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Molecular genetic markers and metabolic disorders in non-alcoholic fatty liver disease 非酒精性脂肪肝的分子遗传标记和代谢紊乱
Pub Date : 2022-01-01 DOI: 10.32364/2587-6821-2022-6-5-206-212
A. B. Krivosheev, V. Maksimov, K.Yu. Boyko, E. E. Levykina, E. Mikhaylova, N. Varaksin, M. Kondratova, I. A. Krivosheeva, A. Autenshlyus
Aim: to assess the probability of unfavorable outcomes of non-alcoholic fatty liver disease (NAFLD) based on clinical, biochemical, and molecular genetic parameters. Patients and Methods: 440 individuals were examined. Among them, 115 patients (84 men and 31 women) aged 23–69 (mean 49.3±1.1 years) were diagnosed with NAFLD and 325 healthy volunteers (172 men and 153 women) aged 25–67 (mean age 47.9±0.6 years) were controls. Molecular genetic testing for TCF7L2 (ТС, СС, and ТТ genotypes) was performed in all participants. The rates of Glu342Lys (PIZ) and Glu264Val (PIS) mutations of α1-antitrypsin gene (SERPINA1) and 282Y and 63D alleles of hemochromatosis (HFE) gene were evaluated. Standard liver function tests (ASAT, ALAT, bilirubin), lipid metabolism (total cholesterol, triglycerides, HDL, LDL), excretory porphyrin metabolism (porphyrin precursors [δ-aminolaevulinic acid and porphobilinogen] and fractions [uroporphyrin and coproporphyrin]), and cytokine profile (interleukins 1β, 6, 8, 10, and 1Ra, tumor necrosis factor/TNF α) were assessed. Results: the rates of TCF7L2 genotype, 282Y and 63D HFE gene alleles were similar in NAFLD patients and healthy controls. Meanwhile, Glu342Lys (PIZ) and Glu264Val (PIS) SERPINA1 gene polymorphisms were significantly more common in NAFLD patients vs. general population. The odds ratio (OR) has demonstrated that Glu342Lys (PIZ) genotype occurrence is 3.9 times greater in the NAFLD group than in healthy controls (NZ + ZZ vs. NN: OR=3.90, 95% CI 1.5–10.5, p=0.007), while Glu264Vol (PIS) genotype occurrence is 6.6 times greater in the NAFLD group than in healthy controls (NS vs. NN: OR=6.6, 95 CI 2.4–18.3, p<0.001). Abnormalities of porphyrin metabolism and cytokine profile were detected in most participants (71.3% and 82.6%, respectively). Unfavorable NAFLD outcomes were reported in 30 patients (26.1%). Conclusions: molecular genetic testing and specific blood biochemistry allows for predicting NAFLD outcome. Describing metabolic disorders allows for assessing the risk of unfavorable outcome. KEYWORDS: non-alcoholic fatty liver disease, molecular genetic testing, TCF7L2 gene, α1-antitrypsin gene (SERPINA1), hemochromatosis gene (HFE), lipid metabolism, porphyrin metabolism, cytokine profile, unfavorable outcome. FOR CITATION: Krivosheev A.B., Maksimov V.N., Boyko K.Yu. et al. Molecular genetic markers and metabolic disorders in non-alcoholic fatty liver disease. Russian Medical Inquiry. 2022;6(5):206–212 (in Russ.). DOI: 10.32364/2587-6821-2022-6-5-206-212.
目的:基于临床、生化和分子遗传学参数评估非酒精性脂肪性肝病(NAFLD)不良结局的概率。患者和方法:440例。其中诊断为NAFLD的患者115例(男性84例,女性31例),年龄23-69岁(平均49.3±1.1岁);对照组325例(男性172例,女性153例),年龄25-67岁(平均47.9±0.6岁)。对所有参与者进行TCF7L2 (ТС、СС和ТТ基因型)的分子基因检测。检测α - 1抗胰蛋白酶基因(SERPINA1) Glu342Lys (PIZ)和Glu264Val (PIS)以及血色素沉着症(HFE)基因282Y和63D等位基因的突变率。标准肝功能测试(ASAT、ALAT、胆红素)、脂质代谢(总胆固醇、甘油三酯、HDL、LDL)、排泄卟啉代谢(卟啉前体[δ-氨基乙酰丙酸和卟啉胆红素原]和部分[uroporphyrin和coproporphyrin])和细胞因子谱(白细胞介素1β、6、8、10和1Ra,肿瘤坏死因子/TNF α)进行评估。结果:NAFLD患者TCF7L2基因型、282Y和63D HFE基因等位基因的发生率与健康对照组相似。同时,Glu342Lys (PIZ)和Glu264Val (PIS) SERPINA1基因多态性在NAFLD患者中比在普通人群中更为常见。比值比(OR)显示,NAFLD组Glu342Lys (PIZ)基因型的发生率是健康对照组的3.9倍(NZ + ZZ vs. NN: OR=3.90, 95% CI 1.5-10.5, p=0.007),而NAFLD组Glu264Vol (PIS)基因型的发生率是健康对照组的6.6倍(NS vs. NN: OR=6.6, 95 CI 2.4-18.3, p<0.001)。在大多数参与者中检测到卟啉代谢和细胞因子谱异常(分别为71.3%和82.6%)。30例患者(26.1%)报告了不良的NAFLD结果。结论:分子基因检测和特异性血液生化可以预测NAFLD的预后。描述代谢紊乱可以评估不良结果的风险。关键词:非酒精性脂肪性肝病,分子基因检测,TCF7L2基因,α1-抗胰蛋白酶基因(SERPINA1),血色素沉着症基因(HFE),脂质代谢,卟啉代谢,细胞因子谱,不良结局。引文:Krivosheev A.B, Maksimov V.N, Boyko K.Yu。et al。非酒精性脂肪肝的分子遗传标记和代谢紊乱。俄罗斯医学调查。2022;6(5):206-212(俄文)。DOI: 10.32364 / 2587-6821-2022-6-5-206-212。
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引用次数: 0
Febuxostat efficacy in patients with gout depending on kidney function 非布司他在痛风患者中的疗效取决于肾功能
Pub Date : 2022-01-01 DOI: 10.32364/2587-6821-2022-6-3-140-147
M. Eliseev, O. Zhelyabina, M. Chikina, M.M. Thakokov
