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Nanomedicine: The Novel Weapon against Parasitic Infections 纳米医学:对抗寄生虫感染的新武器
Pub Date : 2020-11-29 DOI: 10.22037/NBM.V8I4.30416
M. Rahimi, Zahra Arab-Mazar, Sara Rahmati Roodsari
Due to the side effects of drugs and resistance to the used chemicals in the treatment of tropical diseases such as malaria, leishmaniosis, trypanosomiasis and Schistosomiasis, which millions of people around the world are infected, nowadays nanomedicine usage with the production of nanofibers and nanoparticles (nanopowders, nanocrystal or nanocluster). The particles with a diameter of less than 100 nanometers is considered as a special treatment in parasitic diseases1,2. Due to the intracellular nature of some parasites, their treatment is a major challenge for researchers to develop new drugs. Findings show that Chitosan nanoparticles and metals such as silver, gold, and metal oxides have a lethal or inhibitory effect on various parasites, including giardiasis, leishmaniosis, malaria, or toxoplasma and insect larvae1.  The effects of drug release from chitosan nanofibers have also been performed in various external and internal evaluations on lesions caused by Leishmania major and the therapeutic effect of gold and silver nanoparticles on malaria and their concomitant use with bioresonance waves on leishmaniasis2,4. The main purpose of using nanoparticles is to use it as a drug delivery system and to release the drug agent in order to affect the specific site. Recently, the use of particle systems such as nanomedicine as a physical tool to improve the pharmacokinetic properties of various types of drug molecules in vivo is being developed1,4. The endocytic pathway transfers nanoparticles to the site of pathogens. The breakdown of these substances by lysosomal enzymes releases drugs into the phagocytic or lysosomal vesicle, or this process is released into the cytoplasm by a diffusion phenomenon. Specific transmission depends on the physical and chemical nature of the molecules1. In recent years, the use of nanoparticles for the treatment of parasitic diseases has considered, although limited research has conducted in this regard (Table 1). Finally, it can be concluded that according to recent findings on the inhibitory and long-term effects of nanofibers and nanoparticles on different parasites with less side effects than conventional drugs, more effective and less side effects drugs can be developed. Useful vaccines have also been developed to control parasitic diseases.
由于在治疗疟疾、利什曼病、锥虫病和血吸虫病等热带疾病(全世界有数百万人感染这些疾病)时药物的副作用和对所用化学品的耐药性,目前纳米药物的使用伴随着纳米纤维和纳米颗粒(纳米粉末、纳米晶体或纳米团簇)的生产。直径小于100纳米的颗粒被认为是寄生虫病的特殊治疗方法1,2。由于一些寄生虫的细胞内性质,它们的治疗是研究人员开发新药的主要挑战。研究结果表明,壳聚糖纳米颗粒和金属如银、金和金属氧化物对多种寄生虫有致死或抑制作用,包括贾第虫病、利什曼病、疟疾、弓形虫和昆虫幼虫1。壳聚糖纳米纤维的药物释放作用也在各种外部和内部评估中进行了,包括对利什曼原虫引起的病变的影响,以及金和银纳米颗粒对疟疾的治疗效果,以及它们与生物共振波联合使用对利什曼原虫的治疗效果2,4。使用纳米颗粒的主要目的是将其用作药物传递系统,并释放药物制剂以影响特定部位。近年来,利用粒子系统(如纳米医学)作为一种物理工具来改善各种类型药物分子在体内的药代动力学特性正在得到发展。内吞途径将纳米颗粒转移到病原体的位置。这些物质被溶酶体酶分解,释放药物到吞噬细胞或溶酶体囊泡中,或者这个过程通过扩散现象释放到细胞质中。具体的传输取决于分子的物理和化学性质。近年来,虽然在这方面的研究有限,但已经考虑使用纳米颗粒治疗寄生虫病(表1)。最后,可以得出结论,根据最近纳米纤维和纳米颗粒对不同寄生虫的抑制和长期作用的研究结果,其副作用比常规药物小,可以开发出更有效、副作用更小的药物。还开发了控制寄生虫病的有用疫苗。
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引用次数: 1
Docetaxel Enhances the Expression of STING Protein in PC3 Cells, and cGAMP Attenuates this Effect 多西紫杉醇可增强PC3细胞中STING蛋白的表达,而cGAMP可减弱这一作用
Pub Date : 2020-11-29 DOI: 10.22037/NBM.V8I4.30845
Shaghayegh Salimi, M. Rezaei, Z. Mousavi, Roya Atabakhshian, R. Pouriran, S. Ziai
Background: The stimulator of interferon genes (STING) agonist (cGAMP) kills the cancer cells through the activation of the innate immune system. PC3 cells are high in BTK and low in STING. In this study, the effect of adding STING agonist, cGAMP, to docetaxel investigated. Materials and Methods: PC3 cells were treated with docetaxel, cGAMP, and a combination of the docetaxel and cGAMP. Cell toxicity was evaluated by MTT assay, and changes of STING, IRF3, BTK, and DDX41 genes’ expression were quantified by the real-time PCR. STING protein was also detected by Western blotting. Results: The IC50 of docetaxel was 31.1 nM, and cGAMP did not change it significantly but decreased docetaxel toxicity about 30%. Docetaxel increased IRF3, BTK, and DDX41 gene expression significantly, and STING protein about 5 folds. By adding cGAMP to docetaxel STING, IRF3, and BTK, expression decreased several folds. Conclusion: In this in vitro study, cGAMP potentiated docetaxel’s effects and alleviated it.
