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SGLT-2 inhibitors in chronic kidney disease: state of the art 慢性肾脏疾病中的SGLT-2抑制剂:最新进展
Pub Date : 2022-09-12 DOI: 10.32756/0869-5490-2022-3-53-58
I. Sabirov, I. Murkamilov, V. Fomin, Z. Murkamilova, A. Sabirova
All patients with chronic kidney disease (CKD) require treatment to reduce the risk of cardiovascular events and to prevent progression of renal failure. ACE inhibitors and angiotensin receptor blockers are widely used for cardio- and nephroprotection in patients with CKD. Sodium glucose cotransporter type 2 (SGLT-2) inhibitors show significant prospects for reducing morbidity and mortality in this population. SGLT-2 inhibitors have been developed for treatment of patients with type 2 diabetes mellitus. However, evidence from multiple randomized clinical trials suggested that these drugs have cardio- and nephroprotective effects in patients with and without diabetes. Despite a wealth of data, SGLT-2 inhibitors remain underused by nephrologists or cardiologists. This is not surprising since new therapies traditionally take decades from research to clinical implementation due to many barriers, including lack of knowledge, concern about drug side effects, lack of decision support, cost, and clinical inertia. The review article presents data from scientific studies on the renoprotective effect of SGLT-2 inhibitors and the mechanisms of this activity in CKD patients.
所有慢性肾脏疾病(CKD)患者都需要治疗以降低心血管事件的风险并防止肾衰竭的进展。ACE抑制剂和血管紧张素受体阻滞剂被广泛用于CKD患者的心脏和肾脏保护。葡萄糖共转运蛋白2型钠(SGLT-2)抑制剂在降低这一人群的发病率和死亡率方面显示出显著的前景。SGLT-2抑制剂已被开发用于治疗2型糖尿病患者。然而,来自多个随机临床试验的证据表明,这些药物对糖尿病患者和非糖尿病患者具有心脏和肾脏保护作用。尽管有大量的数据,SGLT-2抑制剂仍未被肾病学家或心脏病学家充分使用。这并不奇怪,因为由于缺乏知识、对药物副作用的担忧、缺乏决策支持、成本和临床惯性等许多障碍,新疗法从研究到临床实施传统上需要数十年的时间。这篇综述文章介绍了SGLT-2抑制剂在CKD患者中的肾保护作用及其机制的科学研究数据。
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引用次数: 0
Efficacy and safety of upadacitinib in psoriatic arthritis upadacitinib治疗银屑病关节炎的疗效和安全性
Pub Date : 2022-09-12 DOI: 10.32756/0869-5490-2022-3-38-46
P. Novikov, N. Bulanov, S. Gulyaev, E. Grunina, E. Kuznetsova, T. Shevtsova, S. Moiseev
Psoratic arthritis (PsA) is a common disorder affecting every fifth patient with psoriasis. Typical clinical manifestations of PsA include asymmetric mono/oligoathritis or polyarthritis, spondyloarthritis, enthesitis and dactylitis. More rarely PsA is associated with uveitis and inflammatory bowel disease. Upadacitinib is a selective JAK-kinase inhibitor approved for treatment of PsA. Its efficacy and favorable safety profile in PsA patients were established in two randomized placebocontrolled phase 3 clinical trials (SELECT-PsA 1 and 2). In both studies, upadacitinib was significantly more effective than placebo and improved activity of PsA, psoriatic lesions, enthesitis and dactylitis. Moreover, upadacitinib is approved for treatment of axial spondylitis and, therefore, can be used in patients with any manifestations of PsA. The authors present clinical cases of PsA and discuss indications for upadacitinib administration in such patients.
