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Pulmonary artery thrombosis. Clinical cases 肺动脉血栓临床病例
Pub Date : 2024-01-13 DOI: 10.17816/mechnikov623001
O. Porembskaya, S. Tsaplin, K. Lobastov, Victoria A. Ilina, V. Kravchuk, Sergey A. Sayganov
Accumulating evidence supports the need to consider pulmonary artery thrombosis the separate thrombotic complication, which requires its own treatment algorithms. The aim of the work is to demonstrate the pulmonary artery thrombosis clinical aspects and the effect of the standard thrombotic prophylactic algorithms with clinical examples. Clinical cases of patients with pulmonary artery thrombosis are presented. Pulmonary artery thrombosis is considered to be the thrombotic obstruction of the pulmonary artery branches in the absence of venous and cardiac chambers thrombosis. Patient S. with COVID-19 and 75% of lung involvement was treated in the accordance with the actual COVID-19 treatment recommendations. Enoxaparin sodium 6000 IE once a day followed by the increasing dosage of 8000 IE twice a day was used. To prevent exacerbation tocilizumab was infused, and systemic thrombolytic therapy was performed. On the 6th day after systemic thrombolytic therapy patient died. Examination revealed thrombi in the pulmonary artery branches. Patient P. with continued growth of cerebral left frontoparietal region glioblastoma was hospitalized. Surgical tumor removal was performed a year ago. Conservative therapy, dexamethasone injections and anticoagulant prophylaxis (enoxaparin sodium 4000 IE once a day) were prescribed. After the patient death thrombi were found in the pulmonary artery segmental branches. Outpatient D. had a history of four episodes of dyspnea during the acute respiratory diseases. Computed tomography performed at the time of the third and fourth episodes revealed thrombi in the pulmonary artery segmental branches. The fourth episode occured despite anticoagulant prophylaxis with rivaroxaban (10 mg once a day). Patient was recommended to switch to low molecular weight heparins in case of any disease. There have been no recurrent episodes over the past 8 months. Distinctive features of pulmonary artery thrombosis pathogenesis determine the development of the complication despite anticoagulant prophylaxis. Preventive effect of anti-inflammatory drugs on the pulmonary artery thrombosis development has not been demonstrated.
越来越多的证据表明,有必要将肺动脉血栓形成视为单独的血栓并发症,需要有自己的治疗算法。本文旨在通过临床实例,展示肺动脉血栓形成的临床方面以及标准血栓预防算法的效果。本文介绍了肺动脉血栓形成患者的临床病例。肺动脉血栓形成是指在没有静脉和心腔血栓形成的情况下,肺动脉分支发生血栓性阻塞。患者 S.患有 COVID-19,75% 的肺部受累,按照 COVID-19 的实际治疗建议进行治疗。使用依诺肝素钠 6000 IE,每天一次,然后增加剂量至 8000 IE,每天两次。为防止病情恶化,输注了替西珠单抗,并进行了全身溶栓治疗。全身溶栓治疗后第 6 天,患者死亡。检查发现肺动脉分支有血栓。患者 P.因大脑左额叶区胶质母细胞瘤持续生长而住院治疗。一年前进行了肿瘤手术切除。患者接受了保守治疗、地塞米松注射和抗凝剂预防(依诺肝素钠 4000 IE,每天一次)。患者死亡后,在肺动脉段分支发现了血栓。门诊患者 D 有四次急性呼吸道疾病呼吸困难病史。第三次和第四次发作时进行的计算机断层扫描发现肺动脉节段分支中有血栓。尽管使用了利伐沙班(10 毫克,每天一次)进行抗凝预防,但还是出现了第四次呼吸困难。医生建议患者在出现任何疾病时改用低分子量肝素。在过去的 8 个月里,患者的病情没有反复发作。肺动脉血栓形成发病机制的显著特点决定了尽管使用了抗凝剂预防,并发症仍会发生。抗炎药对肺动脉血栓形成的预防作用尚未得到证实。
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引用次数: 0
Factors of stroke misdiagnosis at the onset of myastenia gravis 肌无力症发病时中风误诊的因素
Pub Date : 2024-01-13 DOI: 10.17816/mechnikov492276
A. R. Alibekov, Vitaliy V. Goldobin, Hosiddin F. Yuldashev, E. Klocheva, Irina A. Lubenets, Aruzhan Zh. Nurmakhanbetova
BACKGROUND: Myasthenia gravis is a rare autoimmune disease,which is difficult to diagnose mainly in the initial stages, when there are single symptoms of the disease or an atypical course. Diagnostic errors are associated with the fact that myasthenia gravis and other diseases of the nervous system have similar symptoms. The most common misdiagnosis in the onset of myasthenia gravis is a stroke. However, the reasons for a false diagnosis remain unspecified and poorly understood. AIM: To determine the factors leading to misdiagnosis of a stroke in the onset of myasthenia gravis. MATERIALS AND METHODS: 133 patients diagnosed with myasthenia gravis were divided into two groups. Patients with misdiagnosed stroke at the onset of myasthenia gravis formed the first group, the rest of the patients – the second group. A comparative assessment was performed according to the age of myasthenia onset, the clinical variant of the onset, primary symptoms, the duration of diagnosis, and the severity of the disease at the time of the correct diagnosis, with the percentage of misdiagnosis calculation. RESULTS: Stroke as misdiagnosis was established more often than others (in 23% of all cases and in 44% of incorrect diagnoses). In the 1st group, complaints of dysarthria and dysphagia were significantly higher, myasthenia gravis began acutely more often, the age of myasthenia onset in patients of the 1st group was statistically higher than in the 2nd. There was no difference between the groups in terms of diagnosis duration, the disease severity, and the history of previous stroke. CONCLUSIONS: Factors leading to stroke misdiagnosis at the onset of myasthenia are advanced age and acute onset with bulbar disorders.
