Association of serum chemerin levels with complications and comorbidity in rheumatoid arthritis
https://doi.org/10.21518/ms2023-398
Abstract
Introduction. Rheumatoid arthritis (RA) is a systemic autoimmune disease as well as a typical inflammatory process. Chemerin is a fat tissue cytokine, which specific receptors were discovered on the surface of the innate immune cells. It is of interest to study the association of chemerin with the complications and comorbidity in RA.
Aim. To study the association between serum chemerin levels with complications and comorbidity in rheumatoid arthritis.
Materials and methods. 88 women with RA were enrolled in our study. ll patients undergone standard clinical and laboratory examination. Serum chemerin, high-sensitive C-reactive protein (hsCRP), anti-citrullinated protein antibodies, insulin and C-peptide levels were determined using ELISA. X-ray absorptiometry was performed. Statistical analysis was performed using conventional methods with a software package Statistica 10.0.
Results. Median chemerin concentration was 463.5 [366–576.5] ng/ml. Chemerin concentration correlated with the age (ρ = 0.232; р = 0.030), weight (ρ = 0.254; р = 0.017) and body mass index (BMI) (ρ = 0.212; р = 0.047), but wasn’t associated with the RA classification criteria. Positive correlation between chemerin concentration and number of painful joints (NPJ) (ρ = 0.213; р = 0.046) and hsCRP (ρ = 0.273; р = 0.010) was observed. Patients with type 2 diabetes mellitus (DM2) had higher chemerin concentration (598.0 ng/ml vs 479.5 ng/ml, Z = -2.68; p = 0.007) and patients with cholecystectomy in anamesis had lower (359.0 ng/ml vs 479.0 ng/ml, Z = 2.02; p = 0.043). Chemerin concentration correlated with systolic and diastolic blood pressure (BP) (ρ = -0.41; р < 0.001 and ρ = -0.27; р = 0.028, respectively).
Conclusions. Chemerin concentration in women with RA correlates with age, weight, BMI, NPJ and hsCRP. Chemerin concentration in patients with comorbid DM2 was higher and in patients comorbid with cholecystectomy in anamnesis was lower. Chemerin concentration correlates negatively with a systolic and diastolic BP.
Keywords
About the Authors
E. V. PapichevRussian Federation
Eugene V. Papichev - Cand. Sci. (Med.), Researcher of the Laboratory of Methods for Treatment and Prevention of Joint Diseases, Research Institute of Clinical and Experimental Rheumatology named after A.B. Zborovsky.
76, Bldg. 2, Zemlyachka St., Volgograd, 400138
Yu. R. Akhverdyan
Russian Federation
Yuri R. Akhverdyan - Cand. Sci. (Med.), Senior Researcher of the Laboratory of Methods for Treatment and Prevention of Joint Diseases, Research Institute of Clinical and Experimental Rheumatology named after A.B. Zborovsky.
76, Bldg. 2, Zemlyachka St., Volgograd, 400138
Yu. V. Polyakova
Russian Federation
Yuliya V. Polyakova - Cand. Sci. (Med.), Researcher of the Laboratory of Methods for Treatment and Prevention of Joint Diseases, Research Institute of Clinical and Experimental Rheumatology named after A.B. Zborovsky.
76, Bldg. 2, Zemlyachka St., Volgograd, 400138
L. E. Sivordova
Russian Federation
Larissa E. Sivordova - Cand. Sci. (Med.), Leading Researcher of the Laboratory of Methods for Treatment and Prevention of Joint Diseases, Research Institute of Clinical and Experimental Rheumatology named after A.B. Zborovsky.
76, Bldg. 2, Zemlyachka St., Volgograd, 400138
B. V. Zavodovsky
Russian Federation
Boris V. Zavodovsky - Dr. Sci. (Med.), Professor, Head of the Laboratory of Methods for Treatment and Prevention of Joint Diseases, Research Institute of Clinical and Experimental Rheumatology named after A.B. Zborovsky.
76, Bldg. 2, Zemlyachka St., Volgograd, 400138
References
1. Bullock J, Rizvi SAA, Saleh AM, Ahmed SS, Do DP, Ansari RA, Ahmed J. Rheumatoid Arthritis: A Brief Overview of the Treatment. Med Princ Pract. 2018;27(6):501–507. https://doi.org/10.1159/000493390.
2. Aletaha D, Smolen JS. Diagnosis and Management of Rheumatoid Arthritis: A Review. JAMA. 2018;320(13):1360–1372. https://doi.org/10.1001/jama.2018.13103.
