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Rise in Levels of Anti-SARS CoV-2 Immunoglubulin G by Covishield Vaccine- A Cohort Study in Rural Medical College, West Bengal, India Covishield疫苗提高抗sars CoV-2免疫球蛋白G水平——印度西孟加拉邦农村医学院的一项队列研究
Pub Date : 2022-01-01 DOI: 10.7860/njlm/2022/52643.2582
J. Rout, Sujash Biswas, Sayari Banerjee, Simit H Kumar, Palash Das, S. Dey
Introduction: The Coronavirus Disease-2019 (COVID-19) pandemic was declared by the World Health Organisation (WHO) on 11th March 2020 caused by Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2). As a preventive measure, valid information concerning the development of antibodies is being collected for assessing the progress towards herd immunity of COVID-19. Aim: To assess the level of Anti-SARS-CoV-2 IgG before and after vaccination by two doses of ChAdOx1 nCoV 19 vaccine in a rural Medical College of West Bengal. Materials and Methods: The present interventional cohort study was conducted in a rural Medical College and Hospital, West Bengal, India, from February 2021 to August 2021. Total 248 willing subjects were included for this interventional study from the same socio-economic and geographical distribution depending upon a vaccine population of a rural Medical College of West Bengal. To measure the anti-SARS-CoV-2 IgG antibody authors used Indian Council of Medical Research-National Institute of Virology (ICMRNIV) certified Anti-SARS-CoV-2 human IgG ELISA COVID KAVACH MERILISA kit and approved protocol by the ICMR. Results: The median age of study population was 39 years (range 25-64) with 97 (39.1%) females and 151 (60.9%) males. It was found that antibody response induced by two doses of vaccination was significantly high (t-value: 28.421, p<0.001) in the vaccinated population. Conclusion: Thus, present study suggests that vaccination may be critical to develop anti-SARS-CoV-2 IgG antibody. This would lead to a better understanding of the immunisation program and prevention of severe disease and deaths due to COVID-19.
2020年3月11日,世界卫生组织(世卫组织)宣布,由严重急性呼吸综合征冠状病毒-2 (SARS-CoV-2)引起的冠状病毒病-2019 (COVID-19)大流行。作为一项预防措施,正在收集有关抗体形成的有效信息,以评估COVID-19群体免疫方面的进展。目的:评价西孟加拉邦农村医学院两剂ChAdOx1 nCoV - 19疫苗接种前后抗sars - cov -2 IgG水平。材料和方法:本介入队列研究于2021年2月至2021年8月在印度西孟加拉邦的一所农村医学院和医院进行。根据西孟加拉邦一所农村医学院的疫苗接种人群,共有248名自愿受试者被纳入这项干预性研究,这些受试者来自相同的社会经济和地理分布。为了检测抗sars - cov -2 IgG抗体,作者使用了印度医学研究委员会-国家病毒学研究所(ICMRNIV)认证的抗sars - cov -2人IgG ELISA试剂盒COVID KAVACH MERILISA试剂盒,并经ICMR批准。结果:研究人群年龄中位数为39岁(25-64岁),女性97例(39.1%),男性151例(60.9%)。结果发现,两剂疫苗诱导的抗体应答在接种人群中显著高(t值:28.421,p<0.001)。结论:本研究提示疫苗接种可能是产生抗sars - cov -2 IgG抗体的关键。这将有助于更好地了解免疫规划和预防COVID-19导致的严重疾病和死亡。
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引用次数: 0
Study of Biomarkers in Cancer Patients Treated with Radiotherapy: A Case-control Study 肿瘤放疗患者的生物标志物研究:一项病例对照研究
Pub Date : 2022-01-01 DOI: 10.7860/njlm/2022/53452.2639
K. P. Patel, Mayur Goradhanbhai Makadia, D. Chaudhari
Introduction: Blood based biomarkers can be useful as prognostic markers because these biomarkers can reflect variations in the tumour microenvironment and the immune system of the host. This study investigates some biomarkers in cancer patients experienced with radiotherapy to evaluate the effect of radiotherapy on the body. Aim: To assess radiotherapy induced changes in the biomarkers like serum total protein, albumin, creatinine and urea in cancer patients and compare to the healthy controls. Materials and Methods: This was a case-control study, conducted in the Biochemistry Department, Baroda Medical College, Gujarat, India, from October 2017 to August 2018. This study enrolled 537 patients, who underwent radiation therapy irrespective of any cancer and 537 healthy controls without any history of cancer or radiation therapy. Serum total protein, albumin, creatinine, and urea were measured. Statistical analysis was performed by descriptive statistics, independent t-test, Frequency, Pearson’s correlation coefficient (r). Results: In each of the groups, out of 537 subjects 185 subjects were females, 61.30±9.03 years was the mean age for females, and 352 subjects were males with a mean age of 61.02±8.93 years. Albumin had negative statistically significant correlation with all parameters. But total protein which was also composed of other acute phase positive reactants had higher values compared to control group which was statistically significant (p<0.001). Conclusion: It was found that patients with cancer, undergoing radiotherapy, suffered from radiation induced changes such as acute phase response, host defense mechanism etc., causing changes in the body which is reflected by biomarkers.
