Mohn Nutrition Research Laboratory, Department of Clinical Science, University of Bergen, Bergen, Norway.
Centre for Nutrition, Department of Clinical Science, University of Bergen, Bergen, Norway.
Br J Nutr. 2024 May 28;131(10):1678-1690. doi: 10.1017/S0007114524000473. Epub 2024 Feb 16.
Elevated plasma concentrations of several one-carbon metabolites are associated with increased CVD risk. Both diet-induced regulation and dietary content of one-carbon metabolites can influence circulating concentrations of these markers. We cross-sectionally analysed 1928 patients with suspected stable angina pectoris (geometric mean age 61), representing elevated CVD risk, to assess associations between dietary macronutrient composition (FFQ) and plasma one-carbon metabolites and related B-vitamin status markers (GC-MS/MS, LC-MS/MS or microbiological assay). Diet-metabolite associations were modelled on the continuous scale, adjusted for age, sex, BMI, smoking, alcohol and total energy intake. Average (geometric mean (95 % prediction interval)) intake was forty-nine (38, 63) energy percent (E%) from carbohydrate, thirty-one (22, 45) E% from fat and seventeen (12, 22) E% from protein. The strongest associations were seen for higher protein intake, i.e. with higher plasma pyridoxal 5'-phosphate (PLP) (% change (95 % CI) 3·1 (2·1, 4·1)), cobalamin (2·9 (2·1, 3·7)), riboflavin (2·4 (1·1, 3·7)) and folate (2·1 (1·2, 3·1)) and lower total homocysteine (tHcy) (-1·4 (-1·9, -0·9)) and methylmalonic acid (MMA) (-1·4 (-2·0, -0·8)). Substitution analyses replacing MUFA or PUFA with SFA demonstrated higher plasma concentrations of riboflavin (5·0 (0·9, 9·3) and 3·3 (1·1, 5·6)), tHcy (2·3 (0·7, 3·8) and 1·3 (0·5, 2·2)) and MMA (2·0 (0·2, 3·9) and 1·7 (0·7, 2·7)) and lower PLP (-2·5 (-5·3, 0·3) and -2·7 (-4·2, -1·2)). In conclusion, a higher protein intake and replacing saturated with MUFA and PUFA were associated with a more favourable metabolic phenotype regarding metabolites associated with CVD risk.
几种一碳代谢物的血浆浓度升高与 CVD 风险增加有关。一碳代谢物的饮食诱导调节和饮食含量都可以影响这些标志物的循环浓度。我们对 1928 名疑似稳定型心绞痛患者(几何平均年龄 61 岁)进行了横断面分析,这些患者代表着升高的 CVD 风险,以评估饮食宏量营养素组成(FFQ)与血浆一碳代谢物和相关 B 族维生素状态标志物(GC-MS/MS、LC-MS/MS 或微生物测定)之间的关联。饮食-代谢物关联在连续尺度上进行建模,调整了年龄、性别、BMI、吸烟、饮酒和总能量摄入。平均(几何均数(95%预测区间))摄入量为 49%(38%,63%)来自碳水化合物,31%(22%,45%)来自脂肪,17%(12%,22%)来自蛋白质。与更高的蛋白质摄入量关联最强,即更高的血浆吡哆醛 5'-磷酸(PLP)(%变化(95%CI)3·1(2·1,4·1))、钴胺素(2·9(2·1,3·7))、核黄素(2·4(1·1,3·7))和叶酸(2·1(1·2,3·1)),更低的总同型半胱氨酸(tHcy)(-1·4(-1·9,-0·9))和甲基丙二酸(MMA)(-1·4(-2·0,-0·8))。用 SFA 替代 MUFA 或 PUFA 的替代分析显示核黄素(5·0(0·9,9·3)和 3·3(1·1,5·6))、tHcy(2·3(0·7,3·8)和 1·3(0·5,2·2))和 MMA(2·0(0·2,3·9)和 1·7(0·7,2·7))的血浆浓度更高,PLP 更低(-2·5(-5·3,0·3)和-2·7(-4·2,-1·2))。总之,较高的蛋白质摄入和用 MUFA 和 PUFA 替代饱和脂肪与与 CVD 风险相关的代谢物的更有利代谢表型相关。