4.5 Article

Circulating Endocannabinoids and Mortality in Hemodialysis Patients

期刊

AMERICAN JOURNAL OF NEPHROLOGY
卷 51, 期 2, 页码 86-95

出版社

KARGER
DOI: 10.1159/000505444

关键词

End stage renal disease; Hemodialysis; Mortality; Endocannabinoid; Endocannabinoid system; 2-arachidonoylglycerol; Anandamide

资金

  1. National Center for Research Resources, National Institutes of Health [UL1 TR001414]
  2. National Center for Advancing Translational Sciences, National Institutes of Health [UL1 TR001414]
  3. UC Irvine Institute for Clinical and Translational Science
  4. Office of Research and Development of the Department of Veterans Affairs [1 IK CX 001043-01A2, IK2-CX001266-01]
  5. NIH (NIDDK) grant [K24-DK091419, K23-DK102903]
  6. AVEO, Inc.
  7. NIH (NIDDK) [R01-DK119498, L30-DK114978]
  8. NIH (NIAID) [R21-AI135500]

向作者/读者索取更多资源

Background: Mortality in patients with end-stage renal disease (ESRD) on maintenance hemodialysis (MHD) remains exceptionally high. While traditional risk factors such as obesity are paradoxically associated with better survival, nontraditional risk factors including cachexia increase the likelihood of poor outcomes. There is accumulating evidence that the endocannabinoid (ECB) system plays a major role in energy preservation and storage, factors which can prevent the deleterious effects of cachexia. Hence, in this study, we evaluated the association of circulating ECB levels with mortality in MHD patients. Methods: Serum concentrations of anandamide (AEA) and 2-arachidonoyl-sn-glycerol (2-AG), major ECB ligands, were measured in MHD patients. Their correlation with various clinical/laboratory indices and association with 12-month all-cause mortality were examined. Results: Serum 2-AG levels positively correlated with body mass index, serum triglycerides and body anthropometric measures. Meanwhile, serum AEA levels correlated positively with serum interleukin-6, and negatively with serum very low-density lipoprotein levels. While increased serum 2-AG levels were associated with reduced risk of all-cause mortality (hazard ratio [HR] 0.52, 95% CI 0.28-0.98), there was no clear association between serum AEA levels and mortality (HR 0.91, 95% CI 0.48-1.72). Conclusions: In MHD patients, the circulating levels of ECB ligand, 2-AG, may play an important role in determining body mass and risk of mortality. These observations were unique to 2-AG as similar findings were not obtained with serum AEA. Future studies need to investigate the mechanisms responsible for these associations and examine the modulation of the ECB system as a potential target for therapy in ESRD.

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