背景:重症肌无力是一种罕见的自身免疫性疾病,主要是在初期阶段难以诊断,因为此时疾病症状单一或病程不典型。诊断错误与重症肌无力和其他神经系统疾病的症状相似有关。肌无力最常见的误诊是中风。然而,造成误诊的原因仍不明确,人们对其了解甚少。目的:确定导致肌无力发病时被误诊为中风的因素。材料与方法:将 133 名确诊为重症肌无力的患者分为两组。肌无力发病时被误诊为中风的患者为第一组,其余患者为第二组。根据肌无力发病年龄、发病临床变异、主要症状、诊断持续时间和正确诊断时的疾病严重程度进行比较评估,并计算误诊百分比。结果:中风的误诊率高于其他疾病(占所有病例的 23%,占误诊病例的 44%)。在第一组中,构音障碍和吞咽困难的主诉明显多于第二组,肌无力的急性起病率更高,第一组患者肌无力的发病年龄在统计学上高于第二组。两组患者在诊断持续时间、疾病严重程度和既往中风史方面没有差异。结论:导致中风误诊的因素肌无力发病时导致中风误诊的因素是高龄和急性发病并伴有球部障碍。
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引用次数: 0
Enamel and dentin of human teeth. Fatigue strength 人类牙齿的珐琅质和牙本质疲劳强度
Pub Date : 2024-01-13 DOI: 10.17816/mechnikov624120
Alexey V. Silin, E. Satygo, A. Maryanovich
The article provides a brief overview of the studies regarding changes in the structure and composition of teeth after eruption. The factors of degenerative changes in tooth structures and their relationship with non-carious lesions have been analyzed. The study makes emphasis on the tooth durability and the factors influencing tissue fatigue, explaining increased tissue wear due to local factors. Understanding mechanisms of metabolism of teeth hard tissues is the key to the stability of restorative treatments and occurrence of non-carious tooth lesions. The evolution of views on this problem is noteworthy. The literature review reveals the initial predominance of mechanical actions, abrasion, and mineralization. It is later complemented by a detailed analysis of the influence of destructive stresses and deformation due to mechanical factors. All the leading works of the 2000s are dedicated to analyzing the ultrastructural features of enamel that affect its mechanical characteristics and can explain both the characteristics of the shape and intensity of mechanical tooth wear during the functioning of the stomatognathic system, as well as the durability of the performed restorations. The literature review covers 74 sources over the past 15 years.
文章简要概述了有关萌出后牙齿结构和组成变化的研究。文章分析了牙齿结构退行性变化的因素及其与非龋性病变的关系。研究强调了牙齿的耐久性和影响组织疲劳的因素,解释了局部因素导致的组织磨损增加。了解牙齿硬组织的新陈代谢机制是修复治疗的稳定性和非龋齿病变发生的关键。关于这一问题的观点演变值得注意。文献综述显示,机械作用、磨损和矿化最初占主导地位。后来又对机械因素造成的破坏性应力和变形的影响进行了详细分析。2000 年代的所有重要著作都致力于分析影响珐琅质机械特性的珐琅质超微结构特征,这些特征既可以解释口颌系统运行过程中牙齿机械磨损的形状和强度特征,也可以解释修复体的耐久性。文献综述涵盖了过去 15 年中的 74 个资料来源。
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引用次数: 0
Strategy of stage treatment for patients with perforated diverticulitis: first experience 穿孔性憩室炎患者的分期治疗策略:初次经验
Pub Date : 2024-01-13 DOI: 10.17816/mechnikov601813
Boris G. Bezmozgin, Evita V. Poryvaeva, Ekaterina A. Pirozhkova, Oleg V. Babkov, I. Yastrebov, I. M. Batyrshin, Dmitry A. Surov, A. Demko
BACKGROUND: The results of surgical treatment of patients with perforative diverticulitis of the colon are still unsatisfactory today. Since the majority of patients undergo Hartmann surgery, the main problem is a large number of stoma patients. Three quarters of them live with a stoma for a long time, which negatively affects their quality of life and increases the cost of treatment. AIM: The purpose of this research work is to improve the immediate results of treating patients with perforative diverticulitis and peritonitis by using staged surgical tactics. MATERIALS AND METHODS: The reaserach included 14 patients with perforative diverticulitis Hinchey grade II-III. The average value of the Mannheim peritoneal index is 18.9 ± 6.3 points. At the first stage of surgical treatment, all the patients underwent colon resection with a zone of perforation of the diverticulum and leaving its muffled ends in the abdominal cavity. After lavage and drainage, temporary closure of the anterior abdominal wall was performed. After 24–48 hours, all the patients underwent colon reconstraction. RESULTS: The average age of the patients was 52.3 ± 12.4 years with 4 women (28.6%) and 10 men (71.4%). The average duration of the first stage was 105.7 ± 27.2 minutes, the second one — 113.2 ± 40.5 minutes. The average hospital-stays were 16.4 ± 7.2 days. There were no anastomosis failures and no lethal outcomes. Complications were noted in 9 patients (64.3%), grade I according to Clavien – Dindo — 83.4%. CONCLUSIONS: The tactics of early surgical treatment is a promising concept for patients with perforative diverticulitis. It provides rapid elimination of the septic focus during the first surgical operation, assumes early reconstruction of the intestine without increasing the number of complications and mortality, and can be used in patients with peritonitis.
