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Features of cytokine balance in patients with osteoarthrosis and atherosclerosis 骨关节病和动脉粥样硬化患者的细胞因子平衡特征
Pub Date : 2020-01-01 DOI: 10.20333/2500136-2020-6-70-74
S. M. Tsvinger, A. Govorin, A. M. Karachenova
The aim of the research is to study the content of some key pro / anti-inflammatory cytokines in patients with osteoarthritis and to evaluate their role in predicting atherogenesis in this category of patients. Material and methods. Patients with primary osteoarthritis of I-III radiological stages were examined. Doppler vessels ultrasound (Doppler ultrasound) of the neck, upper and lower extremities was performed; blood levels of pro / anti-inflammatory cytokines were examined: IL-1β, TNF-α, IL-6, IL- 8, IL-18, MCP-1, IL-17, IL-10, IL-33 by flow cytometry. Results. According to the thickness of intima - media complex, the patients were divided into 2 groups: with a normal thickness of intima - media complex and with atherosclerotic plaque. A significant increase in pro-inflammatory cytokines was revealed in patients with osteoarthritis associated with atherosclerosis compared with those having osteoarthritis with normal thickness of intima-media complex. The level of pro / anti-inflammatory cytokines along with atherosclerosis are closely interconnected. Conclusion. According to the results of the studies obtained, it was found that a long-term subclinical inflammatory process leads to multidirectional disturbances in cytokine balance in patients with osteoarthritis, which probably contributes to the progression of both osteoarthritis and atherosclerosis. A possible factor of early atherosclerosis development in patients with osteoarthritis was also identified.
本研究的目的是研究骨关节炎患者中一些关键的促/抗炎细胞因子的含量,并评估它们在预测这类患者动脉粥样硬化中的作用。材料和方法。对影像学分期为I-III期的原发性骨关节炎患者进行检查。行颈、上、下肢多普勒血管超声(多普勒超声)检查;流式细胞术检测血中促炎性因子IL-1β、TNF-α、IL-6、IL- 8、IL-18、MCP-1、IL-17、IL-10、IL-33的水平。结果。根据内膜-中膜复合体厚度将患者分为内膜-中膜复合体厚度正常组和动脉粥样硬化斑块组。与内膜-中膜复合体厚度正常的骨关节炎患者相比,与动脉粥样硬化相关的骨关节炎患者的促炎细胞因子显著增加。促/抗炎细胞因子水平与动脉粥样硬化密切相关。结论。根据所获得的研究结果,我们发现长期的亚临床炎症过程导致骨关节炎患者细胞因子平衡多向紊乱,这可能与骨关节炎和动脉粥样硬化的进展有关。还确定了骨关节炎患者早期动脉粥样硬化发展的一个可能因素。
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引用次数: 0
Territory operational experience of maternity hospital users in Metropolitan France 法国大城市妇产医院用户的区域运营经验
Pub Date : 2020-01-01 DOI: 10.20333/2500136-2020-4-97-107
K. Kononovich, Crafts, J. Macé
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引用次数: 0
Association of VDR gene polymorphism and ventilation balance in bronchial asthma 支气管哮喘VDR基因多态性与通气平衡的关系
Pub Date : 2020-01-01 DOI: 10.20333/2500136-2020-1-20-26
N. Potapova, I. N. Gaymolenko, N. Strambovskaya
Цель исследования. Изучить роль ассоциации генотипов и аллелей полиморфизма BsmI гена VDR с вентиляционными нарушениями при бронхиальной астме у детей. Материал и методы. За период 2015-2017гг. обследовано 154 ребенка с бронхиальной астмой разной степени тяжести (73 ребенка с легким течением, 22 – со среднетяжелой и 59 – с тяжелой БА) и 34 относительно здоровых ребенка в качестве контрольной группы. Группы обследованных сопоставимы по полу и возрасту. Проведено молекулярно-генетическое типирование полиморфного локуса BsmI c.IVS.G>A гена рецептора VDR (rs1544410, G63980A). Результаты. Генотип GG полиморфизма BsmI c.IVS.G>A гена рецептора VDR встречается у пациентов с бронхиальной астмой в 4,4 раза чаще по сравнению со