Intrapersonal Stability of Plasma Metabolomic Profiles over 10 Years among Women

被引:12
|
作者
Zeleznik, Oana A. [1 ,2 ]
Wittenbecher, Clemens [3 ,4 ]
Deik, Amy [5 ]
Jeanfavre, Sarah [5 ]
Avila-Pacheco, Julian [5 ]
Rosner, Bernard [1 ,2 ]
Rexrode, Kathryn M. [2 ,6 ]
Clish, Clary B. [5 ]
Hu, Frank B. [3 ]
Eliassen, A. Heather [1 ,2 ,7 ]
机构
[1] Brigham & Womens Hosp, Channing Div Network Med, Boston, MA 02115 USA
[2] Harvard Med Sch, Boston, MA 02115 USA
[3] Harvard TH Chan Sch Publ Hlth, Dept Nutr, Boston, MA 02115 USA
[4] German Inst Human Nutr Potsdam Rehbrucke, D-14558 Nuthetal, Germany
[5] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[6] Brigham & Womens Hosp, Div Womens Hlth, Boston, MA 02115 USA
[7] Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
lipids and lipid-related metabolites; polar metabolites; within-person stability; unknown metabolite features; BREAST-CANCER; MEASUREMENT ERROR; RISK; BLOOD; METABOLITES; PROLACTIN; DISEASE; VARIABILITY; BIOMARKERS; OBESITY;
D O I
10.3390/metabo12050372
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In epidemiological studies, samples are often collected long before disease onset or outcome assessment. Understanding the long-term stability of biomarkers measured in these samples is crucial. We estimated within-person stability over 10 years of metabolites and metabolite features (n = 5938) in the Nurses' Health Study (NHS): the primary dataset included 1880 women with 1184 repeated samples donated 10 years apart while the secondary dataset included 1456 women with 488 repeated samples donated 10 years apart. We quantified plasma metabolomics using two liquid chromatography mass spectrometry platforms (lipids and polar metabolites) at the Broad Institute (Cambridge, MA, USA). Intra-class correlations (ICC) were used to estimate long-term (10 years) within-person stability of metabolites and were calculated as the proportion of the total variability (within-person + between-person) attributable to between-person variability. Withinperson variability was estimated among participants who donated two blood samples approximately 10 years apart while between-person variability was estimated among all participants. In the primary dataset, the median ICC was 0.43 (1st quartile (Q1): 0.36; 3rd quartile (Q3): 0.50) among known metabolites and 0.41 (Q1: 0.34; Q3: 0.48) among unknown metabolite features. The three most stable metabolites were N6,N6-dimethyllysine (ICC = 0.82), dimethylguanidino valerate (ICC = 0.72), and N-acetylornithine (ICC = 0.72). The three least stable metabolites were palmitoylethanolamide (ICC = 0.05), ectoine (ICC = 0.09), and trimethylamine-N-oxide (ICC = 0.16). Results in the secondary dataset were similar (Spearman correlation = 0.87) to corresponding results in the primary dataset. Within-person stability over 10 years is reasonable for lipid, lipid-related, and polar metabolites, and varies by metabolite class. Additional studies are required to estimate within-person stability over 10 years of other metabolites groups.
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页数:14
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