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Analysis of mutations spectrum in the ATP7B gene in patients with Wilson disease using massively parallel sequencing. Wilson病患者ATP7B基因突变谱的大规模平行测序分析
Q4 Health Professions Pub Date : 2022-04-17 DOI: 10.51620/0869-2084-2022-67-4-250-256
A. A. Sivtsev, I. Zhalsanova, A. E. Postrigan, E. Fonova, O. Vasilyeva, A. Zarubin, L. I. Minaicheva, A. A. Agafonova, V. V. Petrova, E. Ravzhaeva, O. Salyukova, N. Skryabin
The study aimed to search for mutations in the ATP7B gene using massively parallel sequencing in patients with Wilson disease in the Tomsk region. For 42 patients with suspected Wilson's disease (aged from 1 to 33 years) was performed molecular genetic analysis. Enrichment of the interest genome regions was carried out by the long-range PCR. DNA libraries with ligated adapters were constructed with Nextera DNA Flex (Illumina, USA) kit. Sequencing was performed on the Illumina MiSeq platform (Illumina, USA). As a result of this work, we identified 9 pathogenic genetic variants. All variants were previously described in the literature and were found in patients with Wilson's disease. Five missense mutations, one splice site mutation, and 3 frameshift mutations were identified. In patients with Wilson's disease in the Tomsk region, the most common variant was c.3207C>A, this variant is the most common both in the Russian Federation and in other European populations. Also, a pathogenic variant c.3036dupC was found, which is probably endemic to the Russian Federation.
该研究旨在通过大规模平行测序在托木斯克地区威尔森病患者中寻找ATP7B基因突变。对42例疑似Wilson病患者(年龄1 ~ 33岁)进行分子遗传学分析。通过远程PCR对感兴趣的基因组区域进行富集。连接适配器的DNA文库使用Nextera DNA Flex (Illumina, USA)试剂盒构建。测序在Illumina MiSeq平台(Illumina, USA)上进行。作为这项工作的结果,我们确定了9种致病基因变异。所有的变异都曾在文献中描述过,并在威尔逊氏病患者中发现过。共鉴定出5个错义突变、1个剪接位点突变和3个移码突变。在托木斯克地区的威尔逊氏病患者中,最常见的变异是c.3207C>A,该变异在俄罗斯联邦和其他欧洲人群中最常见。此外,还发现了致病性变种c.3036dupC,这可能是俄罗斯联邦特有的。
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引用次数: 1
Assessment of iron metabolism disorders and adequate treatment of anemic syndrome in patients with breast cancer on the background of adjuvant chemotherapy. 辅助化疗背景下乳腺癌患者铁代谢紊乱及贫血综合征适当治疗的评估
Q4 Health Professions Pub Date : 2022-04-17 DOI: 10.51620/0869-2084-2022-67-4-213-218
V. N. Blindar, G. N. Zubrikhina, T. V. Davydova, M. M. Dobrovolskaya, M. N. Khagazheeva, A. Snegovoy, N. Lyubimova, N. Kushlinskii, D. Ryabchikov
Early and adequate correction of the anemic syndrome (AS) of cancer patients can prevent deterioration in the quality of life and be considered as a reserve for increasing the effectiveness of treatment for breast cancer (BC). The aim of the study was to assess the status of iron using modern methods of ferrokinetics in breast cancer patients on the background of adjuvant chemotherapy for early diagnosis and adequate treatment of AS. The object of the study included 21 breast cancer patients with a relatively favorable prognosis, with luminal types A and B (Her 2 / neu positive or negative), three times negative type. The examination was carried out in the postoperative period, against the background of adjuvant chemotherapy. The main metabolites of ferrokinetics were studied: hepcidin 25 (GP25); ferritin (FR); soluble transferrin receptors (rRTP); transferin (TRF); iron (Fe); erythropoietin (EPO); CRP and IL-6 indicators. AC correction was performed (ferinject, epotin-alpha, B12). 10 (47.6%) patients with breast cancer had AS. Most of them were diagnosed with IDA with microcytic, hypochromic characteristics of erythrocytes, low concentration of FR, Fe, GP25, IL-6, CRP, and high levels of TRP and rRTP. Functional iron deficiency (FDF) was established in some patients. In contrast to patients with IDA, they had a high concentration of FR, CRP and significant production of GP25, IL-6. The EPO level was not optimal for the majority of patients with AS. In isolated cases, during treatment with recombinant erythropoietins, a deficiency of vitamin B12 (cyanocobalamin) was revealed. The rational use of iron preparations, vitamins, and recombinant forms of EPO made it possible to restore Fe metabolism, stabilize the hemoglobin level, and also improve the condition of most breast cancer patients. The obtained data on IL-6, GP25, CRP indicate a certain relationship between them in the development of anemia with VDF in breast cancer patients and the need for further study of the characteristics of iron metabolism in cancer patients.
