巴基斯坦人群阿尔茨海默病发病途径的转录组分析1

IF 2.8 Q2 NEUROSCIENCES Journal of Alzheimer's disease reports Pub Date : 2024-03-19 DOI:10.3233/adr-230146
Tanmoy Mondal, Zarish Noreen, Christopher A. Loffredo, Jheannelle Johnson, Attya Bhatti, Gail Nunlee-Bland, Ruth Quartey, Charles D. Howell, Gemeyel Moses, Thomas Nnanabu, Sharleine T. Cotin, Marika Clark, Vijay Chandra, S. Jana, Bernard Kwabi-Addo, Brent E. Korba, Sharoon Shahzad, Muhammad Farrukh Bhatti, Somiranjan Ghosh
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摘要

背景:阿尔茨海默病(AD)是一种多因素神经退行性疾病,多发于老年人,尤其是在发达国家,目前在巴基斯坦等发展中国家的发病率也在上升。研究目的我们的目标是在巴基斯坦人群中开展一项试点病例对照研究,分析与阿兹海默症发病机制相关的关键基因及其表达水平和相关分子转录组网络。研究方法为了获得与巴基斯坦AD患者发病机制相关的分子网络谱(比较病例和对照),我们使用了高通量qRT-PCR(TaqMan低密度阵列;n = 33名受试者)和Affymetrix阵列(n = 8)以及Ingenuity Pathway Analysis(IPA)来识别与淀粉样蛋白加工和疾病通路相关的特征基因。结果:我们确认了 16 个差异表达的 AD 相关基因,包括在 CAPNS2 和 CAPN1 中观察到的最大倍数变化。全球基因表达研究发现,与健康对照组相比,AD 患者中分别有 61% 和 39% 的基因被显著上调和下调(P 值为 0.05)。关键通路包括淀粉样蛋白加工、神经炎症信号转导和 ErbB4 信号转导等。疾病和失调发展中得分最高的网络是神经系统疾病、机体损伤和异常以及心理障碍。结论我们的试验性研究提供了一种非侵入性的高效方法,通过利用全血将 TLDA 和全局基因表达法相结合,研究 AD 患者的基因表达模式。这为了解淀粉样蛋白加工相关基因的表达状况提供了宝贵的信息,可在未来研究中发挥潜在作用,以确定敏感的早期 AD 生物标志物。
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Transcriptomic Analysis of Alzheimer’s Disease Pathways in a Pakistani Population1
Background: Alzheimer’s disease (AD) is a multifactorial neurodegenerative disorder that is most prevalent in elderly individuals, especially in developed countries, and its prevalence is now increasing in developing countries like Pakistan. Objective: Our goal was to characterize key genes and their levels of expression and related molecular transcriptome networks associated with AD pathogenesis in a pilot case-control study in a Pakistani population. Methods: To obtain the spectrum of molecular networks associated with pathogenesis in AD patients in Pakistan (comparing cases and controls), we used high-throughput qRT-PCR (TaqMan Low-Density Array; n = 33 subjects) coupled with Affymetrix Arrays (n = 8) and Ingenuity Pathway Analysis (IPA) to identify signature genes associated with Amyloid processing and disease pathways. Results: We confirmed 16 differentially expressed AD-related genes, including maximum fold changes observed in CAPNS2 and CAPN1. The global gene expression study observed that 61% and 39% of genes were significantly (p-value 0.05) up- and downregulated, respectively, in AD patients compared to healthy controls. The key pathways include, e.g., Amyloid Processing, Neuroinflammation Signaling, and ErbB4 Signaling. The top-scoring networks in Diseases and Disorders Development were Neurological Disease, Organismal Injury and Abnormalities, and Psychological Disorders. Conclusions: Our pilot study offers a non-invasive and efficient way of investigating gene expression patterns by combining TLDA and global gene expression method in AD patients by utilizing whole blood. This provides valuable insights into the expression status of genes related to Amyloid Processing, which could play potential role in future studies to identify sensitive, early biomarkers of AD in general.
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