S. Gultekin, I. Albayrak, Y. Diler, Ayse Destina Yalcin, B. Arslan
{"title":"阿尔茨海默病患者血浆中的基因表达分析","authors":"S. Gultekin, I. Albayrak, Y. Diler, Ayse Destina Yalcin, B. Arslan","doi":"10.31117/neuroscirn.v7i1.302","DOIUrl":null,"url":null,"abstract":"Alzheimer's disease (AD), which is a neurodegenerative disease, cannot be noticed until severe symptoms are observed. This poses a global challenge as the average human lifespan increases, making it a concern for the entire world population. Early diagnosis can play a crucial role in slowing the progression of the disease, thereby enhancing the quality of life for both the patient and their relatives. AD has been linked to alterations in mRNA expressions. The objective of the presented study was to determine whether there were significant differences in gene expression in blood plasma between Alzheimer's patients and healthy controls. MAPT, APP, Tubb3, TrkB, and CDC42 genes were selected as target genes due to their potential associations with AD. To analyse mRNA expression levels in the control group and AD patients, the real-time PCR (qPCR) method was performed. The findings indicate that MAPT, APP, Tubb3, and CDC42 genes' expression levels were significantly downregulated by 1.09, 1.08, 1.09, and 1.14 times, respectively (p<0.05) in AD patients. Although the TrkB gene expression appeared to be downregulated by 1.03 times in the AD group, it is not statistically different. Given the molecular associations between the pathways of the target genes and AD, changes in the expression of these genes may contribute to the pathogenesis of AD. They may represent potential biomarkers for early diagnosis.","PeriodicalId":36108,"journal":{"name":"Neuroscience Research Notes","volume":"150 ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-03-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Gene expression analysis in plasma of patients with Alzheimer's disease\",\"authors\":\"S. Gultekin, I. Albayrak, Y. Diler, Ayse Destina Yalcin, B. Arslan\",\"doi\":\"10.31117/neuroscirn.v7i1.302\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Alzheimer's disease (AD), which is a neurodegenerative disease, cannot be noticed until severe symptoms are observed. This poses a global challenge as the average human lifespan increases, making it a concern for the entire world population. Early diagnosis can play a crucial role in slowing the progression of the disease, thereby enhancing the quality of life for both the patient and their relatives. AD has been linked to alterations in mRNA expressions. The objective of the presented study was to determine whether there were significant differences in gene expression in blood plasma between Alzheimer's patients and healthy controls. MAPT, APP, Tubb3, TrkB, and CDC42 genes were selected as target genes due to their potential associations with AD. To analyse mRNA expression levels in the control group and AD patients, the real-time PCR (qPCR) method was performed. The findings indicate that MAPT, APP, Tubb3, and CDC42 genes' expression levels were significantly downregulated by 1.09, 1.08, 1.09, and 1.14 times, respectively (p<0.05) in AD patients. Although the TrkB gene expression appeared to be downregulated by 1.03 times in the AD group, it is not statistically different. Given the molecular associations between the pathways of the target genes and AD, changes in the expression of these genes may contribute to the pathogenesis of AD. They may represent potential biomarkers for early diagnosis.\",\"PeriodicalId\":36108,\"journal\":{\"name\":\"Neuroscience Research Notes\",\"volume\":\"150 \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-03-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Neuroscience Research Notes\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.31117/neuroscirn.v7i1.302\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Neuroscience\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuroscience Research Notes","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31117/neuroscirn.v7i1.302","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Neuroscience","Score":null,"Total":0}
引用次数: 0
摘要
阿尔茨海默病(AD)是一种神经退行性疾病,直到出现严重症状时才会被发现。随着人类平均寿命的延长,这种疾病已成为一个全球性挑战,令全世界的人们都感到担忧。早期诊断可在减缓疾病进展方面发挥关键作用,从而提高患者及其亲属的生活质量。注意力缺失症与 mRNA 表达的改变有关。本研究的目的是确定阿尔茨海默病患者和健康对照者血浆中的基因表达是否存在显著差异。由于 MAPT、APP、Tubb3、TrkB 和 CDC42 基因可能与老年痴呆症有关,因此被选为目标基因。为了分析对照组和 AD 患者的 mRNA 表达水平,研究人员采用了实时 PCR(qPCR)方法。结果表明,在AD患者中,MAPT、APP、Tubb3和CDC42基因的表达水平分别显著下调了1.09倍、1.08倍、1.09倍和1.14倍(P<0.05)。虽然TrkB基因的表达在AD组中似乎下调了1.03倍,但没有统计学差异。鉴于目标基因的通路与 AD 之间的分子关联,这些基因表达的变化可能有助于 AD 的发病机制。它们可能是早期诊断的潜在生物标志物。
Gene expression analysis in plasma of patients with Alzheimer's disease
Alzheimer's disease (AD), which is a neurodegenerative disease, cannot be noticed until severe symptoms are observed. This poses a global challenge as the average human lifespan increases, making it a concern for the entire world population. Early diagnosis can play a crucial role in slowing the progression of the disease, thereby enhancing the quality of life for both the patient and their relatives. AD has been linked to alterations in mRNA expressions. The objective of the presented study was to determine whether there were significant differences in gene expression in blood plasma between Alzheimer's patients and healthy controls. MAPT, APP, Tubb3, TrkB, and CDC42 genes were selected as target genes due to their potential associations with AD. To analyse mRNA expression levels in the control group and AD patients, the real-time PCR (qPCR) method was performed. The findings indicate that MAPT, APP, Tubb3, and CDC42 genes' expression levels were significantly downregulated by 1.09, 1.08, 1.09, and 1.14 times, respectively (p<0.05) in AD patients. Although the TrkB gene expression appeared to be downregulated by 1.03 times in the AD group, it is not statistically different. Given the molecular associations between the pathways of the target genes and AD, changes in the expression of these genes may contribute to the pathogenesis of AD. They may represent potential biomarkers for early diagnosis.