早期和适当的纠正癌症患者的贫血综合征(AS)可以防止生活质量的恶化,并被认为是提高乳腺癌(BC)治疗有效性的储备。该研究的目的是在辅助化疗的背景下,利用铁动力学的现代方法评估乳腺癌患者的铁状态,以早期诊断和充分治疗AS。本研究对象包括21例预后较好的乳腺癌患者,腔型为a型和B型(Her 2 / neu阳性或阴性),三倍阴性。在辅助化疗的背景下,术后进行检查。研究了铁动力学的主要代谢产物:hepcidin 25 (GP25);铁蛋白(FR);可溶性转铁蛋白受体;transferin(基金会);铁(Fe);促红细胞生成素(EPO);CRP和IL-6指标。进行AC校正(ferinject, epotin-alpha, B12)。10例(47.6%)乳腺癌患者有AS。多数诊断为IDA,红细胞呈小细胞、低色素特征,FR、Fe、GP25、IL-6、CRP浓度低,TRP、rRTP水平高。部分患者存在功能性铁缺乏(FDF)。与IDA患者相比,他们有高浓度的FR、CRP和显著的GP25、IL-6的产生。大多数AS患者的EPO水平不是最佳的。在个别情况下,在治疗重组促红细胞生成素,缺乏维生素B12(氰钴胺素)被揭示。合理使用铁制剂、维生素和重组EPO,可以恢复铁代谢,稳定血红蛋白水平,改善大多数乳腺癌患者的病情。IL-6、GP25、CRP在乳腺癌患者贫血合并VDF的发生发展中存在一定的关系,需要进一步研究癌症患者铁代谢的特点。
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引用次数: 1
Comparision of fluorimetric and mass spectrometric methods for Fabry disease newborn screening. 法布里病新生儿筛查荧光法与质谱法的比较。
Q4 Health Professions Pub Date : 2022-04-17 DOI: 10.51620/0869-2084-2022-67-4-204-206
D. Orlov, L. Nazarenko, L. I. Didenko, G. Seitova
Fabry disease is an X-linked hereditary lysosomal storage disorder caused by mutations in the GLA gene. Neonatal screening for Fabry disease in males is feasible by measurement of α-galactosidase A activity in DBS using either the mass spectrometric or fluorigenic substrate. The aim of the study: to assess the possibility of introducing the compared methods into the practice of neonatal screening. In the both assays performed a statistically significant difference of the enzyme activity between affected individuals and controls is reported. The slight modification of the fluorimetric method by centrifugation of a 96-well microplate before measurement could improve signal to noise ratio.