Aim: to determine the probability of achieving the target serum uric acid (UA) level during therapy with febuxostat (in the tablet form) in patients with gout stratified depending on kidney function, including patients with type 2 diabetes mellitus (DM2). Patients and Methods: the study included patients over 18 years of age with gout who had not previously taken febuxostat or other urate- lowering drugs for at least 2 weeks before inclusion, with a serum UA level >360 μmoL/L. All were prescribed with febuxostat in the tablet form 80 mg/day. If the target serum UA level was not reached (<360 μmoL/L), the dosage level was increased up to 120 mg/day. Laboratory tests included the determination of blood glucose, creatinine, UA. Initially, patients were divided into groups according to chronic kidney disease (CKD) stages by the level of estimated glomerular filtration rate (eGFR) by CKD-EPI: C1 — high or optimal renal function (>90 mL/min/1.73 m2), C2 — slightly reduced renal function (60–89 mL/min/1.73 m2), C3 — moderately/considerably reduced renal function (30–59 mL/ min/1.73 m2), C4 — significantly reduced renal function (15–29 mL/min/1.73 m2). Patients with DM2 were analyzed separately. The follow-up period covered at least 26 weeks: the primary endpoint was to achieve the target serum UA level, and the eGFR tendency was also evaluated.Results: 136 patients with gout were examined. DM2 was in 38 (27.9%) patients. CKD C0–1 was detected in 30 (22.1%) patients, C2 — in 28 (20.6%), C3 — in 62 (45.6%), C4 — in 16 (11.8%). Febuxostat (in the tablet form) was received at a dose of 80 mg/day in 98 (72.1%) patients, 120 mg/day in 38 (27.9%) patients. There was the following preventive administration of anti-inflammatory therapy: colchicine — 59 (43.4%) patients, NSAIDs — 51 (37.5%) patients, glucocorticosteroids — 12 (8.8%) patients, no drug therapy — 14 (10.3%) patients. UA level significantly decreased in all groups, the average value of Δ MK and the frequency of achieving the target serum UA level were comparable. Achievement of the target serum UA level in general was in 84% of patients; in C0–1, C2, C3, C4 — in 83, 89, 82 and 81% of patients, respectively. The mean eGFR values relative to the baseline increased by the end of the study in all groups, but significant differences were only in patients with C0–1: 101.3±18.1 mL/min/1.73 m2 vs 102.8±28.6 mL/min/1.73 m2 (p=0.002). Of the 38 patients with DM2, 33 (87%) achieved the target serum UA level. In 2 patients with CKD C3, ALT and AST increased up to two norms (when taking febuxostat 120 mg/day). Conclusion: the possibility of achieving the target serum UA level when taking febuxostat (in the tablet form) in patients with gout does not depend on kidney function, including in patients with DM2. KEYWORDS: gout, febuxostat, glomerular filtration rate, chronic kidney disease, diabetes mellitus. FOR CITATION: Eliseev M.S., Zhelyabina O.V., Chikina M.N., Thakokov M.M. Febuxostat efficacy in patients with
目的:确定非布司他(片剂)治疗根据肾功能分层的痛风患者(包括2型糖尿病(DM2)患者)达到目标血清尿酸(UA)水平的概率。患者和方法:研究对象为18岁以上的痛风患者,入组前至少2周未服用非布司他或其他降尿酸药物,且血清UA水平>360 μmoL/L。所有患者均服用非布司他片剂80毫克/天。如果未达到目标血清UA水平(90 mL/min/1.73 m2),则C2 -肾功能轻度下降(60-89 mL/min/1.73 m2), C3 -肾功能中度/明显下降(30-59 mL/min/1.73 m2), C4 -肾功能明显下降(15-29 mL/min/1.73 m2)。DM2患者单独分析。随访时间至少26周:主要终点是达到目标血清UA水平,并评估eGFR趋势。结果:对136例痛风患者进行了检查。38例(27.9%)患者出现DM2。30例(22.1%)检测到CKD C0-1, 28例(20.6%)检测到C2 -, 62例(45.6%)检测到C3 -, 16例(11.8%)检测到C4 -。非布司他(片剂)在98例(72.1%)患者中以80mg /天的剂量服用,在38例(27.9%)患者中以120mg /天的剂量服用。预防性给予抗炎治疗:秋水仙碱59例(43.4%),非甾体抗炎药51例(37.5%),糖皮质激素12例(8.8%),无药物治疗14例(10.3%)。各组血清UA水平均显著降低,Δ MK平均值与达到目标血清UA水平的频率具有可比性。总体而言,84%的患者达到了目标血清UA水平;C0-1、C2、C3、C4 -分别占83%、89%、82%和81%。研究结束时,各组相对于基线的平均eGFR值均有所增加,但仅在C0-1患者中存在显著差异:101.3±18.1 mL/min/1.73 m2 vs 102.8±28.6 mL/min/1.73 m2 (p=0.002)。38例DM2患者中,33例(87%)达到目标血清UA水平。在2例CKD C3患者中,ALT和AST升高到两个标准(当服用非布司他120mg /天时)。结论:痛风患者服用非布司他(片剂)达到目标血清UA水平的可能性不依赖于肾功能,包括DM2患者。关键词:痛风、非布司他、肾小球滤过率、慢性肾病、糖尿病引用本文:Eliseev m.s., Zhelyabina o.v., chinina m.n., Thakokov M.M.。非布司他对痛风患者肾功能的影响。俄罗斯医学调查。2022;6(3):140-147(俄文)。DOI: 10.32364 / 2587-6821-2022-6-3-140-147。
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引用次数: 2
Review of the results of mass screening for the BRCA1/2 gene mutations in patients with different types of malignant neoplasms 不同类型恶性肿瘤患者BRCA1/2基因突变的大规模筛查结果综述
Pub Date : 2022-01-01 DOI: 10.32364/2587-6821-2022-6-6-297-308
A. Stroganova, N. I. Pospekhova, D. A. Golovina, I. Cherepanova, S. Dranko, M. Filippova
