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Hemoglobin
international journal for hemoglobin research
Volume 39, 2015 - Issue 4
143
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Original Article

Molecular Diagnosis of α0-Thalassemia Through Urine DNA: A Novel DNA Source to Facilitate Prevention Programs in Remote Geographical Areas

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Pages 270-273 | Received 22 Sep 2014, Accepted 12 Dec 2014, Published online: 27 May 2015
 

Abstract

We assessed whether urinary DNA sediment was a feasible sample type for the molecular diagnosis of α-thalassemia (α-thal) mutations. Urine samples (5–10 mL) were collected from 218 male and female volunteers. The cells were centrifuged, and DNA was isolated according to the protocol of a commercial DNA isolation kit. Detection of the α0-thal [Southeast Asian (– –SEA) and – –THAI] deletions was performed using quantitative real-time polymerase chain reaction (q-PCR), in addition to conventional gap-PCR. The results revealed that DNA extracted from urinary sediment presented an average DNA content of 11.2 ± 5.5 ng/µL, and the 260/280 ratio indicative of DNA purity, was 1.2 ± 0.2. The overall q-PCR threshold cycle was 31.2 ± 2.3. The melting temperature for the – –SEA deletion was 87.3 ± 0.1 °C, while that of the wild type sequence was 92.5 ± 0.2 °C. There were 16 (7.3%) α0-thal SEA genotypes detected. These results were in agreement with those of the conventional gap-PCR and blood DNA analyses. Thus, DNA from urinary sediment can be efficiently used for the molecular diagnosis of α0-thal mutations. This approach allows for rapid diagnosis, is non invasive, and could be useful for preventing Hb Bart’s (γ4) hydrops fetalis syndrome.

Declaration of interest

This study was supported by the University of Phayao, Phayao, Thailand Endowment Fund. The authors report no conflicts of interest. The authors alone are responsible for the content and writing of this article.

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