背景:干扰素基因刺激剂(STING)激动剂(cGAMP)通过激活先天免疫系统杀死癌细胞。PC3细胞BTK水平高,STING水平低。本研究考察了在多西紫杉醇中加入STING激动剂cGAMP的作用。材料与方法:采用多西他赛、cGAMP、多西他赛与cGAMP联合治疗PC3细胞。MTT法检测细胞毒性,real-time PCR法检测STING、IRF3、BTK、DDX41基因表达变化。Western blotting检测STING蛋白。结果:多西紫杉醇IC50为31.1 nM, cGAMP对其无明显影响,但可使多西紫杉醇毒性降低30%左右。多西紫杉醇显著提高IRF3、BTK、DDX41基因和STING蛋白的表达量约5倍。在多西他赛STING、IRF3和BTK中加入cGAMP,其表达降低数倍。结论:在体外实验中,cGAMP可增强或减轻多西他赛的作用。
{"title":"Docetaxel Enhances the Expression of STING Protein in PC3 Cells, and cGAMP Attenuates this Effect","authors":"Shaghayegh Salimi, M. Rezaei, Z. Mousavi, Roya Atabakhshian, R. Pouriran, S. Ziai","doi":"10.22037/NBM.V8I4.30845","DOIUrl":"https://doi.org/10.22037/NBM.V8I4.30845","url":null,"abstract":"Background: The stimulator of interferon genes (STING) agonist (cGAMP) kills the cancer cells through the activation of the innate immune system. PC3 cells are high in BTK and low in STING. In this study, the effect of adding STING agonist, cGAMP, to docetaxel investigated. \u0000Materials and Methods: PC3 cells were treated with docetaxel, cGAMP, and a combination of the docetaxel and cGAMP. Cell toxicity was evaluated by MTT assay, and changes of STING, IRF3, BTK, and DDX41 genes’ expression were quantified by the real-time PCR. STING protein was also detected by Western blotting. \u0000Results: The IC50 of docetaxel was 31.1 nM, and cGAMP did not change it significantly but decreased docetaxel toxicity about 30%. Docetaxel increased IRF3, BTK, and DDX41 gene expression significantly, and STING protein about 5 folds. By adding cGAMP to docetaxel STING, IRF3, and BTK, expression decreased several folds. \u0000Conclusion: In this in vitro study, cGAMP potentiated docetaxel’s effects and alleviated it.","PeriodicalId":19372,"journal":{"name":"Novelty in Biomedicine","volume":"19 1","pages":"196-204"},"PeriodicalIF":0.0,"publicationDate":"2020-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85286060","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
Evaluation of Beclin1 Effect on Apoptosis in Mouse Infected with Street Rabies Virus Beclin1对街头狂犬病毒感染小鼠细胞凋亡的影响
Pub Date : 2020-11-02 DOI: 10.22037/NBM.V1I1.32599
Homeira Prizad, M. Fazeli, M. Mahmoudi, Alireza Jananni, F. Sheikholeslami
Background: Apoptosis is a programmed cell death in which certain cellular components are packed into small membrane vacuoles by immune cells. Different strains of rabies virus (RABV) have their own biological features, but their effects on apoptosis have been little known. The aim of current research was to evaluate Beclin 1 effect on apoptosis in the mouse infected with the street rabies virus. Materials and Methods: Exogenous Beclin1 overexpressed by the pIRES2-EGFP-Beclin1 vector in the cortex of NMRI mice. To evaluate the apoptosis, TUNEL assay was done on brain tissues of the rabid mice. Results: TUNEL assay data showed that small apoptotic cells were seen in the four groups that received the vector alone or with the SRABV, but no significant changes were observed. There are no signs of apoptosis in mouse normal brain cells. Conclusion: It was previously proven that overexpression of exogenous Beclin1 could induce autophagy but this study showed that overexpression of Beclin 1 does not cause apoptosis in rabies-infected cells.