基于血液的生物标志物可以作为有用的预后标志物,因为这些生物标志物可以反映肿瘤微环境和宿主免疫系统的变化。本研究探讨了放疗后肿瘤患者的一些生物标志物,以评估放疗对机体的影响。目的:探讨放疗对肿瘤患者血清总蛋白、白蛋白、肌酐、尿素等生物标志物的影响,并与健康对照进行比较。材料与方法:本研究为病例对照研究,于2017年10月至2018年8月在印度古吉拉特邦巴罗达医学院生物化学系进行。这项研究招募了537名患者,他们接受了放射治疗,无论是否患有癌症,以及537名没有任何癌症或放射治疗史的健康对照。测定血清总蛋白、白蛋白、肌酐和尿素。采用描述性统计、独立t检验、频率、Pearson相关系数(r)进行统计学分析。结果:每组537例受试者中,女性185例,女性平均年龄61.30±9.03岁,男性352例,平均年龄61.02±8.93岁。白蛋白与各参数呈显著负相关。而由其他急性期阳性反应物组成的总蛋白值高于对照组,差异有统计学意义(p<0.001)。结论:我们发现癌症患者在接受放射治疗后,会发生放射引起的急性期反应、宿主防御机制等变化,引起机体的变化,这些变化通过生物标志物反映出来。
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引用次数: 0
Expression of VEGF and CD34 in Psoriasis Vulgaris: Correlation with Histological Grading by Trozak Histological Assessment Score VEGF和CD34在寻常型银屑病中的表达:与Trozak组织学评分分级的相关性
Pub Date : 2022-01-01 DOI: 10.7860/njlm/2022/53492.2649
R. Sujatha, M. V. Kulkarni, .. Rufaida, Y. Manjunatha
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引用次数: 0
Comparison between Values of Low Density Lipoprotein Cholesterol as Estimated by Direct Enzymatic Method with Calculated Methods Applying Friedewald’s Equation and Novel’s Equation: A Cross-sectional Study 直接酶法测定低密度脂蛋白胆固醇值与应用Friedewald方程和Novel方程计算方法的比较:一项横断面研究
Pub Date : 2022-01-01 DOI: 10.7860/njlm/2022/52146.2594
Maithri Chikkabasavanahalli Manjegowda, Raghunath Hanumantharaya, Mythri Sannamadhu, Medhini Nagaranavile Shivaswamy
Introduction: Lipid profile is routinely used as a screening test to identify the risk of Cardiovascular Diseases (CVD). Elevated Low Density Lipoprotein cholesterol (LDL-c) is an important modifiable risk factor of atherosclerotic CVD. The LDL-c lowering strategy is a known recommendation for the prevention and treatment of CVD. The gold standard method of LDL-c estimation is β-quantification by ultra centrifugation. Other methods include Direct LDL-c measurement (D-LDL-c) using enzymatic assay which is tedious, time consuming and expensive. Hence, calculated method using Friedewald’s equation (F-LDL-c) is routinely used in clinical laboratories in India. Aim: To compare LDL-c values as estimated by direct enzymatic method with LDL-c values obtained by Friedewald’s equation and Novel’s equation, and, also to assess the effects of LDL-c values obtained by both the methods towards the risk stratification of CVD. Materials and Methods: A cross-sectional study, was conducted in the Central Diagnostic Laboratory of Mandya Institute of Medical Sciences, Mandya, Karnataka, India, for a duration of three months from July to September 2020, where, 600 subjects, aged 20-75 years, visiting for routine lipid profile estimation were included. LDL-c was estimated by direct enzymatic method (D-LDL-c) and calculated methods using Friedewald’s {F-LDL-c=TC-HDL-c- (TG/5)} and Novel’s equation {N-LDL-c=TC-HDL-c-(TG/Adjustable factor)}. Values obtained by calculated methods were compared with D-LDL-c values. The LDL-c values obtained were compared at different ranges of Total Cholesterol (TC), Triglycerides (TG) and High-Density Lipoprotein cholesterol (HDL-c). The association between direct and calculated LDL-c values were analysed by Pearson’s correlation. Receiver Operator Characteristic Curve (ROC) analysis was done to predict the better diagnostic method among the calculated methods of LDL-c. Results: The mean±SD of D-LDL-c (115.68±36.94 mg/dL) was high compared to F-LDL-c (106.95±33.48 mg/dL) and N-LDL-c (110.78±32.58 mg/dL). The mean difference between D-LDL-c and N-LDL-c (4.9±4.36 mg/dL) was low compared to F-LDL-c (8.75±3.46 mg/dL). Significant positive correlation was observed between D-LDL-c vs F-LDL-c (r=0.96; p=<0.001) and D-LDL-c vs N-LDLc (r=0.97; p=<0.001). The ROC showed maximum AUC value for N-LDL-c than F-LDL-c at a cut-off value of 100 mg/dL. LDL-c as estimated by Novel’s and Friedewald’s equation led to approximately 5% and 10% less patients being subjects for lipid lowering therapy respectively as compared to D-LDL-c. Conclusion: In conclusion, the use of Novel’s equation for LDL-c estimation instead of Friedewald’s equation could be associated with the small net increase in lipid lowering agent eligible population for primary prevention of atherosclerotic CVD. Replacement of Friedewald’s equation by Novel’s equation would enable for the improved accuracy of LDL-c estimation especially at higher levels of TC, TG and lower levels of HDL-c.
