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Effectiveness of radial Extracorporeal Shock Wave Therapy in Reduces muscle spasms in Stroke Patients; A Systematic Review and Meta-Analysis 桡骨体外冲击波治疗减少脑卒中患者肌肉痉挛的疗效观察系统回顾和荟萃分析
IF 0.2 Q4 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-06-26 DOI: 10.22317/jcms.v9i3.1346
Isam Ali Hameedi, A. Shadmehr, T. Alsaadawi
Objectives: Effectiveness of radial extracorporeal shock wave therapy (rESWT) on pain, range of motion and muscle tone in patients with stroke injuries. Methods: PubMed, EMBASE, Cochrane Library and VIP information were used to collect information for research conducted between the beginning of 2013 and the end of 2022. These studies were randomized controlled trials that used rESWT for muscle spasm in stroke patients with conventional treatments as controls. There are no specific restrictions on the duration of treatment, the type of reESWT, or the severity of symptoms. These studies must have assessed at least one of the following outcome mesurements: visual analog scale (VAS) for pain, Ashwerth measure for muscle tone or external rotation range of motion (ER ROM). RevMan 5.3 software was used to check the quality of included studies. For continuous variables, mean difference (MD) or standardized MD (SMD) with CI 95% were derived. For dichotomous data, event proportions and sample sizes were extracted. Results: In the conducted investigations, it was found that 7 studies investigated the effectiveness of rESWT  treatments after the intervention in comparison with conventional treatment in terms of reducing pain intensity. In total, all 7 studies showed that the rESWT intervention was effective in reducing pain intensity compared to conventional treatments (MD, –0.97 [95% CI, –2.13 to –0.42], P < .00001, I2 = 71%). Compared with traditional treatments, the effectiveness of rESWT plus routine treatments on muscle tone after intervention was assessed in terms of Ashwerth critrion  in 4 trials (SMD, 1.13 [95% CI, 0.46-1.23], P < .00001, I2 =  59%). ER ROM was used to reflect the ROM, which was assessed in 4 RCTs. Because of the limited number of studies, ER ROM was measured immediately after treatment in all included studies. The pooled result of the included studies showed that the heterogeneity was high and unacceptable (MD, 10.31 [95% CI, 2.47–16.18], P < .003, I2 = 81%). Conclusion: The results of this research indicated that rESWT treatment can be used as a safe and non-invasive method to quickly reduce spasticity and increase joint range of motion in stroke patients. But more research on the long-term effects of rESWT as well as the factors influencing its effectiveness to reduce spasticity and comparison with other new treatment protocols is suggested.
目的:桡骨体外冲击波治疗(rESWT)对脑卒中损伤患者疼痛、活动范围和肌肉张力的影响。方法:采用PubMed、EMBASE、Cochrane Library和VIP information收集2013年初至2022年底的研究资料。这些研究是随机对照试验,使用rESWT治疗中风患者的肌肉痉挛,常规治疗作为对照。对于治疗的持续时间、reESWT的类型或症状的严重程度没有特定的限制。这些研究必须评估以下结果测量中的至少一项:疼痛的视觉模拟量表(VAS),肌肉张力的Ashwerth测量或外旋运动范围(ER ROM)。采用RevMan 5.3软件对纳入研究的质量进行检查。对于连续变量,导出CI为95%的均值差(MD)或标准化均值(SMD)。对于二分类数据,提取事件比例和样本量。结果:在已开展的调查中,有7项研究调查了干预后rESWT治疗与常规治疗相比在减轻疼痛强度方面的有效性。总的来说,所有7项研究表明,与常规治疗相比,rESWT干预在减轻疼痛强度方面是有效的(MD, -0.97 [95% CI, -2.13至-0.42],P < 0.00001, I2 = 71%)。与传统治疗相比,4项试验以Ashwerth标准评估rESWT加常规治疗干预后肌张力的有效性(SMD, 1.13 [95% CI, 0.46-1.23], P < 0.00001, I2 = 59%)。ER ROM用于反映ROM,在4个随机对照试验中进行评估。由于研究数量有限,在所有纳入的研究中,ER ROM都是在治疗后立即测量的。纳入研究的汇总结果显示,异质性很高,不可接受(MD, 10.31 [95% CI, 2.47 ~ 16.18], P < 0.003, I2 = 81%)。结论:本研究结果表明,rESWT治疗可作为一种安全、无创的方法,快速减轻脑卒中患者的痉挛,增加关节活动范围。但建议更多的研究rESWT的长期效果以及影响其降低痉挛效果的因素,并与其他新的治疗方案进行比较。
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引用次数: 0
Effect of Adipose Derived Stromal Vascular Fraction on The Early Inflammatory Phase of Burn Wound Healing in Male Rat Model 脂肪源性基质血管组分对雄性大鼠烧伤创面早期炎症期愈合的影响
IF 0.2 Q4 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-06-26 DOI: 10.22317/jcms.v9i3.1331
Laura Noori, K. Fakiha, A. Aljahdali
