Maneerat Yaowapa, Prasongsukarn Kriengchai, Benjathummarak Surachet, Dechkhajorn Wilanee, Chaisri Urai
Department of Tropical Pathology, Faculty of Tropical Medicine, Mahidol University, Bangkok, 10400, Thailand.
Pramongkutklao Hospital and College of Medicine, Bangkok, 10400, Thailand.
Lipids Health Dis. 2016 Jul 18;15:117. doi: 10.1186/s12944-016-0285-5.
Atherosclerosis is a multifactorial disorder of the heart vessels that develops over decades, coupling inflammatory mechanisms and elevated total cholesterol levels under the influence of genetic and environmental factors. Without effective intervention, atherosclerosis consequently causes coronary heart disease (CHD), which leads to increased risk of sudden death. Polymorphonuclear neutrophils play a pivotal role in inflammation and atherogenesis. Human neutrophil peptides (HNPs) or alpha (α)-defensins are cysteine-rich cation polypeptides that are produced and released from activated polymorphonuclear neutrophil granules during septic inflammation and acute coronary vascular disorders. HNPs cause endothelial cell dysfunction during early atherogenesis. In this cross-sectional study, control, hyperlipidemia and CHD groups were representative as atherosclerosis development and CHD complications. We aimed to assess the correlation between α-defensin expression and the development of CHD, and whether it was a useful predictive indicator for CHD risk.
First, DNA microarray analysis was performed on peripheral blood mononuclear cells (PBMCs) from Thai control, hyperlipidemia and CHD male patients (n = 7). Gene expression profiling revealed eight up-regulated genes common between hyperlipidemia and CHD patients, but not controls. We sought to verify and compare α-defensin expression among the groups using: 1) real-time quantitative RT-PCR (qRT-PCR) to determine α-defensin mRNA expression (n = 10), and 2) enzyme-linked immunosorbent assay to determine plasma HNP 1-3 levels (n = 17). Statistically significant differences and correlations between groups were determined by the Mann-Whitney U test or the Kruskal-Wallis test, and the Rho-Spearman correlation, respectively.
We found that α-defensin mRNA expression increased (mean 2-fold change) in the hyperlipidemia (p = 0.043) and CHD patients (p = 0.05) compared with the controls. CHD development moderately correlated with α-defensin mRNA expression (r = 0.429, p = 0.023) and with plasma HNP 1-3 levels (r = 0.486, p = 0.000).
Increased α-defensin expression is a potential inflammatory marker that may predict the risk of CHD development in Thai hyperlipidemia patients.
动脉粥样硬化是一种累及心血管的多因素疾病,在数十年间逐渐发展,在遗传和环境因素的影响下,炎症机制与总胆固醇水平升高相互关联。若不进行有效干预,动脉粥样硬化会导致冠心病(CHD),进而增加猝死风险。多形核中性粒细胞在炎症和动脉粥样硬化形成过程中起关键作用。人中性粒细胞肽(HNPs)或α-防御素是富含半胱氨酸的阳离子多肽,在脓毒症炎症和急性冠状动脉血管疾病期间,由活化的多形核中性粒细胞颗粒产生并释放。在动脉粥样硬化早期,HNPs会导致内皮细胞功能障碍。在这项横断面研究中,对照组、高脂血症组和冠心病组具有动脉粥样硬化发展及冠心病并发症的代表性。我们旨在评估α-防御素表达与冠心病发展之间的相关性,以及它是否是冠心病风险的有效预测指标。
首先,对泰国男性对照组、高脂血症组和冠心病组患者(n = 7)的外周血单核细胞(PBMCs)进行DNA微阵列分析。基因表达谱分析显示,高脂血症患者和冠心病患者共有8个上调基因,而对照组没有。我们试图通过以下方法验证并比较各组间α-防御素的表达情况:1)实时定量逆转录聚合酶链反应(qRT-PCR),以确定α-防御素mRNA表达水平(n = 10);2)酶联免疫吸附测定法,以确定血浆中HNP 1-3水平(n = 17)。分别采用Mann-Whitney U检验或Kruskal-Wallis检验以及Rho-Spearman相关性分析来确定组间的统计学显著差异和相关性。
我们发现,与对照组相比,高脂血症患者(p = 0.043)和冠心病患者(p = 0.05)的α-防御素mRNA表达增加(平均变化2倍)。冠心病的发展与α-防御素mRNA表达(r = 0.429,p = 0.023)以及血浆HNP 1-3水平(r = 0.486,p = 0.000)呈中度相关。
α-防御素表达增加是一种潜在的炎症标志物,可能预测泰国高脂血症患者发生冠心病的风险。