In order to provide a noninvasive prenatal diagnosis of alpha(0)-Thalassemia (Southeast Asian [SEA] deletion), we have developed a real-time quantitative semi-nested polymerase chain reaction (PCR) method for identifying the fetal alpha(0)-Thalassemia in maternal plasma. Analysis was performed using
DNA extracted from 200 muL plasma from 13 pregnant women during 8-20 weeks of gestation who carried fetuses with normal (2), alpha(0)-Thalassemia carrier (8), Hb H disease (1), and homozygous alpha(0)-Thalassemia (
Hb Bart's hydrops fetalis (2). The alpha(0)-
Thalassemia was detected using a two-step PCR. Plasma
DNA was amplified conventionally using alpha(0)-
Thalassemia-specific primers and a portion of the first PCR product was subjected to a semi-nested real-time q-PCR using the
SYBR green I chemistry for fluorescence detection. Calibration curve for alpha(0)-
Thalassemia quantification was prepared by assaying serial dilution of genomic
DNA of an alpha(0)-
Thalassemia carrier. Differences in the C(T) (threshold cycle) values and calculated concentrations of amplified
DNA among normal fetus, alpha(0)-
Thalassemia carrier, Hb H disease, and homozygous alpha(0)-
Thalassemia were clearly observed, which could help in prenatal prediction of the fetal genotype. This noninvasive prenatal detection of alpha(0)-
Thalassemia in maternal plasma should enhance prenatal diagnostic options for this common
genetic disorder in routine
DNA diagnostic setting.