Section of Palliative Care, Department of Medicine, Yale University School of Medicine, New Haven, Conn.
Am J Med. 2016 Jan;129(1):115.e9-115.e16. doi: 10.1016/j.amjmed.2015.07.017. Epub 2015 Jul 31.
Cobalamin (B12) deficiency can lead to irreversible neurocognitive changes if unrecognized. Screening involves measurement of serum cobalamin levels, but the sensitive metabolic indicators of cobalamin deficiency, methylmalonic acid (MMA) and homocysteine (HCys), may be normal when cobalamin values are low and elevated when cobalamin values are normal. Because cobalamin is inactivated by oxidation, the relationship between these metabolites and comorbidities associated with increased oxidative stress (oxidant risks) in subjects with low and low-normal cobalamin levels was studied.
A retrospective record-review was conducted of community-dwelling adults evaluated for cobalamin deficiency during a 12-year period with serum cobalamin values in the low (≤ 200 pg/mL; n = 49) or low-normal (201-300 pg/mL; n = 187) range and concurrent measurement of MMA.
When "No" oxidant risk was present, elevated MMA (>250 nmol/L) and HCys (>12.1 μmol/L) values occurred in 50% and 30% of subjects, respectively (P <.01). In contrast, when "Three or More" oxidant risks were present, mean MMA and HCys values were significantly higher, and elevated MMA and HCys values occurred in 84% and 78% of these subjects, respectively (P ≤.012). Pharmacologic doses of cyanocobalamin significantly decreased metabolite values in ≥ 94% of treated subjects.
In subjects with low or low-normal cobalamin values, metabolic evidence of cobalamin deficiency is more frequent when 3 or more oxidant risks are present. Thus, defining a low serum cobalamin level to screen for cobalamin deficiency may be a "moving target" due to the variable presence and severity of often subtle, confounding clinical conditions in individual subjects.
如果未能识别,钴胺素(B12)缺乏可导致不可逆的神经认知改变。筛查包括血清钴胺素水平的测量,但是当钴胺素值较低时,钴胺素缺乏的敏感代谢指标甲基丙二酸(MMA)和同型半胱氨酸(HCys)可能正常,而当钴胺素值正常时则升高。由于钴胺素被氧化失活,因此研究了低和低正常钴胺素水平的受试者中与增加氧化应激相关的合并症(氧化剂风险)与这些代谢物之间的关系。
对 12 年间因低(≤200pg/ml;n=49)或低正常(201-300pg/ml;n=187)范围内血清钴胺素值而接受钴胺素缺乏评估的社区居住成年人进行了回顾性记录审查,并同时测量了 MMA。
当“无”氧化剂风险存在时,分别有 50%和 30%的受试者出现 MMA(>250nmol/L)和 HCys(>12.1μmol/L)升高(P<.01)。相比之下,当存在“三个或更多”氧化剂风险时,这些受试者的平均 MMA 和 HCys 值显著更高,分别有 84%和 78%的受试者出现 MMA 和 HCys 升高(P≤.012)。氰钴胺素的药理剂量可使≥94%的治疗受试者的代谢物值显著降低。
在低或低正常钴胺素水平的受试者中,当存在 3 个或更多氧化剂风险时,钴胺素缺乏的代谢证据更为常见。因此,由于个体受试者中经常存在微妙的、混杂的临床情况,且其存在和严重程度存在差异,因此定义血清钴胺素水平低以筛查钴胺素缺乏可能是一个“移动目标”。