Abstract
We performed a meta-analysis to estimate whether combined evidence shows the association between the MCP-1-2518A/G polymorphism and susceptibility to autoimmune diseases. Relevant articles dated to July 2014 were acquired from the PubMed, EMBASE, ISI, and CNKI databases. The number of the genotypes and/or alleles for the MCP-1-2518A/G in cases and control subjects was extracted, and statistical analysis was conducted using STATA 11.2 software. Summary odds ratios (ORs) with their 95 % confidence intervals (95 % CIs) were used to calculate the risk of autoimmune diseases with the MCP-1-2518A/G. Significant increased risk of autoimmune diseases could be found for A allele vs. G allele (OR = 1.616, 95 % CI 1.027–2.542, P = 0.038) and AA + AG vs. GG (OR = 1.616, 95 % CI 1.027–2.542, P = 0.038) in Asian patients with rheumatoid arthritis (RA), and for A allele vs. G allele (OR = 1.383, 95 % CI 1.142–1.676, P = 0.022) and AA vs. AG + GG (OR = 1.575, 95 % CI 1.361–1.823, P < 0.001) in European patients with Crohn’s disease (CD). In addition, when comparison of European patients with lupus nephritis (LN) and without LN, significant association between patients with LN and without LN also could be found for AA vs. AG + GG (OR = 0.713, 95 % CI 0.545–0.933, P = 0.014). This meta-analysis showed that the MCP-1-2518-A allele confers susceptibility to Asian patients with RA and European patients with CD.
Similar content being viewed by others
References
Vyse TJ, Todd JA (1996) Genetic analysis of autoimmune disease. Cell 85(3):311–8
Lleo A, Battezzati PM, Selmi C, Gershwin ME, Podda M (2008) Is autoimmunity a matter of sex? Autoimmun Rev 7(8):626–30
Boscolo P, Youinou P, Theoharides TC, Cerulli G, Conti P (2008) Environmental and occupational stress and autoimmunity. Autoimmun Rev 7(4):340–3
Invernizzi P, Gershwin ME (2009) The genetics of human autoimmune disease. J Autoimmun 33(3-4):290–9
Lin JP, Cash JM, Doyle SZ, Peden S, Kanik K, Amos CI, Bale SJ, Wilder RL (1998) Familial clustering of rheumatoid arthritis with other autoimmune diseases. Hum Genet 103(4):475–82
Tait KF, Marshall T, Berman J, Carr-Smith J, Rowe B, Todd JA, Bain SC, Barnett AH, Gough SC (2004) Clustering of autoimmune disease in parents of siblings from the type 1 diabetes Warren repository. Diabet Med 21(4):358–62
Barcellos LF, Kamdar BB, Ramsay PP, DeLoa C, Lincoln RR, Caillier S, Schmidt S, Haines JL, Pericak-Vance MA, Oksenberg JR, Hauser SL (2006) Clustering of autoimmune diseases in families with a high-risk for multiple sclerosis: a descriptive study. Lancet Neurol 5(11):924–31
Morahan G, Peeva V, Mehta M, Williams R (2008) Systems genetics can provide new insights in to immune regulation and autoimmunity. J Autoimmun 31(3):233–6
McCluskey J, Peh CA (1999) The human leucocyte antigens and clinical medicine: an overview. Rev Immunogenet 1(1):3–20
Cen H, Wang W, Leng RX, Wang TY, Pan HF, Fan YG, Wang B, Ye DQ (2013) Association of IFIH1 rs1990760 polymorphism with susceptibility to autoimmune diseases: a meta-analysis. Autoimmunity 46(7):455–62
Lee YH, Rho YH, Choi SJ, Ji JD, Song GG, Nath SK, Harley JB (2007) The PTPN22 C1858T functional polymorphism and autoimmune diseases—a meta-analysis. Rheumatology (Oxford) 46(1):49–56
Vereecke L, Beyaert R, van Loo G (2011) Genetic relationships between A20/TNFAIP3, chronic inflammation and autoimmune disease. Biochem Soc Trans 39(4):1086–91
