Paradoxical role for adiponectin in chronic renal diseases? An example of reverse epidemiology
- PMID: 19236235
- DOI: 10.1517/14728220802658481
Paradoxical role for adiponectin in chronic renal diseases? An example of reverse epidemiology
Abstract
Adiponectin (ADPN) is an adipocyte-derived protein with potential antiatherogenic properties. In the general population, ADPN serum levels are associated with age and body mass index (BMI), type 2 diabetes and presumably cardiovascular disease. The suspected vascular-protective effects are mediated by several mechanisms such as insulin sensitizing, maintaining endovascular homeostasis and anti-inflammatory properties. Patients with chronic kidney disease (CKD) are subjected to an increased cardiovascular risk. The underlying mechanisms are not yet completely understood although in the last few years numerous studies have linked secondary hyperparathyroidism and inflammation to that risk. It is currently not clear whether, in CKD, ADPN plays the same role as it is thought to do in the general population or if the uremic environment overwhelms the vascular-protective impact of ADPN. Therefore, characterizing ADPN levels and kinetics in CKD and comparing its concentrations with surrogate markers of cardiovascular risk in CKD might contribute to a better understanding of adipocytokine signaling in renal disease. The review summarizes the available literature on ADPN measurement, regulation and therapeutic potential in general population and CKD. In our investigations, ADPN was more than twofold increased in hemodialysis patients compared with the general population. ADPN levels were not associated with age, but with lifetime spent on dialysis (vintage) and BMI. The dialysis procedure had no effect on ADPN. To assess the clinical value of ADPN levels as a potential surrogate of cardiovascular risk in or therapeutic target in CKD, end point-driven studies with special regard to the risk behavior in CKD have to be performed.
Similar articles
-
Plasma adiponectin levels for prediction of cardiovascular risk among hemodialysis patients.Ther Apher Dial. 2014 Apr;18(2):185-92. doi: 10.1111/1744-9987.12065. Epub 2013 Jul 3. Ther Apher Dial. 2014. PMID: 24720410
-
Adiponectin, metabolic risk factors, and cardiovascular events among patients with end-stage renal disease.J Am Soc Nephrol. 2002 Jan;13(1):134-141. doi: 10.1681/ASN.V131134. J Am Soc Nephrol. 2002. PMID: 11752030
-
Adiponectin and end-stage renal disease.Hormones (Athens). 2016 Jul;15(3):345-354. doi: 10.14310/horm.2002.1698. Hormones (Athens). 2016. PMID: 27838604 Review.
-
Adiponectin and cardiovascular outcomes among hemodialysis patients.Kidney Blood Press Res. 2012;35(4):247-53. doi: 10.1159/000334649. Epub 2012 Jan 26. Kidney Blood Press Res. 2012. PMID: 22286012
-
Adiponectin and Cognitive Decline.Int J Mol Sci. 2020 Mar 16;21(6):2010. doi: 10.3390/ijms21062010. Int J Mol Sci. 2020. PMID: 32188008 Free PMC article. Review.
Cited by
-
Liver function parameters in hip fracture patients: relations to age, adipokines, comorbidities and outcomes.Int J Med Sci. 2015 Jan 1;12(2):100-15. doi: 10.7150/ijms.10696. eCollection 2015. Int J Med Sci. 2015. PMID: 25589886 Free PMC article.
-
Visceral adipose tissue is associated with insulin resistance in hemodialyzed patients.Med Sci Monit. 2015 Feb 20;21:557-62. doi: 10.12659/MSM.892078. Med Sci Monit. 2015. PMID: 25697647 Free PMC article.
-
Analysis of serum inflammatory mediators in type 2 diabetic patients and their influence on renal function.PLoS One. 2020 Mar 4;15(3):e0229765. doi: 10.1371/journal.pone.0229765. eCollection 2020. PLoS One. 2020. PMID: 32130282 Free PMC article.
-
Development of second generation peptides modulating cellular adiponectin receptor responses.Front Chem. 2014 Oct 17;2:93. doi: 10.3389/fchem.2014.00093. eCollection 2014. Front Chem. 2014. PMID: 25368867 Free PMC article.
-
Circulating adiponectin is associated with renal function independent of age and serum lipids in west africans.Int J Nephrol. 2012;2012:730920. doi: 10.1155/2012/730920. Epub 2012 Aug 22. Int J Nephrol. 2012. PMID: 22957255 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical