[Clinical and Laboratory Characteristics of Primary Autoimmune Hemolytic Anemia Patients with Negative Results of DAT by Tube Test But Positive Results by Microcolumn Gel Assay].

Zhao Wang, Xue-Li Zhou, Li-Jin Bo, Yan Xu, Hui-Juan Liu, Yu-Ping Zhao
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Abstract

Objective: To investigate the clinical features and laboratory characteristics of primary autoimmune hemolytic anemia (AIHA) patients with negative results of direct antiglobulin test (DAT) by tube test but positive results by microcolumn gel assay, in order to provide references for the diagnosis of these patients.

Methods: 59 patients diagnosed with primary AIHA in our hospital from January 2015 to December 2020 were retrospectively analyzed. According to the results of tube test and microcolumn gel assay, the cases were divided into 3 groups, and the clinical and laboratory characteristics of each group were compared.

Results: The cases were grouped as follows: Group I, cases with negative results by both methods of DAT (n=5); Group II, cases with negative results by tube test but positive results by microcolumn gel assay (n=26); Group III, cases with positive results by both methods of DAT (n=28). There was no significant difference in age and sex between Group II and other groups, whereas the positive rate of anti-IgG + anti-C3d of Group II was lower than that in Group III (P=0.015). The main clinical manifestations of Group II were chest tightness, shortness of breath, fatigue, as well as yellow skin and sclera or dark urine, but the incidence rate of these symptoms was not significantly different from other groups. Anemia related indexes in Group II such as red blood cell (RBC) count and hemoglobin (Hb) were lower than the reference intervals, but there was no significant difference compared with other groups. Hemolysis related indexes in Group II such as reticulocyte (Ret) ratio, indirect bilirubin (IBIL), lactate dehydrogenase (LDH) and free-hemoglobin (F-Hb) were higher than the reference intervals, and the latter two items were signficantly higher than those in Group I (P=0.031 and P=0.036). Serum complement C3 and C4 in Group II were higher than those in Group III (P=0.010 and P=0.037).

Conclusion: Anemia severity of primary AIHA patients who were negative of DAT by tube test but positive by microcolumn gel assay was similar to those with negative or positive results by both DAT methods, but the mechanism and degree of complement system involved in hemolysis might be different. Results above may be helpful for laboratory diagnosis of this kind of patients.

【试管试验DAT阴性而微柱凝胶试验阳性的原发性自身免疫性溶血性贫血患者的临床和实验室特点】。
目的:探讨直接抗球蛋白试验(DAT)管试阴性而微柱凝胶试验阳性的原发性自身免疫性溶血性贫血(AIHA)患者的临床特点和实验室特点,为其诊断提供参考。方法:回顾性分析我院2015年1月至2020年12月诊断为原发性AIHA的59例患者。根据试管试验和微柱凝胶试验结果将病例分为3组,比较每组患者的临床和实验室特点。结果:病例分为两组:第一组,两种方法均阴性的病例(n=5);第二组:试管试验阴性,微柱凝胶试验阳性26例;第三组,两种方法均阳性的病例(n=28)。两组患者年龄、性别差异无统计学意义,抗igg +抗c3d阳性率低于三组(P=0.015)。II组的主要临床表现为胸闷、气短、乏力,以及皮肤、巩膜发黄或尿色变深,但这些症状的发生率与其他组无显著差异。II组贫血相关指标如红细胞(RBC)计数、血红蛋白(Hb)均低于参考区间,但与其他组比较差异无统计学意义。II组溶血相关指标网网状红细胞比率(Ret)、间接胆红素(IBIL)、乳酸脱氢酶(LDH)、游离血红蛋白(F-Hb)均高于参考区间,后两项均显著高于I组(P=0.031和P=0.036)。ⅱ组血清补体C3和C4高于ⅲ组(P=0.010和P=0.037)。结论:dda试管试验阴性、微柱凝胶试验阳性的原发性AIHA患者的贫血严重程度与两种方法均阴性或阳性的患者相似,但补体系统参与溶血的机制和程度可能不同。以上结果可为该类患者的实验室诊断提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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