Gene and metabolite expression dependence on body mass index in human myocardium

We hypothesized that body mass index (BMI) dependent changes in myocardial gene expression and energy-related metabolites underlie the biphasic association between BMI and mortality (the obesity paradox) in cardiac surgery. We performed transcriptome profiling and measured a panel of 144 metabolites in 53 and 55, respectively, myocardial biopsies from a cohort of sixty-six adult patients undergoing coronary artery bypass grafting (registration: NCT02908009). The initial analysis identified 239 transcripts with biphasic BMI dependence. 120 displayed u-shape and 119 n-shape expression patterns. The identified local minima or maxima peaked at BMI 28-29. Based on these results and to best fit the WHO classification, we grouped the patients into three groups: BMI < 25, 25 <= BMI <= 32, and BMI > 32. The analysis indicated that protein translation-related pathways were downregulated in 25 <= BMI <= 32 compared with BMI < 25 patients. Muscle contraction transcripts were upregulated in 25 <= BMI <= 32 patients, and cholesterol synthesis and innate immunity transcripts were upregulated in the BMI > 32 group. Transcripts involved in translation, muscle contraction and lipid metabolism also formed distinct correlation networks with biphasic dependence on BMI. Metabolite analysis identified acylcarnitines and ribose-5-phosphate increasing in the BMI > 32 group and alpha-ketoglutarate increasing in the BMI < 25 group. Molecular differences in the myocardium mirror the biphasic relationship between BMI and mortality.

Automated summary

This study investigated changes in myocardial gene expression and energy-related metabolites at different BMI levels in cardiac surgery patients. The analysis revealed that protein translation, muscle contraction, and lipid metabolism pathways showed distinct expression patterns at different BMI ranges. Metabolite analysis showed differences in acylcarnitines, ribose-5-phosphate, and alpha-ketoglutarate levels among different BMI groups. The molecular differences in myocardium reflected the biphasic relationship between BMI and mortality.