Background: germline mutations in the BRCA1 and BRCA2 genes are associated with a high risk of developing cancer of various localizations. Currently, the determination of BRCA status in such patients is important for choosing surgical tactics and determining indications for the administration of multiple chemotherapy drugs. Aim: to evaluate the results of mass genetic screening for mutations in the BRCA1 and BRCA2 genes in patients with various types of malignant neoplasms (MN). Patients and Methods: the results of genetic screening of 5043 patients who are reviewed in the study. The patients had the following diagnoses: breast cancer (BC, n=4216), ovarian cancer (OC, n=481), multiple primary malignant neoplasms (n=174), pancreatic cancer (n=96) and prostate cancer (n=75). Real-time PCR-based genetic testing for eight recurrent BRCA1/2 gene mutations specific for the Russian population was performed for all patients. The study of the entire coding sequence of the BRCA1/2 genes was carried out in 655 patients with negative screening results for mutations using high-resolution melting curve analysis, Sanger sequencing, and massively parallel sequencing. Results and Discussion: among 5043 cancer patients, the total frequency of BRCA mutations was 8%. In patients with BC the recurrent variants accounted for 6.7%, bilateral BC — 13.5%, OC — 17%, multiple primary malignant neoplasms (MPMN) — 13.1%, pancreatic cancer — 3.1%, while in patients with prostate cancer no mutations were found. The frequency of the c.5266dup mutation in the BRCA1 gene was 5.63%. Forty nine patients (0.97%) were carriers of another mutation — p.C61G, which is specific for the Slavic populations. Other variants were found much less frequently (0.1–0.38%). Thus, screening for common mutations helped to determine the prevalence of each of the variants and proved a high frequency of c.5266dup and p.C61G mutations. The analysis of the coding sequence of the BRCA1/2 genes in 655 patients revealed pathogenic mutations (class 5) in 13% of cases. The prevalence of rare variants in patients with BC was 11.1%, bilateral BC — 26.5%, OC — 14.9%, МPМN — 31%, pancreatic cancer — 2.3%, and prostate cancer — 2.5%. In the BRCA1 gene, 41 unique clinically significant mutations were found, and four of them were repeated in unrelated patients. In the BRCA2 gene, 29 unique clinically significant mutations were found, five of which were repeated. Moreover, 19 missense mutations were detected which, according to the databases, were categorized as variants with unknown clinical significance (class 3). They were analyzed using seven pathogenicity prediction algorithms. As a result, five mutations were interpreted by the most algorithms as likely pathogenic or pathogenic (class 4/5), five mutations were re-assessed as variants with unknown significance, and nine variants were identified as clinically insignificant. Conclusion: thus, the Russian population is characterized by the presence of multiple recu
背景:BRCA1和BRCA2基因的种系突变与发生不同部位癌症的高风险相关。目前,确定此类患者的BRCA状态对于选择手术策略和确定多种化疗药物的适应症具有重要意义。目的:评价不同类型恶性肿瘤(MN)患者BRCA1和BRCA2基因突变的大规模基因筛查结果。患者和方法:回顾了5043例患者的遗传筛查结果。诊断为乳腺癌(BC, n=4216)、卵巢癌(OC, n=481)、多发性原发恶性肿瘤(n=174)、胰腺癌(n=96)、前列腺癌(n=75)。对所有患者进行了俄罗斯人群特有的8种复发性BRCA1/2基因突变的实时pcr基因检测。采用高分辨率熔融曲线分析、Sanger测序和大规模平行测序对655例突变筛查结果为阴性的患者进行BRCA1/2基因全编码序列研究。结果与讨论:在5043例癌症患者中,BRCA突变的总频率为8%。在BC患者中,复发变异占6.7%,双侧BC - 13.5%, OC - 17%,多发性原发性恶性肿瘤(MPMN) - 13.1%,胰腺癌- 3.1%,而在前列腺癌患者中未发现突变。BRCA1基因c.5266dup突变频率为5.63%。49名患者(0.97%)携带另一种突变——p.C61G,这是斯拉夫人群特有的。其他变异的发现频率要低得多(0.1-0.38%)。因此,筛选常见突变有助于确定每种变异的患病率,并证明了c.5266dup和p.C61G突变的高频率。对655例患者BRCA1/2基因编码序列的分析显示,13%的病例发生致病性突变(5类)。罕见变异在BC患者中的患病率为11.1%,双侧BC为26.5%,OC为14.9%,МPМN为31%,胰腺癌为2.3%,前列腺癌为2.5%。在BRCA1基因中,发现了41个独特的具有临床意义的突变,其中4个在不相关的患者中重复出现。在BRCA2基因中,发现了29个独特的具有临床意义的突变,其中5个是重复的。此外,检测到19个错义突变,根据数据库,这些突变被归类为具有未知临床意义的变异(3类)。使用7种致病性预测算法对它们进行分析。结果,5个突变被大多数算法解释为可能致病或致病(4/5类),5个突变被重新评估为意义未知的变异,9个变异被确定为临床不显著。结论:因此,俄罗斯人群的特点是存在多种复发性突变,而在不同癌症类型的患者中,c.5266dup和p.C61G的患病率明显高于其他变异的患病率。分析BRCA1/2基因的复发变异体可以鉴定大约。80%的致病突变携带者。使用包含这些变异的面板试剂盒被认为是BRCA1/2基因第一步筛选的廉价且敏感的算法。对所研究的患者群体进行所有编码基因区域的后续调查(测序)是可行的,并且可以显著提高BRCA1/2基因致病性突变的可检测性。关键词:BRCA1突变、BRCA2突变、乳腺癌、卵巢癌、恶性肿瘤引文来源:Stroganova a.m., Pospekhova n.i., Golovina D.A.等。不同类型恶性肿瘤患者BRCA1/2基因突变的大规模筛查结果综述俄罗斯医学调查。2022;6(6):297-308(俄文)。Doi: 10.32364/2587-6821- 2022-6-6-297-308。
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引用次数: 0
Chondroitin sulfate in the treatment of osteoarthritis 硫酸软骨素治疗骨关节炎
Pub Date : 2022-01-01 DOI: 10.32364/2587-6821-2022-6-3-148-152
S. Yakupova, E. A. Fedorova
