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Effect of KRAS and BRAF mutations in metastatic colorectal cancer patients: A systematic review and meta-analysis based on tumor sidedness and KRAS subtypes. KRAS和BRAF突变对转移性结直肠癌患者的影响:基于肿瘤侧边性和KRAS亚型的系统回顾和荟萃分析
Q3 Medicine Pub Date : 2021-01-01 DOI: 10.3233/HAB-210451
Khadijeh Saravani, Morteza Salarzaei, Fateme Parooie

Introduction: Metastatic or recurrent colorectal cancer (MRCRC) has a poor prognosis. The aim of the present meta-analysis was to assess the prevalence of different subtypes of KRAS mutation and BRAF mutation in metastatic CRC patients, and evaluate the relationship between the tumor sidedness and prevalence of KRAS and BRAF mutation.

Methods: We searched MEDLINE/PubMed, the Cochrane Library, and ClinicalTrials.gov from January 2010 to July 2020. The data were extracted independently according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA). The statistical analysis was done using STATA and Meta-Disk 1.4 applications.

Results: Overall, 6699 colorectal cancer patients were included. KRAS and BRAF mutation was reported in 28% and 6% of patients, respectively. The overall prevalence of right primary and left primary metastatic CRC patients with mutated KRAS was 40% and 60%. However, the prevalence BRAF mutated right primary and left primary metastatic CRC patients was 37% and 63%. The overall HR was 2.38 for patients with metastatic CRC who had a mutated type of KRAS. Our study showed a mean overall survival of 35.4 month for KRAS mutant and a 10.12 month survival for BRAF mutant patients with metastatic colorectal cancer patients.

Conclusion: The prevalence of KRAS and BRAF mutations varied significantly according to the location of the tumor. BRAF mutations are more commonly found in metastatic colorectal cancers on the right side. Liver was the most common site of metastases in patients with mutant KRAS and the mortality of patients with mutant KRAS was 2.3 times higher than the patients with wild types. These results help to better describe the population of mCRC patients and can have implications for improving and organizing anti-EGFR therapies. Further research is needed to assess differences in survival through mutation status and primary tumor location.

转移性或复发性结直肠癌(MRCRC)预后较差。本meta分析的目的是评估转移性结直肠癌患者中不同亚型KRAS突变和BRAF突变的患病率,并评估肿瘤的侧边性与KRAS和BRAF突变患病率之间的关系。方法:检索2010年1月至2020年7月的MEDLINE/PubMed、Cochrane图书馆和ClinicalTrials.gov。根据系统评价和荟萃分析首选报告项目(PRISMA)独立提取数据。使用STATA和Meta-Disk 1.4应用程序进行统计分析。结果:共纳入6699例结直肠癌患者。KRAS和BRAF突变分别在28%和6%的患者中报道。KRAS突变的右原发和左原发转移性结直肠癌患者的总体患病率分别为40%和60%。然而,BRAF突变的右侧原发性和左侧原发性转移性CRC患者的患病率分别为37%和63%。KRAS突变型转移性结直肠癌患者的总HR为2.38。我们的研究显示KRAS突变体患者的平均总生存期为35.4个月,BRAF突变体患者合并转移性结直肠癌患者的平均总生存期为10.12个月。结论:KRAS和BRAF突变的发生率因肿瘤部位的不同而有显著差异。BRAF突变更常见于右侧转移性结直肠癌。肝脏是突变型KRAS患者最常见的转移部位,突变型KRAS患者的死亡率是野生型患者的2.3倍。这些结果有助于更好地描述mCRC患者群体,并可能对改善和组织抗egfr治疗具有指导意义。需要进一步的研究来评估通过突变状态和原发肿瘤位置的生存差异。
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引用次数: 6
Relationship between health literacy and quality of life among hemodialysis patients, Tehran, Iran, 2019. 血液透析患者健康素养与生活质量的关系,德黑兰,伊朗,2019。
Q3 Medicine Pub Date : 2021-01-01 DOI: 10.3233/HAB-200423
Yisak Hagos Alemayehu, Khatereh Seylani, Farshad Sharifi, Parvaneh Asgari, Banafsheh Ghorbani, Fatemeh Bahramnezhad

Background: Chronic kidney disease and dialysis are associated with various complications.

Objective: This study aimed to determine the relationship between health literacy and quality of life among patients receiving hemodialysis in hospitals affiliated with Tehran University of Medical Sciences.

