Department of Epidemiology and Biostatistics, School of Public Health, Jilin University, Changchun 130021, China.
Nutrients. 2024 Oct 10;16(20):3436. doi: 10.3390/nu16203436.
There is growing evidence that diet and aging are associated; however, few studies have examined the relationship between macronutrient subtypes and phenotypic age acceleration, and the extent to which BMI (body mass index) mediates this association is unclear. This study included 6911 individuals who were 20 years or older and had participated in the National Health and Nutrition Examination Survey. Daily macronutrient intakes were calculated and classified by the quartile of their subtypes. PhenoAgeAccel was calculated as an aging index using nine chemistry biomarkers. Multivariable linear regression and isocaloric substitution effects were used to evaluate the association of macronutrients with PhenoAgeAccel. Mediation analyses were used to examine the mediation role of BMI in the association. After adjusting for the potential covariates, the consumption of high-quality carbohydrates (β = -1.01, 95% CI: -1.91, -0.12), total protein (β = -2.00, 95% CI: -3.16, -0.84), and plant protein (β = -1.65, 95% CI: -2.52, -0.78) was negatively correlated with PhenoAgeAccel; the consumption of SFAs (β = 1.77, 95% CI: 0.72, 2.81) was positively correlated with PhenoAgeAccel. For every serving of low-quality carbohydrates/animal protein and other calories replaced by one serving of high-quality carbohydrates/plant protein, PhenoAgeAccel would be reduced by about 25 percent. The ratio between BMI-mediated high-quality carbohydrates and PhenoAgeAccel accounted for 19.76% of the total effect, while the ratio between BMI-mediated total fat and PhenoAgeAccel accounted for 30.78% of the total effect. Different macronutrient consumption subtypes are related to PhenoAgeAccel, which is partially mediated by BMI, depending on the quality of macronutrients. Replacing low-quality macronutrients with high-quality macronutrients might slow aging.
越来越多的证据表明饮食和衰老有关;然而,很少有研究探讨宏量营养素亚型与表型年龄加速的关系,以及 BMI(体重指数)在多大程度上介导这种关联尚不清楚。本研究纳入了 6911 名年龄在 20 岁及以上且参加过全国健康与营养调查的个体。计算了每日宏量营养素摄入量,并按亚型的四分位数进行分类。使用 9 种化学生物标志物计算 PhenoAgeAccel 作为衰老指数。多变量线性回归和等热量替代效应用于评估宏量营养素与 PhenoAgeAccel 的关联。中介分析用于检验 BMI 在关联中的中介作用。在调整潜在协变量后,高质量碳水化合物(β = -1.01,95%CI:-1.91,-0.12)、总蛋白(β = -2.00,95%CI:-3.16,-0.84)和植物蛋白(β = -1.65,95%CI:-2.52,-0.78)的消耗与 PhenoAgeAccel 呈负相关;SFA(β = 1.77,95%CI:0.72,2.81)的消耗与 PhenoAgeAccel 呈正相关。每多摄入一份低质量碳水化合物/动物蛋白和其他卡路里,就会使 PhenoAgeAccel 减少约 25%。BMI 介导的高质量碳水化合物和 PhenoAgeAccel 之间的比例占总效应的 19.76%,而 BMI 介导的总脂肪和 PhenoAgeAccel 之间的比例占总效应的 30.78%。不同的宏量营养素摄入亚型与 PhenoAgeAccel 有关,这部分是由 BMI 介导的,取决于宏量营养素的质量。用高质量的宏量营养素替代低质量的宏量营养素可能会减缓衰老。