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印度浦那产前保健诊所孕妇中未确诊的血红蛋白病。

Undiagnosed haemoglobinopathies among pregnant women attending antenatal care clinics in Pune, India.

作者信息

Dharmarajan Sumedha, Pawar Ameya, Bhide Prajkta, Kar Anita

机构信息

School of Health Sciences, Savitribai Phule Pune University (University of Pune), Pune, 411007, India.

Department of Microbiology, Modern College of Arts, Science & Commerce, Pune, India.

出版信息

J Community Genet. 2021 Jul;12(3):337-344. doi: 10.1007/s12687-021-00505-8. Epub 2021 Jan 24.

Abstract

Pregnant women with iron deficiency and those who are carriers of haemoglobinopathies present with anaemia of varying severity. There is no antenatal screening for haemoglobinopathies in India. The objective of this study was to determine the prevalence of undiagnosed haemoglobinopathy carriers in a random sample of pregnant women attending antenatal care clinics in Pune city, India. Biobanked DNA of 360 randomly selected pregnant women was genotyped for six common mutations and two common haemoglobin variants, HbS and HbE. Odds ratios (OR) with 95% confidence intervals were computed to determine association of carrier status with socio-demographic, haematological and clinical characteristics. The prevalence of undiagnosed haemoglobinopathy carriers was 6.3% (95% CI 4.2-9.4%) of which 3.3% (95% CI 1.9-5.7%) were beta thalassaemia carriers. There was an increased odds that beta thalassaemia carriers had moderate anaemia (OR 10.59, 95% CI 1.15-96.90). This study reveals the high prevalence of undiagnosed haemoglobinopathy carriers among pregnant women, indicating the need to immediately implement carrier screening and genetic counselling services across the country.

摘要

缺铁的孕妇以及血红蛋白病携带者会出现不同严重程度的贫血。在印度,没有针对血红蛋白病的产前筛查。本研究的目的是确定在印度浦那市参加产前护理诊所的孕妇随机样本中未确诊的血红蛋白病携带者的患病率。对360名随机选择的孕妇的生物样本库DNA进行基因分型,检测六种常见突变以及两种常见血红蛋白变体,即HbS和HbE。计算95%置信区间的比值比(OR),以确定携带者状态与社会人口统计学、血液学和临床特征之间的关联。未确诊的血红蛋白病携带者患病率为6.3%(95%CI 4.2 - 9.4%),其中3.3%(95%CI 1.9 - 5.7%)为β地中海贫血携带者。β地中海贫血携带者患中度贫血的几率增加(OR 10.59,95%CI 1.15 - 96.90)。这项研究揭示了孕妇中未确诊的血红蛋白病携带者的高患病率,表明有必要在全国立即开展携带者筛查和遗传咨询服务。

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