Liang YL, Wu H, Shen X, Li PQ, Yang XQ, Liang L, Tian WH, Zhang LF (2012) Association of STAT4 rs7574865 polymorphism with autoimmune diseases: a meta-analysis. Mol Biol Rep 39(9):8873–82
Harigai M, Hara M, Yoshimura T, Leonard EJ, Inoue K, Kashiwazaki S (1993) Monocyte chemoattractant protein-1 (MCP-1) in inflammatory joint diseases and its involvement in the cytokine network of rheumatoid synovium. Clin Immunol Immunopathol 69(1):83–91
Hwang SY, Cho ML, Park B, Kim JY, Kim YH, Min DJ, Min JK, Kim HY (2002) Allelic frequency of the MCP-1 promoter -2518 polymorphism in the Korean population and in Korean patients with rheumatoid arthritis, systemic lupus erythematosus and adult-onset Still’s disease. Eur J Immunogenet 29(5):413–6
Banks C, Bateman A, Payne R, Johnson P, Sheron N (2003) Chemokine expression in IBD. Mucosal chemokine expression is unselectively increased in both ulcerative colitis and Crohn’s disease. J Pathol 199(1):28–35
Grimm MC, Elsbury SK, Pavli P, Doe WF (1996) Enhanced expression and production of monocyte chemoattractant protein-1 in inflammatory bowel disease mucosa. J Leukoc Biol 59(6):804–12
Villiger PM, Terkeltaub R, Lotz M (1992) Production of monocyte chemoattractant protein-1 by inflamed synovial tissue and cultured synoviocytes. J Immunol 149(2):722–7
Grandaliano G, Gesualdo L, Ranieri E, Monno R, Montinaro V, Marra F, Schena FP (1996) Monocyte chemotactic peptide-1 expression in acute and chronic human nephritides: a pathogenetic role in interstitial monocytes recruitment. J Am Soc Nephrol 7(6):906–13
Rovin BH, Lu L, Saxena R (1999) A novel polymorphism in the MCP-1 gene regulatory region that influences MCP-1 expression. Biochem Biophys Res Commun 259(2):344–8
Aguilar F, González-Escribano MF, Sánchez-Román J, Núñez-Roldán A (2001) MCP-1 promoter polymorphism in Spanish patients with systemic lupus erythematosus. Tissue Antigens 58(5):335–8
Kim HL, Lee DS, Yang SH, Lim CS, Chung JH, Kim S, Lee JS, Kim YS (2002) The polymorphism of monocyte chemoattractant protein-1 is associated with the renal disease of SLE. Am J Kidney Dis 40(6):1146–52
Tucci M, Barnes EV, Sobel ES, Croker BP, Segal MS, Reeves WH, Richards HB (2004) Strong association of a functional polymorphism in the monocyte chemoattractant protein 1 promoter gene with lupus nephritis. Arthritis Rheum 50(6):1842–9
Nakashima H, Akahoshi M, Shimizu S, Inoue Y, Miyake K, Ninomiya I, Igawa T, Sadanaga A, Otsuka T, Harada M (2004) Absence of association between the MCP-1 gene polymorphism and histological phenotype of lupus nephritis. Lupus 13(3):165–7
Liao CH, Yao TC, Chung HT, See LC, Kuo ML, Huang JL (2004) Polymorphisms in the promoter region of RANTES and the regulatory region of monocyte chemoattractant protein-1 among Chinese children with systemic lupus erythematosus. J Rheumatol 31(10):2062–7
Ye DQ, Hu YS, Li XP, Yang SG, Hao JH, Huang F, Zhang XJ (2005) The correlation between monocyte chemoattractant protein-1 and the arthritis of systemic lupus erythematosus among Chinese. Arch Dermatol Res 296(8):366–71
Sánchez E, Sabio JM, Callejas JL, de Ramón E, Garcia-Portales R, García-Hernández FJ, Jiménez-Alonso J, González-Escribano MF, Martín J, Koeleman BP (2006) Association study of genetic variants of pro-inflammatory chemokine and cytokine genes in systemic lupus erythematosus. BMC Med Genet 7:48
Lima G, Soto-Vega E, Atisha-Fregoso Y, Sánchez-Guerrero J, Vallejo M, Vargas-Alarcón G, Llorente L (2007) MCP-1, RANTES, and SDF-1 polymorphisms in Mexican patients with systemic lupus erythematosus. Hum Immunol 68(12):980–5