здоровыми индивидуумами (26,6 % против 6,0 %) (ОR=5,81, χ2=10,73, р=0,005). Генотип АА преобладает в группе контроля, составляя 53 % против 28 % у пациентов с БА. Не обнаружено статистических различий в частоте распределения генотипов и аллелей полиморфизма BsmI гена рецептора VDR у детей с разной степенью тяжести астмы. Носительство генотипа GG сопровождается резким снижением показателей ОФВ1 и ФЖЕЛ до 41 % и 43 % соответственно среди детей, больных бронхиальной астмой (р<0,05). Заключение. У детей с бронхиальной астмой отмечается более высокая частота встречаемости генотипа GG полиморфизма BsmI c.IVS.G>A гена рецептора VDR. Пациенты-носители генотипа GG полиморфизма G63980A гена VDR имеют резко выраженное снижение ОФВ1 и ФЖЕЛ, что возможно указывает на необратимые изменения архитектуры стенки бронхов и позволяет расценивать его как возможный предиктор вентиляционного дисбаланса при данном заболевании. Данный факт позволяет предполагать определенный вклад данного полиморфизма в реализацию структурной дезорганизации при ремоделировании дыхательных путей. Ключевые слова: бронхиальная астма, дети, полиморфизм гена VDR, вентиляционные нарушения. Конфликт интересов. Авторы декларируют отсутствие явных и потенциальных конфликтов интересов, связанных с публикацией настоящей статьи. Для цитирования: Потапова НЛ, Гаймоленко ИН, Страмбовская НН. Ассоциация полиморфизма гена VDR и вентиляционного баланса при бронхиальной астме. Сибирское медицинское обозрение. 2020;(1):20-26. DOI: 10.20333/2500136-2020-1-20-26
目的研究。研究基因和等位基因BsmI VDR多态性协会的作用,这些基因具有支气管哮喘呼吸障碍。材料和方法。从2015年到2017年。检查了154名患有支气管哮喘的儿童(73名轻度儿童,22名中重儿童和59名重量级儿童)和34名相对健康的对照组儿童。研究小组在性别和年龄上是一致的。BsmI c.IVS的分子-基因特征已经完成。G>A VDR基因(rs154410, G63980A)。结果。GG型多态性BsmI c.IVS。在支气管哮喘患者中,VDR基因的发生率是健康个体的4.4倍(26.6%对6.0%)。aa基因型在控制组中占主导地位,占bah患者53%,占28%。在哮喘不同程度的儿童中,基因和VDR受体多态性BsmI的分布和等位基因没有统计差异。GG型基因载体与fg1和fgl基因分别下降到支气管哮喘儿童的41%和43%。GG型多态性G63980A基因载体G63980A基因基因有明显的下降,表明支气管壁的结构发生了不可逆转的变化,可能被认为是这种疾病的通风不平衡的可能前兆。这一事实表明,这种多态性在重新设计呼吸道时对实现结构性脱节作出了一定贡献。关键词:支气管哮喘、儿童、VDR多态性、呼吸障碍。利益冲突。提交人声称,本文的出版没有明显和潜在的利益冲突。引文:波塔波纳斯,海马伦科,斯特伦博斯。VDR基因多态性协会和支气管哮喘通风平衡协会。西伯利亚医学评论2020;(1): 20 - 26。DOI: 10.20333/2500136 2020 - 1 - 20 - 26
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引用次数: 1
Tuning the Sounds of Service: Essays in Honour of Michael Kleinaltenkamp 调整服务的声音:纪念迈克尔·克莱纳尔滕坎普的随笔
Pub Date : 2020-01-01 DOI: 10.15358/2511-8676-2020-2-3-70
Sascha Raithel, F. Jacob, M. Benkenstein
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引用次数: 0
System-therapeutic view of the experience and behavior in children and adolescents 儿童和青少年的经验和行为的系统治疗观点
Pub Date : 2020-01-01 DOI: 10.20333/2500136-2020-4-108-110
H.-W. Gessmann
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引用次数: 0
Сhronobiological features of females with symptoms of lower urinary tract Сhronobiological有下尿路症状的女性特征
Pub Date : 2020-01-01 DOI: 10.20333/2500136-2020-4-71-76
V. A. Lanina, A. V. Kuz’menko, Y. Vinnik, T. A. Gyaurgiev
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引用次数: 2
miR-204-5p level modulation that induces formation of premetastatic niche in B16 melanoma in vivo model miR-204-5p水平调控诱导B16黑色素瘤体内模型转移前生态位形成
Pub Date : 2020-01-01 DOI: 10.20333/2500136-2020-3-70-77
S. Lavrentev, M. Aksenenko, A. Averchuk, I. S. Zichenko
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引用次数: 0
Structure of unoperated congenital heart diseases in children of Zabaikalsky Territory 扎贝加尔斯基地区未手术先天性心脏病儿童的结构
