Department of Clinical Science, University of Bergen, Norway
Department of Clinical Science, University of Bergen, Norway Department of Heart Disease, Haukeland University Hospital, Bergen, Norway.
Eur J Prev Cardiol. 2015 Jun;22(6):743-52. doi: 10.1177/2047487314529351. Epub 2014 Mar 26.
To investigate whether plasma dimethylglycine was associated with and improved risk prediction of mortality among patients with coronary heart disease (CHD).
By Cox modelling, we explored the association between plasma dimethylglycine and mortality in two independent cohorts of patients with suspected stable angina pectoris (SAP) (n = 4156) and acute myocardial infarction (AMI) (n = 3733). We also assessed any improvement in risk prediction by adding plasma dimethylglycine to established CHD risk factors.
Median follow-up time was 4.7 and 7.0 years among patients with SAP and AMI, respectively. Across both cohorts, elevated plasma dimethylglycine levels were linearly associated with increased risk of all-cause mortality (age and gender adjusted hazard ratios (95% confidence interval, CI) were 1.72 (1.21-2.46) and 1.76 (1.42-2.18) when comparing the fourth versus the first plasma dimethylglycine quartile in patients with SAP and AMI, respectively). There was a particularly strong risk association between plasma dimethylglycine and cardiovascular, as compared with non-cardiovascular, mortality (age and gender adjusted hazard ratios (95% CI) 1.94 (1.21-3.11) and 1.43 (0.83-2.47) among patients with SAP and 1.97 (1.50-2.59) and 1.44 (1.02-2.04) among patients with AMI, respectively). The relationship between dimethylglycine and all-cause and cardiovascular mortality was only slightly attenuated in analyses adjusted for established CHD risk factors. Plasma dimethylglycine also improved risk prediction for all-cause and cardiovascular mortality, and especially among patients with AMI.
Elevated plasma dimethylglycine was associated with and improved risk prediction of mortality in patients with suspected or verified CHD. This relationship was stronger for death from cardiovascular, as compared with non-cardiovascular, causes.
研究血浆二甲氨基乙醇与冠心病(CHD)患者死亡风险的相关性及其对死亡风险的预测价值。
通过 Cox 模型,我们探讨了血浆二甲氨基乙醇与疑似稳定型心绞痛(SAP)(n=4156)和急性心肌梗死(AMI)(n=3733)患者死亡率之间的相关性。我们还评估了将血浆二甲氨基乙醇加入已建立的 CHD 危险因素后,对风险预测的改善程度。
SAP 和 AMI 患者的中位随访时间分别为 4.7 年和 7.0 年。在两个队列中,血浆二甲氨基乙醇水平升高与全因死亡率的增加呈线性相关(SAP 和 AMI 患者中,与第 1 四分位相比,第 4 四分位的年龄和性别调整后的危险比(95%置信区间,CI)分别为 1.72(1.21-2.46)和 1.76(1.42-2.18))。与非心血管死亡相比,血浆二甲氨基乙醇与心血管死亡之间的风险关联更强(SAP 和 AMI 患者中,年龄和性别调整后的危险比(95%CI)分别为 1.94(1.21-3.11)和 1.43(0.83-2.47)和 1.97(1.50-2.59)和 1.44(1.02-2.04))。在校正已建立的 CHD 危险因素后,二甲氨基乙醇与全因和心血管死亡率之间的关系略有减弱。血浆二甲氨基乙醇还可改善全因和心血管死亡率的风险预测,尤其是在 AMI 患者中。
在疑似或确诊 CHD 患者中,血浆二甲氨基乙醇水平升高与死亡率升高相关,并能改善死亡率的预测。与非心血管原因死亡相比,心血管原因死亡的相关性更强。