背景:细胞凋亡是一种程序性细胞死亡,其中某些细胞成分被免疫细胞装入小的膜泡中。不同毒株的狂犬病毒(RABV)具有各自的生物学特性,但其对细胞凋亡的影响尚不清楚。本研究旨在探讨Beclin - 1对街头狂犬病毒感染小鼠细胞凋亡的影响。材料与方法:外源性Beclin1通过pIRES2-EGFP-Beclin1载体在NMRI小鼠皮层过表达。采用TUNEL法观察小鼠脑组织的凋亡情况。结果:TUNEL实验数据显示,单独或与SRABV联合转染四组均可见小细胞凋亡,但未见明显变化。小鼠正常脑细胞无凋亡迹象。结论:先前已证实外源性Beclin1过表达可诱导自噬,但本研究表明Beclin1过表达不会引起狂犬病感染细胞凋亡。
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引用次数: 0
Evaluation of Efficacy of Neuro Muscular Electrical Stimulation and Electro Acupuncture in Improving the Pain and Disability in Patients with the Lumbar Degenerative Intervertebral Disk Disease 神经肌肉电刺激与电针治疗腰椎退行性椎间盘病患者疼痛和残疾的疗效评价
Pub Date : 2020-06-21 DOI: 10.22037/NBM.V1I1.29082
Zeinab Faraji Qomi, Shahin Salehi, O. Hesami, Mehrshad Poorsaed Esfahani, Amir Hosein Abedi Yekta, M. Hassabi, M. Sohrabi, M. Elahi
Background: Chronic low back pain (CLBP) due to the degenerative intervertebral disk diseases is one of the most common musculoskeletal conditions in contemporary societies. A variety of pharmacological, non-pharmacological and surgical options is available for treatment of CLBP. The use of non-pharmacological methods have drastically increased in recent years, offering fewer complications and expenses. This study was conducted to compare the efficacy of the neuromuscular electrical stimulation (NMES) and electro acupuncture (EAP) with exercise therapy alone in patients with chronic low back pain. Materials and Methods: This was a randomized case-controlled clinical trial. Sixty patients with CLBP were randomly assigned to 3 groups (20 cases each) of the EAP with exercise therapy, NMES with exercise therapy, and exercise therapy only. Severity of pain and disability improvement were assessed using the visual analog scale (VAS) and Quebec back pain disability scale respectively. Results: A total of 66 individuals were enrolled, out of which 6 were excluded due to patients’ lack of cooperation. A significant decline in the amounts of Quebec and VAS was observed in the three groups ( p <0.001). The pain and disability improvements did not display any significant difference in the NMES or EAP groups compared to the control group. However, the severity of disability and pain in the NMES group were significantly higher than the EAP group ( p <0.05). Conclusion: These findings may indicate an almost identical efficacy of exercise therapy alone compared to the combination with electrical stimulation techniques in improving the pain and disability in patients suffering CLBP.
