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Genetic predisposition: Some research indicates a potential genetic component, as the condition seems to occur more in individuals with a family history of the syndrome

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doi: 10.1152/ajpcell.00095.2018 57 GuYZhouCPiaoZYuanHJiangHWeiHet al

| doi:10.1007/s10545-007-0666-z Constantin-Teodosiu D, Carlin JI, Cederblad G, Harris RC, Hultman E: Acetyl group accumulation and pyruvate dehydrogenase activity in human muscle during incremental exercise (1991) Acta Physiol Scand | doi:10.1111/j.1748-1716.1991.tb09247.x Diamanti K, Cavalli M, Pan G, et al.: Intra- and inter-individual metabolic profiling highlights carnitine and lysophosphatidylcholine pathways as key molecular defects in type 2 diabetes