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Detection of DNA damage by SCD and Rate of Apoptosis DNA by Gel Electrophoresis among infertile males SCD检测不育男性DNA损伤及凝胶电泳检测DNA凋亡率
Pub Date : 2022-08-25 DOI: 10.21608/jbaar.2022.256197
N. Eskarous, Sobhy Hassab El-Nabi, M. A. Abd El Salam, K. Geba, S. G. GamalEl Din
: Background: DNA damage as Fragmentation has adverse effects on fertilization and embryo development, so it is one of the main causes of a male factor for infertility. Several techniques have been mentioned to elevation this damage. In our study, we determine DNA damage in human spermatozoa by sperm chromatin dispersion (SCD) method and Apoptosis of DNA in human spermatozoa by Optical density in gel electrophoresis in male infertility. Objects and Methods: Semen samples were collected from 100 men and were analyzed by standard light microscopic according to the World Organization (5 th edition) for diagnostic fertility. Furthermore, Sperm DNA damage was determined by using Halosperm Kit, then assessment apoptosis by optical density in Gel Electrophoresis. Results : The mean value of DNA by SCD method in infertile males increased with a value of 47.95±10.96 % when compared with the control value of 21.2 ±2.64 % with (p< 0.00001). On the other hand, the mean value of DNA by measurement of Optical density in Gel Electrophoresis in infertile males decreased with a value of 120.27±18.73 when compare with the control value of 144.4±45 with (p =0.833). Conclusion: by SCD method and other methods for detection of DNA apoptosis by gel electrophoresis addition to routine semen analysis play important role in the diagnosis and management of male infertility.
背景:DNA断裂损伤对受精和胚胎发育有不利影响,是导致男性不育的主要因素之一。已经提到了几种提高这种伤害的技术。在我们的研究中,我们用精子染色质分散(SCD)法和光密度凝胶电泳法测定男性不育症的人精子DNA损伤和DNA凋亡。目的与方法:收集100例男性精液,按照世界生育诊断组织(第5版)标准光镜分析。采用halsperm Kit检测精子DNA损伤,凝胶电泳光密度法检测细胞凋亡。结果:SCD法测定不育男性DNA的平均值为47.95±10.96%,高于对照组的21.2±2.64% (p< 0.00001)。另一方面,通过凝胶电泳光密度测量,不育雄性的DNA平均值为120.27±18.73,低于对照组的144.4±45 (p =0.833)。结论:SCD法及其他方法在精液常规分析的基础上进行DNA凋亡的凝胶电泳检测,对男性不育症的诊断和治疗具有重要意义。
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引用次数: 0
Antimicrobial activity of Lactobacillus acidophilus against pathogenic Escherichia coli isolated from diarrhea patients 嗜酸乳杆菌对腹泻致病性大肠杆菌的抑菌活性研究
Pub Date : 2022-08-22 DOI: 10.21608/jbaar.2022.255697
F. Kadhum
Lactobacillus acidophilus represents a probiotic bacterium that may be found in the mouth, gut, and vaginal canal. Lactobacillus acidophillus may help to relieve diarrhea, bloating, and cramps caused by bacteria that may cause everything from diarrhea to life-threatening colon inflammation. Escherichia coli (hencefourth E. Coil ) bacteria are found in healthy people's intestines as natural flora. Only a very small percentage, like the E. coli O157:H7 variety, can lead to severe stomach discomfort, bloody diarrhea, and vomiting; the rest of the E. coli variety is harmless.