Osteoarthritis (OA) is a common disease in the practice of doctors of various specialties. Leading international organizations regularly update recommendations for the treatment of patients with this disease. The viewpoints of experts differ concerning various interventions. The article issues the use of a drug group — Symptomatic Slow-Acting Drug in Osteoarthritis (SYSADOA), such as glucosamine and chondroitin sulfate (CS). To date, data on the efficacy and good tolerability of these drugs have been accumulating, which is important due to the significant comorbidity in patients with OA. The results of numerous studies reviewed by the authors have suggested a possible mechanism of analgesic and anti-inflammatory action of chondroitin sulfate (CS). In the leading international and national recommendations, CS is included in the treatment regimens of patients with OA, with the clarification that the prescription form has an advantage. The recommendations of the European Society for Clinical and Economic Aspects of Osteoporosis, Osteoarthritis and Musculoskeletal Diseases, (ESCEO) in 2019 strongly recommended the use of high-quality CS as a long-term background treatment. KEYWORDS: osteoarthritis, recommendations, symptomatic slow-acting drug, chondroitin sulfate. FOR CITATION: Yakupova S.P., Fedorova E.A. Chondroitin sulfate in the treatment of osteoarthritis. Russian Medical Inquiry. 2022;6(3):148– 152 (in Russ.). DOI: 10.32364/2587-6821-2022-6-3-148-152.
骨关节炎(OA)是各专科医生的常见病。主要国际组织定期更新治疗该病患者的建议。专家们对各种干预措施的看法不一。本文提出了一组药物的使用-症状性骨关节炎缓释药(SYSADOA),如氨基葡萄糖和硫酸软骨素(CS)。迄今为止,关于这些药物的疗效和良好耐受性的数据不断积累,这一点很重要,因为OA患者存在显著的合并症。作者回顾了大量的研究结果,提出了硫酸软骨素(CS)的镇痛和抗炎作用的可能机制。在主要的国际和国家建议中,CS被纳入OA患者的治疗方案,并澄清处方形式具有优势。2019年,欧洲骨质疏松症、骨关节炎和肌肉骨骼疾病临床和经济方面学会(ESCEO)的建议强烈建议使用高质量的CS作为长期背景治疗。关键词:骨关节炎,推荐,对症缓效药物,硫酸软骨素。引用本文:Yakupova s.p., Fedorova E.A.硫酸软骨素治疗骨关节炎。俄罗斯医学调查。2022;6(3):148 - 152(俄文)。DOI: 10.32364 / 2587-6821-2022-6-3-148-152。
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引用次数: 1
Morphology of regional lymph nodes in experimental prostate carcinogenesis 实验性前列腺癌变的区域淋巴结形态
Pub Date : 2022-01-01 DOI: 10.32364/2587-6821-2022-6-4-171-176
V. Astashov, A. Lomshakov, T. Tsekhmistrenko, O. Vykhristyuk, M. Uloga, Inna Borodina, A. Tolkachev
Background: the migration of tumor cells into blood and lymphatic vessels is a key stage of the metastatic process in malignant neoplasms. Moreover, the presence of tumor cells in the lymph nodes is an indicator of cancer aggressiveness, and the histopathological characteristics of the lymph nodes are one of the important parameters for the treatment prognosis and patient survival Aim: to evaluate changes in the lymph nodes of mice during experimental carcinogenesis in the prostate gland. Material and Methods: the study was conducted on CBA inbred 3-month-old male mice (n=30). To create a model of malignant tumor growth in the prostate gland, a diluted cell strain of transplantable Ehrlich ascites carcinoma was inoculated into the prostate parenchyma. A model of prostate carcinogenesis was created in 18 days by transplanting Ehrlich ascites carcinoma into prostate tissue in mice (n=15; main group). The remaining 15 mice were in the control group. All manipulations with animals were carried out in compliance with the basic ethical principles. After the animals were removed from the experiment, a morphological analysis of the prostate and regional (pelvic) lymph nodes was performed. The area and cellular composition concerning the main structural and functional zones of the pelvic lymph nodes in both groups of animals were evaluated Results: this study showed that the cellular composition changed in the setting of prostate carcinogenesis in the pelvic lymph nodes. In the main group of animals, the number of immunoblasts significantly prevailed in the germinal center of secondary lymphoid nodules versus the control group (p<0,05). An increase in immunoblasts by almost 2 times in mice (experimental group) indicated the inhibition of humoral immunity in prostate carcinogenesis. Also, in the main group, the area of the cortical substance decreased by 14.5% and the area of the paracortex increased by 28.4% versus the control group (p<0,05). Conclusion: the first metastases of prostate cancer appear in regional lymph nodes. On the 18th day of prostate carcinogenesis, the structure of regional lymph nodes undergoes changes: paracortical hyperplasia, a decrease in the area of medullary cords and medullary substance, a decrease in cerebral sinuses KEYWORDS: prostate cancer, carcinogenesis, experiment, Ehrlich ascites carcinoma, lymphangiogenesis, lymph node, regional metastases. FOR CITATION: Astashov V.V., Lomshakov A.A., Tsekhmistrenko T.A. et al. Morphology of regional lymph nodes in experimental prostate carcinogenesis. Russian Medical Inquiry. 2022;6(4):171–176 (in Russ.). DOI: 10.32364/2587-6821-2022-6-4-171-176.