Objectives: Severe burn treatment remains challenging. Research has investigated the efficacy of stem cells and stromal vascular fraction (SVF) in many types of injuries. SVF has advantages for its heterogenous population of cells and avoidance of culturing and ethical issues. SVF can be isolated either enzymatically or mechanically. Enzymatically isolated SVF reduced inflammation and enhanced neovascularization and re-epithelization in the treatment of burn injury. This study highlighted the efficacy of applying mechanically isolated SVF on the early inflammatory phase of deep partial-thickness burn by investigating toll-like receptor 4 (TLR4) signaling pathway. Methods: 30 male Wistar rats with deep partial-thickness burns were assigned into: the control group, silver sulfadiazine (SSD) cream group, and mechanically isolated SVF group. Morphological, histopathological evaluation of inflammation, and immunohistochemical analysis for (TLR4, TNF-α, IL‐1β, and IL-6) were evaluated for the first eight days post-treatment. Results: Morphologically, the SVF group significantly reduced edema and increased wound bed dryness on day one compared to the control group (P=0.0001) and to the SSD group (P=0.001). Histopathologically, the SVF group significantly reduced inflammation four days post-treatment compared with the control group (P=0.045). The SVF group significantly reduced TLR4 protein expression on days four and eight post-treatment compared with the control group (P= 0.001, P= 0.042, respectively). The TNF-α protein expression in the SVF group was significantly lower on days four and eight post-treatment compared with the control group (P= 0.046, P= 0.046, respectively) and with the SSD group (P= 0.008, P= 0.001, respectively). The IL‐1β expression was significantly reduced in the SVF group compared to the control group on day four post-treatment (P= 0.017). There were no significant differences in IL-6 expressions between all groups on both days. Conclusion: The mechanical isolation of SVF has an early anti-inflammatory impact on deep partial-thickness burn injury. This effect could be through inhibiting TLR4, TNF-α, and IL‐1β pathways. This could partially explain the mechanism behind SVF efficacy in the healing process of burn injury.
目的:严重烧伤治疗仍然具有挑战性。干细胞和基质血管组分(SVF)在多种类型损伤中的作用已被研究。SVF的优势在于其细胞群的异质性,避免了培养和伦理问题。SVF可通过酶法或机械法分离。酶分离的SVF在烧伤治疗中减少炎症,增强新生血管和再上皮形成。本研究通过研究toll样受体4 (toll-like receptor 4, TLR4)信号通路,强调了机械分离SVF在深部分厚度烧伤早期炎症期的作用。方法:将30只雄性Wistar大鼠分为:对照组、磺胺嘧啶银乳膏组和机械分离SVF组。在治疗后的前8天,对炎症进行形态学、组织病理学评估,并对(TLR4、TNF-α、IL- 1β和IL-6)进行免疫组织化学分析。结果:形态学上,与对照组(P=0.0001)和SSD组(P=0.001)相比,SVF组在第一天显著减少了水肿,增加了创面干燥度。在组织病理学上,SVF组与对照组相比,治疗4天后炎症明显减轻(P=0.045)。与对照组相比,SVF组在治疗后第4天和第8天显著降低了TLR4蛋白的表达(P= 0.001, P= 0.042)。SVF组在治疗后第4天、第8天TNF-α蛋白表达量显著低于对照组(P= 0.046、P= 0.046)和SSD组(P= 0.008、P= 0.001)。治疗后第4天,SVF组与对照组相比IL - 1β表达显著降低(P= 0.017)。2天各组间IL-6表达差异无统计学意义。结论:机械分离SVF对深度部分厚度烧伤有早期抗炎作用。这种作用可能是通过抑制TLR4、TNF-α和IL - 1β途径实现的。这可以部分解释SVF在烧伤愈合过程中的作用机制。
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引用次数: 0
Dosimetric effects and impacts caused by a carbon fiber table and its accessories in a linear accelerator 直线加速器中碳纤维表及其附件的剂量学效应及影响
IF 0.2 Q4 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-06-26 DOI: 10.22317/jcms.v9i3.1355
H. Alabedi, M. S. Al Musawi, Nabaa Mohammed Ali
Objective : Most contemporary treatment planning systems (TPS) exclude the couch during treatment planning. The present investigation aimed to evaluate the impact of couches and accessories on radiation therapy planning by quantifying the degree of attenuation for two-photon beam energies, 6 MV and 10 MV, at two different field sizes, 5 cm x 5 cm and 10 cm x 10 cm.   Methods: An x-ray radiation beam at two energies (6 MV and 10 MV) generated by a linear accelerator (Elekta Synergy). The output dose was measured using a digital parallel plate ionization chamber of the IBA cc13 type (IBA Dosimetry, Germany), and the readings were recorded with a 2944 Farmer Type chamber. Different commercially available couch tops and accessories evaluated in this study. Results: The results show that the highest attenuation values were observed at 1300 gantry angles for both energies and field sizes. The lowest attenuation values were recorded at 1000 gantry angles with 6 MV energy for 5cm x 5cm and 10cm x 10cm field sizes. The breast board with D level demonstrated the highest attenuation of 6.27% and 5.51% for 6 MV and 10 MV energies, respectively. Conclusion: the findings indicate that the degree of attenuation is not uniform across all angles and may exceed tolerable limits, indicating the need for careful consideration during treatment planning to ensure optimal treatment outcomes.
