Literature DB >> 25945605

High serum chemerin level in CKD patients is related to kidney function, but not to its adipose tissue overproduction.

Joanna Blaszak1, Marek Szolkiewicz2, Elzbieta Sucajtys-Szulc2, Marcin Konarzewski3, Slawomir Lizakowski2, Julian Swierczynski4, Boleslaw Rutkowski2.   

Abstract

Chemerin is an adipokine modulating inflammatory response and affecting glucose and lipid metabolism. These disturbances are common in CKD. The aim of the study was: (a) to evaluate circulating chemerin level at different stages of CKD; (b) to measure subcutaneous adipose tissue chemerin gene expression; (c) to estimate the efficiency of renal replacement therapy in serum chemerin removal. 187 patients were included into the study: a) 58 patients with CKD; (b) 29 patients on hemodialysis; (c) 20 patients after kidney transplantation. 80 subjects constituted control group. Serum chemerin concentration was estimated by ELISA. The adipose tissue chemerin mRNA level was measured by RT-qPCR. The mean serum chemerin concentration in CKD patients was 70% higher than in the control group (122.9 ± 33.7 vs. 72.6 ± 20.7 ng/mL; p < 0.001) and it negatively correlated with eGFR (r = -0.71, p < 0.001). The equally high plasma chemerin level was found in HD patients and a HD session decreased it markedly (115.7 ± 17.6 vs. 101.5 ± 16.4 ng/mL; p < 0.001). Only successful kidney transplantation allowed it to get down to the values noted in controls (74.8 ± 16.0 vs. 72.6 ± 20.7 ng/mL; n.s.). The level of subcutaneous adipose tissue chemerin mRNA in CKD patients was not different than in patients of the control group. The study demonstrates that elevated serum chemerin concentration in CKD patients: (a) is related to kidney function, but not to increased chemerin production by subcutaneous adipose tissue, and (b) it can be efficiently corrected by hemodialysis treatment and normalized by kidney transplantation.

Entities:  

Keywords:  Adipokine; adipose tissue; chemerin; gene expression; renal failure

Mesh:

Substances:

Year:  2015        PMID: 25945605     DOI: 10.3109/0886022X.2015.1040707

Source DB:  PubMed          Journal:  Ren Fail        ISSN: 0886-022X            Impact factor:   2.606


  10 in total

1.  The chemerin knockout rat reveals chemerin dependence in female, but not male, experimental hypertension.

Authors:  Stephanie W Watts; Emma S Darios; Adam E Mullick; Hannah Garver; Thomas L Saunders; Elizabeth D Hughes; Wanda E Filipiak; Michael G Zeidler; Nichole McMullen; Christopher J Sinal; Ramya K Kumar; David J Ferland; Gregory D Fink
Journal:  FASEB J       Date:  2018-06-15       Impact factor: 5.191

2.  Chemerin in peritoneal sepsis and its associations with glucose metabolism and prognosis: a translational cross-sectional study.

Authors:  Paul Horn; Uta Barbara Metzing; Ricardo Steidl; Bernd Romeike; Falk Rauchfuß; Christoph Sponholz; Daniel Thomas-Rüddel; Katrin Ludewig; Andreas L Birkenfeld; Utz Settmacher; Michael Bauer; Ralf Alexander Claus; Christian von Loeffelholz
Journal:  Crit Care       Date:  2016-02-12       Impact factor: 9.097

3.  Low circulating chemerin levels correlate with hepatic dysfunction and increased mortality in decompensated liver cirrhosis.

Authors:  Paul Horn; Christian von Loeffelholz; Franziska Forkert; Sven Stengel; Philipp Reuken; René Aschenbach; Andreas Stallmach; Tony Bruns
Journal:  Sci Rep       Date:  2018-06-18       Impact factor: 4.379

4.  Citrate anion improves chronic dialysis efficacy, reduces systemic inflammation and prevents Chemerin-mediated microvascular injury.

Authors:  Sergio Dellepiane; Davide Medica; Cesare Guarena; Tiziana Musso; Alessandro Domenico Quercia; Gianluca Leonardi; Marita Marengo; Massimiliano Migliori; Vincenzo Panichi; Luigi Biancone; Francesco Pizzarelli; Giovanni Camussi; Vincenzo Cantaluppi
Journal:  Sci Rep       Date:  2019-07-23       Impact factor: 4.379

5.  Chemerin inhibits vascular calcification through ChemR23 and is associated with lower coronary calcium in chronic kidney disease.

Authors:  M Carracedo; A Witasp; A R Qureshi; A Laguna-Fernandez; T Brismar; P Stenvinkel; M Bäck
Journal:  J Intern Med       Date:  2019-07-07       Impact factor: 8.989

6.  Chemerin as a Driver of Hypertension: A Consideration.

Authors:  David J Ferland; Adam E Mullick; Stephanie W Watts
Journal:  Am J Hypertens       Date:  2020-11-03       Impact factor: 2.689

7.  Association of Chemerin and Vascular Endothelial Growth Factor (VEGF) with Diabetic Nephropathy.

Authors:  Shuhua Lin; Jian Teng; Jixia Li; Fang Sun; Dong Yuan; Jing Chang
Journal:  Med Sci Monit       Date:  2016-09-10

8.  Chemerin rs17173608 and vaspin rs2236242 gene variants on the risk of end stage renal disease (ESRD) and correlation with plasma malondialdehyde (MDA) level.

Authors:  Hamid Nomani; Hamid Khanmohamadian; Asad Vaisi-Raygani; Ebrahim Shakiba; Maryam Tanhapour; Zohreh Rahimi
Journal:  Ren Fail       Date:  2018-11       Impact factor: 2.606

Review 9.  The complex effects of adipokines in the patients with kidney disease.

Authors:  Sahar Vahdat
Journal:  J Res Med Sci       Date:  2018-07-26       Impact factor: 1.852

10.  Renal Chemerin Expression is Induced in Models of Hypertensive Nephropathy and Glomerulonephritis and Correlates with Markers of Inflammation and Fibrosis.

Authors:  Alexander Mocker; Karl F Hilgers; Nada Cordasic; Rainer Wachtveitl; Carlos Menendez-Castro; Joachim Woelfle; Andrea Hartner; Fabian B Fahlbusch
Journal:  Int J Mol Sci       Date:  2019-12-11       Impact factor: 5.923

  10 in total

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