背景:结肠穿孔性憩室炎患者的手术治疗效果至今仍不令人满意。由于大多数患者都接受哈特曼手术,因此主要问题是造口患者人数众多。其中四分之三的患者长期带着造口生活,这对他们的生活质量造成了负面影响,并增加了治疗费用。目的:这项研究工作的目的是通过采用分期手术战术,提高治疗穿孔性憩室炎和腹膜炎患者的直接效果。材料与方法:研究对象包括 14 名 Hinchey II-III 级穿孔性憩室炎患者。曼海姆腹膜指数平均值为(18.9 ± 6.3)分。在手术治疗的第一阶段,所有患者都接受了结肠切除术,在憩室穿孔区将其闷头留在腹腔内。洗胃和引流后,对前腹壁进行临时封闭。24-48 小时后,所有患者都接受了结肠重建术。结果:患者平均年龄为(52.3 ± 12.4)岁,其中女性 4 人(28.6%),男性 10 人(71.4%)。第一阶段的平均时间为(105.7 ± 27.2)分钟,第二阶段为(113.2 ± 40.5)分钟。平均住院时间为(16.4 ± 7.2)天。没有吻合失败,也没有死亡病例。9名患者(64.3%)出现并发症,根据克拉维恩-丁多标准,I级并发症占83.4%。结论:对于穿孔性憩室炎患者来说,早期手术治疗是一个很有前景的概念。它能在第一次手术中迅速消除化脓灶,在不增加并发症和死亡率的情况下尽早重建肠道,并可用于腹膜炎患者。
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引用次数: 0
Impact of urate-lowering therapy on the course of chronic kidney disease in patients with asymptomatic hyperuricemia: a meta-analysis of randomized controlled trials 降尿酸治疗对无症状高尿酸血症患者慢性肾病病程的影响:随机对照试验的荟萃分析
Pub Date : 2024-01-13 DOI: 10.17816/mechnikov604850
V. I. Mazurov, Sergey A. Sayganov, A. I. Martynov, R. Bashkinov, Inna Z. Gaydukova, K. V. Sapozhnikov, D. Tolkacheva, N. Sableva, Alexandra Yu. Tsinzerling
The presented study has been carried out to identify the effect of urate-lowering therapy with xanthine oxidase inhibitors on glomerular filtration rate and serum uric acid in patients with asymptomatic hyperuricemia and chronic kidney disease. A systematic review of randomized controlled trials has been conducted; its results based on meta-analysis has been evaluated. A systematic search and selection of publications in Embase, PubMed, Cochrane Library, and eLibrary databases has been performed. The studied drugs were xanthine oxidase inhibitors: allopurinol and febuxostat. The study considered the following parameters such as efficacy endpoints, namely, glomerular filtration rate and serum uric acid after 3–15 months of follow-up. Clinical and methodological heterogeneity of the included randomized controlled trials has been assessed as well as publication bias and risk of systematic error. Synthesis has been performed using bivariate meta-analysis assessing residual statistical heterogeneity. 7 selected randomized controlled trials (1203 patients) have been included in the meta-analysis. This analysis revealed that medication urate-lowering therapy (allopurinol or febuxostat) was associated with higher glomerular filtration rate (+3.0 ml/min/1.73 m2; 95% confidence interval +0.4 to +5.6; p = 0.022) compared with the controls (placebo/no urate-lowering therapy) at 3–15 months of follow-up. Along with this, medication urate-lowering therapy (allopurinol or febuxostat) has been found to result in lower serum uric acid (−3.3 mg/dl; 95% confidence interval −3.8 to −2.8; р 0.001) compared to the controls (placebo / no urate-lowering therapy) at 3–15 months of follow-up. The results of the meta-analysis have demonstrated a positive role of allopurinol and febuxostat in increasing glomerular filtration rate and decreasing serum uric acid in patients with chronic kidney disease and asymptomatic hyperuricemia. The presented data suggest that therapeutic measures aimed at the elimination of asymptomatic hyperuricemia, including the use of xanthine oxidase inhibitors, may be important in slowing the progression of chronic kidney failure and may be additional factors of nephroprotection.
