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两种高效液相色谱仪Bio-Rad Variant-II和Tosoh HLC-723G11在血红蛋白病评估中的比较

Comparison of Two High-Pressure Liquid Chromatography Instruments Bio-Rad Variant-II and Tosoh HLC-723G11 in the Evaluation of Hemoglobinopathies.

作者信息

Chopra Parul, Bhardwaj Sunanda, Negi Pushkar, Arora Anil

机构信息

Department of Hematology and Immunology, National Reference Laboratory, Dr. Lal PathLabs Ltd., Sector-18, Block-E, Rohini, New Delhi, 110085 India.

出版信息

Indian J Hematol Blood Transfus. 2020 Oct;36(4):725-732. doi: 10.1007/s12288-020-01298-5. Epub 2020 Jun 19.

Abstract

Hemoglobin High-performance liquid chromatography (Hb HPLC) is a standard first-line technique for diagnosis of thalassemia and hemoglobinopathies. We compared two HPLC systems for detection and quantification of normal and abnormal Hb fractions. EDTA samples from 100 normal healthy subjects and 107 subjects affected with hemoglobinopathies or carriers were analysed using HPLC systems Tosoh HLC-723G11 and Bio-Rad Variant-II. Retention time (RT) and area of peaks for HbA2, HbF and other structural variants were compared. In discrepant cases samples were run on Sebia Capillary zone electrophoresis (CZE) for confirmation of results (39 out of 107 cases with HbE, HbD Iran, Hb Lepore and HbQ). Measurement of HbA2 and HbF in normal samples and HbF in those with variant Hbs showed good correlation by both analyzers (  = 0.83, 0.9 and 0.99 respectively). HbE co-elutes with HbA2 in Bio-Rad. Correlation done using the apparent HbA2 concentration from Bio-Rad with (HbE + HbA2) from Tosoh G11 showed good correlation (  = 0.97). Correlation of HbS (Eluting at S-window at RT 3.11 min in Tosoh G11 and 4.33 min in Bio-Rad) as well as HbD Punjab (Eluting at D-window at RT 2.82 min in Tosoh G11 and 4.06 min in Bio-Rad) by both instruments was good. HbD Iran (Eluting at E-window at RT 2.69 min in Tosoh G11 and with HbA2 at 3.53 min in Bio-Rad); HbQ (Eluting at C-window at RT 3.78 min in Tosoh G11 and unknown window at 4.7 min in Bio-Rad), HbH (Eluting at P00 window at RT 0.13 min in Tosoh G11 and giving pre-integration peak in Bio-Rad), Hb Lepore (Eluting at P08 window at RT 2.67 min in Tosoh G11 and with HbA2 at 3.46 min in Bio-Rad) gave comparable results. Correlation with findings of CZE was done in few cases when needed. Two automated HPLC instruments demonstrated similar usefulness for screening patients for hemoglobinopathies. However, complex elution patterns as well as co-elution of variants like HbA2, HbE, Hb Lepore, HbD Iran (in Bio-Rad); HbD Iran and HbE (Tosoh G11) pose difficulty in interpretation. A complementary second method like CZE may be required.

摘要

血红蛋白高效液相色谱法(Hb HPLC)是诊断地中海贫血和血红蛋白病的标准一线技术。我们比较了两种用于检测和定量正常及异常血红蛋白组分的HPLC系统。使用HPLC系统Tosoh HLC - 723G11和Bio - Rad Variant - II对来自100名正常健康受试者以及107名患有血红蛋白病或携带者的受试者的乙二胺四乙酸(EDTA)样本进行分析。比较了HbA2、HbF和其他结构变体的保留时间(RT)和峰面积。在结果不一致的情况下,将样本进行Sebia毛细管区带电泳(CZE)以确认结果(107例中有39例为HbE、HbD伊朗型、Hb Lepore和HbQ)。两种分析仪对正常样本中HbA2和HbF的测量以及变异型血红蛋白样本中HbF的测量均显示出良好的相关性(分别为r = 0.83、0.9和0.99)。在Bio - Rad中,HbE与HbA2共洗脱。使用Bio - Rad的表观HbA2浓度与Tosoh G11的(HbE + HbA2)进行相关性分析,结果显示出良好的相关性(r = 0.97)。两种仪器对镰状血红蛋白(在Tosoh G11中于保留时间3.11分钟在S窗口洗脱,在Bio - Rad中于4.33分钟洗脱)以及旁遮普血红蛋白D(在Tosoh G11中于保留时间2.82分钟在D窗口洗脱,在Bio - Rad中于4.06分钟洗脱)的相关性均良好。伊朗血红蛋白D(在Tosoh G11中于保留时间2.69分钟在E窗口洗脱,在Bio - Rad中于3.53分钟与HbA2一起洗脱);血红蛋白Q(在Tosoh G11中于保留时间3.78分钟在C窗口洗脱,在Bio - Rad中于4.7分钟在未知窗口洗脱),血红蛋白H(在Tosoh G11中于保留时间0.13分钟在P00窗口洗脱,在Bio - Rad中给出积分前峰),Hb Lepore(在Tosoh G11中于保留时间2.67分钟在P08窗口洗脱,在Bio - Rad中于3.46分钟与HbA2一起洗脱)给出了可比的结果。必要时,对少数病例进行了与CZE结果的相关性分析。两种自动化HPLC仪器在筛查血红蛋白病患者方面显示出相似的效用。然而,复杂的洗脱模式以及诸如HbA2、HbE、Hb Lepore、伊朗血红蛋白D(在Bio - Rad中);伊朗血红蛋白D和HbE(Tosoh G11)等变体的共洗脱给结果解读带来了困难。可能需要一种像CZE这样的补充性第二种方法。

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Diagnosis of hemoglobinopathies: electrophoresis vs. HPLC.血红蛋白病的诊断:电泳与高效液相色谱法
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