Pubertal Girls With Overweight/Obesity Have Higher Androgen Levels—Can Metabolomics Tell us Why?

代谢组学 超重 内分泌学 内科学 肥胖 化学 生物 医学 生物信息学
作者
Madison E. Calvert,Samantha Molsberry,Kirsten E. Overdahl,Alan K. Jarmusch,Natalie D. Shaw
出处
期刊:The Journal of Clinical Endocrinology and Metabolism [Oxford University Press]
卷期号:109 (5): 1328-1333 被引量:1
标识
DOI:10.1210/clinem/dgad675
摘要

Abstract Context Pubertal girls with higher total body fat (TBF) demonstrate higher androgen levels. The cause of this association is unknown but is hypothesized to relate to insulin resistance. Objective This work aimed to investigate the association between higher TBF and higher androgens in pubertal girls using untargeted metabolomics. Methods Serum androgens were determined using a quantitative mass spectrometry (MS)–based assay. Metabolomic samples were analyzed using liquid chromatography high-resolution MS. Associations between TBF or body mass index (BMI) z score (exposure) and metabolomic features (outcome) and between metabolomic features (exposure) and serum hormones (outcome) were examined using gaussian generalized estimating equation models with the outcome lagged by one study visit. Benjamini-Hochberg false discovery rate (FDR) adjusted P values were calculated to account for multiple testing. RaMP-DB (relational database of metabolomic pathways) was used to conduct enriched pathway analyses among features nominally associated with body composition or hormones. Results Sixty-six pubertal, premenarchal girls (aged 10.9 ± 1.39 SD years; 60% White, 24% Black, 16% other; 63% normal weight, 37% overweight/obese) contributed an average of 2.29 blood samples. BMI and TBF were negatively associated with most features including raffinose (a plant trisaccharide) and several bile acids. For BMI, RaMP-DB identified many enriched pathways related to bile acids. Androstenedione also showed strong positive associations with raffinose and bile acids. Conclusion Metabolomic analyses of samples from pubertal girls did not identify an insulin resistance signature to explain the association between higher TBF and androgens. Instead, we identified potential novel signaling pathways that may involve raffinose or bile acid action at the adrenal gland.

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