嗜酸乳杆菌是一种益生菌,可在口腔、肠道和阴道中发现。嗜酸乳杆菌可能有助于缓解由细菌引起的腹泻、腹胀和痉挛,这些细菌可能导致从腹泻到危及生命的结肠炎症等各种疾病。大肠杆菌(以下简称大肠杆菌)是存在于健康人肠道中的天然菌群。只有非常小的比例,如大肠杆菌O157:H7品种,会导致严重的胃部不适,血性腹泻和呕吐;其余的大肠杆菌品种是无害的。
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引用次数: 0
Genetic study of I kappa B alpha gene promoter polymorphism associated with hepatitis C virus in Egyptian patients 埃及丙型肝炎病毒患者I κ B α基因启动子多态性的遗传学研究
Pub Date : 2022-08-20 DOI: 10.21608/jbaar.2022.255496
Mamoun Ghazalah, Sameer El-Masry, I. Helmy, Ehab Abd-Elkhalek
Background: Host genetic polymorphism is one of the major unalterable major factors for HCV infection, NF-κB proteins play multiple roles in immune response and involve in HCV infection and progression. Aim of the study: To investigate the associations between single nucleotide polymorphism (SNPs) in NF-Kb and the susceptibility as well as resolution of HCV infection. Patients and Methods: This prospective case-control study was conducted at the physical examination center on 150 Egyptian population, including 50 uninfected control cases, 50 cases with spontaneous viral clearance, and 50 cases with persistent HCV infection, they are genotyped for four SNPs (rs11820062, rs230530, rs1056890 and rs3774963) using a Taq Man assay. Results: The current study revealed that the mutation in rs_11820062 of the I kappa B alpha gene significantly increased the risk for HCV infection with a p-value <0.05. Conclusion: This study revealed that genetic variants of the NF-κB pathway genes (rs11820062 T allele) are associated with an increased risk of HCV susceptibility. light polypeptide gene enhancer
背景:宿主基因多态性是HCV感染的主要不可改变的主要因素之一,NF-κB蛋白在免疫应答中发挥多重作用,参与HCV感染和进展。研究目的:探讨NF-Kb单核苷酸多态性(snp)与HCV感染的易感性和消退之间的关系。患者和方法:本前瞻性病例对照研究在体检中心对150名埃及人群进行了研究,其中包括50例未感染的对照病例、50例自发性病毒清除病例和50例持续性HCV感染病例,采用Taq Man法对4个snp (rs11820062、rs230530、rs1056890和rs3774963)进行基因分型。结果:本研究发现I κ B α基因rs_11820062突变显著增加HCV感染的风险,p值<0.05。结论:本研究揭示NF-κB通路基因(rs11820062 T等位基因)的遗传变异与HCV易感性增加相关。轻型多肽基因增强子
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引用次数: 0
Stem cell therapy in renal diseases 肾脏疾病的干细胞治疗
Pub Date : 2022-08-20 DOI: 10.21608/jbaar.2022.255500
Khalil Alhalfawy, Bahgat A. Elfiky, A. Zahran, Z. Kasemy, Mahmoud Zayed
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引用次数: 0
Evaluation of Adiponectin hormone and some biochemical parameters with unstable angina and acute myocardial infarction patients 不稳定型心绞痛及急性心肌梗死患者脂联素激素及相关生化指标的评价
Pub Date : 2022-07-28 DOI: 10.21608/jbaar.2022.251726
Alyaa Majid, Ş. Adem, Anwer Kadhim
The acute coronary syndromes [unstable angina (UA) and acute myocardial infarction (AMI)] are more dangerous than other ischemic heart diseases (IHD) due to acute morphological changes in atherosclerotic plaques which cause (acute ischemia) severe imbalance between myocardium demand and oxygen supply. In this study we investigated adiponectin hormone, creatine kinase(CK), lactate dehydrogenase(LDH), malondialdehyde(MDA), nitric oxide(NO), superoxide dismutase(SOD), and glutathione(GSH) in patients with unstable angina and acute myocardial infarction, This study has been carried out on 100 patients with unstable angina and acute myocardial infarction and 50 healthy subjects. the study shows that there is a significant difference in the concentration of serum Adiponectin, CK, LDH, MDA, NO, SOD, and GSH between (controls, AMI and UA ) in the (male and female ) groups (p≤0.05).
