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老年患者心血管疾病的免疫标志物

Immunological Markers of Cardiovascular Pathology in Older Patients.

作者信息

Bugibayeva Akbota, Kurmanova Almagul, Abzaliyev Kuat, Abzaliyeva Symbat, Kurmanova Gaukhar, Sundetova Diana, Abdykassymova Merei, Bitemirova Raushan, Sagalbayeva Ulzas, Absatarova Karashash, Suleimenova Madina

机构信息

Faculty of Medicine and Healthcare, Al-Farabi Kazakh National University, Almaty 050040, Kazakhstan.

Faculty of Information Technology, Al-Farabi Kazakh National University, Almaty 050040, Kazakhstan.

出版信息

Biomedicines. 2025 Jun 6;13(6):1392. doi: 10.3390/biomedicines13061392.

DOI:10.3390/biomedicines13061392
PMID:40564110
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12189633/
Abstract

The aging process is accompanied by changes in the immunological status of a person. Immunosenescence is considered a significant cause of the development of cardiovascular diseases (CVD) in elderly people. However, to date, the relationship between immune/inflammatory processes and diseases associated with age is considered quite complex and is not fully understood. Immunophenotyping and the intracellular production of cytokines involved in the processes of inflammatory aging will allow us to identify biomarkers that are associated with cardiovascular diseases in the elderly. To identify immunological markers associated with the process of inflammatory aging in older individuals with cardiovascular diseases. CD-phenotyping and intracellular cytokine analysis of peripheral blood using the flow cytometry method were conducted in 52 people over 60 years of age (group 1 had CVD and group 2 did not). Blood samples were stained with monoclonal antibodies (mAb) using Becton Dickinson (BD) reagents for the staining and binding of surface receptors CD4+, CD8+, CD14+, CD19+, CD16+, CD56+, CD59+, CD95+, and HLA DR+ and intracellular receptors TNF, IL-10, GM-CSF, VEGFR-2, IGF, and perforin. In addition, the following parameters were studied: questionnaire data (gender, age, alcohol consumption, smoking, physical activity, and marital status), clinical data (blood pressure (BP), heart rate (HR), body mass index (BMI)), comorbid conditions, and cardiovascular diseases (coronary heart disease (CHD), chronic heart failure (CHF), arterial hypertension (AH), previous myocardial infarction (PICS), diabetes mellitus (DM), atrial fibrillation (AF), and stroke). The older patients with cardiovascular pathology had high levels of monocytes CD14+ ( = 0.014), low levels of CD8+ lymphocytes ( = 0.046), and low intracellular production of GM-CSF ( = 0.013) compared to the older people without CVD. The revealed differences in the expression of CD14+ monocytes indicate their role in the development of cardiovascular pathology associated with age-related changes. A decrease in cytotoxic CD8+ lymphocytes and intracellular GM-CSF production leads to an increased risk of developing cardiovascular diseases in older individuals. These observed changes with age will not only expand existing knowledge about the aging of the regulatory link of the immune system but also help to obtain data to predict CVD in older people. Thus, the obtained results support the use of these immunological markers to identify the risk of circulatory disease and a personalized approach in geriatric practice.

摘要

衰老过程伴随着人体免疫状态的变化。免疫衰老被认为是老年人心血管疾病(CVD)发生发展的一个重要原因。然而,迄今为止,免疫/炎症过程与年龄相关疾病之间的关系被认为相当复杂,尚未完全明确。免疫表型分析以及参与炎症衰老过程的细胞因子的细胞内产生情况,将使我们能够识别与老年人心血管疾病相关的生物标志物。为了识别与患有心血管疾病的老年人炎症衰老过程相关的免疫标志物。对52名60岁以上的人群(第1组患有CVD,第2组未患)采用流式细胞术对外周血进行CD表型分析和细胞内细胞因子分析。使用贝克曼库尔特(BD)试剂,用单克隆抗体(mAb)对血样进行染色,以标记和结合表面受体CD4 +、CD8 +、CD14 +、CD19 +、CD16 +、CD56 +、CD59 +、CD95 +和HLA DR +以及细胞内受体TNF、IL - 10、GM - CSF、VEGFR - 2、IGF和穿孔素。此外,还研究了以下参数:问卷调查数据(性别、年龄、饮酒、吸烟、体育活动和婚姻状况)、临床数据(血压(BP)、心率(HR)、体重指数(BMI))、合并症以及心血管疾病(冠心病(CHD)、慢性心力衰竭(CHF)、动脉高血压(AH)、既往心肌梗死(PICS)、糖尿病(DM)、心房颤动(AF)和中风)。与没有CVD的老年人相比,患有心血管疾病的老年患者单核细胞CD14 +水平较高( = 0.014),CD8 +淋巴细胞水平较低( = 0.046),GM - CSF的细胞内产生水平较低( = 0.013)。所揭示的CD14 +单核细胞表达差异表明它们在与年龄相关变化相关的心血管病理发展中的作用。细胞毒性CD8 +淋巴细胞减少和细胞内GM - CSF产生减少会导致老年人患心血管疾病的风险增加。这些随年龄观察到的变化不仅会扩展关于免疫系统调节环节衰老的现有知识,还将有助于获取数据以预测老年人的CVD。因此,所获得的结果支持使用这些免疫标志物来识别循环系统疾病风险以及在老年医学实践中采取个性化方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0a5/12189633/121c3a4b0819/biomedicines-13-01392-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0a5/12189633/121c3a4b0819/biomedicines-13-01392-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0a5/12189633/121c3a4b0819/biomedicines-13-01392-g001.jpg

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本文引用的文献

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Diagnostics (Basel). 2025 Mar 27;15(7):850. doi: 10.3390/diagnostics15070850.
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