Methods: In this study, a descriptive - correlational study design with 138 sample size was used. Convenience sampling was used to select the study participants. We collected the data on May-September 2019. Data collection was done using the HELIA and KDQOL SF™.

Results: In this study, 133 respondents fully completed the questioners. The mean score of health literacy of the respondents was 49.03 (± 22.37) while the average score of quality of life of the respondents in this study was 53.01 (± 14.86).

Conclusion: Based on the findings, patients receiving haemodialysis had insufficient health literacy and a better quality of life. In order to address the health literacy needs of the patients, consideration of continuous health education and assessment in this patient subpopulation could gradually improve their health literacy and quality of life. Health care providers such as nurses could improve Health Literacy and substantially Quality of Life through interventions aimed at determining existing literacy needs in the long and short term treatment course for individual dialysis patients.

背景:慢性肾脏疾病和透析与各种并发症相关。目的:本研究旨在确定在德黑兰医科大学附属医院接受血液透析患者的健康素养与生活质量之间的关系。方法:本研究采用描述性相关研究设计,样本量为138个。采用方便抽样法选择研究对象。我们收集了2019年5月至9月的数据。使用HELIA和KDQOL SF™完成数据收集。结果:133名被调查者完整完成了问卷。调查对象健康素养平均得分为49.03(±22.37)分,生活质量平均得分为53.01(±14.86)分。结论:根据研究结果,接受血液透析的患者健康素养不足,生活质量较好。为了满足患者的健康素养需求,考虑对该患者亚群进行持续的健康教育和评估,可以逐步提高患者的健康素养和生活质量。护士等卫生保健提供者可以通过旨在确定个别透析患者在长期和短期治疗过程中现有的扫盲需求的干预措施,提高卫生扫盲水平和大幅度提高生活质量。
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引用次数: 2
Serological study of celiac disease in children with dental caries. 龋齿儿童乳糜泻的血清学研究。
Q3 Medicine Pub Date : 2021-01-01 DOI: 10.3233/HAB-210445
Gholamreza Kalvandi, Iraj Shahramian, Abbas Farmany, Shirin Yadegari, Fateme Parooie

Background: Celiac disease is a common gastrointestinal autoimmune disorder. Studies have shown that the prevalence of tooth decay is high in patients with celiac disease. This study was performed to evaluate the serology of celiac disease in children with dental caries.

Methods: Children aged 3 to 12 years who referred to the dental clinic with enamel caries were included in the study. Celiac disease was assessed by measuring serum IgA levels and anti-TTG (Anti TTG (IgA)) antibodies. Then, by analyzing the collected data, the prevalence of celiac disease in children with dental caries and its relationship with various variables were investigated.

Results: 120 children, 56 girls (46.7%) and 64 boys (53.3%) with dental caries were involved in this study. The positive celiac serology rate of studied population was 14 (11.6%). Based on the results of this study, a significant relationship was obtained between maternal education, sex and place of residence and celiac disease (p< 0.05). There were no significant relationships between celiac positive serology in children with dental caries, the number of decayed teeth, and breastfeeding (p> 0.05).

Conclusion: The present study showed that dental caries, might be a red flag indicating possible celiac disease and prevent its complications. On the other hand, pediatricians and dentists should be aware of the oral symptoms of celiac disease. Further studies are needed to plan screening for children with celiac disease.

背景:乳糜泻是一种常见的胃肠道自身免疫性疾病。研究表明,乳糜泻患者中蛀牙的患病率很高。本研究旨在评估患有龋齿的儿童乳糜泻的血清学。方法:以3 ~ 12岁就诊的牙釉质龋患儿为研究对象。通过测定血清IgA水平和抗TTG(抗TTG (IgA))抗体来评估乳糜泻。然后,通过分析收集到的数据,探讨乳糜泻在龋齿儿童中的患病率及其与各变量的关系。结果:本组龋病患儿120例,其中女孩56例(46.7%),男孩64例(53.3%)。研究人群乳糜泻血清学阳性率为14例(11.6%)。本研究结果显示,母亲受教育程度、性别和居住地与乳糜泻有显著相关(p< 0.05)。乳糜泻阳性血清学与龋齿数、母乳喂养无显著相关性(p> 0.05)。结论:目前的研究表明,龋齿可能是乳糜泻的一个危险信号,可以预防其并发症。另一方面,儿科医生和牙医应该了解乳糜泻的口腔症状。需要进一步的研究来计划对患有乳糜泻的儿童进行筛查。
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引用次数: 2
Zero tolerance for complacency by government of West African countries in the face of COVID-19. 面对新冠肺炎疫情,西非国家政府绝不容忍自满。
Q3 Medicine Pub Date : 2021-01-01 DOI: 10.3233/HAB-200413
O Erhabor, T Erhabor, T C Adias, G C Okara, M Retsky