法布里病是一种由GLA基因突变引起的x连锁遗传性溶酶体贮积症。新生儿法布里病的男性筛查是可行的,通过测量α-半乳糖苷酶A活性在DBS使用质谱或荧光底物。该研究的目的是:评估将比较方法引入新生儿筛查实践的可能性。据报道,在这两种分析中,受影响个体和对照组之间的酶活性有统计学意义的差异。在测定前对96孔微孔板进行离心,对荧光测定方法稍作修改,可提高信噪比。
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引用次数: 0
Lactoferrin of oral fluid is normal and in Alzheimer's disease: laboratory and diagnostic aspects (review of literature). 口腔液乳铁蛋白是正常的,在阿尔茨海默病:实验室和诊断方面(文献回顾)。
Q4 Health Professions Pub Date : 2022-04-17 DOI: 10.51620/0869-2084-2022-67-4-207-212
V. Bazarnyi, A. Sidenkova, D. Sosnin
The article discusses the clinical value of determining the lactoferrin protein in oral fluid - one of the representatives of the saliva proteome. The review is based on the analysis of modern literature, including systematic reviews, the results of multicenter prospective studies, review and original articles by leading experts in this field, presented in the databases PubMed, Scopus, CyberLeninka. The problems of the preanalytical stage, methods for determining lactoferrin are highlighted and information about its content in mixed saliva according to various authors is provided. Special attention is paid to the clinical and diagnostic value of the level of salivary lactoferrin in Alzheimer's disease. According to most authors, the diagnostic sensitivity of this parameter ranges from 87 to 100%. Some mechanisms of the relationship between this protein and the central nervous system (CNS) are shown. In conclusion, it is concluded that salivary lactoferrin can be an "indicator" of the formation of amyloid plaques and can be considered as one of the reliable biomarkers of Alzheimer's disease. This opinion is based both on fundamental ideas about the global relationship between innate immunity and the central nervous system, and on clinical data. The special advantage of this laboratory test is its non-invasiveness, which makes it more preferable in comparison with the determination of amyloid and tau proteins in the cerebrospinal fluid and blood.
本文讨论了唾液蛋白质组学的代表之一——口腔液中乳铁蛋白测定的临床价值。本综述基于对现代文献的分析,包括系统综述、多中心前瞻性研究的结果、该领域领先专家的综述和原创文章,并在PubMed、Scopus、CyberLeninka等数据库中发表。重点介绍了分析前阶段存在的问题、测定乳铁蛋白的方法以及不同作者对混合唾液中乳铁蛋白含量的介绍。特别关注唾液乳铁蛋白水平在阿尔茨海默病中的临床和诊断价值。大多数作者认为,该参数的诊断灵敏度在87 - 100%之间。揭示了该蛋白与中枢神经系统(CNS)关系的一些机制。综上所述,唾液乳铁蛋白可作为淀粉样斑块形成的“指示剂”,可作为阿尔茨海默病可靠的生物标志物之一。这一观点既基于先天免疫和中枢神经系统之间整体关系的基本观点,也基于临床数据。这种实验室检测的特殊优点是它的非侵入性,这使得它比测定脑脊液和血液中的淀粉样蛋白和tau蛋白更可取。
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引用次数: 1
Prediction of early recurrencies of uterine body cancer based on monitoring of serum biological markers. 基于血清生物标志物监测的子宫体癌早期复发预测。
Q4 Health Professions Pub Date : 2022-04-17 DOI: 10.51620/0869-2084-2022-67-4-197-203
N. Kovalenko, E. Verenikina, A. Maksimov, O. N. Gladkikh, A. Demidova, E. V. Domashenko
The aim of this work was to optimize the prognosis of early recurrences of uterine cancer by searching for informative laboratory biomarkers. The study included 343 patients with I-IV stages FIGO endometrial adenocarcinoma the ages of 53 and 76 years. In patients before surgery, as well as 3 and 6 months after the end of primary treatment, the concentration of oncological markers CA-125, HE4, DJ-1, DKK-1 was determined in blood serum by ELISA and electrochemiluminescence immunoassay. We analyzed the predictive informativeness of monitoring markers to assess the risk of early recurrences of cancer within two years after surgery. In patients with uterine cancer with the stage of the disease and the degree of tumor differentiation in the blood serum, the concentration of DJ-1 is changed. With myometrial invasion of more than 50%, increased serum levels of three markers - CA-125, HE4, and DJ-1. Depending on the risk of disease recurrence, the assessment of which was determined by intraoperative and histological characteristics, a difference was revealed in the content of HE4 and DJ-1 markers in the blood. It was found that the risk of early recurrence of uterine cancer increased (p<0,05) when the concentration of CA-125 exceeded the level of 29,3 U/ml, HE4 was above 79,3 pmol/l, DJ-1 was above 90,0 ng/ml and DKK-1 above 47,3 pg/ml 6 months after the end of primary treatment. The highest predictive information value was found for monitoring DJ-1 and HE4 in blood serum, which indicates that they are promising for use in continuous monitoring of the course of cancer.
