Laboratoire CLEMENT, 75016 Paris, France.
American Hospital, 92200 Paris, France.
Biomolecules. 2022 Aug 7;12(8):1086. doi: 10.3390/biom12081086.
Methylation is a crucially important ubiquitous biochemical process, which covalently adds methyl groups to a variety of molecular targets. It is the key regulatory process that determines the acquisition of imprinting and epigenetic marks during gametogenesis. Methylation processes are dependent upon two metabolic cycles, the folates and the one-carbon cycles. The activity of these two cycles is compromised by single nucleotide polymorphisms (SNPs) in the gene encoding the Methylenetetrahydrofolate reductase (MTHFR) enzyme. These SNPs affect spermatogenesis and oocyte maturation, creating cytologic/chromosomal anomalies. The two main MTHFR SNP variants C677T (c.6777C>T) and A1298C (c.1298A>C) together with serum homocysteine levels were tested in men with >3 years’ duration of infertility who had failed several ART attempts with the same partner. These patients are often classified as having “idiopathic infertility”. We observed that the genetic status with highest prevalence in this group is the heterozygous C677T, followed by the combined heterozygous C677T/A1298C, and then A1298C; these three variants represent 65% of our population. Only 13.1% of the patients tested are wild type (WT), C677C/A1298A). The homozygous 677TT and the combined heterozygote 677CT/1298AC groups have the highest percentage of patients with an elevated circulating homocysteine level of >15 µMolar (57.8% and 18.8%, respectively, which is highly significant for both). Elevated homocysteine is known to be detrimental to spermatogenesis, and the population with this parameter is not marginal. In conclusion, determination of these two SNPs and serum homocysteine should not be overlooked for patients with severe infertility of long duration, including those with repeated miscarriages. Patients must also be informed about pleiotropic medical implications relevant to their own health, as well as to the health of future children.
甲基化是一种至关重要的普遍存在的生化过程,它将甲基基团共价地添加到各种分子靶标上。它是决定配子发生过程中印迹和表观遗传标记获得的关键调节过程。甲基化过程依赖于两个代谢循环,即叶酸和一碳循环。这些两个循环的活性受到编码亚甲基四氢叶酸还原酶(MTHFR)酶的基因中单核苷酸多态性(SNP)的影响。这些 SNP 影响精子发生和卵母细胞成熟,导致细胞/染色体异常。两种主要的 MTHFR SNP 变体 C677T(c.6777C>T)和 A1298C(c.1298A>C)以及血清同型半胱氨酸水平在不育时间超过 3 年且与同一伴侣多次尝试 ART 失败的男性中进行了测试。这些患者通常被归类为患有“特发性不育症”。我们观察到,该组中患病率最高的遗传状态是杂合性 C677T,其次是杂合性 C677T/A1298C 联合,然后是 A1298C;这三种变体占我们人群的 65%。只有 13.1%的测试患者是野生型(WT),C677C/A1298A)。纯合子 677TT 和杂合子 677CT/1298AC 组中循环同型半胱氨酸水平升高(>15µMolar)的患者比例最高(分别为 57.8%和 18.8%,两者均高度显著)。已知升高的同型半胱氨酸对精子发生有害,并且具有该参数的人群并非微不足道。总之,对于长期严重不育症,包括反复流产的患者,不应忽视这两种 SNP 和血清同型半胱氨酸的测定。还必须告知患者与自身健康以及未来子女健康有关的多效性医学意义。