Relationship between dynamic changes in subpopulations of blood monocytes and the development of complications in patients with acute myocardial infarction

T. Talayeva, O. Parkhomenko, I. Tretyak, O. Dovhan, O. Shumakov
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Dynamic heart echocardiography was also performed on the 1st and 7th day. All patients were divided into 2 groups depending on the dynamical increase (1 group – 21 pts) or decrease (2 group – 29 pts) of classical monocytes (CD14hiCD16–) subpopulation during 7 days of follow-up. The control group included 15 healthy subjects with no signs of coronary heart disease and 23 pts with chronic coronary heart disease without AMI.Results and discussion. In subgroup 1, the percentage of the «classical» fraction of monocytes during the observation increased to 89.0±1.2 %, which was 4.2 % more than on the 1st day and 12.5 % more than in the control group (р<0.05), while the absolute amount of classic monocytes on day 7 increased by 48 % compared to initial value (р<0.01). The percentage of «intermediate» (CD14hiCD16+) blood monocytes in patients of this subgroup on the 1st day of hospitalization was 70 % higher than in the control group, and 42 % higher than in the 2nd subgroup of patients (р<0,001), however, on the 7th day it decreased by 30 % compared to baseline, although it remained by 8 % more than in the control group (the absolute number of «intermediate» monocytes did not change). The activation index (IA) of the «intermediate» monocytes on the first day did not differ between subgroups and was 40 % higher than in the control group (р<0.001). However, in the dynamics of observation, in patients of subgroup 1, this figure did not change, while in subgroup 2 IA decreased by 60 % (р<0.001). Despite the fact that the absolute number of anti-inflammatory («patrolling») (CD14+lowCD16++) monocytes did not change until the 7th day of observation (and their percentage decreased slightly), their IA was significantly lower than in the control group (95 %) and in patients of subgroup 2 (92 %, р<0,001). In patients of subgroup 2, the decrease of the percentage of «classic» monocytes was –7.7 % (from 90.4±0.8 to 83.4±1.2 %). Despite the fact that the number and percentage of intermediate monocytes increased in dynamics, their IA decreased almost 2 times, which may indicate a decrease in the pro-inflammatory ability these monocytes. The percentage and number of «patrolling» monocytes increased in dynamics by 37.4 % (р<0.0001) and by 268.3 % (р<0.01), respectively. IA of patrolling monocytes was almost 12 and 7 times higher than in patients of subgroup 1 on the 1st and 7th day of observation, respectively, which may indicate a significant activation of anti-inflammatory activity of patrolling monocytes. Intracardiac thrombosis was 3.3 times more common in patients of subgroup 1, in this subgroup was also more often noted (compared to the subgroup 2): dilatation of the left ventricle (almost 8 times), reduction of left ventricular ejection fraction (4 times), and pathological post-infarction remodeling of the left ventricle (almost 7 times).Conclusions. The results of the study indicate the important role of different subpopulations of blood monocytes in the processes of myocardial damage and recovery (in particular, the pro-inflammatory role of increasing the number of classical monocytes and increasing the activity of intermediate monocytes, as well as the anti-inflammatory role of increasing the number, percentage and activity of patrolling monocytes) in patients with AMI and can be the basis for developing new approaches to the diagnosis and prevention of complications of this disease.","PeriodicalId":23419,"journal":{"name":"Ukrainian Journal of Cardiology","volume":"28 1","pages":"9-17"},"PeriodicalIF":0.0000,"publicationDate":"2020-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ukrainian Journal of Cardiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31928/1608-635x-2020.4.917","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