本工作的目的是通过寻找信息丰富的实验室生物标志物来优化子宫癌早期复发的预后。该研究包括343例I-IV期FIGO子宫内膜腺癌患者,年龄为53岁至76岁。采用ELISA和电化学发光免疫分析法检测患者术前及初治疗结束后3、6个月血清肿瘤标志物CA-125、HE4、DJ-1、DKK-1的浓度。我们分析了监测指标的预测信息,以评估术后两年内癌症早期复发的风险。子宫癌患者血清中DJ-1的浓度随疾病分期及肿瘤分化程度的不同而变化。当肌层浸润超过50%时,血清中CA-125、HE4和DJ-1三种标志物水平升高。根据疾病复发的风险,其评估由术中和组织学特征决定,血液中HE4和DJ-1标志物的含量存在差异。初步治疗结束6个月后,CA-125浓度超过29.3 U/ml, HE4高于73,3 pmol/l, DJ-1高于90,0 ng/ml, DKK-1高于47.3 pg/ml时,子宫癌早期复发的风险增加(p< 0.05)。检测血清中DJ-1和HE4的预测信息值最高,表明它们有望用于癌症病程的连续监测。
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引用次数: 0
Prospective analysis of laboratory blood parameters in patients with cardiovascular diseases who underwent COVID-19-associated pneumonia. 2019冠状病毒病相关肺炎心血管病患者实验室血液参数的前瞻性分析
Q4 Health Professions Pub Date : 2022-03-25 DOI: 10.51620/0869-2084-2022-67-3-133-139
Tatiana Ivanovna Petelina, N A Musikhina, V D Garanina, E A Gorbatenko, A E Shcherbinina, D V Zhmurov, V A Zhmurov, L I Gapon, N A Galeeva, K S Avdeeva, A A Kapustina, E I Yaroslavskaya

The study of the characteristics and dynamics of laboratory biomarkers in patients with cardiovascular diseases (CVD) undergoing COVID-19-associated pneumonia may be of great clinical importance. The study included 116 patients who underwent COVID-19-associated pneumonia. The patients were divided into 2 groups. The first group included 49 patients without CVD, the second group - 67 patients with CVD. A blood sample was performed in all patients at the time of hospitalization and 3 months after discharge from the hospital. The parameters of general blood count, biochemistry, hemostasis, and biomarkers of inflammation were assessed - concentration of C-reactive protein (CRP), highly sensitive CRP (hs-CRP), homocysteine and IL-6. All patients initially underwent computed tomography of the chest organs. We found that ESR, WBC (leukocytes), NLR (neutrophils/lymphocytes ratio), fibrinogen, LDH (lactate dehydrogenase), LYM/CRP ratio (lymphocytes/CRP) were parameters that significantly distinguished patients in the 1st and 2nd groups. Three months after discharge from the hospital in patients of both groups the increased indicators approached the reference values, however, some parameters such as CRP, ESR, WBC, fibrinogen remained at a higher level in group 2 compared to group 1. Correlation analysis revealed the relationship between parameters of inflammation and hemostasis in the 2nd group of patients, which confirms the presence of latent vascular inflammatory potential in this group. It was revealed that such indicators as lymphocytes, neutrophils, APTT and LDH were associated with the initial volume of lung lesion more than 50%. Increase of these parameters by 1 unit contributes to increase in the volume of lung tissue damage by 6.5%, 6.4%, 11%, and 0.6%, respectively. Thus, dynamic control of laboratory parameters has prognostic value in assessing the nature of the course of COVID-19 associated pneumonia in patients with CVD and developing an algorithm for personalized monitoring of patients in the post-COVID period with the aim of timely correction of therapy to prevent unwanted vascular complications.

