Castillo Luisa F, Pelletier Caitlyn M, Heyden Katarina E, Field Martha S
Division of Nutritional Sciences, Cornell University, Ithaca, New York, NY, USA; email:
Annu Rev Nutr. 2025 Aug;45(1):23-39. doi: 10.1146/annurev-nutr-120524-043056. Epub 2025 May 2.
Folate and vitamin B (B12) are essential cofactors in folate-mediated one-carbon metabolism (FOCM). FOCM includes a series of methyl transfer reactions for methionine regeneration and de novo synthesis of nucleotides, including thymidylate. Deficiency in either folate or B12 can result in negative health outcomes including megaloblastic anemia, with additional neurocognitive impairments observed as a result of B12 deficiency. While folate deficiency is not common in the United States due to mandatory folic acid fortification, B12 deficiency is observed more frequently, particularly in certain subpopulations such as vegetarians/vegans and older adults. Fortification of the food supply with folic acid has been effective to increase folate status and reduce the incidence of birth defects. However, consumption of fortified foods and use of dietary supplements containing folic acid have led to an increase in the proportion of individuals exceeding the tolerable upper intake level of folic acid. Although the interaction between folate and B12 has been appreciated for decades in relation to megaloblastic anemia, it has been recently proposed that elevated serum folate may worsen neurocognitive effects and other metabolic impairments (altered glucose homeostasis, type 2 diabetes in offspring) associated with B12 deficiency. This review highlights molecular mechanisms that may explain the biology underlying these associations with a focus on findings from studies in model systems.
叶酸和维生素B(B12)是叶酸介导的一碳代谢(FOCM)中的必需辅因子。FOCM包括一系列用于甲硫氨酸再生和核苷酸(包括胸苷酸)从头合成的甲基转移反应。叶酸或B12缺乏都可能导致不良健康后果,包括巨幼细胞贫血,B12缺乏还会导致额外的神经认知障碍。虽然由于强制性叶酸强化,美国叶酸缺乏并不常见,但B12缺乏更为常见,尤其是在某些亚人群中,如素食者/纯素食者和老年人。用叶酸强化食品供应有效地提高了叶酸水平并降低了出生缺陷的发生率。然而,食用强化食品和使用含叶酸的膳食补充剂导致超过叶酸可耐受最高摄入量水平的个体比例增加。尽管叶酸和B12之间的相互作用在巨幼细胞贫血方面已被认识数十年,但最近有人提出,血清叶酸升高可能会加重与B12缺乏相关的神经认知效应和其他代谢障碍(后代葡萄糖稳态改变、2型糖尿病)。本综述重点介绍了模型系统研究中的发现,突出了可能解释这些关联背后生物学机制的分子机制。