CNR Institute of Clinical Physiology, Via Moruzzi 1, Pisa, Italy.
CNR Institute of Clinical Physiology, Via Moruzzi 1, Pisa, Italy.
Mutat Res Rev Mutat Res. 2021 Jan-Jun;787:108348. doi: 10.1016/j.mrrev.2020.108348. Epub 2020 Nov 16.
Coronary artery disease (CAD) is the leading cause of morbidity and mortality worldwide. Coronary angiography allows an accurate assessment of the extent and severity of atherosclerotic coronary narrowing, but it provides little characterization of early detection of potentially asymptomatic vulnerable plaque. The identification of the coronary "vulnerable patient" or high-risk plaques remains a major challenge in the treatment of CAD. Recently, growing evidence shows that DNA damage plays a role in the initiation and progression of atherosclerotic plaque. Cytokinesis-block micronucleus (CBMN) assay is one of the most frequently used and validated method for assessing chromosomal damage and genetic instability. Accordingly, the purpose of this systematic review was to retrieve and discuss existing literature on the studies assessing the association between MN and angiographically-proven CAD. A total of 8 studies published between 2001 and 2017 were included in the meta-analysis. Despite a large heterogeneity between studies (I= 99.7 %, p < 0.0001), an overall increase of MN frequencies was found in patients with CAD compared with control group (meta-MR = 1.96; 95 % CI, 1.5-3.2, p = 0.009). A subgroup analysis showed an increase in the frequency of MN formation for both two- vessel (MR = 2.13, 95 % CI: 0.9-6.9, p = 0.08) and three-vessel disease (MR = 2.89, 95 % CI: 1.84-4.55, P = 0.06). Overall, the results of this meta-analysis provide evidence of an association between CBMN and presence, extent and severity of angiographically-assessed CAD. However, the small number of papers analyzed requires further large and more rigorously designed studies, carefully considering a series of clinical confounding factors, such as the quality of the metabolic control, the influence of drugs and radiation imaging treatments.
冠心病(CAD)是全球发病率和死亡率的主要原因。冠状动脉造影可以准确评估动脉粥样硬化性冠状动脉狭窄的程度和严重程度,但对无症状易损斑块的早期检测几乎没有特征描述。确定冠状动脉的“易损患者”或高危斑块仍然是 CAD 治疗的主要挑战。最近,越来越多的证据表明,DNA 损伤在动脉粥样硬化斑块的发生和发展中起作用。胞质分裂阻断微核(CBMN)试验是评估染色体损伤和遗传不稳定性的最常用和最有效的方法之一。因此,本系统评价的目的是检索和讨论评估 MN 与血管造影证实的 CAD 之间相关性的现有文献。共有 8 项发表于 2001 年至 2017 年的研究纳入荟萃分析。尽管研究之间存在很大的异质性(I=99.7%,p<0.0001),但与对照组相比,CAD 患者的 MN 频率总体升高(meta-MR=1.96;95%CI,1.5-3.2,p=0.009)。亚组分析显示,两血管病变(MR=2.13,95%CI:0.9-6.9,p=0.08)和三血管病变(MR=2.89,95%CI:1.84-4.55,P=0.06)患者 MN 形成频率均增加。总的来说,这项荟萃分析的结果提供了证据表明 CBMN 与血管造影评估的 CAD 的存在、程度和严重程度之间存在关联。然而,分析的论文数量较少,需要进一步开展更大和设计更严谨的研究,仔细考虑一系列临床混杂因素,如代谢控制的质量、药物和放射成像治疗的影响。