3. Dougados M. Comorbidities in rheumatoid arthritis. Curr Opin Rheumatol. 2016;28(3):282–288. https://doi.org/10.1097/BOR.0000000000000267.
4. Aviña-Zubieta JA, Choi HK, Sadatsafavi M, Etminan M, Esdaile JM, Lacaille D. Risk of cardiovascular mortality in patients with rheumatoid arthritis: a meta-analysis of observational studies. Arthritis Rheum. 2008;59(12):1690–1697. https://doi.org/10.1002/art.24092.
5. Zborovskaya IA, Aleksandrov AV, Aleksandrov VA, Hortieva SS, Aleksandrova NV, Osmanova GY. Dynamics of quality of life indicators during personalized rehabilitation in patients with rheumatoid arthritis with arterial hypertension. Modern Problems of Science and Education. 2021;(6). (In Russ.) https://doi.org/10.17513/spno.31286.
6. Nasonov EL, Lila AM. Rheumatoid arthritis: achievements and unresolved issues. Terapevticheskii Arkhiv. 2019;91(5):4–7. (In Russ.) https://doi.org/10.26442/00403660.2019.05.000259.
7. Kronzer VL, Crowson CS, Sparks JA, Myasoedova E, Davis JM 3rd. Comorbidities As Risk Factors for Rheumatoid Arthritis and Their Accrual After Diagnosis. Mayo Clin Proc. 2019;94(12):2488–2498. https://doi.org/10.1016/j.mayocp.2019.08.010.
8. Mason A, Holmes C, Edwards CJ. Inflammation and dementia: Using rheumatoid arthritis as a model to develop treatments? Autoimmun Rev. 2018;17(9):919–925. https://doi.org/10.1016/j.autrev.2018.04.001.
9. McInnes IB, Buckley CD, Isaacs JD. Cytokines in rheumatoid arthritis - shaping the immunological landscape. Nat Rev Rheumatol. 2016;12(1):63–68. https://doi.org/10.1038/nrrheum.2015.171.
10. Niu X, Chen G. Clinical biomarkers and pathogenic-related cytokines in rheumatoid arthritis. J Immunol Res. 2014;2014:698192. https://doi.org/10.1155/2014/698192.
11. Fatel ECS, Rosa FT, Simão ANC, Dichi I. Adipokines in rheumatoid arthritis. Adv Rheumatol. 2018;58(1):25. https://doi.org/10.1186/s42358-018-0026-8.
12. Laurindo LF, de Maio MC, Barbalho SM, Guiguer EL, Araújo AC, de Alvares Goulart R et al. Organokines in Rheumatoid Arthritis: A Critical Review. Int J Mol Sci. 2022;23(11):6193. https://doi.org/10.3390/ijms23116193.
13. Abella V, Scotece M, Conde J, López V, Lazzaro V, Pino J et al. Adipokines, metabolic syndrome and rheumatic diseases. J Immunol Res. 2014;2014:343746. https://doi.org/10.1155/2014/343746.
14. Sato H, Kazama JJ, Wada Y, Kuroda T, Narita I, Gejyo F et al. Decreased levels of circulating alpha2-Heremans-Schmid glycoprotein/Fetuin-A (AHSG) in patients with rheumatoid arthritis. Intern Med. 2007;46(20):1685–1691. https://doi.org/10.2169/internalmedicine.46.6269.
15. Zhang S, Rong G, Xu Y, Jing J. Elevated Nesfatin-1 Level in Synovium and Synovial Fluid is Associated with Pro-Inflammatory Cytokines in Patients with Rheumatoid Arthritis. Int J Gen Med. 2021;14:5269–5278. https://doi.org/10.2147/IJGM.S330099.
16. Franco-Trepat E, Alonso-Pérez A, Guillán-Fresco M, Jorge-Mora A, Gualillo O, Gómez-Reino JJ, Gómez Bahamonde R. Visfatin as a therapeutic target for rheumatoid arthritis. Expert Opin Ther Targets. 2019;23(7):607–618. https://doi.org/10.1080/14728222.2019.1617274.
17. Yadav A, Kataria MA, Saini V, Yadav A. Role of leptin and adiponectin in insulin resistance. Clin Chim Acta. 2013;417:80–84. https://doi.org/10.1016/j.cca.2012.12.007.