本研究旨在确定黄嘌呤氧化酶抑制剂降尿酸治疗对无症状高尿酸血症和慢性肾病患者肾小球滤过率和血清尿酸的影响。我们对随机对照试验进行了系统回顾,并对基于荟萃分析的结果进行了评估。在 Embase、PubMed、Cochrane Library 和 eLibrary 数据库中对出版物进行了系统检索和筛选。研究药物为黄嘌呤氧化酶抑制剂:别嘌醇和非布索坦。研究考虑了以下参数作为疗效终点,即随访 3-15 个月后的肾小球滤过率和血清尿酸。对纳入的随机对照试验的临床和方法异质性以及发表偏倚和系统误差风险进行了评估。通过双变量荟萃分析评估了残余统计异质性。荟萃分析包括 7 项选定的随机对照试验(1203 名患者)。分析结果显示,与对照组(安慰剂/无降尿酸治疗)相比,药物降尿酸治疗(别嘌呤醇或非布司他)在随访 3-15 个月时可提高肾小球滤过率(+3.0 ml/min/1.73 m2;95% 置信区间 +0.4 至 +5.6;p = 0.022)。此外,还发现药物降尿酸疗法(别嘌呤醇或非布司他)可降低血清尿酸(-3.3 mg/dl;95% 置信区间 -3.8 至 -2.8;р 0.001),而对照组(安慰剂/无降尿酸疗法)的随访时间为 3-15 个月。荟萃分析结果表明,别嘌醇和非布索坦对提高慢性肾病和无症状高尿酸血症患者的肾小球滤过率和降低血清尿酸有积极作用。所提供的数据表明,旨在消除无症状高尿酸血症的治疗措施,包括使用黄嘌呤氧化酶抑制剂,可能对减缓慢性肾衰竭的进展非常重要,并可能成为保护肾脏的额外因素。
{"title":"Impact of urate-lowering therapy on the course of chronic kidney disease in patients with asymptomatic hyperuricemia: a meta-analysis of randomized controlled trials","authors":"V. I. Mazurov, Sergey A. Sayganov, A. I. Martynov, R. Bashkinov, Inna Z. Gaydukova, K. V. Sapozhnikov, D. Tolkacheva, N. Sableva, Alexandra Yu. Tsinzerling","doi":"10.17816/mechnikov604850","DOIUrl":"https://doi.org/10.17816/mechnikov604850","url":null,"abstract":"The presented study has been carried out to identify the effect of urate-lowering therapy with xanthine oxidase inhibitors on glomerular filtration rate and serum uric acid in patients with asymptomatic hyperuricemia and chronic kidney disease. A systematic review of randomized controlled trials has been conducted; its results based on meta-analysis has been evaluated. \u0000A systematic search and selection of publications in Embase, PubMed, Cochrane Library, and eLibrary databases has been performed. The studied drugs were xanthine oxidase inhibitors: allopurinol and febuxostat. The study considered the following parameters such as efficacy endpoints, namely, glomerular filtration rate and serum uric acid after 3–15 months of follow-up. Clinical and methodological heterogeneity of the included randomized controlled trials has been assessed as well as publication bias and risk of systematic error. Synthesis has been performed using bivariate meta-analysis assessing residual statistical heterogeneity. \u00007 selected randomized controlled trials (1203 patients) have been included in the meta-analysis. This analysis revealed that medication urate-lowering therapy (allopurinol or febuxostat) was associated with higher glomerular filtration rate (+3.0 ml/min/1.73 m2; 95% confidence interval +0.4 to +5.6; p = 0.022) compared with the controls (placebo/no urate-lowering therapy) at 3–15 months of follow-up. Along with this, medication urate-lowering therapy (allopurinol or febuxostat) has been found to result in lower serum uric acid (−3.3 mg/dl; 95% confidence interval −3.8 to −2.8; р 0.001) compared to the controls (placebo / no urate-lowering therapy) at 3–15 months of follow-up. \u0000The results of the meta-analysis have demonstrated a positive role of allopurinol and febuxostat in increasing glomerular filtration rate and decreasing serum uric acid in patients with chronic kidney disease and asymptomatic hyperuricemia. The presented data suggest that therapeutic measures aimed at the elimination of asymptomatic hyperuricemia, including the use of xanthine oxidase inhibitors, may be important in slowing the progression of chronic kidney failure and may be additional factors of nephroprotection.","PeriodicalId":12949,"journal":{"name":"HERALD of North-Western State Medical University named after I.I. Mechnikov","volume":"7 6","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139531673","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Surgical aspects of the treatment of a patient with actinomycosis of the colon complicated by the formation of a colovesical fistula 结肠放线菌病并发结肠瘘管形成患者的外科治疗方法
Pub Date : 2024-01-13 DOI: 10.17816/mechnikov606683
B. Sigua, A. A. Kurkov, E. L. Lataria, O. Kozlova, D. V. Gurzhiy, S. Vinnichuk, A. Efimov, Gleb V. Chizhov, Andrey A. Khvatov, Viacheslav P. Zemlianoi
Actinomycosis is a chronic bacterial infection caused by bacteria from the Actinomycetaceae family. The causes of abdominal actinomycosis are usually destructive appendicitis, prolonged presence of an intrauterine contraceptive or perforation of the colon. Of the internal organs, the left colon and sigmoid colon are most often affected, which often leads to surgical complications. At the same time, diagnosis is significantly difficult due to the nonspecific nature of the clinical presentation, which is similar to that of oncological diseases, and verification of the process is possible only with microscopic examination in a specialized institution. A clinical case demonstrating the difficulties of diagnosis and treatment of widespread abdominal actinomycosis complicated by the development of a colovesical fistula is presented.
