Regional Medical Research Centre for Tribals (ICMR), Nagpur Road, PO-Garha, Jabalpur-482003, Madhya Pradesh, INDIA.
Mediterr J Hematol Infect Dis. 2013 Jun 4;5(1):e2013036. doi: 10.4084/MJHID.2013.036. Print 2013.
Females with sickle cell disease (SCD) often show late onset of menarche. In transgenic sickle cell mouse, deficiency of gene encoding endothelial nitric oxide synthase (eNOS) has been reported to be associated with late onset of menarche. Thus to explore the possible association of eNOS gene polymorphism with age of onset of menarche in SCD females, 3 important eNOS gene polymorphisms- eNOS 4a/b, eNOS 894G>T (rs1799983) and eNOS-786 T>C (rs2070744) and plasma nitrite levels were tested among three groups of females- SCD late menarche, SCD early menarche and control females.
About 39 SCD females comprising of 18 SCD early menarche and 21 SCD late menarche groups were studied along with 48 control females. Genotyping of eNOS gene polymorphisms were done by PCR-RFLP and quantification of plasma nitrite level was performed by ELISA based commercial kits.
SCD late menarche females showed significantly higher prevalence and higher association of heterozygous genotypes, higher frequency of mutant alleles .4a., .T. and .C. as compared to that of control group and SCD early menarche group. The frequency of haplotype .4a-G-C. and haplotype .4b-G-C. (alleles in order of eNOS 4a/b, eNOS 894G>T and eNOS-786 T>C respectively) were found to be significantly high in SCD late menarche compared to combined groups of SCD early menarche and controls. SCD late menarche group had significantly low level of plasma nitrite concentration for all 3 eNOS gene polymorphisms as compared to controls and SCD early menarche females.
eNOS gene polymorphism may influence age of onset of menarche in SCD females.
患有镰状细胞病(SCD)的女性通常出现月经初潮延迟。在转基因镰状细胞小鼠中,已经报道内皮型一氧化氮合酶(eNOS)基因缺失与月经初潮延迟有关。因此,为了探索 eNOS 基因多态性与 SCD 女性月经初潮年龄之间的可能关联,我们在三组女性中检测了三个重要的 eNOS 基因多态性-eNOS 4a/b、eNOS 894G>T(rs1799983)和 eNOS-786 T>C(rs2070744)以及血浆硝酸盐水平-SCD 晚初潮、SCD 早初潮和对照组女性。
我们研究了约 39 名 SCD 女性,包括 18 名 SCD 早初潮和 21 名 SCD 晚初潮组,以及 48 名对照组女性。通过 PCR-RFLP 进行 eNOS 基因多态性的基因分型,并通过基于商业试剂盒的 ELISA 定量检测血浆硝酸盐水平。
与对照组和 SCD 早初潮组相比,SCD 晚初潮女性杂合基因型的患病率和相关性更高,突变等位基因.4a.、.T.和.C.的频率更高。与 SCD 早初潮和对照组的合并组相比,SCD 晚初潮组中.4a-G-C.和.4b-G-C.(按照 eNOS 4a/b、eNOS 894G>T 和 eNOS-786 T>C 的顺序排列的等位基因)的单倍型频率明显更高。与对照组和 SCD 早初潮女性相比,SCD 晚初潮组所有 3 个 eNOS 基因多态性的血浆硝酸盐浓度均显著降低。
eNOS 基因多态性可能影响 SCD 女性的月经初潮年龄。