A novel Coronavirus (SARS-CoV-2) causing a cluster of respiratory infections (Coronavirus Disease 2019, COVID-19) first discovered in Wuhan, China, is responsible for a new illness that has been found to affect the lungs and airways of patients with associated symptoms of fever, cough and shortness of breath. In the light of few cases recorded so far in West Africa there is tendency for complacency. The region needs to make strategic plans based on available evidence to enable them effectively deal with this rapidly evolving pandemic. At this very moment countries like China, Italy, France, Spain, Iran, UK and many others are witnessing sustained and intensive community transmission of this virus and increasing numbers of severe disease and death particularly among elderly patients with other comorbidities. The reality of the seriousness of this pandemic is alarming. Government of member states of ECOWAS need to prepare themselves by building capacity as well as implement evidenced-based steps to mitigate this rapidly evolving pandemic by testing persons presenting with symptoms (fever, cough and shortness of breath), isolating and treating those found positive, tracing and quarantining contacts, implementing social distancing as well as optimizing human and material endowment to allow healthcare workers offer safe quality clinical care for affected patients to prevent secondary infection among healthcare workers.

在中国武汉首次发现的一种新型冠状病毒(SARS-CoV-2)引起了一系列呼吸道感染(2019冠状病毒病,COVID-19),它导致了一种新的疾病,这种疾病已被发现会影响伴有发烧、咳嗽和呼吸短促等相关症状的患者的肺部和呼吸道。鉴于迄今在西非记录的病例很少,人们有自满的倾向。该区域需要根据现有证据制定战略计划,使其能够有效应对这一迅速演变的大流行病。此时此刻,中国、意大利、法国、西班牙、伊朗、英国和许多其他国家正在目睹这种病毒持续和密集的社区传播,严重疾病和死亡人数不断增加,特别是在患有其他合并症的老年患者中。这一流行病的严重性现实令人震惊。西非经共体成员国政府需要做好准备,建设能力,并采取循证措施,对出现症状(发烧、咳嗽和呼吸短促)的人进行检测,隔离和治疗阳性患者,追踪和隔离接触者,以缓解这一迅速演变的大流行病。实施社会距离并优化人力和物质资源,使卫生保健工作者能够为受影响患者提供安全优质的临床护理,以防止卫生保健工作者之间的继发感染。
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引用次数: 4
Age-stratified pediatric reference values of lymphocytes in the Moroccan population. 摩洛哥儿童淋巴细胞的年龄分层参考值。
Q3 Medicine Pub Date : 2021-01-01 DOI: 10.3233/HAB-200432
Aicha El Allam, Sara El Fakihi, Hicham Tahoune, Karima Sahmoudi, Houria Bousserhane, Youssef Bakri, Naima El Hafidi, Fouad Seghrouchni

The number of circulating lymphocytes is altered in a number of diseases including either increase (lymphocytosis) or decrease (lymphocytopenia). Therefore, the assessment of total blood lymphocyte numbers and the relative distribution of lymphocyte subsets is a critical front-line tool in the clinical diagnosis of a number of diseases, including pediatric diseases and disorders. However, the interpretation of this data requires comparison of patient's results to reliable reference values. Blood lymphocyte subpopulation numbers are also subject to genetic polymorphisms, immunogenic and environmental factors and vary greatly between populations. While the best practice reference values should be established within local representative populations of healthy subjects, to date, Caucasian reference values are used in Morocco due to the absence of indigenous reference values. Potential differences in blood lymphocyte subpopulation reference values between Caucasian versus Moroccan populations can adversely affect the diagnosis of pediatric and childhood diseases and disorders such as primary immunodeficiency (PID) in Morocco.

Objective: The aim of this study was to establish the age-stratified normal reference values of blood lymphocyte subsets for the pediatric Moroccan population.