背景:由退变性椎间盘疾病引起的慢性腰痛(CLBP)是当代社会最常见的肌肉骨骼疾病之一。多种药物,非药物和手术选择可用于治疗CLBP。近年来,非药物方法的使用急剧增加,并发症和费用减少。本研究旨在比较神经肌肉电刺激(NMES)和电针(EAP)与单纯运动疗法对慢性腰痛患者的疗效。材料与方法:这是一项随机病例对照临床试验。将60例CLBP患者随机分为EAP联合运动治疗组、NMES联合运动治疗组和仅运动治疗组,每组20例。分别采用视觉模拟量表(VAS)和魁北克背痛残疾量表评估疼痛严重程度和残疾改善程度。结果:共纳入66人,其中6人因患者不配合被排除。三组患者的Quebec评分和VAS评分均显著下降(p <0.001)。与对照组相比,NMES组和EAP组的疼痛和残疾改善没有显示出任何显著差异。而NMES组的残疾程度和疼痛程度均显著高于EAP组(p <0.05)。结论:这些发现可能表明,在改善CLBP患者的疼痛和残疾方面,单独运动疗法与联合电刺激技术的疗效几乎相同。
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引用次数: 0
Effects of low level laser therapy on mucositis in patients under chemotherapy and bone marrow transplantation 低水平激光治疗化疗合并骨髓移植患者黏膜炎的疗效观察
Pub Date : 2020-06-16 DOI: 10.22037/NBM.V1I1.27532
A. Tavakoli, M. Tabarraee, F. Tabeie, M. Mehdizadeh, M. Ghadiani, Leila Izadi Masoole
Background: Oral mucositis is among the most important adverse effects of chemotherapy and bone marrow transplantation and prevention from this side effect is important to improve the situations in patients. Hence, in this study the main aim was to determine the effects of low-level laser therapy on mucositis in patients under chemotherapy and bone marrow transplantation. Materials and Methods: In this randomized controlled clinical trial, 60 consecutive patients under chemotherapy and bone marrow transplantation in a training hospital in 2018 were enrolled and randomly assigned to receive either low-level laser therapy (630 and 780 nm) or off-laser. Finally, the frequency rate and severity of mucositis (grades 0 to 4 according to WHO severity index) were determined and compared across the groups. Results: Mucositis was present in 30% and 56.7% in laser and control groups, respectively with statistically significant difference (p=0.037). The severity of mucositis was same across the laser and control groups (p=0.785). Conclusion: Low-level laser therapy is an effective modality for preventing from mucositis in patients treated by chemotherapy and bone marrow transplantation. Accordingly, utilization of this safe and effective therapeutic method is recommended.
背景:口腔黏膜炎是化疗和骨髓移植最重要的不良反应之一,预防这一副作用对改善患者的情况很重要。因此,本研究的主要目的是确定低水平激光治疗对化疗和骨髓移植患者粘膜炎的影响。材料与方法:随机对照临床试验,选取某培训医院2018年连续接受化疗和骨髓移植的患者60例,随机分为低水平激光治疗组(630和780 nm)和非激光治疗组。最后,确定并比较各组粘膜炎的发生率和严重程度(根据WHO严重程度指数分为0至4级)。结果:激光组黏膜炎发生率为30%,对照组为56.7%,差异有统计学意义(p=0.037)。激光组与对照组的黏膜炎严重程度相同(p=0.785)。结论:低水平激光治疗是预防化疗和骨髓移植患者发生黏膜炎的有效方式。因此,建议使用这种安全有效的治疗方法。
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引用次数: 0
Evaluation of Pregnancy Outcomes in Iranian Women with Uterine Myomas 伊朗子宫肌瘤妇女妊娠结局的评价
Pub Date : 2020-06-16 DOI: 10.22037/NBM.V8I3.29806
Masoumeh Mirzamoradi, Masoumeh Aslanpour, Mina Bakhtiari, R. Jamali, M. Jamali
Background: To investigate the impacts of myomas on the outcomes of pregnancy in Iranian pregnant women with uterine fibroids. Materials and Methods: In this retrospective cohort study, the consequences of myomas on pregnancy were investigated in Iranian pregnant women referred to the perinatology clinic of Mahdieh Hospital (Tehran, Iran). One-hundred and sixty pregnant women diagnosed with uterine myoma were enrolled in the study as the case group. The control group consisted of 160 pregnant women without fibroma. The characteristics of the myomas and their relationships with pregnancy outcomes were surveyed. Results: Non-cephalic presentation, preterm labor, and Cesarean delivery were significantly higher in the case group in comparison with the control group. 106 patients (66.7%) had myomas larger than 5 cm in diameter. Intramural fibroids were seen in 132 (83%) patients. In addition, 133 (83.6%) patients had myomas in the body (corpus) of the uterus. Considering the number of myomas, 124 (78%) patients revealed one myoma in uterus. Uterine myomas during pregnancy rendered an important risk factor for cesarean delivery, breech presentation, and preterm delivery. However, there were no significant correlations between uterine myomas and IUGR, premature membranes rupture, either abortion or bleeding in the first trimester, low birth weight, and severe postpartum bleeding. Conclusion: Our results showed that the presence of myoma could modulate pregnancy outcomes. Our results can be useful in improving the quality of prenatal care and education.
