School of Medicine, Cardiff University, Gwenfro Units 6/7, Wrexham Technology Park, Wrexham LL17 7YP, Wales, United Kingdom.
Biochimie. 2013 May;95(5):1066-76. doi: 10.1016/j.biochi.2012.11.017. Epub 2012 Dec 7.
The classic neurological and psychiatric features associated with vitamin B12 deficiency have been well described and are the subject of many excellent review articles. The advent of sensitive diagnostic tests, including homocysteine and methylmalonic acid assays, has revealed a surprisingly high prevalence of a more subtle 'subclinical' form of B12 deficiency, particularly within the elderly. This is often associated with cognitive impairment and dementia, including Alzheimer's disease. Metabolic evidence of B12 deficiency is also reported in association with other neurodegenerative disorders including vascular dementia, Parkinson's disease and multiple sclerosis. These conditions are all associated with chronic neuro-inflammation and oxidative stress. It is possible that these clinical associations reflect compromised vitamin B12 metabolism due to such stress. Physicians are also increasingly aware of considerable inter-individual variation in the clinical response to B12 replacement therapy. Further research is needed to determine to what extent this is attributable to genetic determinants of vitamin B12 absorption, distribution and cellular uptake.
经典的与维生素 B12 缺乏相关的神经和精神特征已被很好地描述,并成为许多优秀的综述文章的主题。随着敏感诊断测试(包括同型半胱氨酸和甲基丙二酸测定)的出现,一种更为微妙的“亚临床”形式的 B12 缺乏症的发病率令人惊讶地高,尤其是在老年人中。这种情况通常与认知障碍和痴呆症有关,包括阿尔茨海默病。代谢证据表明,B12 缺乏症也与其他神经退行性疾病有关,包括血管性痴呆、帕金森病和多发性硬化症。这些疾病都与慢性神经炎症和氧化应激有关。这些临床关联可能反映了由于这种应激导致的维生素 B12 代谢受损。医生也越来越意识到,B12 替代治疗的临床反应存在很大的个体差异。需要进一步研究以确定这种情况在多大程度上归因于维生素 B12 吸收、分布和细胞摄取的遗传决定因素。