简介:脂质谱通常被用作确定心血管疾病(CVD)风险的筛查试验。低密度脂蛋白胆固醇(LDL-c)升高是动脉粥样硬化性心血管疾病的重要可改变危险因素。降低LDL-c的策略是预防和治疗心血管疾病的一种已知建议。测定LDL-c的金标准方法是超离心β定量法。其他方法包括直接测定LDL-c (D-LDL-c),使用酶分析,这是繁琐,耗时和昂贵的。因此,使用弗里德瓦尔德方程(F-LDL-c)的计算方法是印度临床实验室常规使用的方法。目的:比较直接酶法测得的LDL-c值与Friedewald方程和Novel’s方程测得的LDL-c值,并评价两种方法测得的LDL-c值对心血管疾病风险分层的影响。材料与方法:本研究于2020年7月至9月在印度卡纳塔克邦Mandya医学科学研究所Mandya中央诊断实验室进行了一项横断面研究,为期三个月,其中包括600名年龄在20-75岁之间的受试者,进行常规血脂评估。LDL-c采用直接酶法(D-LDL-c)估算,计算方法采用Friedewald公式{F-LDL-c=TC-HDL-c- (TG/5)}和Novel公式{N-LDL-c=TC-HDL-c-(TG/可调因子)}。将计算得到的值与D-LDL-c值进行比较。在不同的总胆固醇(TC)、甘油三酯(TG)和高密度脂蛋白胆固醇(HDL-c)范围内比较所得LDL-c值。通过Pearson相关分析直接LDL-c值与计算LDL-c值之间的关系。通过Receiver Operator Characteristic Curve (ROC)分析,预测LDL-c计算方法中较好的诊断方法。结果:D-LDL-c的平均值±SD(115.68±36.94 mg/dL)高于F-LDL-c(106.95±33.48 mg/dL)和N-LDL-c(110.78±32.58 mg/dL)。与F-LDL-c(8.75±3.46 mg/dL)相比,D-LDL-c和N-LDL-c的平均差异(4.9±4.36 mg/dL)较低。D-LDL-c与F-LDL-c呈显著正相关(r=0.96;p=<0.001), D-LDL-c vs n - ldl -c (r=0.97;p = < 0.001)。ROC显示N-LDL-c的最大AUC值比F-LDL-c的最大AUC值为100 mg/dL。根据Novel’s和Friedewald’s方程估算的LDL-c与D-LDL-c相比,分别减少了约5%和10%的患者接受降脂治疗。结论:总之,使用Novel’s方程来估计LDL-c而不是Friedewald’s方程可能与降脂剂用于动脉粥样硬化性心血管疾病一级预防的合格人群的净增加有关。用Novel方程代替Friedewald方程可以提高LDL-c估计的准确性,特别是在TC、TG水平较高和HDL-c水平较低的情况下。
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引用次数: 0
Reference Interval of Thyroxine and Thyroid Stimulating Hormone in Cord Blood in Tertiary Care Hospital, Kerala 喀拉拉邦三级医院脐带血甲状腺素和促甲状腺激素的参考区间
Pub Date : 2022-01-01 DOI: 10.7860/njlm/2022/51307.2571
Smitha Kalarikkal Satheesan, S. Sreedharan, Gilsa Engoor Sathiandranathan, Geetha Damodaran Kozhiparambil
Introduction: Even though Congenital hypothyroidism (CH) is one of the most common causes of preventable mental retardation, diagnosis at birth is difficult due to absent or delayed clinical manifestations, owing to the transplacental transfer of maternal thyroid hormones. Delayed diagnosis and treatment can cause irreversible damage to the developing brain. The occurrence of cognitive dysfunction due to CH has reduced significantly in countries where Newborn Screening (NBS) is routinely practiced. Cord blood screening is considered to be an effective method to diagnose congenital hypothyroidism. Aim: To establish reference interval for thyroxine (T3 and T4) and Thyroid Stimulating Hormone (TSH) in cord blood Medical College, Thrissur. Materials and Methods: In the present cross-sectional observational hospital based study, the cord blood samples from 252 deliveries collected over a period of three months from May 2011 at in Government Medical College, Thrissur, Kerala, India. A 5 mL of cord blood samples were collected in a plain non vacuum tube with clot activator from umbilical cord incised 15-20 cm at the time of birth. T3, T4 and TSH was estimated by Enzyme Linked Immuno-sorbent Assay (ELISA) using kits of ELISA reader and Washer. Normality check done by visual inspection of histogram, Q-Q plot, box plot and Kolmogorov-Smirnov test. Results: In total of 153 cord blood samples considered, and final analysis was done on 151 samples (69 males and 82 females) after excluding the samples of babies delivered by Lower Segment Cesarean Section (LSCS). The gestational age was mean 38.48 weeks and mean age of mothers was 24.22 years. More than 90% of the values for TSH is less than 12 mIU/mL and 90% of T4 values is less than 20 µg/dL. Reference interval determined by non parametric ascending rank order. Reference interval established is 0.63-17.033 mIU/L and 9.45-27.173 for TSH and T4 respectively, lower than those reported from studies in other parts of India. The mean value of TSH was 5.084 mIU/L and 87.5% of babies are having TSH values <10 mIU/L. Conclusion: The study was conducted to establish reference intervals for cord blood TSH, T4 and T3 and confirms to the use of cut off values for the screening of CH for TSH as >20 mIU/L.