急性冠状动脉综合征[不稳定心绞痛(UA)和急性心肌梗死(AMI)]比其他缺血性心脏病(IHD)更危险,因为动脉粥样硬化斑块的急性形态学改变导致(急性缺血)心肌需氧量和供氧量严重失衡。本研究对不稳定型心绞痛合并急性心肌梗死患者进行了脂联素、肌酸激酶(CK)、乳酸脱氢酶(LDH)、丙二醛(MDA)、一氧化氮(NO)、超氧化物歧化酶(SOD)和谷胱甘肽(GSH)等激素的测定,并对100例不稳定型心绞痛合并急性心肌梗死患者和50例健康受试者进行了研究。研究表明,(男性和女性)各组(对照组、AMI组和UA组)血清脂联素、CK、LDH、MDA、NO、SOD、GSH浓度差异有统计学意义(p≤0.05)。
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引用次数: 0
Biochemical changes in Egyptian patients infected with COVID-19 埃及新型冠状病毒感染患者的生化变化
Pub Date : 2022-07-28 DOI: 10.21608/jbaar.2022.251729
A. El-Adly, A. Wardany, Mohey Shikhoun
A pandemic-scale outbreak of the newly discovered coronavirus disease 2019 (COVID-19), fast-spreading viral pneumonia, is currently occurring. Due to the disease's overall vulnerability, different age groups have different clinical characteristics and test findings. The purpose of this study was to describe the COVID-19 laboratory results in various age and sex groups. Reverse transcriptase polymerase chain reaction (RT-PCR) for SARS-2 RNA was used in the study, which had 1100 individuals with typical cold symptoms. It was reported that 660 of these cases tested positive for the test, while 440 tested negatives, therefore all cases underwent laboratory testing. Our research revealed that males had higher COVID-19 positivity than females (215/660; 67.4%), with males scoring 445/660; 32.6%). Age does not statistically differ between COVID-19 positive and negative cases. Hematological parameters in blood cells revealed that Lymphocytes differ significantly between COVID-19-infected and uninfected patients as these cells decline in the presence of COVID-19 infection. There are no significant differences in hemoglobin (Hgb percent), red blood cells (RBCs), total white blood cells (WBCS), basophils, neutrophils, monocytes, and eosinophils, as well as blood platelets (PLTS). Erythrocyte sedimentation rate (ESR) is unimportant, whereas COVID-19 infection increases ferritin and C-reactive proteins.
新发现的冠状病毒病2019 (COVID-19),即快速传播的病毒性肺炎,目前正在发生大流行规模的爆发。由于该病的整体易感性,不同年龄组有不同的临床特征和检测结果。本研究的目的是描述不同年龄和性别群体的COVID-19实验室结果。该研究采用SARS-2 RNA逆转录聚合酶链反应(RT-PCR),对1100名典型感冒症状的个体进行了研究。据报告,这些病例中660例检测呈阳性,440例检测呈阴性,因此所有病例都进行了实验室检测。我们的研究显示,男性的COVID-19阳性率高于女性(215/660;67.4%),男性得分为445/660;32.6%)。COVID-19阳性和阴性病例的年龄无统计学差异。血细胞的血液学参数显示,感染COVID-19的患者和未感染COVID-19的患者的淋巴细胞差异显著,这些细胞在感染COVID-19时下降。在血红蛋白(Hgb百分比)、红细胞(rbc)、总白细胞(WBCS)、嗜碱性粒细胞、中性粒细胞、单核细胞和嗜酸性粒细胞以及血小板(PLTS)方面无显著差异。红细胞沉降率(ESR)并不重要,而COVID-19感染会增加铁蛋白和c反应蛋白。
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引用次数: 0
Evaluation of Serum Ferritin in Type-2 Diabetes Mellitus Sudanese Patients 苏丹2型糖尿病患者血清铁蛋白的评价
Pub Date : 2022-07-04 DOI: 10.21608/jbaar.2022.247840
Hayat Ahmed, N. Ali
: Background: Type 2 diabetes mellitus (DM2) is an important health problem worldwide affecting about 8 percent of the population. Diabetes Mellitus is one of the most common chronic diseases in Sudan. These patients have many changes in their blood, and many factors affect the glucose tolerance that is mediated by insulin, one of these changes is S.ferritin level, a marker of iron storage. Increased serum ferritin, reflecting body iron overload, is often associated with insulin resistance. The role of iron in the pathogenesis of diabetes is suggested by an increased incidence of type2 diabetes mellitus in diverse causes of iron overload, and reversal or improvement in glycemic control with a reduction in iron load achieved using either phlebotomy or iron-chelating therapy. Aim: To evaluate serum ferritin level in type-2 Diabetes Mellitus Sudanese Patients. Materials and Method: A case-control study was done in 45diabetic patients and 45normal healthy individuals as a control group, including measurement of serum ferritin by an electrochemiluminescence immunoassay (ECLIA) method full automated chemical analyzer. COBAS e411 machine used Roche HITACHI Kit and quantification of HbA1c level by i-chroma instrument. Results: The study showed that serum ferritin levels were significantly increased in diagnosed cases of type 2 diabetes mellitus in comparison with the age and gender-matched healthy individuals (P. value= 0.008). There was an insignificant correlation between serum ferritin and HbA1c(P. value=0.431). Conclusion: Therefore, the findings of the present study indicate that serum ferritin was increased in diabetes and this increase may contribute to the pathogenesis of this disease as well as to the development of complications. Thus, routine screening for serum ferritin concentration in pre-diabetes and diabetic patients should be done to assess the body's iron stores.
