MTHFR C677T多态性与墨西哥人群急性淋巴细胞白血病的风险

Pub Date : 2022-04-15 DOI:10.31901/24566330.2022/22.03.815
J. P. Meza-Espinoza
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引用次数: 0

摘要

MTHFR基因的C677T多态性在世界各地经常与急性淋巴细胞白血病(ALL)相关。因此,本研究的目的是确定MTHFR C677T多态性是否与墨西哥儿童和成人的ALL相关。对243名ALL患者(136名儿童和107名成人)和379名健康对照进行了病例对照研究。用聚合酶链式反应-限制性片段长度多态性方法对C677T多态性进行基因分型。在儿童、成人和对照组中,T等位基因的频率分别为43%、52%和46%。儿童T等位基因携带者未发现ALL风险[OR=0.81(0.52-1.25),P=0.33],但成人的风险增加[OR=4.98(2.24-11.10),P<0.001]。儿童的研究结果与大多数研究一致,但与成人的研究结果不一致。这些差异可能是由于种族、遗传背景、抽样和方法造成的。
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MTHFR C677T Polymorphism and Risk of Acute Lymphoblastic Leukaemia in Mexican Population
The C677T polymorphism of the MTHFR gene has been frequently associated with acute lymphoblastic leukaemia (ALL) around the world. Therefore, the objective of this study was to determine whether the MTHFR C677T polymorphism is associated with ALL in Mexican children and adults. A case-control study was conducted on 243 patients with ALL (136 children and 107 adults) and 379 healthy controls. Genotyping of the C677T polymorphism was performed by the polymerase chain reaction-restriction fragment length polymorphism method. The frequency of the T allele was forty-three percent, fifty-two percent, and forty-six percent in children, adults, and controls, respectively. No risk of ALL was found for T allele carriers in children [OR=0.81 (0.52-1.25), P=0.33], but an increased risk was detected in adults [OR=4.98 (2.24-11.10), P<0.001]. The findings in children agree with most of the studies but are discordant with those reported in adults. These differences could be due to ethnicity, genetic background, sampling, and methodology.
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