Jiang Fan, Chen Gui-Lan, Li Jian, Xie Xing-Mei, Zhou Jian-Ying, Liao Can, Li Dong-Zhi
a Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center, Southern Medical University , Guangzhou , Guangdong Province , People's Republic of China.
Hemoglobin. 2017 Jul-Nov;41(4-6):248-253. doi: 10.1080/03630269.2017.1378672. Epub 2017 Nov 10.
In this study, we report the experience of a pre gestational thalassemia screening program at a single center in Southern China. Free thalassemia screening, genetic counseling and prenatal diagnosis (PND) for couples planning pregnancy were implemented over a 2-year period. Among a total of 83,062 screened individuals (41,531 couples), the allele frequencies of β-thalassemia (β-thal), - - and - - deletions were 3.79, 5.75 and 0.028%, respectively. Out of the 41,531 couples, 11,039 couples had at least one partner who had a positive screening test; of these, 455 at-risk couples (1.07%) were identified, including 68 (0.16%) for β-thal, 162 (0.39%) for Hb Bart's (γ4) hydrops fetalis, 190 (0.46%) for deletional Hb H (β4) disease and 25 (0.06%) for nondeletional Hb H disease. Of the 455 at-risk couples, 90 were already pregnant and 66 underwent PND at 10-13 weeks' gestation, resulting in 15 affected fetuses. The remaining 355 at-risk couples were still preparing for pregnancy, and they were on the list for follow-up. There is considerable scope for facilitating timely PND through improved organization and screening strategy. The pre pregnancy screening is a feasible and effective approach to thalassemia prevention.
在本研究中,我们报告了中国南方一个单一中心开展的孕前地中海贫血筛查项目的经验。在两年时间里,为计划怀孕的夫妇实施了免费的地中海贫血筛查、遗传咨询和产前诊断(PND)。在总共83,062名筛查对象(41,531对夫妇)中,β地中海贫血(β-thal)、--和--缺失的等位基因频率分别为3.79%、5.75%和0.028%。在41,531对夫妇中,11,039对夫妇至少有一方筛查结果呈阳性;其中,确定了455对高危夫妇(1.07%),包括68对(0.16%)β地中海贫血、162对(0.39%)巴氏水肿胎(γ4)、190对(0.46%)缺失型血红蛋白H(β4)病和25对(0.06%)非缺失型血红蛋白H病。在这455对高危夫妇中,90对已经怀孕,66对在妊娠10 - 13周时接受了产前诊断,结果发现15例胎儿受影响。其余355对高危夫妇仍在准备怀孕,他们在随访名单上。通过改进组织和筛查策略,有很大空间促进及时的产前诊断。孕前筛查是预防地中海贫血的一种可行且有效的方法。