背景:2型糖尿病(DM2)是世界范围内影响约8%人口的重要健康问题。糖尿病是苏丹最常见的慢性病之一。这些患者的血液中有许多变化,许多因素影响胰岛素介导的葡萄糖耐量,其中一个变化是铁蛋白水平,铁蛋白是铁储存的标志。血清铁蛋白升高,反映机体铁超载,常与胰岛素抵抗有关。铁在糖尿病发病机制中的作用是由多种原因引起的铁超载引起的2型糖尿病发病率增加,以及通过静脉切开术或铁螯合治疗减少铁负荷来逆转或改善血糖控制。目的:评价苏丹2型糖尿病患者血清铁蛋白水平。材料与方法:采用电化学发光免疫分析法(ECLIA)全自动化学分析仪对45例糖尿病患者和45例正常健康人进行血清铁蛋白测定,并进行病例对照研究。COBAS e411机采用罗氏日立试剂盒,i-chroma仪定量HbA1c水平。结果:与年龄、性别匹配的健康人相比,诊断为2型糖尿病的患者血清铁蛋白水平明显升高(p值= 0.008)。血清铁蛋白与HbA1c的相关性不显著(P。值= 0.431)。结论:本研究结果提示糖尿病患者血清铁蛋白升高,这种升高可能与糖尿病的发病机制及并发症的发生有关。因此,应对糖尿病前期和糖尿病患者的血清铁蛋白浓度进行常规筛查,以评估机体的铁储备。
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引用次数: 0
A Case Report of Lymphoepithelioma-like, a Variant of Urothelial Carcinoma of the Urinary Bladder 淋巴上皮瘤样膀胱尿路上皮癌1例报告
Pub Date : 2022-06-17 DOI: 10.21608/jbaar.2022.244515
Farouk Hachem, H. Abdallah, A. Ibrahimi, H. Elsayegh, Y. Nouini
Lymphoepithelioma-like carcinoma is an undifferentiated carcinoma with histological features similar to undifferentiated, non-keratinizing carcinoma of the nasopharynx. Lymphoepithelioma-like carcinoma of the urinary bladder is uncommon with a reported incidence of 0.4%1.3% of all bladder cancer. We report a case of a 72 year-old-man with a muscle-invasive lymphoepithelioma-like carcinoma of the bladder who was treated with radical cystectomy with a 12-month follow-up.
淋巴上皮瘤样癌是一种未分化的癌,其组织学特征与鼻咽部未分化、无角化的癌相似。膀胱淋巴上皮瘤样癌并不常见,据报道发病率为0.4%,占所有膀胱癌的1.3%。我们报告一例72岁男性肌肉侵袭性淋巴上皮瘤样膀胱癌患者接受根治性膀胱切除术并随访12个月。
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引用次数: 0
Evaluation of the diagnostic performances of tissue inhibitors of metalloproteinase-1 and fibronectin for heart failure 金属蛋白酶-1和纤维连接蛋白组织抑制剂对心力衰竭诊断价值的评价
Pub Date : 2022-06-01 DOI: 10.21608/jbaar.2022.246476
M. Fouda, B. Zarif, Victoria Samir, Sara A Mekkawy, Mohamed Omran
Previous research has linked an imbalance of the tissue inhibitors of metalloproteinase-1 (TIMP-1) and fibronectin (FN) to heart failure as a part of the extracellular matrix network (ECM) biochemistry profile, which is vital for cardiac homeostasis. This study aimed to assess the diagnostic performance of FN, TIMP-1, and CK-MB in heart failure (HF). Sixty patients (45 with acute and 15 with chronic HF) were recruited. Thirty individuals (20 with ischemic heart diseases, as other cardiac diseases, and 10 healthy individuals) were recruited as a control group. The biotin double antibody sandwich technology determined levels of human fibronectin and tissue inhibitors of metalloproteinase-1. FN was the most effective biomarker in differentiating HF patients from healthy individuals (AUC = 0.850) ( P < 0.001), followed by TIMP (AUC = 0.74) and CK MB (AUC = 0.660). The sensitivity and specificity of FN were 82% and 70%, respectively, at a cutoff of 80 ng/ml. In addition, FN and TIMP had the same AUC (0.71) and efficiency (65%) in distinguishing HF patients from controls, followed by CK-MB (AUC = 0.70). We developed a novel model for HF diagnosis named the HFD model based on three biomarkers (FN, TIMP, and CK MB). The HFD model had an AUC of 0.77 in distinguishing HF patients from healthy individuals, with a sensitivity, specificity, and accuracy reaching 80%. For differentiating HF patients from controls, the HFD model had 0.8 AUC, 76% sensitivity, 75% specificity, and 76% accuracy.