研究心血管疾病(CVD)患者发生covid -19相关性肺炎的实验室生物标志物的特征和动态可能具有重要的临床意义。该研究包括116名患有covid -19相关肺炎的患者。患者分为两组。第一组49例无心血管疾病,第二组67例有心血管疾病。所有患者在住院时和出院后3个月均进行了血液采样。评估一般血细胞计数、生化、止血和炎症生物标志物的参数- c反应蛋白(CRP)、高敏感CRP (hs-CRP)、同型半胱氨酸和IL-6的浓度。所有患者最初都接受了胸部器官的计算机断层扫描。我们发现ESR、WBC(白细胞)、NLR(中性粒细胞/淋巴细胞比值)、纤维蛋白原、LDH(乳酸脱氢酶)、LYM/CRP比值(淋巴细胞/CRP)是区分第一组和第二组患者的显著参数。两组患者出院3个月后各项指标升高均接近参考值,但2组CRP、ESR、WBC、纤维蛋白原等指标仍高于1组。相关分析显示第二组患者炎症与止血参数之间存在相关性,证实该组患者存在血管潜在炎症电位。结果显示,淋巴细胞、中性粒细胞、APTT、LDH等指标与肺病变初始体积的相关性超过50%。这些参数每增加1个单位,肺组织损伤体积分别增加6.5%、6.4%、11%和0.6%。因此,实验室参数的动态控制在评估CVD患者COVID-19相关肺炎病程性质和开发COVID-19后患者个性化监测算法方面具有预后价值,目的是及时纠正治疗,防止不必要的血管并发症。
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引用次数: 1
Efficacy of cephalosporins against enterobacteria isolated from patients with chronic osteomyelitis. 头孢菌素对慢性骨髓炎患者分离肠杆菌的疗效观察。
Q4 Health Professions Pub Date : 2022-03-25 DOI: 10.51620/0869-2084-2022-67-3-158-162
I V Shipitsyna, E V Osipova

Long-term antibiotic therapy, as well as inappropriate use of drugs in the treatment of osteomyelitis, can lead to the appearance of pan-resistant strains. The existing antibiotic prophylaxis regimens for purulent-septic complications are outdated and need to be adjusted. In this regard, it is necessary to monitor the resistance of microorganisms in order to identify ineffective antibacterial drugs. To analyze the resistance profiles of Enterobacteriaceae isolated from patients with chronic osteomyelitis to cephalosporin drugs over a three-year period. The resistance profiles of 912 clinical strains of Enterobacteriaceae were analyzed: Klebsiella pneumoniae (n=349), Proteus sp. (n=208), Escherichia coli (n=176), Enterobacter cloacae (n=179) for the period from 2018-2020 to cephalosporin drugs. In 2018, 66.2% of Enterobacteriaceace were resistant to the 1st generation cephalosporins, in 2019 - 78.7%, in 2020 - 79.5%. Generation II cephalosporins were most active against Proteus sp. bacteria, but a decrease in clinical effect was observed by 2020. Among the third generation cephalosporins in 2018, cefotaxime was most active, but in 2020 the number of resistant strains doubled and amounted to 86.3%. Ceftazidime was active against 47.1% of Enterobacteriaceae isolates in 2018, in 2019 - 45% of strains, in 2020 - 37.2% of bacterial strains. High activity of ceftriaxone was noted only in 2018 against Proteus sp. Preparations of the IV generation in 2018 showed the highest activity against bacteria of the genus Proteus, the least - against bacteria K. pneumoniae. In the period from 2019-2020, a significant decrease in the effectiveness of cefepime was observed.The monitoring of the resistance profiles to antibiotics of the cephalosporin series revealed their low efficacy against Enterobacteriaceae isolated from wounds and fistulas of patients with chronic osteomyelitis, which shows the inexpediency of their empirical use.