背景:探讨子宫肌瘤对伊朗妊娠合并子宫肌瘤妇女妊娠结局的影响。材料和方法:在这项回顾性队列研究中,研究了在Mahdieh医院(伊朗德黑兰)围产期诊所就诊的伊朗孕妇中子宫肌瘤对妊娠的影响。160名被诊断患有子宫肌瘤的孕妇作为病例组参加了这项研究。对照组为160名未患纤维瘤的孕妇。探讨子宫肌瘤的特点及其与妊娠结局的关系。结果:与对照组相比,病例组的非头位表现、早产和剖宫产明显增加。106例(66.7%)肌瘤直径大于5cm。132例(83%)患者可见壁内肌瘤。此外,133例(83.6%)患者在子宫体(体)有肌瘤。考虑到子宫肌瘤的数量,124例(78%)患者发现子宫肌瘤1例。妊娠期子宫肌瘤是剖宫产、臀位分娩和早产的重要危险因素。然而,子宫肌瘤与IUGR、胎膜早破、妊娠早期流产或出血、低出生体重和严重产后出血之间无显著相关性。结论:我们的研究结果表明肌瘤的存在可以调节妊娠结局。我们的研究结果对提高产前护理和教育质量有一定的参考价值。
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引用次数: 1
Daclatasvir/Sofosbuvir versus Ledipasvir/Sofosbuvir in Patients with Hepatitis C Virus Infection Genotypes 1 and 3 Daclatasvir/Sofosbuvir与Ledipasvir/Sofosbuvir对基因型1和3型丙型肝炎病毒感染患者的影响
Pub Date : 2020-06-16 DOI: 10.22037/NBM.V1I1.29735
Narjes Shokatpour, S. Sali, Ali Khahanipour, Sara Abolghasemi, M. Shabani
Background: The new direct-acting antiviral agents (DAAs) with high efficacy, low resistance, and low rate of adverse events (AEs) have shown promising outcomes for hepatitis C virus (HCV) treatment. This study assessed the efficacy and safety of Daclatasvir/Sofosbuvir (DCV/SOF) compared to Ledipasvir/Sofosbuvir (LDV/SOF) in patients with HCV infection in the real-world setting in Iran. Materials and Methods: A total of 42 patients with HCV infection were treated with either LDV/SOF (genotype 1) or DCV/SOF (genotypes 1, 3 or unknown) with or without ribavirin (RBV). Assessment of risk factors, laboratory tests, sustained virologic response at post-treatment week 12 (SVR12), and AEs were performed. Results: The highest risk factor for HCV transmission was major surgery (50.0%), followed by tattooing (40.5%), phlebotomy (40.5%), and dental surgery (40.5%). No statistically significant relationships between genotypes and risk factors were observed. In both treatment groups (LDV/SOF and DCV/SOF), all of the patients (100%) with or without cirrhosis and treatment-experience achieved SVR12. One patient with a history of failed LDV/SOF therapy achieved SVR12 following retreatment with DCV/SOF. Both treatment regimens were well-tolerated. No serious AEs or discontinuation due to AEs was observed. The most common AE across both treatment groups were fatigue (42.9%), followed by anxiety (28.6%). Numerically, more adverse events were found with the LDV/SOF regimen than with the DCV/SOF regimen. Conclusion: Our study showed an excellent safety and efficacy of DCV/SOF and LDV/SOF in Iranian patients infected with HCV. The incidence of AEs among patients treated with LDV/SOF was higher than those receiving SOF/DCV.