放线菌病是一种由放线菌科细菌引起的慢性细菌感染。腹腔放线菌病的病因通常是破坏性阑尾炎、宫内避孕器长期存在或结肠穿孔。在内脏器官中,左结肠和乙状结肠最常受累,这往往会导致手术并发症。同时,由于临床表现的非特异性(与肿瘤疾病的临床表现相似),诊断非常困难,只有在专业机构进行显微镜检查后才能确诊。本文介绍了一个临床病例,该病例显示了广泛腹腔放线菌病并发结肠瘘的诊断和治疗难度。
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引用次数: 0
The influence of comorbid diseases on the profiles of signaling biomarkers (macrophage-derived chemokine, interferon-γ-induced protein 10 kD, soluble CD40 ligand, vascular endothelial growth factor) and severity in patients with COVID-19: clinical studies 合并症对 COVID-19 患者信号生物标志物(巨噬细胞衍生趋化因子、干扰素-γ 诱导的 10 kD 蛋白、可溶性 CD40 配体、血管内皮生长因子)和严重程度的影响:临床研究
Pub Date : 2024-01-13 DOI: 10.17816/mechnikov624558
A. Anisenkova, V. I. Mazurov, S. Apalko, O. Popov, N. Sushentseva, Olga P. Mamaeva, S. V. Mosenko, A. Sarana, Sergey G. Shcherbak
BACKGROUND: Analysis of the effect of comorbid diseases on the concentration of biomarkers will help to deepen the understanding of the pathogenetic mechanisms of the impact of comorbid diseases on the course of COVID-19 and adjust prognostic models for its therapy. AIM: To study the impact of comorbid diseases on the severity and outcomes of COVID-19. In addition, an analysis of the levels of macrophage-derived chemokine, interferon-γ-induced protein 10 kD, soluble CD40 ligand, vascular endothelial growth factor has been carried out in 472 patients with COVID-19, depending on the presence of various forms of comorbid pathology. MATERIALS AND METHODS: To study the concentration of biomarkers an analysis has been conducted in a group of 1648 patients with confirmed COVID-19. The study assessed intergroup differences (disease outcome/severity of disease) in the general group (1648 patients) and in the group of patients without comorbidity (343 patients) — Charlson index less than 2 points. 472 medical histories of patients with COVID-19 have been analyzed, including with certain concentrations of the studied biomarkers and comorbid pathology included in the Charlson Index. For comparison, two samples have been formed: an experimental group consisting of patients with COVID-19 and the presence of a certain comorbid disease and a control group consisting of patients suffering from COVID-19 without a specified comorbid disease. RESULTS: For the first time, data has been obtained indicating that patients with COVID-19 have comorbid conditions with the levels of the studied biomarkers differing significantly from the indicators of the control group. Thus, in patients with arterial hypertension (I10–I15 according to the International Classification of Diseases, 10th revision), chronic heart failure (I50.0), diseases of the vascular system (I70–I79), cerebrovascular diseases (I60–I69), chronic kidney disease (N17–N19), the level of the macrophage-derived chemokine biomarker was significantly lower than in the patients without these diseases. At the same time, in the COVID-19 patients with respiratory diseases (J40–J47), the levels of interferon-γ-induced protein 10 kD and vascular endothelial growth factor were significantly lower than in the patients who did not have lung diseases. CONCLUSIONS: The study findings obtained have confirmed the role of signaling biomarkers in the development of severe forms and death in patients with COVID-19. Significant influence of comorbid pathology on the course of the new coronavirus infection has been shown.