目的:大多数现代治疗计划系统(TPS)在治疗计划中排除了沙发。本研究旨在通过量化两种不同场尺寸(5 cm × 5 cm和10 cm × 10 cm)下双光子束能量(6 MV和10 MV)的衰减程度,评估沙发和配件对放射治疗计划的影响。方法:利用直线加速器(Elekta Synergy)产生两种能量(6 MV和10 MV)的x射线束。输出剂量使用IBA cc13型(IBA dose metry,德国)的数字平行板电离室测量,并用2944 Farmer型电离室记录读数。本研究评估了不同的市售沙发顶和配件。结果:在能量和场大小均为1300个龙门角时,衰减值最高。在5cm × 5cm和10cm × 10cm的电场尺寸下,在1000个龙门角处以6 MV能量记录了最低衰减值。D级胸板在6 MV和10 MV能量下衰减最大,分别为6.27%和5.51%。结论:研究结果表明,各角度的衰减程度并不均匀,可能超过可容忍的限度,在制定治疗计划时需要仔细考虑,以确保最佳的治疗效果。
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引用次数: 0
Molecular detection of mononucleotide biomarkers of microsatellite instability in sporadic colorectal carcinoma patients with clinicopathological correlation 散发性结直肠癌患者微卫星不稳定性单核苷酸生物标志物的分子检测及其临床病理相关性
IF 0.2 Q4 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-06-26 DOI: 10.22317/jcms.v9i3.1348
Wed Thamer Salman Al-Jumaili, Bassam M S Al-Musawi
Objectives: To identify the frequency and types of microsatellite instability among a group of sporadic CRC patients and to correlate the findings with clinicopathological characteristics. Methods: During an 8-month period, all patients with sporadic CRC who attended to two teaching hospitals in Baghdad, Iraq were recruited to this cross-sectional study regardless of age, sex, ethnicity, or tumor characteristics. Demographic, clinical, and histopathological features were recorded. DNA was extracted from FFPE-blocks of the resected tumors and normal tissues. PCR amplification of five microsatellite mononucleotide repeat loci (BAT25, BAT26, NR-21, NR-24, and MONO-27) and 2 pentanucleotide repeat control markers (Penta C and Penta D) was performed to determine the MSI status. Capillary electrophoresis and Genetic Analyzer 3500 (Applied Biosystem, Japan) were used to separate and examine the products. Data were analyzed by Genescan software (Promega, USA). Instability of two or more loci is considered MSI-H. Result: In this study, ages of the 45 recruited patients ranged between 20-80 years, with a mean±SD of 55±12.3 years; of them, 31(68.9%) were ≥50 years; 25 (55.6%) were males. Rectal bleeding was the most frequent presenting feature [22 (48.9%)] patients; 23 (51.1%) of CRCs were located at recto-sigmoid region, 29 (64.4%) were T3 tumors, 34(75.5%) were non-mucinous adenocarcinoma, 39(86.7%) were moderately differentiated, 17 (37.8%) patients had stage III tumors; and 25 (55.5%) had lymphovascular invasion. MSI-H was seen in 5/45 (11.1%) patients; 3(60%) of them were ≥50 years, 4(80%) were males, 3(60%) were smokers, 2 (40%) presented with intestinal obstruction and altered bowel habits each; 4(80%) had T3 tumors, 3(60%) had mucinous adenocarcinomas [p=0.004], 2(40%) had stage II tumor and stage III each. Conclusion: The frequency of MSI-H among the recruited patients with CRC was 5/45 (11.1%) and it was significantly associated with mucinous adenocarcinoma subtype. NR-24 and NR-21 were the most prevalent instable markers.