Brown KS, Nackos E, Morthala S, Jensen LE, Whitehead AS, Von Feldt JM (2007) Monocyte chemoattractant protein-1: plasma concentrations and A(-2518)G promoter polymorphism of its gene in systemic lupus erythematosus. J Rheumatol 34(4):740–6
Wang YY, Deng DQ, Mao CZ, Xu BY, Hu LP (2007) Study on the association between MCP-1-2518 promoter polymorphism and systemic lupus erythematosus in Chinese Him in Yunnan Province. Int J Immunol 1:5–8
Hoshi D, Okamoto H, Kaneko H, Ichikawa N, Terai C, Yamanaka H, Kamatani N (2008) Association of a polymorphism in the monocyte chemoattractant protein-1/CCL2 gene and lupus nephritis in systemic lupus erythematosus patients. Clin Exp Rheumatol 26(5):972–3
Piotrowski P, Lianeri M, Gasik R, Roszak A, Olesińska M, Jagodziński PP (2010) Monocyte chemoattractant protein-1 -2518 A/G single nucleotide polymorphism might be associated with renal disease and thrombocytopenia of SLE. J Biomed Biotechnol 13:265
Malafronte P, Vieira JM Jr, Pereira AC, Krieger JE, Barros RT, Woronik V (2010) Association of the MCP-1-2518 A/G polymorphism and no association of its receptor CCR2–64 V/I polymorphism with lupus nephritis. J Rheumatol 37(4):776–82
Aranda F, Wingeyer SP, Muñoz SA, Allievi A, Orden A, Trobo R, Alvarez A, Eimon A, Barreira JC, Schneeberger E, Sarano J, Hofman J, de Larrañaga G (2012) The -2518 A/G polymorphism in the monocyte chemoattractant protein 1 gene is associated with the risk of developing systemic lupus erythematosus in Argentinean patients: a multicenter study. Eur Cytokine Netw 23(1):7–11
Lee YH, Kim HJ, Rho YH, Choi SJ, Ji JD, Song GG (2003) Functional polymorphisms in matrix metalloproteinase-1 and monocyte chemoattractant protein-1 and rheumatoid arthritis. Scand J Rheumatol 32(4):235–9
González-Escribano MF, Torres B, Aguilar F, Rodríguez R, García A, Valenzuela A, Núñez-Roldán A (2003) MCP-1 promoter polymorphism in Spanish patients with rheumatoid arthritis. Hum Immunol 64(7):741–4
Herfarth H, Göke M, Hellerbrand C, Mühlbauer M, Vogl D, Schölmerich J, Rogler G (2003) Polymorphism of monocyte chemoattractant protein 1 in Crohn’s disease. Int J Colorectal Dis 18(5):401–5
Palmieri O, Latiano A, Salvatori E, Valvano MR, Bossa F, Latiano T, Corritore G, di Mauro L, Andriulli A, Annesec V (2010) The -A2518G polymorphism of monocyte chemoattractant protein-1 is associated with Crohn’s disease. Am J Gastroenterol 105(7):1586–94
Karrer S, Bosserhoff AK, Weiderer P, Distler O, Landthaler M, Szeimies RM, Müller-Ladner U, Schölmerich J, Hellerbrand C (2005) The -2518 promotor polymorphism in the MCP-1 gene is associated with systemic sclerosis. J Invest Dermatol 124(1):92–8
Navratilova Z, Lukac J, Mrazek F, Kriegova E, Bucova M, Bosak V, Petrek M (2008) MCP-1-2518 A/G single nucleotide polymorphism in Slovak patients with systemic sclerosis. Mediators Inflamm 20:40–3
Carulli MT, Spagnolo P, Fonseca C, Welsh KI, Dubois RM, Black CM, Denton CP (2008) Single-nucleotide polymorphisms in CCL2 gene are not associated with susceptibility to systemic sclerosis. J Rheumatol 35(5):839–44
Radstake TR, Vonk MC, Dekkers M, Schijvenaars MM, Treppichio WL, Lafyatis R, Riemekasten G, van den Hoogen F, Coenen MJ (2009) The -2518A > G promoter polymorphism in the CCL2 gene is not associated with systemic sclerosis susceptibility or phenotype: results from a multicenter study of European Caucasian patients. Hum Immunol 70(2):130–3