背景:分析合并疾病对生物标志物浓度的影响有助于加深理解合并疾病对 COVID-19 病程影响的发病机制,并调整其治疗的预后模型。目的:研究合并症对COVID-19严重程度和预后的影响。此外,还对 472 例 COVID-19 患者的巨噬细胞衍生趋化因子、γ-干扰素诱导的 10 kD 蛋白、可溶性 CD40 配体、血管内皮生长因子的水平进行了分析,这取决于是否存在各种形式的合并病症。材料与方法:为了研究生物标志物的浓度,对 1648 名确诊为 COVID-19 的患者进行了分析。该研究评估了普通组(1648 名患者)和无合并症患者组(343 名患者)(Charlson 指数小于 2 点)的组间差异(疾病结果/疾病严重程度)。对 472 名 COVID-19 患者的病史进行了分析,其中包括所研究的生物标志物的某些浓度和夏尔森指数中包含的合并病症。为了进行比较,还组成了两个样本:一个实验组由患有 COVID-19 并存在某种合并症的患者组成,另一个对照组由没有特定合并症的 COVID-19 患者组成。结果:首次获得的数据表明,COVID-19 患者患有合并症,所研究的生物标志物水平与对照组的指标有显著差异。因此,在患有动脉高血压(根据国际疾病分类第 10 次修订版,I10-I15)、慢性心力衰竭(I50.0)、血管系统疾病(I70-I79)、脑血管疾病(I60-I69)、慢性肾脏疾病(N17-N19)的患者中,巨噬细胞衍生趋化因子生物标志物的水平明显低于没有这些疾病的患者。同时,在 COVID-19 呼吸系统疾病患者(J40-J47)中,干扰素-γ诱导蛋白 10 kD 和血管内皮生长因子的水平明显低于没有肺部疾病的患者。结论:研究结果证实了信号生物标志物在 COVID-19 患者的重症发展和死亡中的作用。合并病症对新型冠状病毒感染病程的影响显著。
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引用次数: 0
Assessment of the physical development of children with and without high thrombogenic risk factors in the Health Center for Children 评估儿童保健中心有血栓形成高危因素和无血栓形成高危因素儿童的身体发育情况
Pub Date : 2023-12-14 DOI: 10.17816/mechnikov472110
L.A. Elizarieva, Marina Yu. Galaktionova, L. Strozenko, Yuriy F. Lobanov, I.Yu. Boldenkova
BACKGROUND: Up to 65% diseases associated with pathological thrombus have been described; more than 100 thrombogenic risk factors leading to vascular accidents have been studied. It is known that physical development is an important indicator of health in children. The relationship between the presence of thrombogenic risk factors in various disorders of physical development in children has been studied. AIM: To determine the relationship between physical development disorders in children and the presence of thrombogenic risk factors. MATERIALS AND METHODS: The study included 396 children aged 14–18 years, who underwent physical growth assessment using the sigma deviation method and genetic testing to determine polymorphisms of folate cycle genes and polymorphisms of thrombophilia genes. Statistical processing was carried out using the application package Statistica 10.0 (StatSoft, Inc., USA). RESULTS: The analysis of anthropometric indicators in children showed that in the group of the patients with thrombogenic risk factors, height and body weight values with average physical disharmonious development due to excess weight were statistically significantly higher than age-reference indicators. CONCLUSIONS: Based on the results of the study, it has been shown that disharmony in physical development in children with high thrombogenic risk factors may be one of the risk factors for the development of thrombotic conditions.
背景:已描述的与病理性血栓相关的疾病多达 65%;已研究的导致血管意外的血栓风险因素超过 100 个。众所周知,身体发育是儿童健康的重要指标。已对儿童身体发育的各种障碍中存在的血栓形成危险因素之间的关系进行了研究。目的:确定儿童身体发育障碍与血栓形成危险因素之间的关系。材料与方法:该研究包括 396 名 14-18 岁的儿童,他们使用西格玛偏差法进行了身体发育评估,并进行了基因检测,以确定叶酸循环基因的多态性和血栓性疾病基因的多态性。统计处理使用 Statistica 10.0 应用软件包(StatSoft, Inc.)结果:对儿童人体测量指标的分析表明,在有血栓形成危险因素的患者组中,因体重过重导致身体发育不协调的平均身高和体重值在统计学上明显高于年龄参考指标。结论:研究结果表明,具有高血栓形成危险因素的儿童身体发育不协调可能是导致血栓形成的危险因素之一。
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引用次数: 0
Dynamics of clinical manifestations and cytokine levels in patients with rheumatoid arthritis associated with upadacitinib therapy 类风湿性关节炎患者的临床表现和细胞因子水平与达达替尼治疗的动态关系
Pub Date : 2023-12-14 DOI: 10.17816/mechnikov567926
N. Lapkina, A. A. Baranov, N. Levshin, J. A. Malysheva, V. Amirdzhanova, A. S. Artyukhov
BACKGROUND: Recently, it has become evident that despite extensive data obtained from randomised placebo-controlled trials, which are still the golden standard for assessing the efficacy and safety of therapy, there are still some fundamentally important questions regarding the optimal management of patients with rheumatoid arthritis. In this regard, it is extremely relevant to assess the results of therapy in real clinical practice. Currently, much attention is paid to the study of the level of proinflammatory cytokines, both as markers of inflammatory activity of rheumatoid arthritis and monitoring the prognosis of anti-inflammatory therapy efficacy. In Russia, there are no works devoted to the study of cytokine concentration dynamics in patients with rheumatoid arthritis on