目的:确定一组散发性CRC患者中微卫星不稳定的频率和类型,并将其与临床病理特征相关联。方法:在8个月的时间里,所有在伊拉克巴格达两家教学医院就诊的散发性CRC患者被招募到这项横断面研究中,无论年龄、性别、种族或肿瘤特征如何。记录人口统计学、临床和组织病理学特征。从切除的肿瘤和正常组织的FFPE块中提取DNA。对5个微卫星单核苷酸重复基因座(BAT25、BAT26、NR-21、NR-24和MONO-27)和2个五核苷酸重复控制标记(Penta C和Penta D)进行PCR扩增,以确定MSI状态。毛细管电泳和遗传分析仪3500(Applied Biosystem,Japan)用于分离和检查产物。数据通过Genescan软件(Promega,USA)进行分析。两个或多个基因座的不稳定性被认为是MSI-H。结果:在本研究中,45名招募患者的年龄在20-80岁之间,平均±SD为55±12.3岁;其中≥50岁者31例(68.9%);男性25例(55.6%)。直肠出血是最常见的表现特征[22例(48.9%)]患者;23例(51.1%)CRC位于直肠乙状结肠区,29例(64.4%)为T3肿瘤,34例(75.5%)为非粘液腺癌,39例(86.7%)为中分化,17例(37.8%)为III期肿瘤;淋巴管侵犯25例(55.5%)。MSI-H见于5/45(11.1%)患者;其中3人(60%)≥50岁,4人(80%)为男性,3人(6%)为吸烟者,2人(40%)分别出现肠梗阻和排便习惯改变;4例(80%)患有T3肿瘤,3例(60%)患有粘液腺癌[p=0.004],2例(40%)分别患有II期和III期肿瘤。结论:MSI-H在招募的CRC患者中的频率为5/45(11.1%),并且与粘液腺癌亚型显著相关。NR-24和NR-21是最普遍的不稳定标记。
{"title":"Molecular detection of mononucleotide biomarkers of microsatellite instability in sporadic colorectal carcinoma patients with clinicopathological correlation","authors":"Wed Thamer Salman Al-Jumaili, Bassam M S Al-Musawi","doi":"10.22317/jcms.v9i3.1348","DOIUrl":"https://doi.org/10.22317/jcms.v9i3.1348","url":null,"abstract":"Objectives: To identify the frequency and types of microsatellite instability among a group of sporadic CRC patients and to correlate the findings with clinicopathological characteristics. \u0000Methods: During an 8-month period, all patients with sporadic CRC who attended to two teaching hospitals in Baghdad, Iraq were recruited to this cross-sectional study regardless of age, sex, ethnicity, or tumor characteristics. Demographic, clinical, and histopathological features were recorded. DNA was extracted from FFPE-blocks of the resected tumors and normal tissues. PCR amplification of five microsatellite mononucleotide repeat loci (BAT25, BAT26, NR-21, NR-24, and MONO-27) and 2 pentanucleotide repeat control markers (Penta C and Penta D) was performed to determine the MSI status. Capillary electrophoresis and Genetic Analyzer 3500 (Applied Biosystem, Japan) were used to separate and examine the products. Data were analyzed by Genescan software (Promega, USA). Instability of two or more loci is considered MSI-H. \u0000Result: In this study, ages of the 45 recruited patients ranged between 20-80 years, with a mean±SD of 55±12.3 years; of them, 31(68.9%) were ≥50 years; 25 (55.6%) were males. Rectal bleeding was the most frequent presenting feature [22 (48.9%)] patients; 23 (51.1%) of CRCs were located at recto-sigmoid region, 29 (64.4%) were T3 tumors, 34(75.5%) were non-mucinous adenocarcinoma, 39(86.7%) were moderately differentiated, 17 (37.8%) patients had stage III tumors; and 25 (55.5%) had lymphovascular invasion. MSI-H was seen in 5/45 (11.1%) patients; 3(60%) of them were ≥50 years, 4(80%) were males, 3(60%) were smokers, 2 (40%) presented with intestinal obstruction and altered bowel habits each; 4(80%) had T3 tumors, 3(60%) had mucinous adenocarcinomas [p=0.004], 2(40%) had stage II tumor and stage III each. \u0000Conclusion: The frequency of MSI-H among the recruited patients with CRC was 5/45 (11.1%) and it was significantly associated with mucinous adenocarcinoma subtype. NR-24 and NR-21 were the most prevalent instable markers.","PeriodicalId":42860,"journal":{"name":"Journal of Contemporary Medical Sciences","volume":" ","pages":""},"PeriodicalIF":0.2,"publicationDate":"2023-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45703340","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
Case report: Identification of a rare homozygous missense variant in the PKLR gene reported for the first time in transfusion-dependent Saudi Patient 病例报告:首次在沙特输血依赖患者中发现PKLR基因中一种罕见的纯合错义变体
IF 0.2 Q4 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-06-26 DOI: 10.22317/jcms.v9i3.1354
Rawabi Zahed, B. Sajer
Red cell pyruvate kinase deficiency is one of the most common erythrocytic glycolytic pathway defects connected with congenital non-spherocytic anemia. The condition inherited as an autosomal recessive Mendelian trait is caused by mutations in the PKLR gene located on chromosome 1q21. Pyruvate kinase enzyme is crucial in the energy-producing glycolysis pathway that provides red blood cells with the primary source of energy (ATP). We report here a case of a Saudi female patient that was initially diagnosed at a few months old with beta-thalassemia major and was treated with regular blood transfusions and iron overload management. At the time of our sample collection, the patient was recently transferred to King Abdul Aziz University Hospital. Genetic testing was performed to identify the disease-contributing variant of beta-thalassemia using TaqMan genotyping of six common beta-thalassemia variants (negative results). NGS targeted HBB gene sequencing which did not reveal any related variants. MLPA was performed to rule out alpha thalassemia diagnosis. The use of whole genome sequencing revealed a rare missense variant in the PKLR gene c.1015G>A (D339N) in a homozygous state that correlates to her severe phenotype. Documenting this incident will aid medical staff in providing appropriate care to similar cases and highlights the importance of following up with the diagnosis investigation process to minimize misdiagnosis incidences.
