普通人群中功能性钴胺素缺乏症的患病率及相关死亡率风险:与钴胺素缺乏症不同的未被关注的表型。

IF 6.8 4区 医学 Q1 NUTRITION & DIETETICS
Yan Liu, Yi Gao, Yige Liu, Yiying Zhang, Shanjie Wang, Bo Yu
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引用次数: 0

摘要

背景:目前的指南将监测和管理钴胺素(Cbl)缺乏症列为优先事项,但对功能性 Cbl 缺乏症(Cbl 敏感性降低)的处理不够充分。本研究旨在调查功能性 Cbl 缺乏症的患病负担,并研究与 Cbl 缺乏症相比,功能性 Cbl 缺乏症与美国成年人死亡风险的前瞻性关联:该队列研究纳入了 1999 年至 2014 年期间年龄≥20 岁的 22,513 名美国参与者,并随访至 2019 年 12 月 31 日。采用Cbl和甲基丙二酸(MMA)水平的二元分类组合评估Cbl敏感性,Cbl的临界值为400 pg/mL,MMA的临界值为250 nmol/L。功能性 Cbl 缺乏症的定义是 MMA 和 Cbl 水平升高。血清 Cbl 水平 结果:在这项研究中,约有 2.1% 的美国成年人患有 Cbl 缺乏症,而经年龄调整后的功能性 Cbl 缺乏症患病率为 4.5%,相当于约 1,000 万美国成年人。在 10.7 年的中位随访期内,共有 4636 例死亡记录。与 MMA lowCbllow 组(MMA ≤250 nmol/L,Cbl ≤400 pg/mL)相比,MMAhighCblhigh 组的全因、心血管和癌症相关死亡率的多变量调整危险比为 1.76(95% 置信区间 [CI]:1.53-2.02,p p = 0.089)。相比之下,在调整了类似的混杂因素后,与 Cbl 缺乏相关的死亡风险变得不显著。虽然Cbl补充剂或高于推荐水平的膳食摄入量可能会缓解Cbl缺乏症,但它们似乎并不能降低功能性Cbl缺乏症的患病率或与之相关的死亡风险:结论:与 Cbl 缺乏症相比,功能性 Cbl 缺乏症更为常见,并且与普通人群死亡风险的增加有显著关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prevalence of Functional Cobalamin Deficiency and Relevant Mortality Risk in the General Population: An Unheeded Phenotype Distinct from Cobalamin Deficiency.

Background: Current guidelines prioritize monitoring and managing cobalamin (Cbl) deficiency but insufficiently address the issue of functional Cbl deficiency (decreased Cbl sensitivity). This study aims to investigate the prevalence burden of functional Cbl deficiency and to examine its prospective association with mortality risk, compared to Cbl deficiency, among United States (US) adults.

Method: The cohort study included 22,513 US participants aged ≥20 years from 1999 to 2014 and was followed up through December 31, 2019. Cbl sensitivity was assessed using a combination of binary classifications for Cbl and methylmalonic acid (MMA) levels, with cutoff values set at 400 pg/mL for Cbl and 250 nmol/L for MMA. Functional Cbl deficiency was defined as elevated MMA and Cbl levels. Serum Cbl levels <148 pmol/L (200 pg/mL) were classified as Cbl deficiency.

Results: In this study, approximately 2.1% of US adults had Cbl deficiency, while the age-adjusted prevalence of functional Cbl deficiency was 4.5%, corresponding to an estimated 10 million US adults. Over a median follow-up period of 10.7 years, there were 4636 recorded deaths. Compared to the MMAlowCbllow group (MMA ≤250 nmol/L, Cbl ≤400 pg/mL), the multivariable-adjusted hazard ratios for all-cause, cardiovascular, and cancer-related mortality in the MMAhighCblhigh group were 1.76 (95% confidence interval [CI]: 1.53-2.02, p < 0.001), 2.17 (95% CI: 1.78-2.67, p < 0.001), and 1.38 (95% CI: 0.95-2.00, p = 0.089). In contrast, the mortality risk associated with Cbl deficiency became insignificant after adjusting for similar confounders. While Cbl supplementation or dietary intake above recommended levels might alleviate Cbl deficiency, they do not appear to reduce the prevalence of functional Cbl deficiency or its associated mortality risk.

Conclusion: Compared with Cbl deficiency, functional Cbl deficiency is more frequent and is significantly associated with increased mortality risk in the general population.

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