长期抗生素治疗,以及在骨髓炎治疗中不适当使用药物,可导致泛耐药菌株的出现。现有的化脓性脓毒症的抗生素预防方案已经过时,需要调整。在这方面,有必要监测微生物的耐药性,以识别无效的抗菌药物。分析三年来慢性骨髓炎患者分离的肠杆菌科细菌对头孢菌素类药物的耐药性。分析912株肠杆菌科临床菌株2018-2020年对头孢菌素类药物的耐药情况:肺炎克雷伯菌(349株)、变形杆菌(208株)、大肠杆菌(176株)、阴沟肠杆菌(179株)。2018年对第一代头孢菌素耐药率为66.2%,2019年为78.7%,2020年为79.5%。第二代头孢菌素对变形杆菌最有效,但到2020年临床效果有所下降。在第三代头孢菌素中,2018年头孢噻肟活性最高,但到2020年耐药菌株数量翻了一番,达到86.3%。头孢他啶在2018年、2019年和2020年分别对47.1%、45%和37.2%的肠杆菌科菌株有活性。头孢曲松仅在2018年对变形杆菌有较高的活性,2018年第四代制剂对变形杆菌属细菌的活性最高,对肺炎克雷伯菌的活性最低。在2019-2020年期间,观察到头孢吡肟的有效性显着下降。对头孢菌素系列抗生素的耐药性监测显示,头孢菌素系列抗生素对慢性骨髓炎患者伤口和瘘管中分离的肠杆菌科细菌的疗效较低,表明其临床应用的不适宜。
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引用次数: 2
Prevalence of causative agents of transmissive tick-borned ricketsious in the Crimean peninsula. 克里米亚半岛传播蜱传佝偻病病原体的流行情况。
Q4 Health Professions Pub Date : 2022-03-25 DOI: 10.51620/0869-2084-2022-67-3-170-176
M T Gafarova, E I Bondarenko, K D Maliy, E E Alieva, I L Evstafiev, N N Tovpinec, N K Malaya, A V Kubyshkin

The paper presents the results of a study of the prevalence of Ixodid ticks - potential carriers of tick-borne rickettsiosis pathogens. Ectoparasites were collected in various natural and climatic zones of the Crimean Peninsula within the year 2016-2018. As a result of screening with the help of real-time PCR analysis (PCR-RT), a genetic marker (a section of the gltA gene) of the rickettsia group of tick-borne spotted fever was detected in ticks. The most common DNA marker of rickettsia was found in ticks in the eastern regions of the steppe zone - 50,6 %, in the north-western part of the steppe zone this value was 12,0 %. The least amount of rickettsia target DNA was detected in ticks collected in the mountain forest and south bank zones - 4,5 %. As a result of sequencing of positive DNA samples from fragments of the gltA, ompA, ompB, and sca4 genes, the species composition of rickettsias was established. The DNA of 8 species of rickettsia was identified: Circulation of three R. conorii, R. massiliae, R. sibirica subsp. mongolotimonae, R. slovaca, R. aeschlimannii, R. monacensis, R. helvetica, R. raoultii. R. massiliae, R. slovaca, and R. helvetica were established in the Crimean Peninsula for the first time. The peculiarities of the geographical distribution of the identified rickettsia species were determined, which was due to the spread of mites-carriers of pathogens. The revealed diversity of rickettsia species and their vectors, due to the isolation of the areas of the main feeding animals and the established routes of migratory birds, suggests the circulation of other rickettsia species on the territory of the Crimean Peninsula. The obtained results suggest that the diseases of tick-borne rickettsiosis in the Crimean Peninsula can be caused not only by R. conorii, as previously thought, but also by other types of rickettsii.

本文介绍了一项研究的结果,流行的伊克斯蜱-蜱传立克次体病病原体的潜在载体。在2016-2018年期间,在克里米亚半岛的各个自然和气候带收集了体外寄生虫。通过实时荧光定量PCR (PCR- rt)筛选,在蜱中检测到蜱传斑疹热立克次体群的遗传标记(gltA基因片段)。立克次体DNA标记在草原带东部地区最常见,为50.6%,在草原带西北部地区最常见,为12.0%。在山区森林和南岸地区采集的蜱中检测到的立克次体靶DNA含量最少,为4.5%。通过对gltA、ompA、ompB和sca4基因片段的阳性DNA样本测序,确定了立克次体的物种组成。鉴定出8种立克次体的DNA,其中3种为恙螨、马氏恙螨、西伯利亚恙螨亚种。蒙古田鼠、斯洛伐克田鼠、埃斯克利曼田鼠、monacensis、helvetica、raoultii。R. massiliae、R. slovaca和R. helvetica是首次在克里米亚半岛发现。确定了已鉴定立克次体物种地理分布的特殊性,这是由于病原体载体螨的传播。由于主要取食动物的地区与候鸟的既定路线隔绝,立克次体物种及其媒介的多样性表明,在克里米亚半岛领土上还存在其他立克次体物种的传播。所得结果表明,克里米亚半岛的蜱传立克次体病不仅可能像以前认为的那样由conorii r引起,还可能由其他类型的立克次体引起。