The aim – to determine the extent of different subpopulations of blood monocytes in acute myocardial infarction (AMI) with ST-segment elevation patients on day 1 and 7 and to evaluate the relationship between their content and the dynamics of changes and the risk of complications after AMI.Materials and methods. The composition of individual subpopulations of monocytes in the peripheral venous blood (and general clinical and biochemical blood tests) was evaluated in 50 pts with STEMI (who were admitted within 6 hours after the onset of the disease) at admission (before primary PCI) and on day 7. All patients received standard recommended therapy. Dynamic heart echocardiography was also performed on the 1st and 7th day. All patients were divided into 2 groups depending on the dynamical increase (1 group – 21 pts) or decrease (2 group – 29 pts) of classical monocytes (CD14hiCD16–) subpopulation during 7 days of follow-up. The control group included 15 healthy subjects with no signs of coronary heart disease and 23 pts with chronic coronary heart disease without AMI.Results and discussion. In subgroup 1, the percentage of the «classical» fraction of monocytes during the observation increased to 89.0±1.2 %, which was 4.2 % more than on the 1st day and 12.5 % more than in the control group (р<0.05), while the absolute amount of classic monocytes on day 7 increased by 48 % compared to initial value (р<0.01). The percentage of «intermediate» (CD14hiCD16+) blood monocytes in patients of this subgroup on the 1st day of hospitalization was 70 % higher than in the control group, and 42 % higher than in the 2nd subgroup of patients (р<0,001), however, on the 7th day it decreased by 30 % compared to baseline, although it remained by 8 % more than in the control group (the absolute number of «intermediate» monocytes did not change). The activation index (IA) of the «intermediate» monocytes on the first day did not differ between subgroups and was 40 % higher than in the control group (р<0.001). However, in the dynamics of observation, in patients of subgroup 1, this figure did not change, while in subgroup 2 IA decreased by 60 % (р<0.001). Despite the fact that the absolute number of anti-inflammatory («patrolling») (CD14+lowCD16++) monocytes did not change until the 7th day of observation (and their percentage decreased slightly), their IA was significantly lower than in the control group (95 %) and in patients of subgroup 2 (92 %, р<0,001). In patients of subgroup 2, the decrease of the percentage of «classic» monocytes was –7.7 % (from 90.4±0.8 to 83.4±1.2 %). Despite the fact that the number and percentage of intermediate monocytes increased in dynamics, their IA decreased almost 2 times, which may indicate a decrease in the pro-inflammatory ability these monocytes. The percentage and number of «patrolling» monocytes increased in dynamics by 37.4 % (р<0.0001) and by 268.3 % (р<0.01), respectively. IA of patrolling monocytes was almost 12 and 7 times higher than in patients of subgroup 1 on the 1st and 7th day of observation, respectively, which may indicate a significant activation of anti-inflammatory activity of patrolling monocytes. Intracardiac thrombosis was 3.3 times more common in patients of subgroup 1, in this subgroup was also more often noted (compared to the subgroup 2): dilatation of the left ventricle (almost 8 times), reduction of left ventricular ejection fraction (4 times), and pathological post-infarction remodeling of the left ventricle (almost 7 times).Conclusions. The results of the study indicate the important role of different subpopulations of blood monocytes in the processes of myocardial damage and recovery (in particular, the pro-inflammatory role of increasing the number of classical monocytes and increasing the activity of intermediate monocytes, as well as the anti-inflammatory role of increasing the number, percentage and activity of patrolling monocytes) in patients with AMI and can be the basis for developing new approaches to the diagnosis and prevention of complications of this disease.
急性心肌梗死患者血单核细胞亚群动态变化与并发症发生的关系
目的-确定急性心肌梗死(AMI) st段抬高患者血液单核细胞不同亚群在第1天和第7天的程度,并评估其含量与AMI后动态变化和并发症风险之间的关系。材料和方法。对50例STEMI患者(发病后6小时内入院)在入院时(初次PCI前)和第7天外周静脉血中单个单核细胞亚群的组成(以及一般临床和生化血液检查)进行评估。所有患者均接受标准推荐治疗。术后第1、7天分别行动态心脏超声心动图检查。根据7天随访期间经典单核细胞(CD14hiCD16 -)亚群的动态增加(1组- 21例)或减少(2组- 29例),将所有患者分为两组。对照组包括15名无冠心病征象的健康受试者和23名无AMI的慢性冠心病患者。结果和讨论。在亚组1中,观察期间单核细胞“经典”部分的百分比增加到89.0±1.2%,比第1天增加4.2%,比对照组增加12.5% (p <0.05),而第7天经典单核细胞的绝对数量比初始值增加48% (p <0.01)。该亚组患者在住院第一天的“中间”(CD14hiCD16+)血液单核细胞百分比比对照组高70%,比第二亚组患者高42%(< 0.001),然而,在第7天,与基线相比下降了30%,尽管仍比对照组高8%(“中间”单核细胞的绝对数量没有变化)。第一天“中间”单核细胞的激活指数(IA)在亚组之间没有差异,比对照组高40% (p <0.001)。然而,在动态观察中,在亚组1患者中,这一数字没有变化,而在亚组2患者中,IA下降了60% (p <0.001)。尽管事实上抗炎(“巡逻”)(CD14+低cd16 ++)单核细胞的绝对数量直到观察的第7天才发生变化(并且它们的百分比略有下降),但它们的IA显著低于对照组(95%)和亚组2患者(92%,< 0.001)。在亚组2患者中,“经典”单核细胞百分比下降了- 7.7%(从90.4±0.8下降到83.4±1.2%)。尽管中间单核细胞的数量和百分比动态增加,但它们的IA下降了近2倍,这可能表明这些单核细胞的促炎能力下降。“巡逻”单核细胞的百分比和数量分别动态增加了37.4%(<0.0001)和268.3%(<0.01)。观察第1天和第7天,巡逻单核细胞的IA分别比1亚组患者高近12倍和7倍,这可能表明巡逻单核细胞的抗炎活性明显激活。心内血栓形成在亚组1患者中是3.3倍,在这个亚组中也更常见(与亚组2相比):左心室扩张(近8倍),左心室射血分数降低(4倍),以及病理性梗死后左心室重构(近7倍)。本研究结果表明,不同亚群血单核细胞在心肌损伤和恢复过程中的重要作用(特别是增加经典单核细胞数量和增加中间单核细胞活性的促炎作用,以及增加数量的抗炎作用)。AMI患者中巡逻单核细胞的百分比和活性),可以作为开发诊断和预防这种疾病并发症的新方法的基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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