银屑病关节炎(PsA)是影响五分之一银屑病患者的常见疾病。PsA的典型临床表现包括不对称单/少关节炎或多关节炎、脊柱炎、鼻炎和指突炎。更罕见的是,PsA与葡萄膜炎和炎症性肠病有关。Upadacitinib是一种选择性jak激酶抑制剂,被批准用于治疗PsA。在两项随机安慰剂对照的3期临床试验(SELECT-PsA 1和2)中,upadacitinib在PsA患者中的疗效和良好的安全性得到了证实。在这两项研究中,upadacitinib明显比安慰剂更有效,并改善了PsA、银屑病病变、鼻炎和指炎的活性。此外,upadacitinib被批准用于治疗轴性脊柱炎,因此可用于任何PsA表现的患者。作者介绍了PsA的临床病例,并讨论了此类患者更新他替尼的适应症。
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引用次数: 0
Heart involvement in Fabry disease: clinical features, cardiac MRI and speckle-tracking echocardiography 法布里病累及心脏:临床特征、心脏MRI和斑点跟踪超声心动图
Pub Date : 2022-09-12 DOI: 10.32756/0869-5490-2022-3-22-29
A. Moiseev, E. Mershina, A. Safarova, E. Tao, N. Bulanov, V. Sholomova, Z. Kobalava, E. Pavlikova, S. Moiseev, V. Fomin
To evaluate the frequency and clinical features of heart involvement in Fabry disease (FD) and diagnostic value of cardiac MRI and speckle-tracking echocardiography.
探讨法布里病(FD)心脏受累的频率、临床特征及心脏MRI和斑点跟踪超声心动图的诊断价值。
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引用次数: 1
The socioeconomic burden of paracetamol adverse reactions over 10 years in Russia 俄罗斯10年来扑热息痛不良反应的社会经济负担
Pub Date : 2022-09-12 DOI: 10.32756/0869-5490-2022-3-60-66
G.I. Sirayeva, A. Kolbin, A. Kalyapin, Y. Balykina
To evaluate the socioeconomic burden of paracetamol adverse reactions.
评价扑热息痛不良反应的社会经济负担。
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引用次数: 0
Pharmaceutical care for patients with headache: a systematic review of clinical studies 头痛患者的药物治疗:临床研究的系统回顾
Pub Date : 2022-09-12 DOI: 10.32756/0869-5490-2022-3-47-52
O. Reshetko, A. I. Grishin
The article presents an overview of studies of pharmaceutical care for patients with different types of headache. Various methods were used, including education of pharmacists, questionnaires for patients and specialists, interviews, the use of special protocols and algorithms for providing pharmaceutical care, patient modelling.
本文综述了不同类型头痛患者的药学服务研究。使用了各种方法,包括对药剂师进行教育,对患者和专家进行问卷调查,访谈,使用特殊协议和算法提供药物护理,患者建模。
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引用次数: 2
Classic homocystinuria: etiology, natural history and treatment 经典同型半胱氨酸尿:病因、自然病史及治疗
Pub Date : 2022-09-12 DOI: 10.32756/0869-5490-2022-3-30-37
S. Moiseev, N. Chebotareva, N. Bulanov, P. Novikov, E. Shchegoleva, T. Shevtsova, E. Tao, E. Filatova
Classic homocystinuria is a rare autosomal recessive disorder of methionine metabolism resulting from a deificiency of cystathionine beta-synthase that is involved in transsulfuration of homocysteine. The disorder is caused by mutations of CBS gene. Lack of enzyme is associated with accumulation of homocysteine that induce various toxicities, e.g. endothelial dysfunction and increased risk of thrombosis. Clinical manifestations of classic homocystinuria include ectopia lentis and/or severe myopia, skeletal abnormalities (marfanoid habitus, generalized osteoporosis and bone deformity), mental retardation, seizures, psychiatric and behavioral disorderts, venous and arterial thrombosis. Some patients with milder form of the disease can present only with thromboembolic events in adulthood. Diagnosis of classic homocystinuria should by established by biochemical (elevated plasma homocysteine and methionine and low cistathione) and genetic (homozygous and compound heterozygous mutations of CBS gene) tests. Low methionine diet, vitamin B6, folic acid and betaine anhydrous, a methylating agent, can be used to reduce homocysteine levels, to prevent progression of the homocystinuria and thromboembolic events.