Methods: We measured the concentration of lymphocyte subpopulations by flow cytometry from 83 Moroccan healthy subjects stratified into 5 age groups of 0-1, 1-2, 2-6, 6-12 and > 12-18 (adult).

Results: The absolute and relative amounts of the main lymphocyte subsets of T-cells, B cells and Natural Killer (NK) cells were measured and compared to previously described reference values from Cameroonian, Turkish, American and Dutch populations. Additionally, we also observed an age-related decline in the absolute population sizes of lymphocyte subsets within our study group. Relative proportions of CD3+CD4+ helper T lymphocytes decreased with increasing age and by 12 years-adult age, both proportions of CD3+CD4+ helper T lymphocytes and CD3+CD8+ cytotoxic T lymphocytes, as well as CD3-CD19+ B lymphocytes were also decreased. Finally, we compared the median values and range of our Moroccan study group with that of published results from Cameroon, Turkey, USA and Netherlands and observed significant differences in median and mean values of absolute number and relative proportions of lymphocyte subsets especially at 0-1 years and 1-2 years age groups. Above age 12 years, the Moroccan values were lower. For NK cells, the Moroccan values are also lower.

Conclusions: The results of this study have a significant impact in improving the threshold values of the references intervals routinely used in the diagnosis of paediatric diseases such as PIDs or mother-to-child transmitted HIV within the Moroccan population.

