Serum Metabolite Profile Associated with Sex-Dependent Visceral Adiposity Index and Low Bone Mineral Density in a Mexican Population.
Berenice Palacios-GonzálezGuadalupe León-ReyesBerenice Rivera-ParedezIsabel Ibarra-GonzálezMarcela Vela AmievaYvonne Nicole FloresSamuel Canizales-QuinterosJorge SalmerónRafael Velázquez-CruzPublished in: Metabolites (2021)
Recent evidence shows that obesity correlates negatively with bone mass. However, traditional anthropometric measures such as body mass index could not discriminate visceral adipose tissue from subcutaneous adipose tissue. The visceral adiposity index (VAI) is a reliable sex-specified indicator of visceral adipose distribution and function. Thus, we aimed to identify metabolomic profiles associated with VAI and low bone mineral density (BMD). A total of 602 individuals from the Health Workers Cohort Study were included. Forty serum metabolites were measured using the targeted metabolomics approach, and multivariate regression models were used to test associations of metabolomic profiles with anthropometric, clinical, and biochemical parameters. The analysis showed a serum amino acid signature composed of glycine, leucine, arginine, valine, and acylcarnitines associated with high VAI and low BMD. In addition, we found a sex-dependent VAI in pathways related to primary bile acid biosynthesis, branched-chain amino acids, and the biosynthesis of pantothenate and coenzyme A (CoA). In conclusion, a metabolic profile differs by VAI and BMD status, and these changes are gender-dependent.
Keyphrases
- bone mineral density
- insulin resistance
- adipose tissue
- body composition
- amino acid
- postmenopausal women
- high fat diet
- metabolic syndrome
- high fat diet induced
- body mass index
- skeletal muscle
- type diabetes
- weight gain
- healthcare
- public health
- mental health
- weight loss
- mass spectrometry
- ms ms
- cell wall
- data analysis
- drug delivery
- fatty acid
- drug induced
- climate change