Facultad de Medicina, Benemérita Universidad Autónoma de Puebla, Calle 13 Sur 2901 Colonia Volcanes, C.P. 72420, Puebla, Puebla, Mexico.
Facultad de nutrición, Benemérita Universidad Autónoma de Puebla, Calle 13 Sur 2901 Colonia Volcanes, C.P. 72420, Puebla, Puebla, Mexico.
High Blood Press Cardiovasc Prev. 2021 May;28(3):263-270. doi: 10.1007/s40292-021-00441-1. Epub 2021 Mar 5.
Every 10 years, an adult's basal metabolic rate (BMR), independent of their BMI, decreases 1-2% due to skeletal muscle loss, thus decreasing an adult's energy requirement and promoting obesity. Increased obesity augments the risk of developing Metabolic Syndrome (MetS); however, an adult's healthy lifestyle, which increases BMR, can mitigate MetS development. To compare different BMRs for certain ages, Metabolic age (Met-age) was developed.
To assess the association between Met-age and MetS and to determine if Met-age is an indicator of high-risk individuals for MetS.
Four hundred thirty-five attendees at 2 clinics agreed to participate and gave signed informed consent. MetS risk was assessed by the ESF-I questionnaire. Met-age was determined using a TANITA bio-analyzer. Strengthen of association was determined by calculating Spearman's rho and predictability was evaluated by the area-under-a-receiver-operating characteristic curve (AUC). Difference-in-age (DIA) = [chronological age - Met-age].
There was a difference between the low-risk (n = 155) and the high-risk (n = 280) groups' Met-age (37.8±16.7 v. 62.9±17.3) and DIA (1.3±17.4 v. - 10.5±20.8, p < 0.001). There was a positive correlation between the ESF-I questionnaire and Met-age (rho = - 0.624, p < 0.001) and a negative correlation for DIA (rho = - 0.358, p < 0.001). Met-age was strongly predictive (AUC = 0.84, 95% CI 0.80-0.88), suggesting a 45.5 years cutoff (sensitivity = 83.2%, specificity = 72.3%). DIA was a good predictor (AUC = 0.68, 95% CI 0.63-0.74) with a - 11.5 years cutoff (sensitivity = 52.5%, specificity = 82.8%).
Met-age highly associated with and is an indicator of high-risk individuals for MetS. This would suggest that increases in Met-age are associated with augmented MetS severity, independent of the individual's chronological age.
每 10 年,由于骨骼肌流失,成年人的基础代谢率(BMR)会降低 1-2%,这与 BMI 无关,从而降低了成年人的能量需求,促进了肥胖的发生。肥胖的增加增加了患代谢综合征(MetS)的风险;然而,成年人健康的生活方式会增加 BMR,可以减轻 MetS 的发展。为了比较不同年龄的 BMR,开发了代谢年龄(Met-age)。
评估 Met-age 与 MetS 的相关性,并确定 Met-age 是否是 MetS 高危人群的指标。
2 家诊所的 435 名参与者同意参加并签署了知情同意书。MetS 风险通过 ESF-I 问卷进行评估。使用 TANITA 生物分析仪确定 Met-age。关联强度通过计算 Spearman's rho 来确定,预测能力通过接受者操作特征曲线下面积(AUC)来评估。差异年龄(DIA)= [实际年龄-代谢年龄]。
低风险组(n=155)和高风险组(n=280)的 Met-age (37.8±16.7 v. 62.9±17.3)和 DIA(1.3±17.4 v. -10.5±20.8,p<0.001)存在差异。ESF-I 问卷与 Met-age 呈正相关(rho=-0.624,p<0.001),与 DIA 呈负相关(rho=-0.358,p<0.001)。Met-age 具有很强的预测能力(AUC=0.84,95%CI 0.80-0.88),提示 45.5 岁的截断值(敏感性=83.2%,特异性=72.3%)。DIA 是一个很好的预测指标(AUC=0.68,95%CI 0.63-0.74),提示-11.5 岁的截断值(敏感性=52.5%,特异性=82.8%)。
Met-age 与 MetS 高度相关,是 MetS 高危人群的指标。这表明,代谢年龄的增加与 MetS 严重程度的增加有关,而与个体的实际年龄无关。