the background upadacitinib therapy, which proves the relevance of the following study. AIM: To investigate the dynamics of clinical and laboratory values of inflammatory activity of the disease and cytokines in patients with rheumatoid arthritis associated with upadacitinib therapy. MATERIALS AND METHODS: We examined 10 patients with a reliable diagnosis of rheumatoid arthritis: patients’ age was 46.30 ± 10.20 years and disease duration was 12.00 (3.00–21.00) years. All the patients had moderate to high disease activity: Disease Activity Score-28 with erythrocyte sedimentation rate 5.48 (4.50–5.80), Clinical Disease Activity Index 28.00 (19.50–32.00) and Simple Disease Activity Index 29.18 (19.51–33.05). All the patients included in the study were treated with upadacitinib at a dose of 15 mg once a day against the background of the therapy with methotrexate, leflunomide, non-steroidal anti-inflammatory drugs and glucocorticoids. Observation was carried out before treatment and after 3, 6 months of therapy. Serum levels of 15 cytokines: interleukin-1β, -4, -6, -10, -17A, -17F, -21, -22, -23, -25, -31, -33, tumor necrosis factor-alpha, interferon gamma, soluble СD40 ligand were studied using multiplex xMAP technology. RESULTS: After 3 and 6 months of upadacitinib therapy, there was a significant decrease in Disease Activity Score-28 with erythrocyte sedimentation rate 3.78 (2.53–4.20) and 3.5 (2.00–3.68), Clinical Disease Activity Index 12.00 (5.00–17.34) and 9.0 (3.00–11.00), Simple Disease Activity Index 12.38 (5.02–17.00) and 9.61 (3.06–11.60), erythrocyte sedimentation rate 19.0 (11.0–26.0), 7.0 (4.0–18.0), CRP 0.56 (0.50–1.99), 0.71 (0.51–1.1). The values of erythrocyte sedimentation rate decreased after 3 months of treatment (baseline 21.0 (15.0–25.0) mm/hour, after 3 months 14,0 (11,0–17,0) mm/hour. After 6 months of upadacitinib therapy, there was a significant decrease in interleukin-10 (p 0.05) and interleukin-33 (p 0.01) levels compared to baseline. On the contrary, the level of interleukin-25 increased by the 6th month of treatment (p 0.01). CONCLUSIONS: The results of the study indicate the effectiveness of upadacitinib in rheumatoid arthritis, and also prov
背景:随机安慰剂对照试验仍是评估疗效和安全性的黄金标准,尽管从随机安慰剂对照试验中获得了大量数据,但最近人们发现,在类风湿关节炎患者的最佳治疗方面仍存在一些根本性的重要问题。因此,在实际临床实践中对治疗效果进行评估极为重要。目前,促炎细胞因子水平的研究备受关注,它既是类风湿性关节炎炎症活动的标志,又能监测抗炎治疗效果的预后。在俄罗斯,还没有专门研究类风湿性关节炎患者在接受达达替尼治疗时细胞因子浓度动态的著作,这证明了以下研究的相关性。目的:研究与奥达替尼治疗相关的类风湿关节炎患者的临床和实验室炎症活动值及细胞因子的动态变化。材料与方法:我们对 10 名确诊为类风湿性关节炎的患者进行了检查:患者年龄为 46.30 ± 10.20 岁,病程为 12.00(3.00-21.00)年。所有患者均有中度至高度疾病活动:疾病活动度评分 28 分,红细胞沉降率 5.48(4.50-5.80),临床疾病活动度指数 28.00(19.50-32.00),单纯疾病活动度指数 29.18(19.51-33.05)。所有参与研究的患者都在接受甲氨蝶呤、来氟米特、非甾体抗炎药和糖皮质激素治疗的基础上接受了达达替尼治疗,剂量为每天一次,每次15毫克。在治疗前和治疗 3、6 个月后进行观察。使用多重 xMAP 技术研究了血清中 15 种细胞因子的水平:白细胞介素-1β、-4、-6、-10、-17A、-17F、-21、-22、-23、-25、-31、-33、肿瘤坏死因子-α、γ 干扰素、可溶性 СD40 配体。结果:达帕替尼治疗3个月和6个月后,疾病活动度评分-28显著下降,红细胞沉降率分别为3.78(2.53-4.20)和3.5(2.00-3.68),临床疾病活动指数为12.00(5.00-17.34)和 9.0(3.00-11.00),单纯疾病活动指数 12.38(5.02-17.00)和 9.61(3.06-11.60),红细胞沉降率 19.0(11.0-26.0)、7.0(4.0-18.0),CRP 0.56(0.50-1.99)、0.71(0.51-1.1)。治疗 3 个月后,红细胞沉降率值有所下降(基线为 21.0(15.0-25.0)毫米/小时,3 个月后为 14.0(11.0-17.0)毫米/小时。达帕替尼治疗 6 个月后,白细胞介素-10(p 0.05)和白细胞介素-33(p 0.01)的水平与基线相比显著下降。相反,白细胞介素-25的水平在治疗第6个月时有所上升(p 0.01)。结论:研究结果表明,奥达帕替尼对类风湿性关节炎具有疗效,同时也为进一步研究该疾病细胞因子依赖性炎症的发病机制提供了依据。
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引用次数: 0
Studying zonulin levels in patients with inflammatory bowel disease and peripheral arthritis 研究炎症性肠病和外周关节炎患者的 zonulin 水平
Pub Date : 2023-12-14 DOI: 10.17816/mechnikov582014
G. Khusainova, Olga B. Nesmeyanova, A. I. Dolgushina, O.S. Abramovskikh, V. Genkel, K. Nikushkina