先前的研究将金属蛋白酶-1 (TIMP-1)和纤维连接蛋白(FN)的组织抑制剂失衡与心力衰竭联系起来,作为细胞外基质网络(ECM)生物化学谱的一部分,这对心脏稳态至关重要。本研究旨在评估FN、TIMP-1和CK-MB在心力衰竭(HF)中的诊断价值。60例患者(45例急性心衰,15例慢性心衰)被招募。30人(20人患有缺血性心脏病和其他心脏病,10人健康)作为对照组。生物素双抗体夹心技术测定人纤维连接蛋白和金属蛋白酶-1组织抑制剂的水平。FN是区分HF患者与健康人最有效的生物标志物(AUC = 0.850) (P < 0.001),其次是TIMP (AUC = 0.74)和CK MB (AUC = 0.660)。FN的敏感性为82%,特异性为70%,截止值为80 ng/ml。此外,FN和TIMP在区分HF患者和对照组方面具有相同的AUC(0.71)和效率(65%),其次是CK-MB (AUC = 0.70)。我们基于三种生物标志物(FN、TIMP和CK MB)开发了一种新的心衰诊断模型,命名为HFD模型。HFD模型区分HF患者和健康人的AUC为0.77,敏感性、特异性和准确性均达到80%。对于区分HF患者和对照组,HFD模型的AUC为0.8,灵敏度为76%,特异性为75%,准确性为76%。
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引用次数: 1
The Role of CD3 and CD8 in Preterm Preeclamptic women by using Immunohistochemical technique 免疫组化技术研究CD3和CD8在早产子痫前期妇女中的作用
Pub Date : 2022-06-01 DOI: 10.21608/jbaar.2022.246929
A. Abbood
Preterm birth (PTB) and PE are the two major causes of perinatal mortality, morbidity, and long-range neurological disability. PTB defined as delivery before 37 weeks gestation, has become an epidemic in developed countries, Indeed PTB and PE are leading causes of maternal and neonatal death worldwide. The immunohistochemical study show: - The staining intensity for PE immunohistochemical showed the greatest (+2) intensity was recorded at 52% for anti-CD3 lymphocyte biomarker. Also, followed by 28% of (+1) Intensity was comparable biomarkers. (12%) of +3 and 8% for 0 intensity when compared with Tonsil control positive and placental tissue control negative. On the other hand, the staining intensity for PE immunohistochemical shows the greatest frequency of (0) intensity was recorded for anti-CD8 cytotoxic T-cell biomarker with 52 % then +1 (28%) and 20% for +2 when compared with skin control positive and negative.
早产(PTB)和PE是围产期死亡率、发病率和长期神经功能障碍的两个主要原因。产妇结核定义为妊娠37周前分娩,在发达国家已成为一种流行病。事实上,产妇结核和肺痨是全世界孕产妇和新生儿死亡的主要原因。免疫组化研究表明:- PE免疫组化染色强度显示,抗cd3淋巴细胞生物标志物的染色强度最高(+2),为52%。此外,28%的(+1)强度是可比较的生物标志物。与扁桃体控制阳性和胎盘组织控制阴性相比,+3强度为12%,0强度为8%。另一方面,PE免疫组化染色强度显示,与皮肤对照阳性和阴性相比,抗cd8细胞毒性t细胞生物标志物的(0)强度频率最高,为52%,为+1(28%),为+2(20%)。
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引用次数: 0
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