Long-term retrospective observation study to evaluate effects of adiponectin on skeletal muscle in renal transplant recipients

Sci Rep. 2020 Jul 1;10(1):10723. doi: 10.1038/s41598-020-67711-1.

Abstract

Although it has been reported that chronic kidney disease exacerbates sarcopenia progression, the mechanisms of the process remain unclear. Fifty-one patients who underwent renal transplantation at our hospital since 1998 (31 males and 20 females; aged 29-52 years at the time of transplantation) were retrospectively examined for the relationships among the psoas muscle index (PMI), intramuscular adipose tissue content (IMAC), serum adiponectin fractions (high-/low-molecular-weight) and new-onset diabetes after transplantation (NODAT). Before transplantation, age at kidney transplantation negatively correlated with PMI and positively correlated with IMAC (rS = - 0.427, p < 0.01; rS = 0.464, p < 0.01, respectively). Both at 1 and 5 years after transplantation, PMI was higher than before transplantation (p < 0.01). IMAC transiently decreased to - 0.39 at 1 year after kidney transplantation but subsequently increased to - 0.36 at 5 years after kidney transplantation. Multivariate analyses revealed that the mean increase in high-molecular weight adiponectin concentrations was an exacerbating factor for the mean change in PMI (p = 0.003). Moreover, the mean increases in IMAC were exacerbating factors for NODAT. In conclusion, the increase in the PMI is associated with high-molecular weight adiponectin levels after renal transplantation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adiponectin / metabolism*
  • Adipose Tissue / metabolism
  • Adipose Tissue / pathology*
  • Adult
  • Age of Onset
  • Diabetes Mellitus / etiology*
  • Diabetes Mellitus / metabolism
  • Diabetes Mellitus / pathology
  • Female
  • Humans
  • Kidney Transplantation / adverse effects*
  • Male
  • Middle Aged
  • Muscle, Skeletal / metabolism*
  • Psoas Muscles / metabolism
  • Psoas Muscles / pathology*
  • Retrospective Studies
  • Risk Assessment
  • Risk Factors
  • Sarcopenia / etiology*
  • Sarcopenia / metabolism
  • Sarcopenia / pathology
  • Transplant Recipients

Substances

  • ADIPOQ protein, human
  • Adiponectin