Kumar Munish, Sharma Tanavi, Patel Krishna, Chinnapparaj Shobia, Dixit Ravi, Gendle Chandrashekhar, Aggarwal Ashish, Takkar Aastha, Gupta Tulika, Singla Navneet, Pal Arnab, Salunke Pravin, Dhandapani Sivashanmugam, Chabra Rajesh, Chatterjee Aditi, Gowda Harsha, Bhagat Hemant
Division of Neuro-anesthesia, Department of Anesthesia and Intensive Care, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Institute of Bioinformatics, International Tech Park, Bangalore, India.
OMICS. 2024 May;28(5):234-245. doi: 10.1089/omi.2024.0070. Epub 2024 May 7.
Cerebral vasospasm (CV) is a significant complication following aneurysmal subarachnoid hemorrhage (aSAH), and lacks a comprehensive molecular understanding. Given the temporal trajectory of intracranial aneurysm (IA) formation, its rupture, and development of CV, altered gene expression might be a molecular substrate that runs through these clinical events, influencing both disease inception and progression. Utilizing RNA-Seq, we analyzed tissue samples from ruptured IAs with and without vasospasm to identify the dysregulated genes. In addition, temporal gene expression analysis was conducted. We identified seven dysregulated genes in patients with ruptured IA with vasospasm when compared with those without vasospasm. We found 192 common genes when the samples of each clinical subset of patients with IA, that is, unruptured aneurysm, ruptured aneurysm without vasospasm, and ruptured aneurysm with vasospasm, were compared with control samples. Among these common genes, , , , and displayed temporal expression (progressive increase) with the pathological progression of disease that is formation of aneurysm, its rupture, and consequently the development of vasospasm. We validated the temporal gene expression pattern of at both the transcript and protein levels and emerges as a crucial gene implicated in the pathological progression of disease. In addition, and appear to be pivotal genes for CV development. To the best of our knowledge, this is the first study to compare the transcriptome of aneurysmal tissue samples of aSAH patients with and without CV. The findings collectively provide new insights on the molecular basis of IA and CV and new leads for translational research.
脑血管痉挛(CV)是动脉瘤性蛛网膜下腔出血(aSAH)后的一种严重并发症,目前对其分子机制尚缺乏全面了解。鉴于颅内动脉瘤(IA)形成、破裂及CV发展的时间轨迹,基因表达改变可能是贯穿这些临床事件的分子基础,影响疾病的发生和进展。我们利用RNA测序技术分析了有或无血管痉挛的破裂IA组织样本,以鉴定失调基因。此外,还进行了基因表达的时间分析。与无血管痉挛的患者相比,我们在有血管痉挛的破裂IA患者中鉴定出7个失调基因。当将IA患者各临床亚组(即未破裂动脉瘤、无血管痉挛的破裂动脉瘤和有血管痉挛的破裂动脉瘤)的样本与对照样本进行比较时,我们发现了192个共同基因。在这些共同基因中, 、 、 和 随着疾病的病理进展(即动脉瘤形成、破裂以及随后的血管痉挛发展)呈现出时间表达(逐渐增加)。我们在转录本和蛋白质水平上验证了 的时间基因表达模式, 成为参与疾病病理进展的关键基因。此外, 和 似乎是CV发展的关键基因。据我们所知,这是第一项比较有或无CV的aSAH患者动脉瘤组织样本转录组的研究。这些发现共同为IA和CV的分子基础提供了新见解,并为转化研究提供了新线索。