Steinmetz OM, Panzer U, Harendza S, Mertens PR, Ostendorf T, Floege J et al (2004) No association of the -2518 MCP-1 A/G promoter polymorphism with incidence and clinical course of IgA nephropathy. Nephrol Dial Transplant 19(3):596–601
Mori H, Kaneko Y, Narita I, Goto S, Saito N, Kondo D, Sato F, Ajiro J, Saga D, Ogawa A, Sakatsume M, Ueno M, Tabei K, Geivo F (2005) Monocyte chemoattractant protein-1 A-2518G gene polymorphism and renal survival of Japanese patients with immunoglobulin A nephropathy. Clin Exp Nephrol 9(4):297–303
Egger M, Smith GD, Phillips AN (1997) Meta-analysis: principles and procedures. BMJ 315(7121):1533–7
Alzawawy A, Zohary M, Ablordiny M, Eldalie M (2009) Estimation of monocyte-chemoattractantprotein-1 (Mcp-1) level in patients with lupus nephritis. Int J Rheum Dis 12(4):311–8
Marks SD, Shah V, Pilkington C, Tullus K (2010) Urinary monocyte chemoattractant protein-1 correlates with disease activity in lupus nephritis. Pediatr Nephrol 25(11):2283–8
Anaya JM (2010) The autoimmune tautology. Arthritis Res Ther 12(6):147
Acknowledgments
We thank all our colleagues working in the Department of Rheumatology and Clinical Immunology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Key Laboratory of Rheumatology and Clinical Immunology.
Disclosures
None.
Author information
Authors and Affiliations
Corresponding author
Additional information
Si Chen and Chuiwen Deng contributed equally to this work.
Electronic supplementary material
Below is the link to the electronic supplementary material.
Fig. S1
Forest plots of all models for SSc in overall meta-analysis. (GIF 172 kb)
Fig. S2
Forest plots of all models for SLE in overall meta-analysis. (GIF 298 kb)
Fig. S3
Forest plots of all models for SLE in stratified meta-analysis (GIF 285 kb)
Fig. S4
Forest plots of all models for IgAN in overall meta-analysis. (GIF 254 kb)
Fig. S5
Forest plots of all models for RA in overall meta-analysis. (GIF 192 kb)
Fig. S6
Forest plots of other models for CD in overall meta-analysis and forest plots of other models for RA in stratified meta-analysis. (GIF 209 kb)
Fig. S7
Forest plots of other models for SLE with LN patients vs. controls in overall meta-analysis (GIF 133 kb)
Fig. S8
Forest plots of all models for SLE with LN patients vs. controls in stratified meta-analysis. (GIF 228 kb)
Fig. S9
Forest plots of all models for SLE without LN patients vs. controls in overall meta-analysis. (GIF 270 kb)
Fig. S10
Forest plots of all models for SLE without LN patients vs. controls in stratified meta-analysis. (GIF 279 kb)
Fig. S11
Forest plots of all models for SLE with LN patients vs. SLE without LN patients in overall meta-analysis. (GIF 254 kb)
Fig. S12
Forest plots of other models for SLE with LN patients vs. SLE without LN patients in stratified meta-analysis. (GIF 210 kb)
Fig. S13
The results of sensitivity analysis from SLE without LN patients vs. controls. (GIF 188 kb)
Fig. S14
The results of sensitivity analysis from SLE with LN patients vs. controls. (GIF 205 kb)
Fig. S15
The results of sensitivity analysis from SLE with LN patients vs. SLE without LN patients. (GIF 204 kb)
Rights and permissions
About this article
Cite this article
Chen, S., Deng, C., Hu, C. et al. Association of MCP-1-2518A/G polymorphism with susceptibility to autoimmune diseases: a meta-analysis. Clin Rheumatol 35, 1169–1179 (2016). https://doi.org/10.1007/s10067-015-3060-5
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10067-015-3060-5