经典同型半胱氨酸尿是一种罕见的常染色体隐性蛋氨酸代谢疾病,由参与同型半胱氨酸转硫的半胱氨酸-合成酶缺乏引起。这种疾病是由CBS基因突变引起的。酶的缺乏与同型半胱氨酸的积累有关,从而诱发各种毒性,例如内皮功能障碍和血栓形成风险增加。典型同型半胱氨酸尿的临床表现包括异位性晶状体和/或严重近视、骨骼异常(类马氏体质、全身性骨质疏松症和骨畸形)、智力低下、癫痫发作、精神和行为障碍、静脉和动脉血栓形成。一些病情较轻的患者在成年期只能出现血栓栓塞事件。典型同型半胱氨酸尿的诊断应通过生化检测(血浆同型半胱氨酸、蛋氨酸升高、顺胱甘肽水平降低)和遗传检测(CBS基因纯合和复合杂合突变)来确定。低蛋氨酸饮食、维生素B6、叶酸和无水甜菜碱(一种甲基化剂)可用于降低同型半胱氨酸水平,以防止同型半胱氨酸尿的进展和血栓栓塞事件。
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引用次数: 0
Cardio- and nephroprotective effects of antihypertensive therapy in nonadherent hypertensive patients 抗高血压治疗对非依从性高血压患者的心脏和肾保护作用
Pub Date : 2022-09-12 DOI: 10.32756/0869-5490-2022-3-16-21
S. Simenyura, Z. Sizova, N. N. Shindryaeva, A.V. Legoshina
To evaluate the impact of various regimens of antihypertensive treatment on blood pressure and target organs in nonadherent hypertensive patients.
目的:评价不同降压治疗方案对非黏附性高血压患者血压及靶器官的影响。
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引用次数: 0
Comparative efficacy of olokizumab and tocilizumab in hospitalized patients with COVID-19 olokizumab与tocilizumab在COVID-19住院患者中的比较疗效
Pub Date : 2022-09-12 DOI: 10.32756/0869-5490-2022-3-9-15
M. Brovko, P. Novikov, E. Nabatchikova, N. Bulanov, E. Tao, P. Potapov, L. Akulkina, N. Soloveva, S. Moiseev
To compare the efficacy of olokizumab and tocilizumab in reducing the risk of invasive mechanical ventilation or death in hospitalized patients with COVID-19.
比较olokizumab和tocilizumab在降低COVID-19住院患者有创机械通气或死亡风险方面的疗效。
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引用次数: 0
Venous congestion on the VExUS scale in patients with decompensated heart failure 失代偿性心力衰竭患者的静脉充血
Pub Date : 2022-06-04 DOI: 10.32756/0869-5490-2022-2-27-31
R. Aslanova, Z. Kobalava, A. Safarova, M. Vatsik-Gorodetskaya, V. Efimova, E. Cabello Montoya Flora, A. O. Kurlaeva, A. Abramov
Persistent venous congestion in patients with decompensated heart failure (DCHF) increases the risk of rehospitalization and death. VExUS protocol that evaluates the systemic hepatic-renal congestion in addition to assessing the inferior vena cava is regarded as a promising non-invasive ultrasound method to assess venous congestion in these patients.
失代偿性心力衰竭(DCHF)患者持续静脉充血增加再住院和死亡的风险。除了评估下腔静脉外,还评估全身性肝肾充血的VExUS方案被认为是一种有前途的无创超声方法来评估这些患者的静脉充血。
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引用次数: 0
Clinical and pharmacological features and place of irbesartan in the treatment of cardiovascular diseases 厄贝沙坦治疗心血管疾病的临床、药理特点及地位
Pub Date : 2022-06-04 DOI: 10.32756/0869-5490-2022-2-57-62
E. V. Rebrova, E. Shikh, A.Yu. Ryazanovа
Irbesartan belongs to a group of angiotensin II receptor blockers that are used worldwide for the treatment of patients with hypertension, type 2 diabetes, and impaired renal function. Irbesartan can be administered alone or in combination with other antihypertensive drugs (for example, hydrochlorothiazide), if blood pressure control cannot be achieved with monotherapy. The mechanism of action of Irbesartan is mainly due to the selective blockade of AT1 receptors and, as a consequence, a decrease in the vasopressor effect of angiotensin II. The review article summarizes pharmacokinetic and pharmacodynamic properties and clinical data on the tolerability and safety of Irbesartan.
厄贝沙坦属于血管紧张素II受体阻滞剂,在世界范围内用于治疗高血压、2型糖尿病和肾功能受损患者。如果单药不能控制血压,厄贝沙坦可单独使用或与其他降压药(如氢氯噻嗪)联合使用。厄贝沙坦的作用机制主要是由于选择性阻断AT1受体,从而降低血管紧张素II的血管加压作用。本文综述了厄贝沙坦的药代动力学和药效学特性以及耐受性和安全性的临床资料。
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Clinical pharmacology and therapy
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