背景:新型直接作用抗病毒药物(DAAs)具有高效、低耐药和低不良事件发生率(ae),在丙型肝炎病毒(HCV)治疗中显示出良好的结果。本研究评估了Daclatasvir/Sofosbuvir (DCV/SOF)与Ledipasvir/Sofosbuvir (LDV/SOF)在伊朗HCV感染患者中的疗效和安全性。材料与方法:42例HCV感染患者分别用利巴韦林(RBV)治疗LDV/SOF(基因型1)或DCV/SOF(基因型1、3或未知)。评估危险因素、实验室检测、治疗后第12周的持续病毒学反应(SVR12)和ae。结果:HCV传播的最高危险因素是大手术(50.0%),其次是纹身(40.5%)、静脉切开(40.5%)和牙科手术(40.5%)。基因型与危险因素之间无统计学意义的关系。在两个治疗组(LDV/SOF和DCV/SOF)中,所有有或没有肝硬化和治疗经验的患者(100%)都达到了SVR12。1例LDV/SOF治疗失败的患者在再次接受DCV/SOF治疗后达到了SVR12。两种治疗方案的耐受性都很好。未观察到严重不良反应或因不良反应而停药。两个治疗组中最常见的AE是疲劳(42.9%),其次是焦虑(28.6%)。数值上,LDV/SOF方案比DCV/SOF方案发现了更多的不良事件。结论:本研究显示,DCV/SOF和LDV/SOF治疗伊朗HCV患者具有良好的安全性和有效性。LDV/SOF组的ae发生率高于SOF/DCV组。
{"title":"Daclatasvir/Sofosbuvir versus Ledipasvir/Sofosbuvir in Patients with Hepatitis C Virus Infection Genotypes 1 and 3","authors":"Narjes Shokatpour, S. Sali, Ali Khahanipour, Sara Abolghasemi, M. Shabani","doi":"10.22037/NBM.V1I1.29735","DOIUrl":"https://doi.org/10.22037/NBM.V1I1.29735","url":null,"abstract":"Background: The new direct-acting antiviral agents (DAAs) with high efficacy, low resistance, and low rate of adverse events (AEs) have shown promising outcomes for hepatitis C virus (HCV) treatment. This study assessed the efficacy and safety of Daclatasvir/Sofosbuvir (DCV/SOF) compared to Ledipasvir/Sofosbuvir (LDV/SOF) in patients with HCV infection in the real-world setting in Iran. \u0000Materials and Methods: A total of 42 patients with HCV infection were treated with either LDV/SOF (genotype 1) or DCV/SOF (genotypes 1, 3 or unknown) with or without ribavirin (RBV). Assessment of risk factors, laboratory tests, sustained virologic response at post-treatment week 12 (SVR12), and AEs were performed. \u0000Results: The highest risk factor for HCV transmission was major surgery (50.0%), followed by tattooing (40.5%), phlebotomy (40.5%), and dental surgery (40.5%). No statistically significant relationships between genotypes and risk factors were observed. In both treatment groups (LDV/SOF and DCV/SOF), all of the patients (100%) with or without cirrhosis and treatment-experience achieved SVR12. One patient with a history of failed LDV/SOF therapy achieved SVR12 following retreatment with DCV/SOF. Both treatment regimens were well-tolerated. No serious AEs or discontinuation due to AEs was observed. The most common AE across both treatment groups were fatigue (42.9%), followed by anxiety (28.6%). Numerically, more adverse events were found with the LDV/SOF regimen than with the DCV/SOF regimen. \u0000Conclusion: Our study showed an excellent safety and efficacy of DCV/SOF and LDV/SOF in Iranian patients infected with HCV. The incidence of AEs among patients treated with LDV/SOF was higher than those receiving SOF/DCV.","PeriodicalId":19372,"journal":{"name":"Novelty in Biomedicine","volume":"21 1","pages":"171-181"},"PeriodicalIF":0.0,"publicationDate":"2020-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80043987","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
Comparison of efficacy between manipulation and exercise therapy in the treatment of patients with Sacroiliac joint dysfunction: A randomized clinical trial 手法与运动疗法治疗骶髂关节功能障碍的疗效比较:一项随机临床试验
Pub Date : 2020-06-16 DOI: 10.22037/NBM.V1I1.26180
D. Elyaspour, R. Nikray, F. Nouri, J. Hashemi
Background: Sacroiliac joint dysfunction is one of the main sources of lower back pain affects 16-30% of these patients. Various treatments had proposed for subluxation and sacroiliac syndrome but the current evidence on this subject is not confirmatory and few surveys have assessed the efficacy of manipulation in the treatment of this condition. The present study aimed to compare the efficacy of manipulation with exercise therapy in patients with sacroiliac pain syndrome. Materials and Methods: In this single-blinded clinical trial, the 30 patients categorized (to two groups) to receive either manipulation or exercise therapy. Required data gathered via medical history and the Persian translation of the Beck and Oswestry questionnaires and the pain assessed according to the visual analogue scale (VAS). Data entered into SPSS v.22 software for analysis. Results: Changes in VAS (p=0.011) and Oswestry score (p=0.012) after one week were significantly greater in the manipulation group. In addition, changes in the Oswestry disability index (ODI) score in the manipulation group of one week and one month after treatment were significantly different from the pre-treatment. Conclusion: Based on the findings of this survey, manipulation had a better efficacy on pain severity and disability of patients with sacroiliac pain syndrome, compared to exercise therapy and considering its low risks and non-invasiveness, its application by trained physicians recommended.
