Department of Nutrition, University of California-Davis, One Shields Avenue, Davis, CA 95616, USA.
USDA-ARS Western Human Nutrition Research Center, 430 West Health Sciences Drive, Davis, CA 95616, USA.
Nutrients. 2022 Mar 25;14(7):1376. doi: 10.3390/nu14071376.
TMAO is elevated in individuals with cardiometabolic diseases, but it is unknown whether the metabolite is a biomarker of concern in healthy individuals. We conducted a cross-sectional study in metabolically healthy adults aged 18-66 years with BMI 18-44 kg/m and assessed the relationship between TMAO and diet, the fecal microbiome, and cardiometabolic risk factors. TMAO was measured in fasted plasma samples by liquid chromatography mass spectrometry. The fecal microbiome was assessed by 16S ribosomal RNA sequencing and recent food intake was captured by multiple ASA24 dietary recalls. Endothelial function was assessed via EndoPAT. Descriptive statistics were computed by fasting plasma TMAO tertiles and evaluated by ANOVA and Tukey's post-hoc test. Multiple linear regression was used to assess the relationship between plasma TMAO and dietary food intake and metabolic health parameters. TMAO concentrations were not associated with average intake of animal protein foods, fruits, vegetables, dairy, or grains. TMAO was related to the fecal microbiome and the genera , , , and were enriched in individuals in the lowest versus the highest TMAO tertile. TMAO was positively associated with α-diversity and compositional differences were identified between groups. TMAO was not associated with classic cardiovascular risk factors in the healthy cohort. Similarly, endothelial function was not related to fasting TMAO, whereas the inflammatory marker TNF-α was significantly associated. Fasting plasma TMAO may not be a metabolite of concern in generally healthy adults unmedicated for chronic disease. Prospective studies in healthy individuals are necessary.
氧化三甲胺(TMAO)在患有心脏代谢疾病的个体中升高,但尚不清楚该代谢物是否是健康个体中值得关注的生物标志物。我们对年龄在 18-66 岁、体重指数(BMI)为 18-44 kg/m²且代谢健康的成年人进行了一项横断面研究,评估了 TMAO 与饮食、粪便微生物群和心脏代谢危险因素之间的关系。通过液相色谱-质谱法在空腹血浆样本中测量 TMAO。通过 16S 核糖体 RNA 测序评估粪便微生物群,通过多次 ASA24 饮食回忆捕获近期食物摄入量。通过 EndoPAT 评估内皮功能。通过空腹血浆 TMAO 三分位值计算描述性统计数据,并通过方差分析和 Tukey 事后检验进行评估。使用多元线性回归评估血浆 TMAO 与饮食食物摄入量和代谢健康参数之间的关系。TMAO 浓度与动物蛋白食物、水果、蔬菜、乳制品或谷物的平均摄入量无关。TMAO 与粪便微生物群有关,并且在最低 TMAO 三分位与最高 TMAO 三分位的个体中,属 、 、 和 得到富集。TMAO 与 α 多样性呈正相关,并且在组间鉴定出组成差异。在健康队列中,TMAO 与经典心血管危险因素无关。同样,内皮功能与空腹 TMAO 无关,而炎症标志物 TNF-α 则与之显著相关。在未服用慢性疾病药物的一般健康成年人中,空腹血浆 TMAO 可能不是值得关注的代谢物。需要在健康个体中进行前瞻性研究。