Chatterjee Tridip, Chakravarty Amit, Chakravarty Sudipa
a Department of Human Genetics , Institute of Genetic Medicine and Genomic Science , Kolkata , West Bengal , India.
b Thalassaemia Foundation, Salt Lake , Kolkata , West Bengal , India.
Hemoglobin. 2015;39(6):384-8. doi: 10.3109/03630269.2015.1068799. Epub 2015 Oct 1.
We evaluated population screening programs (1999-2011), conducted by the Thalassaemia Foundation, Kolkata, India, for the first time in Eastern India in different districts of West Bengal, for prevention of thalassemia comprising screening of heterozygotes and β-thalassemia intermedia (β-TI) cases [β(+), β(++), β(0)/β(+), β(E)/β(E) (codon 26 or HBB: c.79G > A), Hb-E-β-thalassemia (Hb E-β-thal)]. Among 18,166 cases, we found 2092 heterozygotes and 2245 β-TI individuals (who had no information about their disorders). Results were evaluated with standard hematological analyses including erythrocyte indices, hemoglobin (Hb) typing and quantification. Participants were divided into five groups (children, pre-marriage cases, pre-pregnancy cases, affected family members, pregnant women). The objectives of this evaluation were to fix cut-off values of red blood cells (RBCs), mean corpuscular volume (MCV), mean corpuscular Hb (MCH), red blood cell distribution width (RDW) and Hb A2, as the standard World Health Organization (WHO) guidelines were not strictly followed in mass-scale screening programs. We have observed many dilemmas in considering the status of the thalassemia subject, due to presence of some other clinical conditions such as iron deficiency anemia, α-thalassemia (α-thal), δ-thalassemia (δ-thal), clinically silent Hb variants, and some cases of non hemoglobinopathies (such as pregnancy) along with thalassemia. The MCV values varied greatly in different conditions of hemoglobinopathies, whereas MCH provided a more stable measurement. We found an MCH value of <27.0 pg is a suitable cut-off point for screening in this population. Participants with an MCH of <27.0 pg should be investigated further to confirm or exclude a diagnosis of β-thal trait.
我们首次对印度加尔各答地中海贫血基金会在印度东部西孟加拉邦不同地区开展的人群筛查项目(1999 - 2011年)进行了评估,该项目旨在预防地中海贫血,包括对杂合子和中间型β地中海贫血(β-TI)病例[β(+)、β(++)、β(0)/β(+)、β(E)/β(E)(密码子26或HBB:c.79G > A)、血红蛋白E-β地中海贫血(Hb E-β-thal)]进行筛查。在18166例病例中,我们发现了2092例杂合子和2245例β-TI个体(他们对自己的病情一无所知)。通过包括红细胞指数、血红蛋白(Hb)分型和定量在内的标准血液学分析对结果进行了评估。参与者被分为五组(儿童、婚前病例、孕前病例、受影响的家庭成员、孕妇)。此次评估的目的是确定红细胞(RBC)、平均红细胞体积(MCV)、平均红细胞血红蛋白含量(MCH)、红细胞分布宽度(RDW)和Hb A2的临界值,因为在大规模筛查项目中并未严格遵循世界卫生组织(WHO)的标准指南。由于存在一些其他临床情况,如缺铁性贫血、α地中海贫血(α-thal)、δ地中海贫血(δ-thal)、临床无症状的Hb变异体,以及一些非血红蛋白病病例(如妊娠)合并地中海贫血,我们在考虑地中海贫血患者的状况时遇到了许多困境。在不同的血红蛋白病情况下,MCV值差异很大,而MCH提供了更稳定的测量结果。我们发现MCH值<27.0 pg是该人群筛查的合适临界点。MCH<27.0 pg的参与者应进一步检查以确认或排除β地中海贫血特征的诊断。