红细胞丙酮酸激酶缺乏是与先天性非球形细胞性贫血相关的最常见的红细胞糖酵解途径缺陷之一。这种遗传为常染色体隐性孟德尔性状的疾病是由位于染色体1q21上的PKLR基因突变引起的。丙酮酸激酶在产生能量的糖酵解途径中至关重要,该途径为红细胞提供主要能量来源(ATP)。我们在这里报告了一例沙特女性患者,她在几个月大时最初被诊断为严重β地中海贫血,并接受了定期输血和铁过载治疗。在我们采集样本时,患者最近被转移到阿卜杜勒·阿齐兹国王大学医院。使用六种常见β地中海贫血变异体的TaqMan基因分型进行基因检测,以确定β地中海贫血的致病变异体(阴性结果)。NGS靶向HBB基因测序,未发现任何相关变异。进行MLPA以排除α地中海贫血的诊断。全基因组测序的使用揭示了PKLR基因c.1015G>a(D339N)中一种罕见的错义变体,该变体处于纯合状态,与她的严重表型相关。记录这一事件将有助于医务人员为类似病例提供适当的护理,并强调跟进诊断调查过程的重要性,以最大限度地减少误诊发生率。
{"title":"Case report: Identification of a rare homozygous missense variant in the PKLR gene reported for the first time in transfusion-dependent Saudi Patient","authors":"Rawabi Zahed, B. Sajer","doi":"10.22317/jcms.v9i3.1354","DOIUrl":"https://doi.org/10.22317/jcms.v9i3.1354","url":null,"abstract":"Red cell pyruvate kinase deficiency is one of the most common erythrocytic glycolytic pathway defects connected with congenital non-spherocytic anemia. The condition inherited as an autosomal recessive Mendelian trait is caused by mutations in the PKLR gene located on chromosome 1q21. Pyruvate kinase enzyme is crucial in the energy-producing glycolysis pathway that provides red blood cells with the primary source of energy (ATP). We report here a case of a Saudi female patient that was initially diagnosed at a few months old with beta-thalassemia major and was treated with regular blood transfusions and iron overload management. At the time of our sample collection, the patient was recently transferred to King Abdul Aziz University Hospital. Genetic testing was performed to identify the disease-contributing variant of beta-thalassemia using TaqMan genotyping of six common beta-thalassemia variants (negative results). NGS targeted HBB gene sequencing which did not reveal any related variants. MLPA was performed to rule out alpha thalassemia diagnosis. The use of whole genome sequencing revealed a rare missense variant in the PKLR gene c.1015G>A (D339N) in a homozygous state that correlates to her severe phenotype. Documenting this incident will aid medical staff in providing appropriate care to similar cases and highlights the importance of following up with the diagnosis investigation process to minimize misdiagnosis incidences.","PeriodicalId":42860,"journal":{"name":"Journal of Contemporary Medical Sciences","volume":" ","pages":""},"PeriodicalIF":0.2,"publicationDate":"2023-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47930982","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
The role of Neuropsychological assessment in the Differential Diagnoses of Late-Onset Depression, Dementia, and Mild Cognitive Impairment 神经心理学评估在晚期抑郁症、痴呆症和轻度认知障碍鉴别诊断中的作用
IF 0.2 Q4 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-06-26 DOI: 10.22317/jcms.v9i3.1233
G. Morkavuk, Gokce Sirvanli
Objective: The present study aimed to compare the neuropsychological test parameters of dementia, depression, and MCI patients and determine the disease-specific test characteristics and their relationship with electroencephalography.Methods: Ninety-one patients who were admitted to the neurology outpatient clinic with forgetfulness complaints between October 2019 and March 2022 and whose neuropsychological tests were performed were included in the study. The files of these 91 patients were reviewed retrospectively and their sociodemographic data were recorded. Furthermore, the EEG results which were taken during the patients' evaluation period due to forgetfulness were evaluated. Neuropsychological tests were compared between patients with dementia, MCI and depression. It was also investigated whether there was a relationship between NPT test parameters and EEG in patients with EEG results.Results: The study was completed with 87 patients. Of these 87 patients, 54 were female and 33 were male. Twenty-four patients had depression, 16 MCI, and 47 dementia. All of the dementia patients had Alzheimer's type dementia. When dementia, depression, and MCI groups were compared, the age difference was statistically significant (p=0.001). The mean age of the depression group was 66.5, the MCI group was 73.5, and the dementia group was 77. WMS-I, WMS-II, WMS-III, WMS-IV, similarities test, clock drawing test, trail making test, shape copying, language, and mood evaluation tests were statistically significantly different between the groups.  There was no statistically significant difference between the groups regarding gender, education level, dominant hand, and occupation. EEG background activity frequencies were also examined between the groups, and there was no statistically significant difference.Conclusion: In conclusion, when evaluating patients who present with the complaint of forgetfulness, a detailed neuropsychological evaluation must be performed in addition to other diagnostic tests. Sensitive tests should be included to confirm the diagnosis, especially in cases where being in between for the differential diagnosis. Thus, further studies are needed on this subject.