背景:骶髂关节功能障碍是16-30%的患者腰痛的主要原因之一。对于半脱位和骶髂综合征,已经提出了多种治疗方法,但目前关于该主题的证据尚不确定,并且很少有调查评估手法治疗该病症的疗效。本研究旨在比较手法与运动疗法对骶髂疼痛综合征患者的疗效。材料和方法:在这项单盲临床试验中,30名患者分为两组,接受手法治疗或运动治疗。通过病史和Beck和Oswestry问卷的波斯语翻译收集所需数据,并根据视觉模拟量表(VAS)评估疼痛。数据输入SPSS v.22软件进行分析。结果:手法组1周后VAS评分(p=0.011)和Oswestry评分(p=0.012)变化显著大于手法组。此外,手法组在治疗后1周和1个月的Oswestry残疾指数(ODI)评分变化与治疗前有显著差异。结论:根据本调查结果,手法治疗对骶髂疼痛综合征患者的疼痛程度和残疾程度的改善效果优于运动治疗,考虑到其低风险和无创性,建议由经过培训的医师应用。
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引用次数: 0
Twin in compared with singleton pregnancies complicated by Preterm premature rupture of membranes (PPROM) 双胎妊娠合并胎膜早破(PPROM)的比较
Pub Date : 2020-06-16 DOI: 10.22037/NBM.V1I1.24855
Masoumeh Mirzamoradi, Maral Baleshi, N. Rahmati, V. Hazari, M. Daraei, Z. Heidar
Background: Our purpose was to compare the latency periods of preterm premature rupture of the membranes (PPROM) in twin compared with singleton pregnancies from 24 to 34 weeks' gestation and assessment of respiratory distress syndrome (RDS) between twins and singletons. Materials and Methods: Between 2010 and 2014 in Mahdieh Hospital, Tehran, Iran, data on all women with singleton and twin gestations complicated by PPROM were reviewed. Latencies between singleton and twin pregnancies were compared. An additional comparing according to PPROM at under, equal and above 30 weeks' gestation was surveyed in these groups. In addition, their latencies compared among them. Use of surfactant consumption and need for intubation were measured during hospitalization between twins and singletons. Results: The mean latencies of singleton and twin pregnancies were statistically significant without comparing the gestational age at PPROM (8.22±7.4 vs. 5.54±3.36 days, p=0.001). When PPROM occurred at or = 30 weeks' gestation, latency was significantly different in singleton and twin pregnancies (6.3±5.85 vs. 2.42±2.60 days, p=0.002). There were significant differences in the use of surfactant and intubation between twin and singletons (p<0.05). Conclusion: This study provides the basis for effective patient counseling and managing pregnancies with PPROM. Overall, in pregnancies with PPROM at > or = 30 weeks' gestation, latency in twins was significantly shorter than in singleton pregnancies. For fetal lung maturity, the use of surfactant and intubation increased in twins compared with singletons.
