García-García Inés, García-Fragoso Lourdes, Renta Jessicca, Arce Sylvia, Cadilla Carmen L
Department of Pediatrics, Neonatology Section, Medical Sciences Campus, University of Puerto Rico, GPO Box 365067, San Juan, PR, USA.
P R Health Sci J. 2002 Mar;21(1):17-9.
Homozygosity for a common polymorphism in the 5,10 methylenetetrahydrofolate reductase (MTHFR) gene (C677T) has been associated to an increased risk of neural tube defects as well as derangements in folate, homocysteine, and hematological parameters. This study analyzed the relationship between folate levels, the erythrocyte volume, and the presence of homozygosity for the C677T polymorphism in a group of 126 Puerto Rican healthy women of childbearing age. Blood samples were analyzed for erythrocyte mean corpuscular volume (MCV), mean erythrocyte hemoglobin content (MCH), folate, and RBC folate. Homozygosity for the C677T mutation was determined by PCR. Thirty-two percent (32%) of women used a folic acid supplement during the three months prior to sampling. Mean folate and RBC folate levels were within the normal range. Individuals homozygous for the MTHFR C677T polymorphism had no elevation of MCV (p = 0.70) or MCH (p = 0.68). Women in the lower quartile of folate levels did not show differences in their MCV or MCH. In this sample of Puerto Rican women, homozygosity for the C677T MTHFR polymorphism was not associated to elevations of MCV or MCH even in the presence of lower folate levels.
5,10-亚甲基四氢叶酸还原酶(MTHFR)基因常见多态性(C677T)的纯合性与神经管缺陷风险增加以及叶酸、同型半胱氨酸和血液学参数紊乱有关。本研究分析了126名波多黎各育龄健康女性中叶酸水平、红细胞体积与C677T多态性纯合性之间的关系。对血样进行红细胞平均体积(MCV)、平均红细胞血红蛋白含量(MCH)、叶酸和红细胞叶酸分析。通过聚合酶链反应(PCR)确定C677T突变的纯合性。32%的女性在采样前三个月使用了叶酸补充剂。平均叶酸和红细胞叶酸水平在正常范围内。MTHFR C677T多态性纯合个体的MCV(p = 0.70)或MCH(p = 0.68)没有升高。叶酸水平处于下四分位数的女性其MCV或MCH没有差异。在这个波多黎各女性样本中,即使存在较低的叶酸水平,C677T MTHFR多态性的纯合性也与MCV或MCH升高无关。