Department of Epidemiology and Biostatistics, School of Public Health, Jiamusi University, Jiamusi, People's Republic of China.
Department of Integrated Traditional Chinese and Western Medicine, First Affiliated Hospital of Harbin Medical University, Harbin, People's Republic of China.
Am J Clin Nutr. 2024 May;119(5):1122-1132. doi: 10.1016/j.ajcnut.2024.02.009. Epub 2024 Apr 2.
Elevated serum methylmalonic acid (MMA), a marker of cobalamin (vitamin B12) deficiency, has been linked to cancer progression. However, the impact of MMA or cobalamin on mortality risk in cancer survivors remains unknown.
To explore the relationship between MMA, serum, dietary, and supplement of cobalamin, MMA metabolism-related genes, and poor prognosis in adult cancer survivors.
We analyzed data from 1988 cancer survivors aged ≥20 y. Patients were selected from the National Health and Nutrition Examination Survey and followed up until December 31, 2019. Weighted Cox proportional hazard regression was used to estimate hazard ratios (HRs) and the corresponding 95% confidence intervals (CIs) for mortality risk assessment. Genomic analysis identified MMA metabolism-related genes linked to early death in a 33-cancer-type cohort from The Cancer Genome Atlas.
Among 1988 participants, 872 deaths occurred over a 10-year follow-up. Higher serum MMA levels were significantly linked to increased long-term mortality risk (tertile 3 compared with tertile 1: adjusted HR: 1.37; 95% CI: 1.11, 1.70; P-trend < 0.001). No associations were found between serum, dietary, and supplement of cobalamin and cancer survivor mortality (each P-trend > 0.143). However, MMA-associated mortality was notable in patients without deficiency. When combining cobalamin and MMA categories, multivariate-adjusted HR (95% CI) for all-cause mortality was 2.06 (95% CI: 1.60, 2.65) in participants with >250 nmol/L and cobalamin >295.1 pmol/L compared with those with MMA ≤250 nmol/L and cobalamin >295.1 pmol/L. Moreover, reduced transcriptional levels of MMA metabolism-related genes, indicating decreased mitochondrial MMA metabolism capability, are linked to an unfavorable prognosis in certain cancer types.
Serum MMA was associated with long-term mortality risk in adult cancer survivors, which was more significant among individuals with higher levels of serum cobalamin. These findings suggest that mortality related to MMA was attributed to the insufficient flux of MMA metabolism, not cobalamin deficiency.
血清甲基丙二酸(MMA)水平升高是钴胺素(维生素 B12)缺乏的标志物,与癌症进展有关。然而,MMA 或钴胺素对癌症幸存者的死亡风险的影响尚不清楚。
探讨 MMA、血清、饮食和补充钴胺素、MMA 代谢相关基因与成年癌症幸存者不良预后之间的关系。
我们分析了 1988 名年龄≥20 岁的癌症幸存者的数据。这些患者是从国家健康和营养调查中选择的,并随访至 2019 年 12 月 31 日。使用加权 Cox 比例风险回归来估计死亡率风险评估的风险比(HR)和相应的 95%置信区间(CI)。基因组分析确定了与癌症基因组图谱中 33 种癌症类型队列中早期死亡相关的 MMA 代谢相关基因。
在 1988 名参与者中,有 872 人在 10 年的随访中死亡。较高的血清 MMA 水平与长期死亡风险增加显著相关(第 3 三分位与第 1 三分位相比:调整后的 HR:1.37;95%CI:1.11,1.70;P-趋势<0.001)。血清、饮食和补充钴胺素与癌症幸存者死亡率之间无关联(每项 P-趋势>0.143)。然而,在没有缺乏症的患者中,MMA 相关性死亡率很明显。当结合钴胺素和 MMA 类别时,MMA 代谢相关基因多变量调整后的 HR(95%CI)对于所有原因死亡率为 2.06(95%CI:1.60,2.65),与 MMA≤250nmol/L 和 cobalamin>295.1 pmol/L 的参与者相比,参与者>250 nmol/L 和 cobalamin>295.1 pmol/L。此外,MMA 代谢相关基因的转录水平降低,表明线粒体 MMA 代谢能力下降,与某些癌症类型的不良预后有关。
血清 MMA 与成年癌症幸存者的长期死亡率风险相关,在血清钴胺素水平较高的个体中更为显著。这些发现表明,与 MMA 相关的死亡率归因于 MMA 代谢通量不足,而不是钴胺素缺乏。