血清转铁蛋白受体在阿尔及利亚西部130例缺铁性贫血诊断中的作用

Beddek Fatima, A. Demmouche
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引用次数: 2

摘要

贫血是妊娠期最常见的疾病之一。最常见的原因是缺铁。使用血清铁蛋白<15 ng/ml诊断缺铁性贫血相对容易。然而,由于铁蛋白是急性相反应物,住院或生病患者缺铁性贫血的诊断可能很困难,因为即使在缺铁的情况下,血清铁蛋白也可能正常或升高。可溶性转铁蛋白受体测定(sT-fR)在这些情况下可能是有用的,因为它反映了铁的需求与供应的程度,而且它不是急性相反应物。目的:我们研究的目的是确认sT-fR的价值和特异性,并将其纳入阿尔及利亚实验室铁状态的常规参数表中以鉴别诊断贫血。患者和方法:本研究纳入130例患者,分为三组:对照组40例健康成人(男性22例,女性18例)。第2组,在Sidi Bel Abbes大学医院“Abdelkader Hassani”血液科住院的30名患者(11名男性和19名女性),代表了c反应蛋白(CRP <10 mg/L)率的纯缺铁性贫血(无任何相关疾病(IDA))的受试者组。第三组是Sidi Bel Abbes大学医院内科住院的60名慢性贫血(ACD)贫血患者(36名男性和24名女性)。每位患者进行全血细胞计数、铁状态、sT-fR测定和炎症平衡(CRP)。所有这些检查均在新鲜血浆和血清中立即进行;采用免疫比浊法测定。使用Statview软件(1998年)对数据进行统计分析(均值和标准差、相关系数、正态性检验和均值比较)。P值(P<0.05)为有统计学意义,所有P值均采用双侧分布的t检验函数计算。结果:对照组(健康人)铁含量正常。所有参数在100%的受试者中男女均处于正常范围。第二组的结果与IDA的所有参数完全一致,它的铁状态非常紊乱,代表了这种贫血:贫血(Hb <120 g/L);微细胞增多症(MCV <80 fl);循环池(血清铁降低,高转铁蛋白血症);储备不足(铁蛋白<30 μg/L),促红细胞生成需要高铁(高sT-fR)。在第三组中,很难解释铁蛋白水平(非常高),它与其他参数相矛盾,这导致我们讨论这组的同质性。由于我们研究的关键参数存在性别影响(血红蛋白、铁蛋白和sT-fR在两性中存在异质性(P<0.001),因此将结果在男性和女性之间分开分析。对结果进行了分析,讨论了sT-fR对铁状态的敏感性以及各参数对贫血特异性诊断的信息贡献。结论:本研究允许我们推荐使用sT-fR检测,因为它在探索成人红细胞生成和鉴别诊断贫血方面非常有前景,正常范围为:男性和绝经后女性2.65 ~ 4.39 mg/L,绝经前女性2.03 ~ 3.69 mg/L,希望建立一个国际范围的参考值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of Serum Transferrin Receptor in Diagnosis of Iron Deficiency Anemia:Report of 130 Cases in West of Algeria
Introduction: Anemia is one of the most common disorders in pregnancy. The most common cause is iron deficiency. Iron deficiency anemia is relatively easy to diagnose using a serum ferritin of <15 ng/ml. However, because ferritin is an acute phase reactant, the diagnosis of iron deficiency anemia in hospitalised or ill patients may be difficult, since serum ferritin may be normal or raised, even in the face of iron deficiency. Soluble transferrin receptor assay (sT-fR) may be useful in these situations because it reflects the degree of iron requirement in relation to supply, and it is not an acute phase reactant. Aim: The aims of our study are to affirm the value and specificity of sT-fR and integrate it in the list of routine parameters of iron status in the differential diagnosis of anemia in our laboratories in Algeria. Patients and Method: Our study included 130 patients divided into three groups: control group with 40 healthy adult (22 men and 18 women). Group 2, with 30 patients (11 men and 19 women) hospitalized at the hematology department of the University Hospital “Abdelkader Hassani” of Sidi Bel Abbes, which represents the group of subjects with purely iron deficiency anemia without any associated disease (IDA) having rates of C-reactive protein (CRP <10 mg/L), and the third group with 60 anemic patients with anemia of chronic disease (ACD) (36 men and 24 women) hospitalized at the department of Internal Medicine of the University Hospital of Sidi Bel Abbes. Each patient underwent a complete blood count, an iron status, and the sT-fR assays, and inflammatory balance (CRP). All these examinations were performed immediately on fresh plasma and serum; assays were performed by immunoturbidimetric method. Statistical analyzes of the data (mean and standard deviation, correlation coefficients, tests for normality and comparison of means) were performed using the software Statview (1998). A P-value (P<0.05) was considered statistically significant, all P values are calculated by the t-test function using bilateral distribution. Results: The control group (healthy subjects) has a normal iron status. All parameters with levels in normal ranges in both sexes for 100% of subjects. The outcome of the second group is in perfect agreement with IDA for all of its parameters, it has a very disturbed iron status representative of this anemia: anemia (Hb <120 g/L); microcytosis (MCV <80 fl); circulating pool (serum iron decreased high transferrinemia); reserves depleted (ferritin <30 μg/L) and erythropoietic needs high iron (high sT-fR). In the third group it's difficult to interpret ferritin levels (very higher), it's in contradiction with the other parameters, which leads us to discuss the homogeneity of this group. Because there is gender effect on key parameters of our study (hemoglobin, ferritin and sT-fR are heterogeneous in both sexes (P<0.001), the results were analyzed separately between men and women. Analyses of results were done for discussing the sensitivity of the sT-fR on iron status and the informative contribution of each parameter to the specific diagnosis of anemia. Conclusion: This study has allowed us to recommend for the use of sT-fR assays, because it is very promising for the exploration of erythropoiesis and the differential diagnosis of anemia in adults, with a normal range of: 2.65 to 4.39 mg/L in men and postmenopausal women and 2.03 to 3.69 mg/L in premenopausal women, in the hope of establishing an international range of reference values.
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