虽然先天性甲状腺功能减退症(CH)是可预防的智力低下最常见的原因之一,但由于母体甲状腺激素经胎盘转移,临床表现缺失或延迟,在出生时诊断困难。延迟诊断和治疗会对发育中的大脑造成不可逆转的损害。在新生儿筛查(NBS)常规实施的国家,由于CH引起的认知功能障碍的发生率显著降低。脐带血筛查被认为是诊断先天性甲状腺功能减退症的有效方法。目的:建立脐带血患者甲状腺素(T3、T4)和促甲状腺激素(TSH)水平的参考区间。材料和方法:在本以医院为基础的横断面观察性研究中,从2011年5月起三个月内在印度喀拉拉邦特里苏瑟尔政府医学院收集了252例分娩的脐带血样本。取新生儿出生时切开15 ~ 20 cm脐带,在带凝块激活剂的普通非真空管中采集5 mL脐带血。采用酶联免疫吸附法(ELISA)测定T3、T4和TSH。通过直方图、Q-Q图、箱形图和Kolmogorov-Smirnov检验进行正态性检验。结果:共纳入153份脐带血样本,剔除下段剖宫产(LSCS)新生儿样本后,最终分析151份脐带血样本(男69份,女82份)。平均胎龄38.48周,平均年龄24.22岁。90%以上的TSH值小于12 mIU/mL, 90%的T4值小于20µg/dL。参考区间由非参数升序决定。建立的TSH和T4参考区间分别为0.63-17.033 mIU/L和9.45-27.173 mIU/L,低于印度其他地区的研究报告。TSH平均值为5.084 mIU/L, 87.5%的婴儿TSH值为20 mIU/L。
{"title":"Reference Interval of Thyroxine and Thyroid Stimulating Hormone in Cord Blood in Tertiary Care Hospital, Kerala","authors":"Smitha Kalarikkal Satheesan, S. Sreedharan, Gilsa Engoor Sathiandranathan, Geetha Damodaran Kozhiparambil","doi":"10.7860/njlm/2022/51307.2571","DOIUrl":"https://doi.org/10.7860/njlm/2022/51307.2571","url":null,"abstract":"Introduction: Even though Congenital hypothyroidism (CH) is one of the most common causes of preventable mental retardation, diagnosis at birth is difficult due to absent or delayed clinical manifestations, owing to the transplacental transfer of maternal thyroid hormones. Delayed diagnosis and treatment can cause irreversible damage to the developing brain. The occurrence of cognitive dysfunction due to CH has reduced significantly in countries where Newborn Screening (NBS) is routinely practiced. Cord blood screening is considered to be an effective method to diagnose congenital hypothyroidism. Aim: To establish reference interval for thyroxine (T3 and T4) and Thyroid Stimulating Hormone (TSH) in cord blood Medical College, Thrissur. Materials and Methods: In the present cross-sectional observational hospital based study, the cord blood samples from 252 deliveries collected over a period of three months from May 2011 at in Government Medical College, Thrissur, Kerala, India. A 5 mL of cord blood samples were collected in a plain non vacuum tube with clot activator from umbilical cord incised 15-20 cm at the time of birth. T3, T4 and TSH was estimated by Enzyme Linked Immuno-sorbent Assay (ELISA) using kits of ELISA reader and Washer. Normality check done by visual inspection of histogram, Q-Q plot, box plot and Kolmogorov-Smirnov test. Results: In total of 153 cord blood samples considered, and final analysis was done on 151 samples (69 males and 82 females) after excluding the samples of babies delivered by Lower Segment Cesarean Section (LSCS). The gestational age was mean 38.48 weeks and mean age of mothers was 24.22 years. More than 90% of the values for TSH is less than 12 mIU/mL and 90% of T4 values is less than 20 µg/dL. Reference interval determined by non parametric ascending rank order. Reference interval established is 0.63-17.033 mIU/L and 9.45-27.173 for TSH and T4 respectively, lower than those reported from studies in other parts of India. The mean value of TSH was 5.084 mIU/L and 87.5% of babies are having TSH values <10 mIU/L. Conclusion: The study was conducted to establish reference intervals for cord blood TSH, T4 and T3 and confirms to the use of cut off values for the screening of CH for TSH as >20 mIU/L.","PeriodicalId":31115,"journal":{"name":"National Journal of Laboratory Medicine","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"71270076","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
Differential Expression of SLC25A38 Gene in Patients of Acute Lymphoblastic Leukaemia SLC25A38基因在急性淋巴细胞白血病患者中的差异表达
Pub Date : 2022-01-01 DOI: 10.7860/njlm/2022/50387.2578
P. Prakash, S Kumar, Sanjay Kumar, hraddha Raj, Poonam Sinha
Introduction: The SLC25A38 gene produces protein that belongs to the mitochondrial solute carrier family, SLC25. It is implicated in apoptotic pathways, which regulate intrinsic caspase-dependent apoptosis. Aim: To determine level of expression of SLC25A38 gene in patients of Acute Lymphoblastic Leukaemia (ALL). Materials and Methods: A cross-sectional study was done in the Department of Biochemistry, Indira Gandhi Institute of Medical Sciences, Patna, Bihar, India, from April 2019 to March 2020. The study included 30 leukaemia patients out of which 25 were adult males and five were adult females and 10 healthy volunteers were included as the control group. Level of expression of SLC25A38 gene normalised to Glyceraldehyde 3-phosphate Dehydrogenase (GAPDH) gene relative to normal healthy volunteers among the ALL patients was measured using quantitative real time polymerase chain reaction. All data collected were analysed using Statistical Package for the Social Sciences (SPSS) version 16.0 software. Results: An average of 5.3 fold expression of SLC25A38 gene normalised to GAPDH relative to normal healthy volunteer among the ALL patients was seen. The fold of expression was determined by 2-∆∆Ct method. There was a positive correlation between blast cell abundance and level of SLC25A38 gene expression (Pearson’s r=0.408, p=0.025). The expression level was found to be associated with the proportion of blast cells in the bone marrow. Conclusion: High expression of SLC25A38 gene is a common feature in ALL and may be a novel biomarker for prognosis and diagnosis, as well as a potential therapeutic target for ALL.