背景:我们的目的是比较24 ~ 34周双胞胎与单胎妊娠的胎膜早破(PPROM)潜伏期,以及双胞胎与单胎妊娠呼吸窘迫综合征(RDS)的评估。材料和方法:回顾2010 - 2014年伊朗德黑兰Mahdieh医院所有单胎和双胎合并PPROM的妇女的资料。比较单胎和双胎妊娠的潜伏期。另外比较各组妊娠30周以下、30周及30周以上的PPROM。此外,对它们的延迟进行了比较。在双胞胎和单胎住院期间测量表面活性剂用量和插管需求。结果:单胎妊娠和双胎妊娠的平均潜伏期(8.22±7.4天比5.54±3.36天,p=0.001)差异有统计学意义。当PPROM发生在妊娠30周或= 30周时,单胎妊娠和双胎妊娠的潜伏期有显著差异(6.3±5.85天和2.42±2.60天,p=0.002)。双胎和单胎在表面活性剂和插管的使用上有显著差异(p = 30周妊娠),双胞胎的潜伏期明显短于单胎妊娠。对于胎儿肺成熟度,使用表面活性剂和插管在双胞胎比单胎增加。
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引用次数: 0
The Effect of Epoetin Alfa and Sodium Valproate in patients with Myelodysplastic Syndrome 肾上腺素和丙戊酸钠在骨髓增生异常综合征患者中的作用
Pub Date : 2020-06-16 DOI: 10.22037/NBM.V1I1.27537
Seyed Ashkan Hosseini, M. Tabarraee, M. Ghadiani
Background: Myelodysplastic syndrome (MDS) is an important precancerous disease leading to blood malignancies. Prompt diagnosis and treatment would result in better outcome in patients. Purpose of the study was to determine the effect of Epoetin Alfa and Sodium Valproate in patients with MDS. Materials and Methods: In this interventional quasi-experimental study, 50 consecutive patients with MDS from Taleghani Hospital (Tehran, Iran) in 2016-2017 were enrolled. They underwent treatment for eight months with 10000 units per month from Epoetin Alfa plus 200 mg TDS from Sodium Valproate. The hematological response was determined according to the hemoglobin, platelet, and neutrophil. Results: Hematological response was present in 68%. The packed cell treatment were decreased significantly (P=0.040) and 56% of patients had no receipt of packed cells after treatment. Conclusion: It is concluded that Epoetin Alfa plus Sodium Valproate was effective in treatment of patients with Myelodysplastic syndrome and use of this combination therapy is recommended.
背景:骨髓增生异常综合征(MDS)是一种重要的导致血液恶性肿瘤的癌前病变。及时诊断和治疗可使患者获得较好的预后。本研究的目的是确定促生成素和丙戊酸钠在MDS患者中的作用。材料与方法:在这项介入性准实验研究中,入组了2016-2017年来自伊朗德黑兰Taleghani医院的50例MDS患者。他们接受了8个月的治疗,每月10000单位的促生成素加上200毫克的丙戊酸钠TDS。根据血红蛋白、血小板和中性粒细胞测定血液学反应。结果:68%的患者出现血液学反应。填充细胞治疗明显减少(P=0.040), 56%的患者治疗后没有收到填充细胞。结论:促生成素联合丙戊酸钠治疗骨髓增生异常综合征是有效的,推荐使用该联合疗法。
{"title":"The Effect of Epoetin Alfa and Sodium Valproate in patients with Myelodysplastic Syndrome","authors":"Seyed Ashkan Hosseini, M. Tabarraee, M. Ghadiani","doi":"10.22037/NBM.V1I1.27537","DOIUrl":"https://doi.org/10.22037/NBM.V1I1.27537","url":null,"abstract":"Background: Myelodysplastic syndrome (MDS) is an important precancerous disease leading to blood malignancies. Prompt diagnosis and treatment would result in better outcome in patients. Purpose of the study was to determine the effect of Epoetin Alfa and Sodium Valproate in patients with MDS. Materials and Methods: In this interventional quasi-experimental study, 50 consecutive patients with MDS from Taleghani Hospital (Tehran, Iran) in 2016-2017 were enrolled. They underwent treatment for eight months with 10000 units per month from Epoetin Alfa plus 200 mg TDS from Sodium Valproate. The hematological response was determined according to the hemoglobin, platelet, and neutrophil. Results: Hematological response was present in 68%. The packed cell treatment were decreased significantly (P=0.040) and 56% of patients had no receipt of packed cells after treatment. Conclusion: It is concluded that Epoetin Alfa plus Sodium Valproate was effective in treatment of patients with Myelodysplastic syndrome and use of this combination therapy is recommended.","PeriodicalId":19372,"journal":{"name":"Novelty in Biomedicine","volume":"60 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2020-06-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87758096","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
期刊
Novelty in Biomedicine
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