BACKGROUND: Currently, disruption of the barrier function of the intestinal mucosa is considered one of the key mechanisms in the pathogenesis of extraintestinal manifestations of inflammatory bowel diseases, especially damage to the musculoskeletal system. AIM: To study the relationship between the level of zonulin in blood serum and the parameters of the immune status in patients with inflammatory bowel diseases in combination with peripheral arthritis. MATERIALS AND METHODS: 97 patients with ulcerative colitis and Crohn’s disease have been examined, with peripheral arthritis verified in 47 patients; the control group included 50 patients without peripheral arthritis. Zonulin, tumor necrosis factor α, interleukin-1β, -10, -17A, -23 were determined in blood serum using standard kits for direct enzyme immunoassay. RESULTS: Patients with peripheral arthritis were younger with an earlier onset of inflammatory bowel diseases (p 0.001). When assessing the concentration of serum zonulin in the patients with and without arthritis, no significant differences have been found. In the patients with peripheral arthritis, zonulin concentration directly correlated with the level of interleukin-17A (r = 0.323; p = 0.039), interleukin-23 (r = 0.321; p = 0.041). CONCLUSIONS: According to the data obtained, the use of zonulin as a marker of peripheral arthritis in inflammatory bowel diseases is not recommended. Nevertheless, the correlation of zonulin and the concentrations of interleukin-17А and -23 demonstrates its role in the regulation of mucosal immunity in the development of extraintestinal manifestations of inflammatory bowel diseases.
背景:目前,肠黏膜屏障功能的破坏被认为是炎症性肠病肠外表现,尤其是肌肉骨骼系统损伤的关键发病机制之一。目的:研究合并外周关节炎的炎症性肠病患者血清中 zonulin 水平与免疫状态参数之间的关系。材料与方法:研究对象为 97 名溃疡性结肠炎和克罗恩病患者,其中 47 名患者证实患有外周关节炎;对照组包括 50 名无外周关节炎的患者。使用直接酶联免疫测定标准试剂盒测定血清中的左旋胰岛素、肿瘤坏死因子α、白细胞介素-1β、-10、-17A、-23。结果:外周关节炎患者年龄较轻,炎症性肠病发病较早(P 0.001)。在评估关节炎患者和非关节炎患者的血清zonulin浓度时,未发现明显差异。在外周关节炎患者中,佐纳林浓度与白细胞介素-17A(r = 0.323; p = 0.039)、白细胞介素-23(r = 0.321; p = 0.041)的水平直接相关。结论:根据所获得的数据,不建议使用 zonulin 作为炎症性肠病外周关节炎的标志物。然而,佐凝蛋白与白细胞介素-17А和-23浓度之间的相关性表明,佐凝蛋白在炎症性肠病肠道外表现的发展过程中起到了调节粘膜免疫的作用。
{"title":"Studying zonulin levels in patients with inflammatory bowel disease and peripheral arthritis","authors":"G. Khusainova, Olga B. Nesmeyanova, A. I. Dolgushina, O.S. Abramovskikh, V. Genkel, K. Nikushkina","doi":"10.17816/mechnikov582014","DOIUrl":"https://doi.org/10.17816/mechnikov582014","url":null,"abstract":"BACKGROUND: Currently, disruption of the barrier function of the intestinal mucosa is considered one of the key mechanisms in the pathogenesis of extraintestinal manifestations of inflammatory bowel diseases, especially damage to the musculoskeletal system. \u0000AIM: To study the relationship between the level of zonulin in blood serum and the parameters of the immune status in patients with inflammatory bowel diseases in combination with peripheral arthritis. \u0000MATERIALS AND METHODS: 97 patients with ulcerative colitis and Crohn’s disease have been examined, with peripheral arthritis verified in 47 patients; the control group included 50 patients without peripheral arthritis. Zonulin, tumor necrosis factor α, interleukin-1β, -10, -17A, -23 were determined in blood serum using standard kits for direct enzyme immunoassay. \u0000RESULTS: Patients with peripheral arthritis were younger with an earlier onset of inflammatory bowel diseases (p 0.001). When assessing the concentration of serum zonulin in the patients with and without arthritis, no significant differences have been found. In the patients with peripheral arthritis, zonulin concentration directly correlated with the level of interleukin-17A (r = 0.323; p = 0.039), interleukin-23 (r = 0.321; p = 0.041). \u0000CONCLUSIONS: According to the data obtained, the use of zonulin as a marker of peripheral arthritis in inflammatory bowel diseases is not recommended. Nevertheless, the correlation of zonulin and the concentrations of interleukin-17А and -23 demonstrates its role in the regulation of mucosal immunity in the development of extraintestinal manifestations of inflammatory bowel diseases.","PeriodicalId":12949,"journal":{"name":"HERALD of North-Western State Medical University named after I.I. Mechnikov","volume":"17 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-12-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138972879","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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HERALD of North-Western State Medical University named after I.I. Mechnikov
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