SLC25A38基因产生的蛋白质属于线粒体溶质载体家族SLC25。它涉及凋亡途径,调节内在的caspase依赖性凋亡。目的:探讨急性淋巴细胞白血病(ALL)患者SLC25A38基因的表达水平。材料与方法:横断面研究于2019年4月至2020年3月在印度比哈尔邦巴特那英迪拉甘地医学科学研究所生物化学系进行。该研究包括30名白血病患者,其中25名成年男性,5名成年女性,10名健康志愿者作为对照组。采用实时定量聚合酶链反应检测ALL患者SLC25A38基因转化为甘油醛3-磷酸脱氢酶(GAPDH)基因相对于正常健康志愿者的表达水平。所有收集的数据均使用SPSS 16.0版社会科学统计软件包进行分析。结果:ALL患者SLC25A38基因转化为GAPDH的平均表达量是正常健康志愿者的5.3倍。2-∆∆Ct法测定表达倍数。胚细胞丰度与SLC25A38基因表达水平呈正相关(Pearson’s r=0.408, p=0.025)。其表达水平与骨髓中母细胞的比例有关。结论:SLC25A38基因高表达是ALL的共同特征,可能是一种新的预后和诊断生物标志物,也是ALL潜在的治疗靶点。
{"title":"Differential Expression of SLC25A38 Gene in Patients of Acute Lymphoblastic Leukaemia","authors":"P. Prakash, S Kumar, Sanjay Kumar, hraddha Raj, Poonam Sinha","doi":"10.7860/njlm/2022/50387.2578","DOIUrl":"https://doi.org/10.7860/njlm/2022/50387.2578","url":null,"abstract":"Introduction: The SLC25A38 gene produces protein that belongs to the mitochondrial solute carrier family, SLC25. It is implicated in apoptotic pathways, which regulate intrinsic caspase-dependent apoptosis. Aim: To determine level of expression of SLC25A38 gene in patients of Acute Lymphoblastic Leukaemia (ALL). Materials and Methods: A cross-sectional study was done in the Department of Biochemistry, Indira Gandhi Institute of Medical Sciences, Patna, Bihar, India, from April 2019 to March 2020. The study included 30 leukaemia patients out of which 25 were adult males and five were adult females and 10 healthy volunteers were included as the control group. Level of expression of SLC25A38 gene normalised to Glyceraldehyde 3-phosphate Dehydrogenase (GAPDH) gene relative to normal healthy volunteers among the ALL patients was measured using quantitative real time polymerase chain reaction. All data collected were analysed using Statistical Package for the Social Sciences (SPSS) version 16.0 software. Results: An average of 5.3 fold expression of SLC25A38 gene normalised to GAPDH relative to normal healthy volunteer among the ALL patients was seen. The fold of expression was determined by 2-∆∆Ct method. There was a positive correlation between blast cell abundance and level of SLC25A38 gene expression (Pearson’s r=0.408, p=0.025). The expression level was found to be associated with the proportion of blast cells in the bone marrow. Conclusion: High expression of SLC25A38 gene is a common feature in ALL and may be a novel biomarker for prognosis and diagnosis, as well as a potential therapeutic target for ALL.","PeriodicalId":31115,"journal":{"name":"National Journal of Laboratory Medicine","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"71270108","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 Comparison of Rapid Screening Test and ELISA for the Diagnosis of Hepatitis B Surface Antigen in Patients Attending a Tertiary Care Hospital, Tamil Nadu, India 印度泰米尔纳德邦一家三级医院患者乙型肝炎表面抗原快速筛查试验与ELISA诊断的比较
Pub Date : 2022-01-01 DOI: 10.7860/njlm/2022/50412.2580
P. Prabha, D. Saikeerthana, V. Vijayashree, M. Gogan
Introduction: Hepatitis B virus infection is a major public health problem and leading cause of death worldwide. World Health Organisation (WHO) estimates that in 2015 about 257 million population were living with chronic Hepatitis B virus infection with a global prevalence of 3.5%. Among the several viral antigens of Hepatitis B, Hepatitis B Surface Antigen (HBsAg) is an important viral antigen which is recognised as a superior marker for Hepatitis B virus detection. For proper diagnosis of infection as well as disease management and prevention, identification of appropriate test kit is necessary. Aim: To compare the