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Cross-Sectional Associations between Homoarginine Intermediate Phenotypes and Atrial Fibrillation in the Community—The Gutenberg Health Study

机译:精氨酸中型表型和社区心房颤动之间的跨部门关联—古登堡健康研究

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摘要

Homoarginine has come into the focus of interest as a biomarker for cardiovascular disease. Atrial fibrillation (AF) causes a substantial increase in morbidity and mortality. Whether circulating homoarginine is associated with occurrence or persistence of AF and may serve as a new predictive biomarker remains unknown. We measured plasma levels of homoarginine in the population-based Gutenberg health study (3761 patients included, of them 51.7% males), mean age 55.6 ± 10.9 years-old. Associations between homoarginine and intermediate electrocardiographic and echocardiographic phenotypes and manifest AF were examined. Patients with AF (124 patients, of them 73.4% males) had a mean age 64.8 ± 8.6 years-old compared to a mean age of 55.3 ± 10.9 in the population without AF (p-value < 0.001) and showed a less beneficial risk factor profile. The median homoarginine levels in individuals with and without AF were 1.9 μmol/L (interquartile range (IQR) 1.5–2.5) and 2.0 μmol/L (IQR 1.5–2.5), respectively, p = 0.56. In multivariable-adjusted regression analyses homoarginine was not statistically significantly related to electrocardiographic variables. Among echocardiographic variables beta per standard deviation increase was −0.12 (95% confidence interval (CI) −0.23–(−0.02); p = 0.024) for left atrial area and −0.01 (95% CI −0.02–(−0.003); p = 0.013) for E/A ratio. The odds ratio between homoarginine and AF was 0.91 (95% CI 0.70–1.16; p = 0.45). In our large, population-based cross-sectional study, we did not find statistically significant correlations between lower homoarginine levels and occurrence or persistence of AF or most standard electrocardiographic phenotypes, but some moderate inverse associations with echocardiographic left atrial size and E/A. Homoarginine may not represent a strong biomarker to identify individuals at increased risk for AF. Further investigations will be needed to elucidate the role of homoarginine and cardiac function.
机译:高精氨酸作为心血管疾病的生物标志物已成为人们关注的焦点。心房颤动(AF)导致发病率和死亡率大幅增加。循环中的高精氨酸是否与房颤的发生或持续存在有关,并可能作为一种新的预测性生物标志物尚不清楚。在基于人群的古登堡健康研究中,我们测量了高精氨酸的血浆水平(包括3761例患者,其中51.7%为男性),平均年龄为55.6±10.9岁。检查了高精氨酸与中间心电图和超声心动图表型与明显房颤之间的关联。 AF患者(124例患者,其中男性占73.4%)的平均年龄为64.8±8.6岁,而无AF患者的平均年龄为55.3±10.9(p值<0.001),并且显示出较低的风险因素资料。有或没有房颤的个体中高精氨酸水平分别为1.9μmol/ L(四分位间距(IQR)1.5-2.5)和2.0μmol/ L(IQR 1.5-2.5),p = 0.56。在多变量校正回归分析中,高精氨酸与心电图变量在统计学上无显着相关性。在超声心动图变量中,每个标准偏差的增加值对于左心房面积为-0.12(95%置信区间(CI)-0.23-(-0.02); p = 0.024)和-0.01(95%CI -0.02-(-0.003) p = 0.013)。高精氨酸和AF之间的比值比为0.91(95%CI 0.70-1.16; p = 0.45)。在我们基于人群的大型横断面研究中,我们未发现较低的高精氨酸水平与AF或大多数标准心电图表型的发生或持续存在统计学上的显着相关性,但与超声心动图左心房大小和E / A呈中等程度的负相关。高精氨酸可能不能代表一个强有力的生物标志物,以识别AF风险增加的个体。需要进一步的研究来阐明高精氨酸和心脏功能的作用。

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