在许多疾病中,循环淋巴细胞的数量发生改变,包括增加(淋巴细胞增多)或减少(淋巴细胞减少)。因此,评估血液淋巴细胞总数和淋巴细胞亚群的相对分布是临床诊断包括儿科疾病和障碍在内的许多疾病的关键一线工具。然而,对这些数据的解释需要将患者的结果与可靠的参考值进行比较。血液淋巴细胞亚群数量也受遗传多态性、免疫原性和环境因素的影响,在人群之间差异很大。虽然最佳做法参考值应在当地健康受试者的代表性人群中确定,但由于缺乏土著参考值,迄今为止,摩洛哥使用的是高加索参考值。高加索人与摩洛哥人之间血液淋巴细胞亚群参考值的潜在差异可能对儿科和儿童疾病的诊断产生不利影响,如摩洛哥原发性免疫缺陷(PID)。目的:本研究的目的是为摩洛哥儿童建立按年龄分层的血淋巴细胞亚群正常参考值。方法:采用流式细胞术检测83名摩洛哥健康受试者淋巴细胞亚群浓度,将其分为0-1、1-2、2-6、6-12和> 12-18(成人)5个年龄组。结果:测量了t细胞、B细胞和自然杀伤(NK)细胞的主要淋巴细胞亚群的绝对和相对数量,并与先前描述的喀麦隆、土耳其、美国和荷兰人群的参考值进行了比较。此外,我们还观察到,在我们的研究组中,淋巴细胞亚群的绝对种群大小与年龄相关。随着年龄的增长,CD3+CD4+辅助性T淋巴细胞的相对比例下降,到12 -成年时,CD3+CD4+辅助性T淋巴细胞和CD3+CD8+细胞毒性T淋巴细胞以及CD3- cd19 + B淋巴细胞的比例也下降。最后,我们将摩洛哥研究组的中位数和范围与喀麦隆、土耳其、美国和荷兰发表的结果进行了比较,发现淋巴细胞亚群绝对数量和相对比例的中位数和平均值存在显著差异,特别是在0-1岁和1-2岁年龄组。在12岁以上,摩洛哥的数值较低。对于NK细胞,摩洛哥值也较低。结论:这项研究的结果对提高参考区间的阈值具有重大影响,这些阈值通常用于诊断儿科疾病,例如在摩洛哥人口中诊断aids或母婴传播艾滋病毒。
{"title":"Age-stratified pediatric reference values of lymphocytes in the Moroccan population.","authors":"Aicha El Allam,&nbsp;Sara El Fakihi,&nbsp;Hicham Tahoune,&nbsp;Karima Sahmoudi,&nbsp;Houria Bousserhane,&nbsp;Youssef Bakri,&nbsp;Naima El Hafidi,&nbsp;Fouad Seghrouchni","doi":"10.3233/HAB-200432","DOIUrl":"https://doi.org/10.3233/HAB-200432","url":null,"abstract":"<p><p>The number of circulating lymphocytes is altered in a number of diseases including either increase (lymphocytosis) or decrease (lymphocytopenia). Therefore, the assessment of total blood lymphocyte numbers and the relative distribution of lymphocyte subsets is a critical front-line tool in the clinical diagnosis of a number of diseases, including pediatric diseases and disorders. However, the interpretation of this data requires comparison of patient's results to reliable reference values. Blood lymphocyte subpopulation numbers are also subject to genetic polymorphisms, immunogenic and environmental factors and vary greatly between populations. While the best practice reference values should be established within local representative populations of healthy subjects, to date, Caucasian reference values are used in Morocco due to the absence of indigenous reference values. Potential differences in blood lymphocyte subpopulation reference values between Caucasian versus Moroccan populations can adversely affect the diagnosis of pediatric and childhood diseases and disorders such as primary immunodeficiency (PID) in Morocco.</p><p><strong>Objective: </strong>The aim of this study was to establish the age-stratified normal reference values of blood lymphocyte subsets for the pediatric Moroccan population.</p><p><strong>Methods: </strong>We measured the concentration of lymphocyte subpopulations by flow cytometry from 83 Moroccan healthy subjects stratified into 5 age groups of 0-1, 1-2, 2-6, 6-12 and > 12-18 (adult).</p><p><strong>Results: </strong>The absolute and relative amounts of the main lymphocyte subsets of T-cells, B cells and Natural Killer (NK) cells were measured and compared to previously described reference values from Cameroonian, Turkish, American and Dutch populations. Additionally, we also observed an age-related decline in the absolute population sizes of lymphocyte subsets within our study group. Relative proportions of CD3+CD4+ helper T lymphocytes decreased with increasing age and by 12 years-adult age, both proportions of CD3+CD4+ helper T lymphocytes and CD3+CD8+ cytotoxic T lymphocytes, as well as CD3-CD19+ B lymphocytes were also decreased. Finally, we compared the median values and range of our Moroccan study group with that of published results from Cameroon, Turkey, USA and Netherlands and observed significant differences in median and mean values of absolute number and relative proportions of lymphocyte subsets especially at 0-1 years and 1-2 years age groups. Above age 12 years, the Moroccan values were lower. For NK cells, the Moroccan values are also lower.</p><p><strong>Conclusions: </strong>The results of this study have a significant impact in improving the threshold values of the references intervals routinely used in the diagnosis of paediatric diseases such as PIDs or mother-to-child transmitted HIV within the Moroccan population.</p>","PeriodicalId":53564,"journal":{"name":"Human Antibodies","volume":"29 1","pages":"85-94"},"PeriodicalIF":0.0,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3233/HAB-200432","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38656882","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: 2
Over-expression of IL-6 coding gene in the peripheral blood of migraine with aura patients. 先兆偏头痛患者外周血IL-6编码基因的过表达。
Q3 Medicine Pub Date : 2021-01-01 DOI: 10.3233/HAB-210442
Mahdi Ramezani, Alireza Komaki, Mohammad Mahdi Eftekharian, Mehrdokht Mazdeh, Soudeh Ghafouri-Fard

Migraine is a common disorder which is placed among the top ten reasons of years lived with disability. Cytokines are among the molecules that contribute in the pathophysiology of migraine. In the current study, we evaluated expression levels of IL-6 coding gene in the peripheral blood of 120 migraine patients (54 migraine without aura and 66 migraine with aura patients) and 40 healthy subjects. No significant difference was detected in expression of IL-6 between total migraine patients and healthy controls (Posterior beta = 0.253, P value = 0.199). The interaction effect between gender and group was significant (Posterior beta =-1.274, P value = 0.011), therefore, we conducted subgroup analysis within gender group. Such analysis revealed that while expression of this gene is not different between male patients and male controls (Posterior beta =-0.371, P value > 0.999), it was significantly over-expressed in female patients compared with female controls (Posterior beta = 0.86, P= 0.002). Expression of IL-6 was significantly higher in patients with aura compared with controls (Posterior beta = 0.63, adjusted P value = 0.019). However, expression of this cytokine coding gene was not different between patients without aura and healthy subjects (Posterior beta = 0.193, adjusted P value = 0.281). Therefore, IL-6 might be involved in the pathophysiology of migraine among females and migraine with aura among both sexes.