背景:肿瘤细胞向血液和淋巴管的迁移是恶性肿瘤转移过程的关键阶段。此外,淋巴结内肿瘤细胞的存在是肿瘤侵袭性的一个指标,淋巴结的组织病理学特征是治疗预后和患者生存的重要参数之一。目的:评价实验性前列腺癌变过程中小鼠淋巴结的变化。材料与方法:选用CBA近交系3月龄雄性小鼠30只。为了建立前列腺恶性肿瘤生长模型,将可移植的埃利希腹水癌稀释细胞株接种到前列腺实质中。将埃利希腹水癌移植至小鼠前列腺组织,于18 d建立前列腺癌模型(n=15;主要组)。其余15只小鼠作为对照组。所有对动物的操作都遵循基本的伦理原则。将动物从实验中取出后,对前列腺和区域(盆腔)淋巴结进行形态学分析。对两组动物盆腔淋巴结主要结构区和功能区的面积和细胞组成进行了评估。结果:本研究表明盆腔淋巴结前列腺癌发生后细胞组成发生了变化。主组动物继发性淋巴结节生发中心的免疫母细胞数量显著高于对照组(p< 0.05)。小鼠(实验组)免疫母细胞增加近2倍,表明前列腺癌发生过程中体液免疫受到抑制。与对照组相比,主组皮质物质面积减少14.5%,副皮质面积增加28.4% (p< 0.05)。结论:前列腺癌的第一次转移发生在区域淋巴结。在前列腺癌变第18天,区域淋巴结结构发生改变:皮质旁增生,髓索及髓质面积减少,脑窦减少。关键词:前列腺癌,癌变,实验,埃利希腹水癌,淋巴管生成,淋巴结,区域转移。引文:Astashov v.v., Lomshakov a.a., Tsekhmistrenko T.A.等。实验性前列腺癌变的区域淋巴结形态。俄罗斯医学调查。2022;6(4):171-176(俄文)。DOI: 10.32364 / 2587-6821-2022-6-4-171-176。
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引用次数: 0
Selecting anticoagulant therapy in patients with cirrhosis 肝硬化患者抗凝治疗的选择
Pub Date : 2022-01-01 DOI: 10.32364/2587-6821-2022-6-5-286-292
N. Arykan, A. Shestopalov, E.E. Khvorostinina, A.O. Alekseeva, K. Asaturyan
Patients with liver diseases have a higher risk of hemostatic disorders. Meanwhile, despite a well-established opinion on a low risk of thromboses in cirrhosis, thromboembolic events cannot be totally ruled out in these patients. Increased risks of thrombotic events and venous thromboembolism in cirrhosis are accounted for by external (immobilization, surgeries, infections, comorbidities) and internal factors (reduced synthesis of anticoagulants, increased levels of estrogens). Practically, the selection of anticoagulant therapy in cirrhosis is difficult because of divergent hemostatic disorders and requires continuous and careful monitoring of hemostasis. In 2019, the American Gastroenterological Association (AGA) released guidelines on anticoagulant therapy in patients with cirrhosis and pulmonary embolism. We describe a patient with cirrhosis and pulmonary embolism. A management strategy was tailored to the AGA guidelines, the Russian Society on Liver Research guidelines, and the Russian Gastroenterological Association on Fibrosis and Cirrhosis and Complication Diagnosis and Treatment guidelines. This example of successful selection of anticoagulant therapy, multidisciplinary approach, and dynamic evaluation of all available methods of hemostasis control will be useful for practitioners. KEYWORDS: cirrhosis, hemostasis, thrombosis, hemorrhage, venous thromboembolism, pulmonary embolism, thromboelastometry, anticoagulant, low-molecular-weight heparin. FOR CITATION: Arykan N.G., Shestopalov A.E., Khvorostinina E.E. et al. Selecting anticoagulant therapy in patients with cirrhosis. Russian Medical Inquiry. 2022;6(5):286–292 (in Russ.). DOI: 10.32364/2587-6821-2022-6-5-286-292.