18. Ku IA, Farzaneh-Far R, Vittinghoff E, Zhang MH, Na B, Whooley MA. Association of low leptin with cardiovascular events and mortality in patients with stable coronary artery disease: the Heart and Soul Study. Atherosclerosis. 2011;217(2):503–508. https://doi.org/10.1016/j.atherosclerosis.2010.10.047.
19. Farooqi IS, Jebb SA, Langmack G, Lawrence E, Cheetham CH, Prentice AM et al. Effects of recombinant leptin therapy in a child with congenital leptin deficiency. N Engl J Med. 1999;341(12):879–884. https://doi.org/10.1056/NEJM199909163411204.
20. Bozaoglu K, Bolton K, McMillan J, Zimmet P, Jowett J, Collier G et al. Chemerin is a novel adipokine associated with obesity and metabolic syndrome. Endocrinology. 2007;148(10):4687–4694. https://doi.org/10.1210/en.2007-0175.
21. Kaur J, Adya R, Tan BK, Chen J, Randeva HS. Identification of chemerin receptor (ChemR23) in human endothelial cells: chemerin-induced endothelial angiogenesis. Biochem Biophys Res Commun. 2010;391(4):1762–1768. https://doi.org/10.1016/j.bbrc.2009.12.150.
22. Muruganandan S, Parlee SD, Rourke JL, Ernst MC, Goralski KB, Sinal CJ. Chemerin, a novel peroxisome proliferator-activated receptor gamma (PPARgamma) target gene that promotes mesenchymal stem cell adipogenesis. J Biol Chem. 2011;286(27):23982–23995. https://doi.org/10.1074/jbc.M111.220491.
23. Issa ME, Muruganandan S, Ernst MC, Parlee SD, Zabel BA, Butcher EC et al. Chemokine-like receptor 1 regulates skeletal muscle cell myogenesis. Am J Physiol Cell Physiol. 2012;302(11):C1621–C1631. https://doi.org/10.1152/ajpcell.00187.2011.
24. Ernst MC, Issa M, Goralski KB, Sinal CJ. Chemerin exacerbates glucose intolerance in mouse models of obesity and diabetes. Endocrinology. 2010;151(5):1998–2007. https://doi.org/10.1210/en.2009-1098.
25. Weigert J, Neumeier M, Wanninger J, Filarsky M, Bauer S, Wiest R et al. Systemic chemerin is related to inflammation rather than obesity in type 2 diabetes. Clin Endocrinol (Oxf). 2010;72(3):342–348. https://doi.org/10.1111/j.1365-2265.2009.03664.x.
26. Wittamer V, Franssen JD, Vulcano M, Mirjolet JF, Le Poul E, Migeotte I et al. Specific recruitment of antigen-presenting cells by chemerin, a novel processed ligand from human inflammatory fluids. J Exp Med. 2003;198(7):977–985. https://doi.org/10.1084/jem.20030382.
27. Chakaroun R, Raschpichler M, Klöting N, Oberbach A, Flehmig G, Kern M, et al. Effects of weight loss and exercise on chemerin serum concentrations and adipose tissue expression in human obesity. Metabolism. 2012;61(5):706–714. https://doi.org/10.1016/j.metabol.2011.10.008.
28. Bodvall B. The Postcholecystectomy Syndromes. Clin Gastroenterol. 1973;2(1):103–126. https://doi.org/10.1016/S0300-5089(21)00336-9.
29. Gu P, Jiang W, Lu B, Shi Z. Chemerin is associated with inflammatory markers and metabolic syndrome phenotypes in hypertension patients. Clin Exp Hypertens. 2014;36(5):326–332. https://doi.org/10.3109/10641963.2013.827697.
30. Malik AA, Wani ML, Tak SI, Irshad I, Ul-Hassan N. Association of dyslipidaemia with cholilithiasis and effect of cholecystectomy on the same. Int J Surg. 2011;9(8):641–642. https://doi.org/10.1016/j.ijsu.2011.08.003.
31. Watts SW, Dorrance AM, Penfold ME, Rourke JL, Sinal CJ, Seitz B et al. Chemerin connects fat to arterial contraction. Arterioscler Thromb Vasc Biol. 2013;33(6):1320–1328. https://doi.org/10.1161/ATVBAHA.113.301476.
Review
For citations:
Papichev EV, Akhverdyan YR, Polyakova YV, Sivordova LE, Zavodovsky BV. Association of serum chemerin levels with complications and comorbidity in rheumatoid arthritis. Meditsinskiy sovet = Medical Council. 2023;(21):136-142. (In Russ.) https://doi.org/10.21518/ms2023-398