偏头痛是一种常见的疾病,是导致残疾的十大原因之一。细胞因子是参与偏头痛病理生理的分子之一。在本研究中,我们评估了120名偏头痛患者(54名无先兆偏头痛患者和66名有先兆偏头痛患者)和40名健康受试者外周血中IL-6编码基因的表达水平。总体偏头痛患者与健康对照组IL-6表达差异无统计学意义(后验β = 0.253, P值= 0.199)。性别与组间交互作用显著(后验β =-1.274, P值= 0.011),因此我们在性别组内进行亚组分析。分析结果显示,该基因在男性患者与男性对照组的表达量无差异(后验β =-0.371, P值> 0.999),而在女性患者中与女性对照组相比明显过表达(后验β = 0.86, P= 0.002)。有先兆的患者IL-6表达明显高于对照组(后验β = 0.63,校正P值= 0.019)。然而,该细胞因子编码基因在无先兆患者和健康受试者之间的表达无差异(后验β = 0.193,调整P值= 0.281)。因此,IL-6可能参与了女性偏头痛和男性先兆偏头痛的病理生理过程。
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引用次数: 3
Radiomics, aptamers and nanobodies: New insights in cancer diagnostics and imaging. 放射组学,适体体和纳米体:癌症诊断和成像的新见解。
Q3 Medicine Pub Date : 2021-01-01 DOI: 10.3233/HAB-200436
Abdullah O Alamoudi

At present, cancer is a major health issue and the second leading cause of mortality worldwide. Researchers have been working hard on investigating not only improved therapeutics but also on early detection methods, both critical to increasing treatment efficacy and developing methods for disease prevention. Diagnosis of cancers at an early stage can promote timely medical intervention and effective treatment and will result in inhibiting tumor growth and development. Several advances have been made in the diagnostics and imagining technologies for early tumor detection and deciding an effective therapy these include radiomics, nanobodies, and aptamers. Here in this review, we summarize the main applications of radiomics, aptamers, and the use of nanobody-based probes for molecular imaging applications in diagnosis, treatment planning, and evaluations in the field of oncology to develop quantitative and personalized medicine. The preclinical data reported to date are quite promising, and it is predicted that nanobody-based molecular imaging agents will play an important role in the diagnosis and management of different cancer types in near future.

目前,癌症是一个主要的健康问题,也是全世界第二大死亡原因。研究人员一直在努力研究改进的治疗方法和早期检测方法,这对提高治疗效果和开发疾病预防方法都至关重要。癌症的早期诊断可以促进及时的医疗干预和有效的治疗,并将导致抑制肿瘤的生长和发展。在早期肿瘤检测和确定有效治疗的诊断和成像技术方面取得了一些进展,包括放射组学、纳米体和适体体。本文综述了放射组学、适体体和纳米探针在肿瘤诊断、治疗计划和评估方面的主要应用,以发展定量和个性化医疗。目前所报道的临床前数据都很有前景,预计在不久的将来,基于纳米体的分子显像剂将在不同类型癌症的诊断和治疗中发挥重要作用。
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引用次数: 3
Prevalence of HLA DQ 2, 8 in children with celiac disease. 乳糜泻患儿HLA dq2,8的患病率
Q3 Medicine Pub Date : 2021-01-01 DOI: 10.3233/HAB-200437
Seyed Mohsen Dehghani, Naqi Dara, Behrooz Gharesifar, Iraj Shahramian, Fatemeh Dalili, Morteza Salarzaei

Objective: Celiac disease is a chronic disease that affect small bowel by making its villi become atrophic. Various environmental and genetic factors have been identify as inducing factors for celiac disease. Most of the patients has one of the HLA DQ forms. Although the prevalence of these genes are variable in different areas of the world, we do not have a comprehensive information about this issue in our region. Thus the aim of present study is to investigate the prevalence of HLA DQ typing of patients who visited Emam Reza Gastroenterology clinic of Shiraz(IRAN).

Methods: In this case-control study all under 18 years old children who were diagnosed with celiac disease and have visited Emam Reza gastroenterology clinic were investigated. The diagnosis of celiac disease was made by history, physical exam, serologic test, and histopathology of duodenal biopsy. Blood sample was taken and HLA typing performed using PCR method at Motahari clinic cytology laboratory. Also those people who neither them self nor their first degree relatives were not case of celiac disease and underwent HLA typing for other reason were identified as control group. The statistical analysis was done using SPSS 18 software. The p value < 0.05 was identified as statistically significant.