肝病患者发生止血障碍的风险较高。与此同时,尽管肝硬化血栓形成的风险较低,但不能完全排除这些患者的血栓栓塞事件。肝硬化血栓形成事件和静脉血栓栓塞的风险增加是由外部因素(固定、手术、感染、合并症)和内部因素(抗凝血剂合成减少、雌激素水平升高)造成的。实际上,肝硬化患者抗凝治疗的选择是困难的,因为有多种不同的止血障碍,需要持续仔细地监测止血情况。2019年,美国胃肠病学协会(AGA)发布了肝硬化和肺栓塞患者抗凝治疗指南。我们描述了一个肝硬化和肺栓塞的病人。根据AGA指南、俄罗斯肝脏研究学会指南和俄罗斯胃肠病学协会纤维化和肝硬化及并发症诊断和治疗指南制定了管理策略。这个成功选择抗凝治疗的例子,多学科的方法,动态评估所有可用的止血控制方法将是有用的从业人员。关键词:肝硬化,止血,血栓形成,出血,静脉血栓栓塞,肺栓塞,血栓弹性测量,抗凝剂,低分子肝素。引用本文:Arykan N.G, Shestopalov A.E, Khvorostinina E.E.等。肝硬化患者抗凝治疗的选择。俄罗斯医学调查。2022;6(5):286-292(俄文)。DOI: 10.32364 / 2587-6821-2022-6-5-286-292。
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引用次数: 1
Ultrasound guided transrectal polyfocal biopsy in prostate cancer diagnosis 超声引导下经直肠多灶活检在前列腺癌诊断中的应用
Pub Date : 2022-01-01 DOI: 10.32364/2587-6821-2022-6-6-309-313
A. Berezhnoy, S. Dunaevskaya, S.I. Auzina
Background: prostate cancer (PCa) is a topic of special interest in the modern urologic oncology. PCa is associated with high rates of morbidity and mortality among the male population in Russia and worldwide. The current diagnostic algorithm for PCa detection includes a digital rectal examination to check the prostate, and a PSA test to measure levels of prostate specific antigen (PSA) in the blood, and a prostate biopsy followed by morphological verification. Aim: to analyze the results of transrectal ultrasound guided polyfocal biopsies of the prostate, performed from 2021 to 2022 in patients who underwent diagnosis and treatment at the Clinical Hospital "RZD-Meditsina" of the city of Krasnoyarsk. Patients and Methods: in all cases the evaluation of patients included the measurement of a total PSA (PSAtotal) concentration, standard examination, and the preparation for biopsy. The ultrasound guided prostate biopsy was performed in the hospital setting. After the procedure, all patients were followed up to control and prevent possible complications. Histological examination of the biomaterial included the verification of malignant neoplasms or benign lesions in the prostate tissue, Gleason score, and other morphological characteristics. Results: findings of 220 transrectal ultrasound guided prostate biopsies were analyzed. The median age of patients was 64 (44–89) years. Benign prostatic hyperplasia (BPH) was diagnosed in 112 (51%) patients, prostate cancer — in 108 (49%) patients. PSA level varied from 0.48 to 37.9 ng/ml in the BPH patients, and from 4.48 to 100.0 ng/ml in the PCa group. The median prostate volume was 74.61 (10.26–134.80) cm3 in the PCa group, and 153.45 (116.22–185.50) cm3 in the patients with BPH. Most of PCa patients had Gleason score ≤7 representing moderately differentiated tumors. Post-biopsy complications were observed in 141 (64.09%) patients and included hematuria, short-term rectal bleeding, chronic prostatitis exacerbation. All complications were cured successfully treated using conservative therapy. Conclusion: PCa can be diagnosed even in patients with low PSATotal levels or the normal prostate volume . Moderately differentiated tumors (Gleason score ≤7) predominated in the population of patients. These data are consistent with the effective early detection of PCa. Patients should be closely monitored in the early post-operative period after a diagnostic prostate biopsy to prevent potential complications. KEYWORDS: prostate cancer, biopsy, prostate, transrectal puncture biopsy, ultrasound navigation. FOR CITATION: Berezhnoy A.G., Dunaevskaya S.S., Auzina S.I. Ultrasound guided transrectal polyfocal biopsy in prostate cancer diagnosis. Russian Medical Inquiry. 2022;6(6):309–313 (in Russ.). DOI: 10.32364/2587-6821-2022-6-6-309-313.
背景:前列腺癌(PCa)是现代泌尿肿瘤学中一个特别感兴趣的话题。前列腺癌与俄罗斯和全世界男性人口的高发病率和高死亡率有关。目前用于前列腺癌检测的诊断算法包括直肠指检检查前列腺,PSA测试测量血液中前列腺特异性抗原(PSA)的水平,以及形态学验证后的前列腺活检。目的:分析2021年至2022年在克拉斯诺亚尔斯克市“RZD-Meditsina”临床医院接受诊断和治疗的患者经直肠超声引导前列腺多灶活检的结果。患者和方法:在所有病例中,对患者的评估包括总PSA (PSAtotal)浓度的测量、标准检查和活检准备。超声引导前列腺活检在医院进行。术后对所有患者进行随访,以控制和预防可能的并发症。生物材料的组织学检查包括前列腺组织中恶性肿瘤或良性病变的验证,Gleason评分和其他形态学特征。结果:对220例经直肠超声引导下的前列腺活检结果进行分析。患者的中位年龄为64(44-89)岁。112例(51%)诊断为良性前列腺增生,108例(49%)诊断为前列腺癌。前列腺增生患者的PSA水平从0.48到37.9 ng/ml不等,前列腺增生组的PSA水平从4.48到100.0 ng/ml不等。前列腺癌组中位前列腺体积为74.61 (10.26-134.80)cm3,前列腺增生组中位前列腺体积为153.45 (116.22-185.50)cm3。多数PCa患者Gleason评分≤7分,为中分化肿瘤。141例(64.09%)患者出现活检后并发症,包括血尿、短期直肠出血、慢性前列腺炎加重。所有并发症均经保守治疗成功治愈。结论:前列腺素水平低或前列腺体积正常均可诊断前列腺癌。患者中以中度分化肿瘤(Gleason评分≤7)为主。这些数据与前列腺癌的有效早期检测一致。在诊断性前列腺活检术后早期应密切监测患者,以防止潜在的并发症。关键词:前列腺癌,活检,前列腺,经直肠穿刺活检,超声导航。引用本文:Berezhnoy a.g., Dunaevskaya s.s., Auzina S.I.超声引导下经直肠前列腺癌多灶活检诊断。俄罗斯医学调查。2022;6(6):309-313(俄文)。DOI: 10.32364 / 2587-6821-2022-6-6-309-313。
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引用次数: 0
Early gastric cancer: clinical case 早期胃癌临床1例
Pub Date : 2022-01-01 DOI: 10.32364/2587-6821-2022-6-6-334-340
O. Malikhova, V. E. Ryabova, V. Lozovaya, A. Tumanyan, M. A. Krylovetskaya, Z.V. Halaev
