Abstract

BackgroundIndividuals’ peak bone mineral density (BMD) achieved and maintained at ages 20–40 years is the most powerful predictor of low bone mass and osteoporotic fractures later in life. The aim of this study was to identify metabolomic factors associated with peak BMD variation in US Caucasian women.MethodsA total of 136 women aged 20–40 years, including 65 subjects with low and 71 with high hip BMD, were enrolled. The serum metabolites were assessed using a liquid chromatography-mass spectrometry (LC-MS) method. The partial least-squares discriminant analysis (PLS-DA) method and logistic regression models were used, respectively, to examine the associations of metabolomic profiles and individual metabolites with BMD.ResultsThe low and high BMD groups could be differentiated by the detected serum metabolites using PLS-DA (Ppermutation = 0.008). A total of 14 metabolites, including seven amino acids and amino acid derivatives, five lipids (including three bile acids), and two organic acids, were significantly associated with the risk for low BMD. Most of these metabolites are novel in that they have never been linked with BMD in humans earlier. The prediction model including the newly identified metabolites significantly improved the classification of the groups with low and high BMD. The area under the receiver operating characteristic curve without and with metabolites were 0.88 (95% CI: 0.83–0.94) and 0.97 (95% CI: 0.94–0.99), respectively (P for the difference = 0.0004).ConclusionMetabolomic profiling may improve the risk prediction of osteoporosis among Caucasian women. Our findings also suggest the potential importance of the metabolism of amino acids and bile acids in bone health.

Highlights

  • Individuals’ peak bone mineral density (BMD) achieved and maintained at ages 20–40 years is the most powerful predictor of low bone mass and osteoporotic fractures later in life

  • We identified a total of 192 metabolites with known identities and passed quality control using the liquid chromatography-mass spectrometry (LC-MS) metabolomics platform

  • Our study found that three bile acids in human serum were associated with BMD, further supporting the potentially important role of bile acids in bone health

Read more

Summary

Introduction

Individuals’ peak bone mineral density (BMD) achieved and maintained at ages 20–40 years is the most powerful predictor of low bone mass and osteoporotic fractures later in life. Osteoporosis is the most common metabolic bone disease, mainly characterized by low bone mineral density (BMD) and deteriorated bone quality/strength, with subsequent increased risk of low trauma osteoporotic fractures. Osteoporosis afflicts over 200 million people worldwide [1] It has become a serious public health concern due to its climbing prevalence with the population aging and high morbidity, mortality, and health expenditures caused by osteoporotic fractures [2, 3]. A Mendelian randomization study used the genome-phenotype association data from the US population and metabolomics-phenotype association data from the UK and indirectly identified some metabolites associated with BMD [12]. Promising findings were obtained from these studies, it is still unclear if the findings could be generalized to other race/ethnicity populations since metabolomic profiles have strong genetic determination and are significantly influenced by age and menopause status [13, 14]

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call