目的:本研究旨在比较痴呆、抑郁和MCI患者的神经心理测试参数,并确定疾病特异性测试特征及其与脑电图的关系。方法:在2019年10月至2022年3月期间,91名因健忘投诉而入住神经科门诊并进行神经心理测试的患者被纳入研究。对这91名患者的档案进行了回顾性审查,并记录了他们的社会人口学数据。此外,评估了在患者因健忘而进行评估期间取得的脑电图结果。对痴呆、MCI和抑郁症患者的神经心理测试进行比较。还调查了有脑电图结果的患者的NPT测试参数与脑电图之间是否存在关系。结果:本研究共完成87例患者。在这87名患者中,54名为女性,33名为男性。24名患者患有抑郁症,16名MCI,47名痴呆症。所有痴呆症患者都患有阿尔茨海默氏症。当比较痴呆、抑郁和MCI组时,年龄差异具有统计学意义(p=0.001)。抑郁组的平均年龄为66.5岁,MCI组为73.5岁,痴呆组为77岁。WMS-I、WMS-II、WMS-III、WMS-IV、相似性测试、时钟绘制测试、轨迹制作测试、形状复制、语言和情绪评估测试在各组之间具有统计学显著差异。在性别、教育水平、优势手和职业方面,两组之间没有统计学上的显著差异。两组之间的脑电图背景活动频率也进行了检查,没有统计学上的显著差异。结论:总之,在评估出现健忘症状的患者时,除了其他诊断测试外,还必须进行详细的神经心理学评估。应包括敏感测试来确认诊断,尤其是在介于鉴别诊断之间的情况下。因此,需要对这一问题进行进一步的研究。
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引用次数: 0
Genetic polymorphisms of DPYD in patients with breast cancer on capecitabine therapy 癌症患者卡培他滨治疗中DPYD基因多态性的研究
IF 0.2 Q4 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-06-26 DOI: 10.22317/jcms.v9i3.1350
Raaid Fadhl Abbas, A. Sahib, Hasanain Shakir Mahmood, Karar Kadhim Mohsin, Ali Amal Aldeen Majeed
 Objectives:   Breast cancer is the primary cause of death in Iraqi women aged 30–54 years. The study examined the relationship between (G > A) (rs3918290) and (rs55886062, T >G) DPYD gene polymorphisms, their haplotypes, and capecitabine serum concentrations in postmenopausal Iraqi women with breast cancer in postmenopausal women. During capecitabine chemotherapy. Methods: The study included 200 women: 100 apparently health (45-75 years old) and 100 with breast cancer (40-70 years old). This study, conducted between July and October 2022 at the oncology centre at Imam al-Hussain medical city in Kerbala, Iraq, plasma levels of Capacetabine and 5fu were measured in  breast cancer patients who had been taking capecitabine for at least three months. All participants gave informed consent. Results: Capecitabine, and 5FU concentrations in breast cancer patients differed significantly, As the results showed, Capecitabine, and 5FU had a significantly higher concentration of them in patients with the TT allele than in those with the CC and CT alleles for the polymorphism (IVS14 + 1G > A) (rs3918290) and in patients with DPYD*13 (rs55886062) with the CC allele rather than the AA and AC alleles. Mutant allele carriers had increased Capecitabine concentrations (p<0.001). Conclusion: Ca15.3, serum calcium, and estradiol all exist in bodily serum, making them a potentially useful novel diagnostic biomarker for patients with breast cancer due to their high levels of stability, as well as the biological properties of tumors, such as serum calcium and estrogen.