Gastric cancer (GC) is one of the most common types of malignant neoplasms in Russia and worldwide. In recent decades, GC incidence and mortality have been declining. However, gastric cancer remains one of the leading causes of morbidity and mortality, facilitating further improvements of GC diagnostics and treatment. As known, early gastric cancer is a tumor limited to the gastric mucosa or the submucosal layer of the stomach wall. The detection of early-stage GC is the goal of screening programs. The rapid development of endoscopic technologies and the introduction of the ZOOM endoscopy and narrow-band imaging for precise diagnostics have dramatically improved the quality and effectiveness of patient examinations. These advances have underpinned the increased detection of early gastric cancer. Early gastric cancer can be completely cured. Until recently, the gold standard treatment for GC, including its early stages, was radical resection and gastrectomy. This treatment approach is fully justified and ideal from the perspective of oncology. At the same time, it is associated with postoperative complications and deaths, as well as with a substantial decrease in the quality of life in long term GC survivors. Latest endoscopic technologies enable to perform organ-preserving operations in patients with early GC. As a result, it is possible to reduce dramatically the probability of postoperative complications and to improve the quality of life of patients. As of today, the optimization of endoscopic techniques for the treatment of early GC, as well as the search and implementation of new techniques are considered as the most important issues. The article presents a review of key endoscopic methods used for diagnosis and treatment of GC and a clinical case of a patient with early subcardial stomach cancer. KEYWORDS: oncology, gastric cancer, early gastric cancer, dysplastic changes in the stomach mucosa, endoscopy, endoscopic diagnostics, endoscopic resection, OVESCO. FOR CITATION: Malikhova O.A., Ryabova V.E., Lozovaya V.V. et al. Early gastric cancer: clinical case. Russian Medical Inquiry. 2022;6(6):334– 340 (in Russ.). DOI: 10.32364/2587-6821-2022-6-6-334-340.
胃癌(GC)是俄罗斯和世界范围内最常见的恶性肿瘤之一。近几十年来,胃癌的发病率和死亡率一直在下降。然而,胃癌仍然是发病率和死亡率的主要原因之一,促进了胃癌诊断和治疗的进一步改进。众所周知,早期胃癌是一种局限于胃粘膜或胃壁粘膜下层的肿瘤。早期GC的检测是筛选程序的目标。内窥镜技术的快速发展以及用于精确诊断的ZOOM内窥镜和窄带成像的引入,极大地提高了患者检查的质量和有效性。这些进展为早期胃癌的检测提供了基础。早期胃癌是可以完全治愈的。直到最近,胃癌的金标准治疗,包括其早期阶段,是根治性切除和胃切除术。从肿瘤学的角度来看,这种治疗方法是完全合理和理想的。同时,它与术后并发症和死亡有关,并与长期胃癌幸存者的生活质量大幅下降有关。最新的内镜技术使早期胃癌患者能够进行器官保存手术。因此,有可能大大减少术后并发症的概率,提高患者的生活质量。目前,内镜下治疗早期胃癌的技术优化,以及新技术的寻找和实施被认为是最重要的问题。本文就胃癌的主要内镜诊断和治疗方法及1例早期心下胃癌的临床病例作一综述。关键词:肿瘤学,胃癌,早期胃癌,胃粘膜发育异常改变,内镜检查,内镜诊断,内镜切除,OVESCO。出处:Malikhova o.a., Ryabova v.e., Lozovaya V.V.等。早期胃癌临床1例。俄罗斯医学调查。2022;6(6):334 - 340(俄文)。DOI: 10.32364 / 2587-6821-2022-6-6-334-340。
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引用次数: 1
Prospects of using interferon inducers of the double stranded RNA type for the treatment of viral and bacterial infections 双链RNA型干扰素诱导剂治疗病毒和细菌感染的前景
Pub Date : 2022-01-01 DOI: 10.32364/2587-6821-2022-6-11-643-649
O. Radaeva, A. V. Taganov, E. A. Rogozhina
The article highlights the role of the interferon system in the host defense against infections, primarily those caused by viral agents. The authors explain the effect of double stranded RNA (dsRNA)-based products used as interferon inducers (II) from a pathogenesis standpoint. The key advantage of interferon inducers is a broad spectrum of antiviral activity based on immunomodulating and secondary etiotropic effects. The addition of the so-called early-type II (the production of interferon occurs 2 — 6 hours after administration) to the treatment schemes promotes a timely and adequate immune response and helps to achieve a therapeutic effect. Despite a long-standing interest in the natural dsRNA, the imperfection of the described methods of its synthesis provided the impetus for finding and developing techniques aimed at creating an efficient and safe product. A novel technology of sodium ribonucleinate production enabled to receive an active bacterial endotoxin-free pharmaceutical substance and to minimize the concentration of related impurities which considerably increased the product safety. The innovative solutions underpinning the production of an advanced interferon inducer of the double stranded RNA type will significantly expand the potential applications of interferon therapy. KEYWORDS: antivirals, interferons, interferon inducers, Radamin Viro, sodium ribonucleinate. FOR CITATION: Radaeva O.A., Taganov A.V., Rogozhina E.A. Prospects of using interferon inducers of the double stranded RNA type for the treatment of viral and bacterial infections. Russian Medical Inquiry. 2022;6(11):643–649 (in Russ.). DOI: 10.32364/2587-6821- 2022-6-11-643-649.
