Islam Md Tarikul, Sarker Suprovath Kumar, Talukder Shezote, Bhuyan Golam Sarower, Rahat Asifuzzaman, Islam Nafisa Nawal, Mahmud Hasan, Hossain Mohammad Amir, Muraduzzaman A K M, Rahman Jakia, Qadri Syeda Kashfi, Shahidullah Mohammod, Mannan Mohammad Abdul, Tahura Sarabon, Hussain Manzoor, Saha Narayan, Akhter Shahida, Nahar Nazmun, Begum Firoza, Shirin Tahmina, Akhteruzzaman Sharif, Qadri Syed Saleheen, Qadri Firdausi, Mannoor Kaiissar
Laboratory of Genetics and Genomics, Institute for Developing Science and Health Initiatives, Mohakhali, Dhaka, Bangladesh.
Department of Genetic Engineering & Biotechnology, University of Dhaka, Dhaka, Bangladesh.
BMC Genet. 2018 Aug 10;19(1):58. doi: 10.1186/s12863-018-0664-1.
Like glucose-6-phosphate dehydrogenase (G6PD) deficient hemizygous males and homozygous females, heterozygous females could also manifest hemolytic crisis, neonatal hyperbilirubinemia or kernicterus upon exposure to oxidative stress induced by certain foods such as fava beans, drugs or infections. Although hemizygous males and homozygous females are easily detected by conventional G6PD enzyme assay method, the heterozygous state could be missed by the conventional methods as the mosaic population of both normal and deficient RBCs circulates in the blood. Thus the present study aimed to apply high resolution melting (HRM) curve analysis approach to see whether HRM could be used as a supplemental approach to increase the chance of detection of G6PD heterozygosity.
Sixty-three clinically suspected females were evaluated for G6PD status using both enzyme assay and HRM analysis. Four out of sixty-three participants came out as G6PD deficient by the enzyme assay method, whereas HRM approach could identify nine participants with G6PD variants, one homozygous and eight heterozygous. Although only three out of eight heterozygous samples had G6PD enzyme deficiency, the HRM-based heterozygous G6PD variants detection for the rest of the samples with normal G6PD enzyme activities could have significance because their newborns might fall victim to serious consequences under certain oxidative stress.
In addition to the G6PD enzyme assay, HRM curve analysis could be useful as a supplemental approach for detection of G6PD heterozygosity.
与葡萄糖-6-磷酸脱氢酶(G6PD)缺乏的半合子男性和纯合子女性一样,杂合子女性在接触某些食物(如蚕豆)、药物或感染诱导的氧化应激时,也可能出现溶血危机、新生儿高胆红素血症或核黄疸。虽然通过传统的G6PD酶检测方法很容易检测出半合子男性和纯合子女性,但由于正常和缺陷红细胞的嵌合群体在血液中循环,传统方法可能会漏检杂合子状态。因此,本研究旨在应用高分辨率熔解(HRM)曲线分析方法,看看HRM是否可以作为一种补充方法来增加检测G6PD杂合性的机会。
使用酶检测和HRM分析对63名临床疑似女性的G6PD状态进行了评估。酶检测方法显示63名参与者中有4名G6PD缺乏,而HRM方法可以识别出9名有G6PD变异的参与者,其中1名纯合子和8名杂合子。虽然8个杂合子样本中只有3个有G6PD酶缺乏,但对于其余G6PD酶活性正常的样本,基于HRM的杂合子G6PD变异检测可能具有重要意义,因为他们的新生儿在某些氧化应激下可能会受到严重影响。
除了G6PD酶检测外,HRM曲线分析可作为检测G6PD杂合性的补充方法。