also cause transient impairment of awareness, interfering with daily activities.
Various factors can trigger epilepsy, including genetic factors, brain damage, metabolic causes, and unknown etiology. Diagnosis of epilepsy involves electroencephalography (EEG), which...
Various factors can trigger epilepsy, including genetic factors, brain damage, metabolic causes, and unknown etiology. Diagnosis of epilepsy involves electroencephalography (EEG), which...
1.2K
Genome-wide Association Studies-GWAS
15.3K
Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
GWAS does not require the identification of the target gene involved in...
15.3K
Single Nucleotide Polymorphisms-SNPs
17.9K
A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
17.9K
Antiepileptic Drugs: Modulators of Neurotransmitter Release Mediated by SV2A Protein
834
Antiepileptic drugs, such as levetiracetam (Keppra) and brivaracetam (Briviact), have emerged as crucial tools in managing epilepsy. These medications exert their therapeutic effects by targeting the synaptic vesicle protein SV2A, a transmembrane glycoprotein primarily found in the brain.
SV2A is a transmembrane glycoprotein located predominantly in the brain, modulating the release of neurotransmitters for neuronal communication. Both levetiracetam and brivaracetam exhibit a high affinity for...
SV2A is a transmembrane glycoprotein located predominantly in the brain, modulating the release of neurotransmitters for neuronal communication. Both levetiracetam and brivaracetam exhibit a high affinity for...
834
Seizures: Classification
1.4K
Epilepsy is primarily characterized by unpredictable seizures, either provoked by an identifiable factor, such as injury or illness, or unprovoked, occurring spontaneously without apparent cause.
Seizures are typically classified into two main categories: focal and generalized seizures.
Focal Seizures
Focal seizures originate from specific regions of the brain. These seizures are further sub-classified into two types:
Seizures are typically classified into two main categories: focal and generalized seizures.
Focal Seizures
Focal seizures originate from specific regions of the brain. These seizures are further sub-classified into two types:
1.4K