本文强调了干扰素系统在宿主防御感染中的作用,主要是那些由病毒制剂引起的感染。作者从发病机制的角度解释了以双链RNA (dsRNA)为基础的产品用作干扰素诱导剂(II)的作用。干扰素诱导剂的主要优势是基于免疫调节和继发性致病因作用的广谱抗病毒活性。在治疗方案中加入所谓的早期II型(干扰素的产生发生在给药后2 - 6小时),可促进及时和充分的免疫反应,并有助于达到治疗效果。尽管人们长期对天然dsRNA感兴趣,但所描述的合成方法的不完善为寻找和开发旨在创造高效和安全产品的技术提供了动力。一种新的核糖核酸酸钠生产技术能够获得活性细菌无内毒素药物物质,并将相关杂质的浓度降至最低,从而大大提高了产品的安全性。创新的解决方案支持生产先进的双链RNA型干扰素诱导剂,将显著扩大干扰素治疗的潜在应用。关键词:抗病毒药物,干扰素,干扰素诱导剂,Radamin Viro,核糖核酸酸钠引文:Radaeva o.a., Taganov a.v., Rogozhina E.A.使用双链RNA型干扰素诱导剂治疗病毒和细菌感染的前景。俄罗斯医学调查,2022;6(11):643-649。Doi: 10.32364/2587-6821- 2022-6-11-643-649。
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引用次数: 3
Patient management with maxillary sinus cysts 上颌窦囊肿的治疗
Pub Date : 2022-01-01 DOI: 10.32364/2587-6821-2022-6-7-411-415
S. Karpishchenko, A.Y. Zernitsky, O. Vereshchagina, E. Bolozneva, E. A. Zueva, A.I. Kuprik
Cystic lesions of the maxillary sinuses include cysts, polyps and neoplasms. Maxillary sinus cysts are benign lesions that are commonly an incidental finding during X–ray, since any symptoms do not accompany their presence. An urgent problem is the development of differential diagnostics, the determination of indications for surgical treatment and the optimal treatment tactics for patients with cystic lesions of the maxillary sinuses. The authors describe their experience in patient management with maxillary sinus cysts. 175 patients (mean age — 44.93 years) with lesions in the maxillary sinus were examined and surgically operated. All patients underwent a comprehensive clinical examination aimed at a differential diagnosis of maxillary sinus pathology: cysts, polyps and neoplasms. All patients underwent endoscopic endonasal surgery: in 135 cases it was conducted via the inferior nasal meatus, in 40 patients — via the middle nasal meatus due to the large size of the cyst. Histology confirmed the established diagnosis during the clinical and instrumental examination. The postoperative period proceeded with no abnormalities. After 6 months, the patients underwent a control computed tomography of paranasal sinuses. In all cases, there was a complete cyst removal and restoration of sinus pneumatization. Thus, the differential diagnosis concerning cystic lesions of the maxillary sinus should be based on clinical manifestations and the results of X-ray techniques and follow-up of patients with scanty symptoms and signs. The optimal treatment method of maxillary sinus cysts is the endoscopic endonasal approach, followed by morphological examination. KEYWORDS: benign lesion, maxillary sinus cyst, cystic lesion, differential diagnosis, endoscopy, endoscopic endonasal approach. FOR CITATION: Karpishchenko S.A., Zernitsky A.Y., Vereshchagina O.E. et al. Patient management with maxillary sinus cysts. Russian Medical Inquiry. 2022;6(7):411–415 (in Russ.). DOI: 10.32364/2587-6821-2022-6-7-411-415.
上颌窦囊性病变包括囊肿、息肉和肿瘤。上颌窦囊肿是一种良性病变,通常在x线检查时偶然发现,因为没有任何症状伴随。一个紧迫的问题是鉴别诊断的发展,确定手术治疗的适应症和最佳治疗策略的患者的囊肿性上颌窦病变。作者描述了他们在上颌窦囊肿患者管理的经验。对175例上颌窦病变患者(平均年龄44.93岁)进行了检查和手术治疗。所有患者都接受了全面的临床检查,目的是鉴别诊断上颌窦病理:囊肿,息肉和肿瘤。所有患者均行鼻内窥镜手术:135例经下鼻道,40例因囊肿较大经中鼻道。组织学证实了临床和仪器检查的既定诊断。术后未见异常。6个月后,患者接受了鼻窦炎计算机断层扫描。在所有病例中,都有一个完整的囊肿切除和窦气化恢复。因此,对上颌窦囊性病变的鉴别诊断应根据临床表现、x线检查结果及对症状体征不明显患者的随访。上颌窦囊肿的最佳治疗方法是鼻内窥镜入路,然后进行形态学检查。关键词:良性病变,上颌窦囊肿,囊性病变,鉴别诊断,内镜检查,内镜鼻内入路。引文:Karpishchenko S.A, Zernitsky A.Y, Vereshchagina O.E.等。上颌窦囊肿的治疗。俄罗斯医学调查。2022;6(7):411-415(俄文)。DOI: 10.32364 / 2587-6821-2022-6-7-411-415。
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引用次数: 0
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Russian Medical Inquiry
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