Pub Date : 2020-01-01 DOI: 10.20333/2500136-2020-6-83-89
A. Ignatieva, O. F. Sibira, I. Gaimolenko
The aim of the research is to study the morbidity by appealability and some characteristics of congenital heart diseases in children of Zabaikalsky Territory. Material and methods. A retrospective clinical and anamnestic analysis of children with congenital heart diseases without surgical treatment, who were hospitalized, was carried out. The analysis included 3 year-observation. CHD diagnosed is an inclusion criterion; while surgical treatment of heart diseases is exclusion criterion. Statistical data processing was carried out using Microsoft Excel 2007, Statistica v.10.0 software package. χ2 test (Pearson) was used to compare two independent groups by qualitative characteristics. The results were considered statistically significant (reliable) at the achieved significance level of p <0.05. Results. In Zabaikalsky Territory, approximately 200 children with congenital heart disease without surgical treatment are hospitalized annually; the average age is 3 years. Fifty-three per cent of children applied for inpatient care for the first time, 44% of them were children at their first year. Gender distribution indicates the highest incidence of the pathology in girls. In CHD structure, atrial septal defects are on the first place, while interventricular septal defects are on the second. Combination of ASD and IVSD was observed with approximately equal frequency. Chronic heart failure associated with CHD was registered in 77% of children. In most cases CHF, stage 1, was diagnosed (63%). In 2/3 of cases, pulmonary hypertension of various severity was detected. Analysis of place of residence of children with CHD in the Zabaikalsky Territory shows that children from areas with the highest population density are hospitalized more often. Conclusion. The problem of congenital heart diseases in children of Zabaikalsky Territory is of current importance due to the widespread prevalence and high specific gravity among all internal organ defects in children of this region.
本研究的目的是了解扎贝加尔斯基地区儿童先天性心脏病的患病率及一些特点。材料和方法。对未经手术治疗而住院的先天性心脏病患儿进行回顾性临床和记忆分析。分析包括3年的观察。诊断为冠心病为纳入标准;而心脏疾病的手术治疗是排除标准。统计数据处理采用Microsoft Excel 2007、Statistica v.10.0软件包。采用χ2检验(Pearson)比较两个独立组的质量特征。在p <0.05达到显著性水平时,认为结果具有统计学意义(可靠)。结果。在扎贝卡尔斯基地区,每年约有200名未接受手术治疗的先天性心脏病儿童住院;平均年龄为3岁。53%的儿童是第一次申请住院治疗,其中44%是一岁的儿童。性别分布表明女孩的发病率最高。在冠心病结构中,房间隔缺损排在首位,室间隔缺损排在第二位。ASD和IVSD合并出现的频率大致相等。与冠心病相关的慢性心力衰竭在77%的儿童中出现。在大多数病例中,诊断为1期CHF(63%)。2/3的病例检测到不同程度的肺动脉高压。对扎贝卡尔斯基地区冠心病儿童居住地的分析表明,来自人口密度最高地区的儿童更常住院。结论。扎贝卡尔斯基地区儿童先天性心脏病问题目前十分重要,因为该地区儿童的所有内脏器官缺陷普遍存在,而且比重很高。
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引用次数: 0
Problem of informed consent personalization when providing dental services 提供牙科服务时的知情同意个人化问题
Pub Date : 2020-01-01 DOI: 10.20333/2500136-2020-4-92-96
A. U. Yagodina, S. Korotin, A. Petrachev
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引用次数: 0
The eff ect of inhaled anesthetics on jugular oximetry during aneurysms clipping of intracranial arteries 颅内动脉动脉瘤夹闭术中吸入麻醉剂对颈静脉血氧测定的影响
Pub Date : 2020-01-01 DOI: 10.20333/2500136-2020-3-86-91
N. Dovbysh, A. Gritsan, D. A. Kurnosov, N. A. Stepanenko
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引用次数: 0
期刊
Journal of Software Maintenance and Evolution: Research and Practice
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