Division of Endocrinology, Metabolism, and Nutrition, Duke University Medical Center, Durham, NC 27710, USA.
Metabolism. 2013 Jul;62(7):961-9. doi: 10.1016/j.metabol.2013.01.007. Epub 2013 Feb 1.
To identify novel biomarkers through metabolomic profiles that distinguish metabolically well (MW) from metabolically unwell (MUW) individuals, independent of body mass index (BMI).
MATERIALS/METHODS: This study was conducted as part of the Measurement to Understand the Reclassification of Disease of Cabarrus/Kannapolis (MURDOCK) project. Individuals from 3 cohorts were classified as lean (BMI<25kg/m²), overweight (BMI≥25kg/m², BMI<30kg/m²) or obese (BMI≥30kg/m²). Cardiometabolic abnormalities were defined as: (1) impaired fasting glucose (≥100mg/dL and ≤126mg/dL); (2) hypertension; (3) triglycerides ≥150mg/dL; (4) HDL-C <40mg/dL in men, <50mg/dL in women; and (5) insulin resistance (calculated Homeostatic Model Assessment (HOMA-IR) index of >5.13). MW individuals were defined as having <2 cardiometabolic abnormalities and MUW individuals had≥two cardiometabolic abnormalities. Targeted profiling of 55 metabolites used mass-spectroscopy-based methods. Principal components analysis (PCA) was used to reduce the large number of correlated metabolites into clusters of fewer uncorrelated factors.
Of 1872 individuals, 410 were lean, 610 were overweight, and 852 were obese. Of lean individuals, 67% were categorized as MUW, whereas 80% of overweight and 87% of obese individuals were MUW. PCA-derived factors with levels that differed the most between MW and MUW groups were factors 4 (branched chain amino acids [BCAA]) [p<.0001], 8 (various metabolites) [p<.0001], 9 (C4/Ci4, C3, C5 acylcarnitines) [p<.0001] and 10 (amino acids) [p<.0002]. Further, Factor 4, distinguishes MW from MUW individuals independent of BMI.
BCAA and related metabolites are promising biomarkers that may aid in understanding cardiometabolic health independent of BMI category.
通过代谢组学谱识别新的生物标志物,将代谢良好(MW)与代谢不良(MUW)个体区分开来,与体重指数(BMI)无关。
材料/方法:本研究作为卡巴拉斯/坎纳波利斯(MURDOCK)项目疾病再分类测量(Measurement to Understand the Reclassification of Disease of Cabarrus/Kannapolis,MURDOCK)项目的一部分进行。将来自 3 个队列的个体分为瘦(BMI<25kg/m²)、超重(BMI≥25kg/m²,BMI<30kg/m²)或肥胖(BMI≥30kg/m²)。心血管代谢异常定义为:(1)空腹血糖受损(≥100mg/dL 和≤126mg/dL);(2)高血压;(3)甘油三酯≥150mg/dL;(4)男性 HDL-C <40mg/dL,女性<50mg/dL;(5)胰岛素抵抗(计算的稳态模型评估(HOMA-IR)指数>5.13)。MW 个体定义为有<2 种心血管代谢异常,MUW 个体有≥2 种心血管代谢异常。使用基于质谱的方法对 55 种代谢物进行靶向分析。主成分分析(PCA)用于将大量相关代谢物减少为较少的不相关因素群。
在 1872 名个体中,410 名个体为瘦,610 名个体为超重,852 名个体为肥胖。在瘦个体中,67%被归类为 MUW,而超重个体中有 80%,肥胖个体中有 87%为 MUW。MW 和 MUW 组之间水平差异最大的 PCA 衍生因子是因子 4(支链氨基酸[BCAA])[p<.0001]、因子 8(各种代谢物)[p<.0001]、因子 9(C4/Ci4、C3、C5 酰基肉碱)[p<.0001]和因子 10(氨基酸)[p<.0002]。此外,因子 4 可区分 MW 和 MUW 个体,与 BMI 无关。
BCAA 和相关代谢物是有前途的生物标志物,可能有助于在不考虑 BMI 类别的情况下理解心血管代谢健康。