目标:癌症是伊拉克30-54岁妇女死亡的主要原因。该研究检测了(G>A)(rs3918290)和(rs55886062,T>G)DPYD基因多态性、其单倍型和卡培他滨血清浓度在绝经后患有乳腺癌症的伊拉克绝经后妇女中的关系。卡培他滨化疗期间。方法:研究对象包括200名女性:100名明显健康(45-75岁)和100名患有癌症(40-70岁)。这项研究于2022年7月至10月在伊拉克克尔巴拉Imam al-Hussain医疗城的肿瘤中心进行,测量了服用卡培他滨至少三个月的癌症患者的血浆卡帕他滨和5fu水平。所有参与者均表示知情同意。结果:乳腺癌症患者的卡培他滨、5FU浓度差异显著,5FU在TT等位基因患者中的多态性(IVS14+1G>a)显著高于CC和CT等位基因的患者(rs3918290),在DPYD*13患者中(rs55886062)具有CC等位基因而不是AA和AC等位基因。突变等位基因携带者卡培他滨浓度升高(p<0.001)。结论:Ca15.3、血清钙和雌二醇均存在于人体血清中,由于其高水平的稳定性以及肿瘤的生物学特性,如血清钙和雌激素,使其成为癌症患者潜在的有用的新型诊断生物标志物。
{"title":"Genetic polymorphisms of DPYD in patients with breast cancer on capecitabine therapy","authors":"Raaid Fadhl Abbas, A. Sahib, Hasanain Shakir Mahmood, Karar Kadhim Mohsin, Ali Amal Aldeen Majeed","doi":"10.22317/jcms.v9i3.1350","DOIUrl":"https://doi.org/10.22317/jcms.v9i3.1350","url":null,"abstract":" Objectives:   Breast cancer is the primary cause of death in Iraqi women aged 30–54 years. The study examined the relationship between (G > A) (rs3918290) and (rs55886062, T >G) DPYD gene polymorphisms, their haplotypes, and capecitabine serum concentrations in postmenopausal Iraqi women with breast cancer in postmenopausal women. During capecitabine chemotherapy. \u0000Methods: The study included 200 women: 100 apparently health (45-75 years old) and 100 with breast cancer (40-70 years old). This study, conducted between July and October 2022 at the oncology centre at Imam al-Hussain medical city in Kerbala, Iraq, plasma levels of Capacetabine and 5fu were measured in  breast cancer patients who had been taking capecitabine for at least three months. All participants gave informed consent. \u0000Results: Capecitabine, and 5FU concentrations in breast cancer patients differed significantly, As the results showed, Capecitabine, and 5FU had a significantly higher concentration of them in patients with the TT allele than in those with the CC and CT alleles for the polymorphism (IVS14 + 1G > A) (rs3918290) and in patients with DPYD*13 (rs55886062) with the CC allele rather than the AA and AC alleles. Mutant allele carriers had increased Capecitabine concentrations (p<0.001). \u0000Conclusion: Ca15.3, serum calcium, and estradiol all exist in bodily serum, making them a potentially useful novel diagnostic biomarker for patients with breast cancer due to their high levels of stability, as well as the biological properties of tumors, such as serum calcium and estrogen.","PeriodicalId":42860,"journal":{"name":"Journal of Contemporary Medical Sciences","volume":" ","pages":""},"PeriodicalIF":0.2,"publicationDate":"2023-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49105610","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
A potential role of extracellular DNA in biofilm and ciprofloxacin resistance 细胞外DNA在生物膜和环丙沙星耐药性中的潜在作用
IF 0.2 Q4 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-04-26 DOI: 10.22317/jcms.v9i2.1338
Hind Tahseen Ibrahim, Ali A. Mussa, Harith Jabbar Fahad Al-Mathkhury
Objectives: This study aims to broaden our knowledge of the role of eDNA in bacterial biofilms and antibiotic-resistance gene transfer among isolates. Methods: Staphylococcus aureus, E. coli, and Pseudomonas aeruginosa were isolated from different non-repeated 170 specimens. The bacterial isolates were identified using morphological and molecular methods. Different concentrations of genomic DNA were tested for their potential role in biofilms formed by study isolates employing microtiter plate assay. Ciprofloxacin resistance was identified by detecting a mutation in gyrA and parC. Results: The biofilm intensity significantly decreased (P < 0.05) concerning S. aureus isolates and insignificantly (P > 0.05) concerning E. coli isolates. Yet, one E. coli isolate's biofilm was significantly decreased (P < 0.05) linearly with increasing eDNA. Of considerable interest, the addition of eDNA led to a significant increase (P < 0.05) in the biofilm of the two-tested P. aeruginosa isolates. Moreover, eDNA participated in transferring Ciprofloxacin resistance to the sensitive isolate when it presents in its biofilm. Conclusion: eDNA has a dual effect on bacterial biofilms either supportive or suppressive following bacterial species per se. Also, it seems to play an important role in antibiotic resistance within the biofilm.
目的:本研究旨在拓宽我们对eDNA在细菌生物膜和分离株间抗生素耐药性基因转移中的作用的了解。方法:从170个不同的非重复标本中分离出金黄色葡萄球菌、大肠杆菌和铜绿假单胞菌。采用形态学和分子生物学方法对分离菌株进行鉴定。采用微量滴定板法测试不同浓度的基因组DNA在研究分离株形成的生物膜中的潜在作用。通过检测gyrA和parC中的一个突变来鉴定对环丙沙星的耐药性。结果:金黄色葡萄球菌和大肠杆菌的生物膜强度分别显著降低(P<0.05)和不显著降低(P>0.05)。然而,一个大肠杆菌分离株的生物膜随着eDNA的增加而显著线性降低(P<0.05)。值得关注的是,eDNA的添加导致两个测试的铜绿假单胞菌分离株的生物膜显著增加(P<0.05)。此外,当敏感分离物存在于其生物膜中时,eDNA参与将环丙沙星耐药性转移到敏感分离物。结论:eDNA对细菌生物膜本身具有支持或抑制的双重作用,并且在生物膜内的抗生素耐药性中起着重要作用。
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引用次数: 0
Isolation, identification and comparative analysis of 16S rRNA of Multidrug-resistant Bacteria Clinically isolated from Al Qassim Region Hospitals in Saudi Arabia 沙特阿拉伯Al-Qassim地区医院临床分离的多药耐药菌16S rRNA的分离、鉴定和比较分析
IF 0.2 Q4 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-04-26 DOI: 10.22317/jcms.v9i2.1337
H.S. Alkhowaiter, Othman Alyahyawy, Abdullah Abdulhafeez Aljeddawi, Salah El-Deen Mohamed Abo-Aba
Objective:   This study concluded that the antibiotic resistance and gene transfer across bacterial strains in the hospital setting are two possible explanations for the observed sequence changes in the target microorganisms. Methods:   The 16S rDNA genes of all isolates were effectively amplified using PCR, and detailed identification results were derived from GenBank databases. The BLAST search resulted in the classification of 28 isolates into five strains. The GC content of bacterial sequences varies greatly between single species. Results:  16S rDNA was utilized to identify bacterial species from isolates strains results demonstrated that identification of bacterial strains. Sequences varied between and within strains, also, variation are noticed in genomic nucleotide content of isolated and identified strains. Results of the present study demonstrated that the observed heterogeneity in the sequences of our target bacterial strains may be linked to antibiotic resistance and gene transfer between bacteria that evolved as a result of the hospital environment. Conclusion:  This study concluded that antibiotic-resistant bacteria are capable of transferring copies of their DNA encoding a resistance mechanism to other bacteria, even those that are distantly related to them. the observed heterogeneity in the sequences of our target bacterial strains may be linked to antibiotic resistance and gene transfer between bacteria that evolved as a result of the hospital environment.