results of rapid screening tests and ELISA for the diagnosis of HBsAg. Materials and Methods: A cross-sectional study was conducted from July 2019-August 2019 in a tertiary care hospital. A total of 200 blood samples received for HBsAg testing were centrifuged. Serum of all the 200 blood samples were tested for HBsAg using both rapid Immuno Chromatographic Card (ICT) method (HEPAVIEW - one step test for HBsAg, Viola Diagnostic System, A Division of Tulip Diagnostics Pvt., Ltd.) and Enzyme Linked Immuno Sorbent Assays (ELISA) (Merilisa HBsAg- Meril Diagnostics Pvt., Ltd.) method. Data for rapid card method and ELISA were noted and entered into MS excel spread sheet and analysed. Results: Among the total 200 blood samples tested by HbsAg rapid card, five samples were positive and the remaining 195 were negative. For rapid card test, the sensitivity was 83.4%, specificity 100%, Positive Predictive Value (PPV) 100% and Negative Predictive Value (NPV) 99.4% and for ELISA the sensitivity, specificity, PPV and NPV were all 100%. Conclusion: The overall performance of the rapid ICT for HBsAg was less sensitive to ELISA. So, only ELISA can be encouraged in all setups irrespective of their developmental and economical status not only to prevent the complications of Hepatitis B infection but also for early diagnosis and better treatment of patients.
乙型肝炎病毒感染是一个主要的公共卫生问题,也是全世界死亡的主要原因。世界卫生组织(世卫组织)估计,2015年约有2.57亿人患有慢性乙型肝炎病毒感染,全球流行率为3.5%。在乙型肝炎的几种病毒抗原中,乙型肝炎表面抗原(HBsAg)是一种重要的病毒抗原,被认为是检测乙型肝炎病毒的优良标记。为正确诊断感染以及管理和预防疾病,确定适当的检测试剂盒是必要的。目的:比较快速筛查试验与ELISA法诊断乙型肝炎表面抗原的结果。材料与方法:于2019年7月- 2019年8月在某三级医院进行横断面研究。取200份血样进行HBsAg离心检测。采用快速免疫层析卡(ICT)法(HEPAVIEW - HBsAg一步检测,Viola诊断系统,Tulip Diagnostics Pvt., Ltd.)和酶联免疫吸附测定(ELISA)法(Merilisa HBsAg- Meril Diagnostics Pvt., Ltd.)检测所有200份血样的血清HBsAg。记录快速卡法和酶联免疫吸附试验的数据并输入MS excel电子表格进行分析。结果:采用HbsAg快速卡检测的200份血样中,阳性5份,阴性195份。快速卡法敏感性为83.4%,特异性为100%,阳性预测值(PPV)为100%,阴性预测值(NPV)为99.4%;ELISA法敏感性、特异性、PPV和NPV均为100%。结论:快速ICT检测HBsAg的总体性能对ELISA的敏感性较低。因此,无论其发展和经济状况如何,只有ELISA才能在所有机构中得到鼓励,不仅可以预防乙型肝炎感染的并发症,而且可以早期诊断和更好地治疗患者。
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引用次数: 1
Relationship between Iron Profile and Thyroid Profile in Hypothyroid Patients 甲状腺功能减退患者铁谱与甲状腺谱的关系
Pub Date : 2022-01-01 DOI: 10.7860/njlm/2022/48551.2556
Santosh Kumar, J. Keshari, R. Kumari, P. Prakash, U. Kumar, Ved Prakash
Introduction: Thyroid hormone biosynthesis is dependent on iron metabolism. Changes in iron metabolism and its deficiency may cause a change in the profile of thyroid hormone. Such interferences caused can lead to hypothyroidism in case of anaemia or the other way round. Aim: To find a relationship between various parameters of iron profile to that of thyroid profile in hypothyroid patients when compared to normal healthy subjects. Materials and Methods: Present case-control study was conducted on 50 hypothyroid patients and 50 healthy subjects of same age, in the Department of Endocrinology, IGIMS, Patna between April 2017 to June 2018. Serum ferritin and Serum T3, T4, and Thyroid Stimulating Hormone (TSH) were estimated by Chemiluminescence Immuno Assay (CLIA) method. Serum iron estimation was done using TPTZ (2,4,6-Tripyridyl-s-triazine) method and Total Iron Binding Capacity (TIBC) estimation was done by Nitroso PSAP method. All statistical test and analysis were performed in Statistical Package for the Social Science (SPSS) 16.0. The differences between mean values of groups for each test variable were tested by Student’s t-test after testing for homogeneity of variance and normality test (Kolmogorov-Smirnov test). Results: The mean age of the hypothyroid patients was 30.28±10.5 years while it was 31.14±10.4 years in control group. It was observed from the study that mean serum ferritin level and iron level were significantly lower in hypothyroid subjects compared to control groups (p<0.001) while TIBC was significantly higher (p<0.001). Serum ferritin and iron were found to be negatively correlated with TSH (-0.695 and -0.541) and positively correlated to T3 and T4, respectively. Conclusion: Evaluating iron profile in thyroid disorder may be an aid to the treatment modality and disease outcome
甲状腺激素的生物合成依赖于铁的代谢。铁代谢的变化及其缺乏可能导致甲状腺激素的变化。在贫血或其他情况下,这种干扰会导致甲状腺功能减退。目的:探讨甲状腺功能减退患者铁谱各参数与正常健康人甲状腺谱的关系。材料与方法:本病例对照研究于2017年4月至2018年6月在巴特那IGIMS内分泌科进行,选取50例甲状腺功能减退患者和50例同龄健康受试者。采用化学发光免疫分析法(CLIA)测定血清铁蛋白和血清T3、T4、促甲状腺激素(TSH)水平。血清铁含量测定采用TPTZ(2,4,6-三吡啶-s-三嗪)法,总铁结合能力(TIBC)测定采用亚硝基PSAP法。所有统计检验和分析均在社会科学统计软件包(SPSS) 16.0进行。各检验变量组间均值的差异在方差齐性检验和正态性检验(Kolmogorov-Smirnov检验)后,采用Student 's t检验。结果:甲状腺功能减退患者平均年龄30.28±10.5岁,对照组平均年龄31.14±10.4岁。研究发现,甲状腺功能减退患者的平均血清铁蛋白水平和铁水平显著低于对照组(p<0.001),而TIBC显著高于对照组(p<0.001)。血清铁蛋白和铁分别与TSH呈负相关(-0.695和-0.541),与T3和T4呈正相关。结论:评价甲状腺疾病患者的铁谱对治疗方式和预后有一定的指导意义
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引用次数: 0
Primary Extranodal Non-Hodgkin’s Lymphoma: An Observational Study at a Tertiary Care Teaching Centre in Northern India 原发性结外非霍奇金淋巴瘤:印度北部三级保健教学中心的一项观察性研究
Pub Date : 2022-01-01 DOI: 10.7860/njlm/2022/50589.2583
Mili Jain, Shivanjali Raghuvanshi, S. Bhalla, P. Agarwal, Ashutosh Kumar, U. Singh, M. Goel
Introduction: Extranodal Non-Hodgkin’s Lymphoma (NHL) constitutes approximately one fourth of all NHL. The data regarding extranodal NHL from India is however limited. Aim: To evaluate the epidemiological and histomorphological patterns of extranodal NHL in a tertiary care institute in Northern India. Materials and Methods: The retrospective observational study was conducted on data of biopsy sections retrieved from the archives for a period of four years (January 2016 to December 2019), 130 extranodal NHL cases (90 males, 40 females) that were analysed for histological features and immunohistochemical subtype. All statistical analysis was done by Statistical Package for Social Sciences (SPSS) software. The values were represented in number, percentage, mean and ratio. Results: Total of 362 cases of NHL were reported. Out of which, 130 (36%) cases were of extranodal NHL. Male to female ratio being was 2.25:1. Mean age of presentation was 38.5 years. Paediatric cases constituted (32/130; 24.6%) cases. Head and neck was the most common site (52/130; 40%) followed by Gastrointestinal Tract (GIT) (21/130; 16.2%) and central nervous system (13/130; 10%). Amongst the paediatric cases, head and neck (11/32; 34.4%) was the most common site, followed by GIT (8/32; 25%). Amongst head and neck lymphomas, nasal cavity and Waldeyer Ring were the most common sites followed by orbit and oral cavity. Common sites among the GIT lymphomas were stomach, small intestine and large intestine. The B-cell NHL constituted 81/130 (62.3%), T-cell NHL 20/130 (15.4%) and NHL (Unclassified) were 29/130 (22.3%). Amongst B-cell type NHL, Diffuse Large B Cell Lymphoma (DLBCL) was the most common subtype. Conclusion: Extranodal NHL diagnosis is challenging due to morphological similarities with non haematopoietic tumours. Lineage determination by Immunohistochemistry (IHC) serves as the key to diagnosis. In our population, head and neck was the most common site, with B-cell NHL being the most common subtype.
