Section of Preventive Medicine and Epidemiology, Department of Medicine, Boston University School of Medicine, Boston, MA, United States of America.
Center for Biostatistics in AIDS Research, Harvard T.H. Chan School of Public Health, Boston, MA, United States of America.
PLoS One. 2021 Sep 7;16(9):e0254577. doi: 10.1371/journal.pone.0254577. eCollection 2021.
Circulating levels of the endogenous inhibitor of nitric oxide synthase, asymmetric dimethylarginine (ADMA), are positively associated with the prevalence of metabolic syndrome (MetS) in cross-sectional investigations. It is unclear if circulating ADMA and other methylarginines are associated with incident MetS prospectively.
We related circulating ADMA, symmetric dimethylarginine (SDMA), L-arginine (ARG) concentrations (measured with a validated tandem mass spectrometry assay) and the ARG/ADMA ratio to MetS and its components in 2914 (cross-sectional analysis, logistic regression; mean age 58 years, 55% women) and 1656 (prospective analysis, Cox regression; mean age 56 years, 59% women) individuals from the Framingham Offspring Study who attended a routine examination.
Adjusting for age, sex, smoking, and eGFR, we observed significant associations of ADMA (direct) and ARG/ADMA (inverse) with odds of MetS (N = 1461 prevalent cases; Odds Ratio [OR] per SD increment 1.13, 95%CI 1.04-1.22; and 0.89, 95%CI 0.82-0.97 for ADMA and ARG/ADMA, respectively). Upon further adjustment for waist circumference, systolic and diastolic blood pressure, glucose, high-density lipoprotein cholesterol, and triglycerides, we observed a positive relation between SDMA and MetS (OR per SD increment 1.15, 95% CI 1.01-1.30) but the other associations were rendered statistically non-significant. We did not observe statistically significant associations between any of the methylarginines and the risk of new-onset MetS (752 incident events) over a median follow-up of 11 years.
It is unclear whether dimethylarginines play an important role in the incidence of cardiometabolic risk in the community, notwithstanding cross-sectional associations. Further studies of larger samples are needed to replicate our findings.
在横断面研究中,内源性一氧化氮合酶抑制剂不对称二甲基精氨酸(ADMA)的循环水平与代谢综合征(MetS)的患病率呈正相关。目前尚不清楚循环 ADMA 和其他甲基精氨酸是否与前瞻性 MetS 相关。
我们将循环 ADMA、对称二甲基精氨酸(SDMA)、L-精氨酸(ARG)浓度(用经过验证的串联质谱测定法测量)与 ARG/ADMA 比值与 Framingham 后代研究中的 2914 名(横断面分析,逻辑回归;平均年龄 58 岁,55%女性)和 1656 名(前瞻性分析,Cox 回归;平均年龄 56 岁,59%女性)参加常规检查的个体中的 MetS 及其成分相关联。
在调整年龄、性别、吸烟和 eGFR 后,我们观察到 ADMA(直接)和 ARG/ADMA(间接)与 MetS 的几率显著相关(N=1461 例现患病例;ADMA 每 SD 增加 1.13,95%CI 1.04-1.22;ARG/ADMA 为 0.89,95%CI 0.82-0.97)。进一步调整腰围、收缩压和舒张压、血糖、高密度脂蛋白胆固醇和甘油三酯后,我们观察到 SDMA 与 MetS 之间存在正相关关系(每 SD 增加 1.15,95%CI 1.01-1.30),但其他关联则变得无统计学意义。在中位数为 11 年的随访中,我们没有观察到任何一种甲基精氨酸与新发生的 MetS 风险之间存在统计学显著的关联(752 例新发事件)。
尽管存在横断面关联,但二甲精氨酸在社区中心血管代谢风险的发生中是否起重要作用尚不清楚。需要更大样本量的进一步研究来复制我们的发现。