Zhang Guiying, Tang Xuelei, Li Qifu, Lin Rong
Department of Biology, Hainan Medical University, Haikou, China.
Department of Neurology, The First Affiliated Hospital of Hainan Medical University, Haikou, China.
Open Life Sci. 2024 Feb 23;19(1):20220818. doi: 10.1515/biol-2022-0818. eCollection 2024.
Stroke is a debilitating condition that often leads to disability and death. The increasing prevalence of stroke has drawn worldwide attention. Extensive evidence indicates a crucial role of genetic determinants in the occurrence and perpetuation of stroke. An Icelandic study identified a significant correlation of the phosphodiesterase 4D () single-nucleotide polymorphism (SNP) rs2910829 with stroke susceptibility. However, subsequent studies reported in Chinese populations were contradictory. We implemented a meta-analysis to inspect whether SNP rs2910829 is related to stroke susceptibility in Chinese populations and subsequently performed an analysis to predict its potential functions. Finally, we analysed data from 24 studies comprising 7,484 Chinese stroke patients and 7,962 control individuals. Compared with the CC genotype, the TT genotype was associated with increased susceptibility to stroke (pooled odds ratio [OR] 1.28, 95% confidence interval [CI] 1.13-1.46, < 0.001), whereas the CT genotype was not. Correspondingly, a significant association was detected under the recessive model (TT vs CT + CC: OR 1.30, 95% CI 1.15-1.47, < 0.001). Similar results were obtained in large artery atherosclerosis (LAA) stroke but not in small vessel stroke. Bioinformatics analysis also revealed that SNP rs2910829 and its linked SNPs might be implicated in transcriptional regulation. This meta-analysis reveals significant relationships between the SNP rs2910829 and susceptibility to stroke and subtype-LAA stroke in Chinese individuals, and further investigations are warranted to evaluate this effect.
中风是一种使人衰弱的疾病,常常导致残疾和死亡。中风患病率的不断上升已引起全球关注。大量证据表明遗传因素在中风的发生和持续发展中起关键作用。一项冰岛的研究发现磷酸二酯酶4D()单核苷酸多态性(SNP)rs2910829与中风易感性之间存在显著相关性。然而,随后在中国人群中进行的研究结果却相互矛盾。我们进行了一项荟萃分析,以检验SNP rs2910829是否与中国人群的中风易感性相关,随后进行了分析以预测其潜在功能。最后,我们分析了来自24项研究的数据,这些研究包括7484名中国中风患者和7962名对照个体。与CC基因型相比,TT基因型与中风易感性增加相关(合并比值比[OR] 1.28,95%置信区间[CI] 1.13 - 1.46,< 0.001),而CT基因型则不然。相应地,在隐性模型下检测到显著关联(TT与CT + CC相比:OR 1.30,95% CI 1.15 - 1.47,< 0.001)。在大动脉粥样硬化(LAA)性中风中获得了类似结果,但在小血管中风中未获得。生物信息学分析还显示,SNP rs2910829及其连锁SNP可能参与转录调控。这项荟萃分析揭示了SNP rs2910829与中国个体中风易感性以及亚型LAA性中风之间的显著关系,有必要进一步开展研究来评估这种效应。