结外非霍奇金淋巴瘤(NHL)约占所有NHL的四分之一。然而,来自印度的结外NHL数据有限。目的:评估结外NHL在印度北部三级医疗机构的流行病学和组织学模式。材料与方法:回顾性观察研究从2016年1月至2019年12月的4年档案中检索的130例结外NHL(男性90例,女性40例)的活检切片数据,分析其组织学特征和免疫组织化学亚型。所有统计分析均采用SPSS (statistical Package for Social Sciences)软件进行。数值以数字、百分比、平均值和比率表示。结果:共报告NHL病例362例。其中,130例(36%)为结外NHL。男女比例为2.25:1。平均出现年龄为38.5岁。儿科病例占32/130;24.6%)的病例。头颈部是最常见的部位(52/130;40%),其次是胃肠道(GIT) (21/130;16.2%)和中枢神经系统(13/130;10%)。在儿科病例中,头颈部(11/32;34.4%)是最常见的部位,其次是GIT (8/32;25%)。在头颈部淋巴瘤中,鼻腔和Waldeyer环是最常见的部位,其次是眼眶和口腔。胃肠道淋巴瘤的常见部位为胃、小肠和大肠。b细胞NHL占81/130 (62.3%),t细胞NHL占20/130 (15.4%),NHL(未分类)占29/130(22.3%)。在B细胞型NHL中,弥漫性大B细胞淋巴瘤(DLBCL)是最常见的亚型。结论:结外NHL的诊断是具有挑战性的,因为它与非造血肿瘤的形态学相似。免疫组化(IHC)系系测定是诊断的关键。在我们的人群中,头颈部是最常见的部位,b细胞NHL是最常见的亚型。
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引用次数: 0
Analysis of Blood and Blood Component Wastage and its Reasons among Various Departments in a Tertiary Care Teaching Hospital in Southern India 印度南部某三级教学医院各科室血液及血液成分浪费分析及原因分析
Pub Date : 2022-01-01 DOI: 10.7860/njlm/2022/51736.2606
C. Ravikanth, B. Babu, R. Arun, K. Babu
Introduction: The main aim of many blood centers are to supply sufficient amount of safe blood and blood components whenever required. Shortage of blood may be due to low donation rate, inadequate storage, improper transportation and wastage at ward side. Wastage of blood can have a negative impact on blood transfusion services. Aim: To determine the rates of wastage of blood and blood components units at the ward side and identify the various reasons for wastage and explain the strategies to reduce the wastage rate. Materials and Methods: This retrospective study was conducted in the Department of Transfusion Medicine, Sri Venkateswara Institute of Medical Sciences, Tirupati, Andhra Pradesh, India from January 2018 to December 2020. The data was collected from the blood centre record. All blood and blood components issued during the study period were included in the study. The number, type and blood group of blood and blood components issued, the number of blood units wasted after issue, and the reason for wastage was collected. The collected data were entered in Microsoft excel and analysed using Statistical Package for the Social Science (SPSS) version 21.0. Descriptive statistics were performed as necessary. Results: During the study period, a total of 69198 units of blood and blood components were issued to different wards and operation theatres in the hospital. Among the total issues, 26863 (38.82%) were in the form of Packed Red Blood Cells (PRBC), 3968 (5.73%) in the form of Whole Blood (WB), 26069 (37.67%) in the form of Fresh Frozen Plasma (FFP), 11272 (16.29%) in the form of Random Donor Platelets (RDP), 933 (1.35%) in the form of Cryoprecipitate (CP) and 93 (0.13%) in the form of Single Donor Platelets (SDP). Among issued, 115 (0.17%) of blood and blood components were wasted with packed red cells accounting for 51 (44.35%). Among the various reasons, 43 (37.39%) was due to demise of patients before transfusion was initiated, followed by non requirement by the patients due to no loss/minimal loss blood during surgery 24 (20.87%). Majority of blood and blood components were wasted by the Department of Emergency Medicine (EMD) 36 (31.3%) followed by the Department of Neurology 20 (17.39%) and Orthopaedics 12 (10.43%). Conclusion: Implementation of proper blood transfusion policies and continuous educational programs in coordination with clinicians and staff nurses at ward side and operation theatres will help to decrease the blood wastage at ward side.
许多血液中心的主要目的是在需要时提供足够的安全血液和血液成分。血液短缺可能是由于献血率低、储存不足、运输不当和病区浪费所致。血液浪费可能对输血服务产生负面影响。目的:了解病区血液及血液成分单位的流失率,找出造成流失率的各种原因,并阐述降低流失率的对策。材料与方法:本回顾性研究于2018年1月至2020年12月在印度安得拉邦蒂鲁帕蒂Sri Venkateswara医学科学研究所输血医学系进行。数据是从血液中心的记录中收集的。研究期间发放的所有血液和血液成分均纳入研究。收集发放的血液和血液成分的数量、类型和血型,发放后浪费的血液单位数,浪费的原因。收集的数据在Microsoft excel中输入,并使用社会科学统计软件包(SPSS) 21.0版进行分析。必要时进行描述性统计。结果:研究期间,共向医院各病房、手术室发放血液及血液成分69198份。其中,包装红细胞(PRBC) 26863份(38.82%),全血(WB) 3968份(5.73%),新鲜冷冻血浆(FFP) 26069份(37.67%),随机供血小板(RDP) 11272份(16.29%),冷冻沉淀(CP) 933份(1.35%),单供血小板(SDP) 93份(0.13%)。其中,血液及血液成分浪费115份(0.17%),其中红细胞堆积51份(44.35%)。在各种原因中,43例(37.39%)是由于患者在开始输血前死亡,其次是患者因术中无失血量或失血量最小而不需要输血24例(20.87%)。浪费最多的是急诊科(EMD) 36例(31.3%),其次是神经内科(17.39%)和骨科(10.43%)。结论:实施正确的输血政策,并与病区及手术室的临床医生和护士协调开展持续的教育项目,有助于减少病区的血液浪费。
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引用次数: 0
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National Journal of Laboratory Medicine
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