Results: A total of 139 patients with celiac disease and 146 normal children were studied. The mean age of the patient with celiac disease were 9.1 years old with standard deviation of 3.4 years old. 64% of the celiac patients were girls and 36% were boys. While this proportion was 54.4% for boy and 48.6% for girls in control group. The most common HLA in celiac patients group were HLA DQ2 and 8 but the most common ones in control group were HLA DQ 8 and 5. Failure to Thrive were the most common signs of the celiac patients with a prevalence of 60 children. Total IgA titer were normal in 98.6% of the patients and TTG IgA titer were positive in 93.5% of the patients. The most common co existing disease with the celiac disease were diabetes with a prevalence of 30 children (66.7%).

Conclusion: present study reveals that the prevalence of the HLA DQ2 and 8 among patients with celiac disease is 72.6% and 53% in our normal population.

目的:乳糜泻是一种通过使小肠绒毛萎缩而影响小肠的慢性疾病。各种环境和遗传因素已被确定为乳糜泻的诱发因素。大多数患者有一种HLA DQ型。虽然这些基因的流行率在世界不同地区是不同的,但我们没有关于本地区这一问题的全面信息。因此,本研究的目的是调查到设拉子(伊朗)伊玛目礼萨胃肠病学诊所就诊的患者HLA - DQ分型的流行情况。方法:在本病例对照研究中,调查了所有18岁以下就诊于Emam Reza胃肠病学诊所的诊断为乳糜泻的儿童。乳糜泻的诊断是通过病史、体格检查、血清学检查和十二指肠活检的组织病理学来确定的。在Motahari临床细胞学实验室采集血样,采用PCR法进行HLA分型。同时,那些既不是自身也不是直系亲属没有乳糜泻但因其他原因进行HLA分型的人被确定为对照组。采用SPSS 18软件进行统计分析。p值< 0.05为差异有统计学意义。结果:共对139例乳糜泻患者和146例正常儿童进行了研究。乳糜泻患者平均年龄9.1岁,标准差3.4岁。64%的乳糜泻患者是女孩,36%是男孩。而在对照组中,男孩和女孩的这一比例分别为54.4%和48.6%。乳糜泻患者组最常见的HLA为HLA DQ2和8,对照组最常见的HLA为HLA dq8和5。发育不良是乳糜泻患者最常见的症状,共有60名儿童患有乳糜泻。98.6%的患者总IgA滴度正常,93.5%的患者TTG IgA滴度阳性。与乳糜泻合并最常见的疾病是糖尿病,患病率为30例(66.7%)。结论:本研究显示,乳糜泻患者HLA DQ2和8在正常人群中的患病率分别为72.6%和53%。
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引用次数: 1
Immunogenicity of biologics used in the treatment of inflammatory bowel disease. 用于治疗炎性肠病的生物制剂的免疫原性。
Q3 Medicine Pub Date : 2021-01-01 DOI: 10.3233/HAB-210449
Mariam Bqain, Alex Efimov, David Baker, Angray S Kang

Purpose of the review: Here we critically evaluate the literature on immunotherapy failure in inflammatory bowel disease patients. In particular anti-drug antibody production, and subsequently loss of response as the primary cause of immunotherapy failure in IBD patients. The benefits of shifting from the "standard" empirical dose escalation approach to therapeutic drug monitoring with anti-TNFα therapy is explored.

Recent findings: The American Gastroenterology Association and British Society of Gastroenterology both currently recommend the use of reactive therapeutic drug monitoring to guide treatment, following loss of response in inflammatory bowel disease patients with active disease. However, further research is required to prove the efficacy of a proactive therapeutic drug monitoring approach alone in remitted IBD patients.

Summary: A combination of personalised monitoring approach for anti-drug antibodies and therapeutic drug monitoring could provide beneficial treatment outcome for people with inflammatory bowel disease by predicting drug failure prior to clinical symptoms and allowing timely switching to an alternative drug.