目的:本研究得出结论,在医院环境中,抗生素耐药性和菌株间的基因转移是观察到的目标微生物序列变化的两种可能解释。方法:利用聚合酶链式反应对所有分离株的16S rDNA基因进行有效扩增,并从GenBank数据库中获得详细的鉴定结果。BLAST搜索结果将28个分离株分为5个菌株。细菌序列的GC含量在单个物种之间变化很大。结果:利用16S rDNA对分离菌株进行菌种鉴定。菌株之间和菌株内部的序列各不相同,分离和鉴定的菌株的基因组核苷酸含量也存在差异。本研究的结果表明,在我们的目标菌株序列中观察到的异质性可能与抗生素耐药性和因医院环境而进化的细菌之间的基因转移有关。结论:这项研究得出结论,抗生素耐药性细菌能够将其编码耐药性机制的DNA拷贝转移到其他细菌,即使是与它们亲缘关系较远的细菌。在我们的目标菌株序列中观察到的异质性可能与抗生素耐药性和由于医院环境而进化的细菌之间的基因转移有关。
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引用次数: 0
Serum Antioxidant Status in Sickle Cell Disease Patients: Implications for Oxidative Stress and Disease Severity 镰状细胞病患者血清抗氧化状态:对氧化应激和疾病严重程度的影响
IF 0.2 Q4 MEDICINE, GENERAL & INTERNAL Pub Date : 2023-04-26 DOI: 10.22317/jcms.v9i2.1336
Zainab Ali Hadi, F. J. Al-Tu’ma, Atheer Hameid Odda, Hawra Almuhafdah
Objectives: The main aim of this subject is to determine the oxidative status of Iraqi sickle cell anemic patients and then correlated with various biomarkers. Methods: In this study, blood samples from 100 sickle cell anemic subjects were analyzed, and then compared with control group which consisting of 50 individuals without sickle cell anemia was established. Various biochemical techniques were employed to measure different oxidative stress markers and inflammatory mediators. Serum samples were collected from blood to determine the levels of antioxidants such as catalase (CAT), glutathione peroxidase (G-Px), reduced glutathione (GSH), and lipid-peroxidation product malondialdehyde (MDA). Results: The results revealed that the levels of serum antioxidant activity (CAT), GSH, and G-Px were significantly reduced with (P < 0.05) in sickle cell anemic patients as compared with apparently control group. In contrast, the MDA level was significantly higher in sickle cell anemic patients than that found in the apparently control group. Conclusion: In this work, there is an increased oxidative stress in sickle cell anemic patients, which is accompanied by a decrease in antioxidant activity and a rise in lipid peroxidation, leading to the intensification of sickle cell anemic symptoms in patients.
目的:本课题的主要目的是确定伊拉克镰状细胞性贫血患者的氧化状态,并与各种生物标志物进行相关性研究。方法:本研究对100例镰状细胞性贫血患者的血样进行分析,并与50例无镰状细胞性贫血的对照组进行比较。采用多种生化技术测量不同的氧化应激标志物和炎症介质。采集血清样本,测定过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(G-Px)、还原性谷胱甘肽(GSH)和脂质过氧化产物丙二醛(MDA)等抗氧化剂水平。结果:与明显对照组相比,镰状细胞贫血患者血清抗氧化活性(CAT)、GSH、G-Px水平显著降低(P < 0.05)。相比之下,镰状细胞性贫血患者的MDA水平明显高于明显对照组。结论:在本研究中,镰状细胞性贫血患者存在氧化应激增高,同时伴随着抗氧化活性降低和脂质过氧化升高,导致患者镰状细胞性贫血症状加重。
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引用次数: 0
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Journal of Contemporary Medical Sciences
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