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引用次数: 4
Beta coronaviruses and human endocrine system: new data (review of literature). 冠状病毒与人体内分泌系统:新数据(文献综述)。
Q4 Health Professions Pub Date : 2022-03-25 DOI: 10.51620/0869-2084-2022-67-3-140-146
S V Bulgakova, E V Treneva, N O Zakharova

A new dangerous respiratory disease COVID-19 was first reported in China in December 2019, the pathogen SARS-Coronavirus 2 (SARS-CoV-2), belonging to the beta coronavirus genus, which, in addition to SARS-CoV-2, includes SARS-CoV-1 and MERS-CoV. The genome of SARS-CoV-2 is almost 80% similar to SARS-CoV-1 and 50% to MERS-CoV. The mechanisms of infection of SARS-CoV-1 and SARS-CoV-2 are also similar and occur through the binding of the virus to the type 2 angiotensin-converting enzyme protein (ACE2), which is widely represented in the human body with predominant expression in endocrine tissues. In this connection, SARS-CoV-1 and SARS-CoV-2 affect the organs of the endocrine system, causing damage and hormonal changes that affect the prognosis of the course of COVID-19. This literature review is devoted to the analysis of changes in the organs of the endocrine system that occur during infection with SARS-CoV-1 and SARS-CoV-2, as well as the potential effect of hormones on susceptibility to SARS-CoV-2.

2019年12月,中国首次报道了一种新的危险呼吸道疾病COVID-19,病原体sars -冠状病毒2 (SARS-CoV-2),属于β冠状病毒属,除SARS-CoV-2外,还包括SARS-CoV-1和MERS-CoV。SARS-CoV-2的基因组几乎与SARS-CoV-1相似80%,与MERS-CoV相似50%。SARS-CoV-1和SARS-CoV-2的感染机制也相似,都是通过病毒与2型血管紧张素转换酶蛋白(ACE2)结合而发生的,ACE2在人体中广泛存在,主要表达于内分泌组织。因此,SARS-CoV-1和SARS-CoV-2会影响内分泌系统的器官,造成损害和激素变化,从而影响COVID-19病程的预后。本文献综述旨在分析SARS-CoV-1和SARS-CoV-2感染期间内分泌系统器官的变化,以及激素对SARS-CoV-2易感性的潜在影响。
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引用次数: 0
Diagnostic cytokine marker of male infertility - interleukin 4. 男性不育症的细胞因子诊断标志物-白细胞介素4。
Q4 Health Professions Pub Date : 2022-03-25 DOI: 10.51620/0869-2084-2022-67-3-151-157
O V Bukharin, M D Kuzmin, N B Perunova, I A Nikiforov, I N Chainikova, E V Ivanova

Analysis of the study is to assess the diagnostic significance of cytokines in the sperm plasma of men of reproductive age (20 - 45 years) of two groups: of patients with chronic bacterial prostatitis, not complicated by infertility and with loss of fertility. The study of sperm plasma - the WHO standard. Determination of the level of cytokines in seminal plasma - by enzyme immunoassay («Cytokine», Russia). Two methods of mathematical statistics were used: discriminant analysis and classification trees (decision trees).The similarity of interpretations of discriminant analysis and decision tree was noted, where the main role in both cases belongs to the cytokine IL-4. The level of sperm IL-4 in combination with therapeutic monitoring can be used for the medical management of patients with chronic prostatitis in order to prevent the development of infertility and to develop methods for screening diagnostics of fertility disorders in men.

分析本研究的目的是评估两组育龄男性(20 - 45岁):慢性细菌性前列腺炎、未合并不孕症和丧失生育能力患者的精子血浆中细胞因子的诊断意义。精子血浆的研究-世界卫生组织标准。精浆中细胞因子水平的测定-通过酶免疫分析法(«细胞因子»,俄罗斯)。采用两种数理统计方法:判别分析和分类树(决策树)。注意到判别分析和决策树解释的相似性,其中两种情况下的主要作用都属于细胞因子IL-4。精子IL-4水平结合治疗监测可用于慢性前列腺炎患者的医疗管理,以预防不孕症的发展,并制定男性生育障碍的筛查诊断方法。
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引用次数: 2
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Klinichescheskaya Laboratornaya Diagnostika
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