回顾的目的:在这里,我们批判性地评价炎症性肠病患者免疫治疗失败的文献。特别是抗药物抗体的产生,以及随后的反应丧失是IBD患者免疫治疗失败的主要原因。从“标准”经验剂量递增方法转向抗tnf - α治疗药物监测的好处进行了探讨。最近的发现:美国胃肠病学协会和英国胃肠病学协会目前都推荐使用反应性治疗药物监测来指导治疗炎症性肠病患者的活动性疾病。然而,需要进一步的研究来证明主动治疗药物监测方法在缓解的IBD患者中的有效性。摘要:抗药物抗体的个性化监测方法和治疗性药物监测相结合,可以在临床症状出现之前预测药物失效,并允许及时切换到替代药物,从而为炎症性肠病患者提供有益的治疗结果。
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引用次数: 1
Comparative evaluation of SARS-CoV-2 IgG assays against nucleocapsid and spike antigens. SARS-CoV-2 IgG对核衣壳和刺突抗原检测的比较评价。
Q3 Medicine Pub Date : 2021-01-01 DOI: 10.3233/HAB-210440
Mitra Rezaei, Mohammadhadi Sadeghi, Alireza Korourian, Payam Tabarsi, Mihan Porabdollah, Elham Askari, Esmaeil Mortaz, Shima Mahmoudi, Majid Marjani, Ali Akbar Velayati

Background: There are few studies to compare antibody response against anti-spike (S) and anti- nucleoprotein (N) SARS-CoV-2.

Objective: The aim of this study was to evaluate the IgG antibody production against S and N antigens of the virus and their correlation with the time and severity of the disease.

Methods: The IgG antibodies against S and N antigens of SARS-CoV-2 in serum specimens of 72 symptomatic patients who tested real-time reverse transcription polymerase chain reaction positive for SARS-CoV-2 were detected using the ELISA technique. Different antibody response was compared and the correlation with the time from disease onset and the severity was evaluated.

Results: Forty-eight of 72 (67%) patients tested positive for anti-SARS-CoV-2 antibodies, while 24 (33%) did not have detectable antibodies. Comparison of antibody levels for N and S antibodies showed that they correlate with each other well (r= 0.81; P< 0.001). However, sensitivity of anti-S SARS-CoV-2 IgG and anti-N SARS-CoV-2 IgG was 30% and 60%, during the first 7 days after symptom onset (r= 0.53; P= 0.111), but increased to 73% and 68% at more than 1-week post symptom onset (r= 0.89, P= 0.111), respectively. Cases with positive IgG response showed a decreased CD8+ T cells percentage compared to the negative IgG groups (26 ± 14 vs. 58 ± 32, p= 0.066 in anti-N IgG group and 28 ± 15 vs. 60 ± 45, p= 0.004 in anti-S IgG group, respectively).

Conclusion: Nearly one-third of the confirmed COVID-19 patients had negative serology results. Lower percent positivity at early time points after symptom onset (less than 1 week) was seen using anti-S SARS-COV-2 IgG kit compare to the anti-N SARS-CoV-2 IgG; therefore, clinicians should interpret negative serology results of especially anti-S SARS-CoV-2 IgG with caution.

背景:比较抗刺突(S)抗体和抗核蛋白(N)抗体对SARS-CoV-2反应的研究很少。目的:评价病毒S抗原和N抗原IgG抗体的产生及其与发病时间和严重程度的相关性。方法:采用ELISA技术检测72例SARS-CoV-2实时逆转录聚合酶链反应阳性患者血清中SARS-CoV-2 S、N抗原IgG抗体。比较不同抗体反应,并评价与发病时间和严重程度的相关性。结果:72例患者中48例(67%)检测出抗sars - cov -2抗体阳性,24例(33%)未检测到抗体。N抗体和S抗体的抗体水平比较表明,它们之间的相关性很好(r= 0.81;P < 0.001)。而在症状出现后的前7天,抗- s - cov -2 IgG和抗- n - cov -2 IgG的敏感性分别为30%和60% (r= 0.53;P= 0.111),但在症状出现后1周以上分别增加到73%和68% (r= 0.89, P= 0.111)。IgG阳性组CD8+ T细胞百分比较IgG阴性组降低(抗n IgG组为26±14比58±32,p= 0.066;抗s IgG组为28±15比60±45,p= 0.004)。结论:近三分之一的新冠肺炎确诊患者血清学结果为阴性。使用抗s - SARS-COV-2 IgG试剂盒与抗n - SARS-COV-2 IgG相比,在症状出现后(不到1周)的早期时间点的阳性率较低;因此,临床医生应谨慎解释血清学阴性结果,特别是抗SARS-CoV-2 IgG。
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引用次数: 6
期刊
Human Antibodies
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