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Published in: Rheumatology International 12/2012

01-12-2012 | Original Article

PAI-1 mRNA expression and plasma level in rheumatoid arthritis: relationship with 4G/5G PAI-1 polymorphism

Authors: José Francisco Muñoz-Valle, Sandra Luz Ruiz-Quezada, Edith Oregón-Romero, Rosa Elena Navarro-Hernández, Eduardo Castañeda-Saucedo, Ulises De la Cruz-Mosso, Berenice Illades-Aguiar, Marco Antonio Leyva-Vázquez, Natividad Castro-Alarcón, Isela Parra-Rojas

Published in: Rheumatology International | Issue 12/2012

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Abstract

Rheumatoid arthritis (RA) is a chronic inflammatory disease affecting the synovial membrane, cartilage and bone. PAI-1 is a key regulator of the fibrinolytic system through which plasminogen is converted to plasmin. The plasmin activates the matrix metalloproteinase system, which is closely related with the joint damage and bone destruction in RA. The aim of this study was to investigate the relationship between 4G/5G PAI-1 polymorphism with mRNA expression and PAI-1 plasma protein levels in RA patients. 113 RA patients and 123 healthy subjects (HS) were included in the study. The 4G/5G PAI-1 polymorphism was determined by polymerase chain reaction–restriction fragment length polymorphism method; the PAI-1 mRNA expression was determined by real-time PCR; and the soluble PAI-1 (sPAI-1) levels were quantified using an ELISA kit. No significant differences in the genotype and allele frequencies of 4G/5G PAI-1 polymorphism were found between RA patients and HS. However, the 5G/5G genotype was the most frequent in both studied groups: RA (42%) and HS (44%). PAI-1 mRNA expression was slightly increased (0.67 fold) in RA patients with respect to HS (P = 0.0001). In addition, in RA patients, the 4G/4G genotype carriers showed increased PAI-1 mRNA expression (3.82 fold) versus 4G/5G and 5G/5G genotypes (P = 0.0001), whereas the sPAI-1 plasma levels did not show significant differences. Our results indicate that the 4G/5G PAI-1 polymorphism is not a marker of susceptibility in the Western Mexico. However, the 4G/4G genotype is associated with high PAI-1 mRNA expression but not with the sPAI-1 levels in RA patients.
Literature
1.
go back to reference McInnes IB, Schett G (2007) Cytokines in the pathogenesis of rheumatoid arthritis. Nat Rev Immunol 7:429–442PubMedCrossRef McInnes IB, Schett G (2007) Cytokines in the pathogenesis of rheumatoid arthritis. Nat Rev Immunol 7:429–442PubMedCrossRef
2.
go back to reference Pope RM (2002) Apoptosis as a therapeutic tool in rheumatoid arthritis. Nat Rev Immunol 2:527–535PubMedCrossRef Pope RM (2002) Apoptosis as a therapeutic tool in rheumatoid arthritis. Nat Rev Immunol 2:527–535PubMedCrossRef
3.
go back to reference Ha H, Oh EY, Lee HB (2009) The role of plasminogen activator inhibitor 1 in renal and cardiovascular diseases. Nat Rev Nephrol 5:203–211PubMedCrossRef Ha H, Oh EY, Lee HB (2009) The role of plasminogen activator inhibitor 1 in renal and cardiovascular diseases. Nat Rev Nephrol 5:203–211PubMedCrossRef
4.
go back to reference Ma Z, Paek D, Oh CK (2009) Plasminogen activator inhibitor-1 and asthma: role in the pathogenesis and molecular regulation. Clin Exp Allergy 39:1136–1144PubMedCrossRef Ma Z, Paek D, Oh CK (2009) Plasminogen activator inhibitor-1 and asthma: role in the pathogenesis and molecular regulation. Clin Exp Allergy 39:1136–1144PubMedCrossRef
5.
go back to reference Eriksson P, Kallin PB, van’t Hooft FM et al (1995) Allele-specific increase in basal transcription of the plasminogen-activator inhibitor 1 gene is associated with myocardial infarction. Proc Natl Acad Sci USA 92:1851–1855PubMedCrossRef Eriksson P, Kallin PB, van’t Hooft FM et al (1995) Allele-specific increase in basal transcription of the plasminogen-activator inhibitor 1 gene is associated with myocardial infarction. Proc Natl Acad Sci USA 92:1851–1855PubMedCrossRef
6.
go back to reference Wong TY, Poon P, Szeto CC et al (2000) Association of plasminogen activator inhibitor-1 4G/4G genotype and type 2 diabetic nephropathy in Chinese patients. Kidney Int 57:632–638PubMedCrossRef Wong TY, Poon P, Szeto CC et al (2000) Association of plasminogen activator inhibitor-1 4G/4G genotype and type 2 diabetic nephropathy in Chinese patients. Kidney Int 57:632–638PubMedCrossRef
7.
go back to reference Margaglione M, Cappucci G, Colaizzo D et al (1998) The PAI-1 Gene Locus 4G/5G polymorphism is associated with a family history of coronary artery disease. Arterioscler Thromb Vasc Biol 18:152–156PubMedCrossRef Margaglione M, Cappucci G, Colaizzo D et al (1998) The PAI-1 Gene Locus 4G/5G polymorphism is associated with a family history of coronary artery disease. Arterioscler Thromb Vasc Biol 18:152–156PubMedCrossRef
8.
go back to reference Margaglione M, Cappucci G, d’Addedda M et al (1998) PAI-1 plasma levels in a general population without clinical evidence of atherosclerosis: relation to environmental and genetic determinants. Arterioscler Thromb Biol 18:562–567CrossRef Margaglione M, Cappucci G, d’Addedda M et al (1998) PAI-1 plasma levels in a general population without clinical evidence of atherosclerosis: relation to environmental and genetic determinants. Arterioscler Thromb Biol 18:562–567CrossRef
9.
go back to reference Morange PE, Henry M, Tregouët D et al (2000) The A −844 G polymorphism in the PAI-1 gene is associated with a higher risk of venous thrombosis in factor V Leiden Carriers. Arterioscler Thromb Vasc Biol 20:1387–1391PubMedCrossRef Morange PE, Henry M, Tregouët D et al (2000) The A −844 G polymorphism in the PAI-1 gene is associated with a higher risk of venous thrombosis in factor V Leiden Carriers. Arterioscler Thromb Vasc Biol 20:1387–1391PubMedCrossRef
10.
go back to reference van der Laan MH, Slagboom PE, Meulenbelt I et al (1998) A functional polymorphism in the promotor of plasminogen activator inhibitor-1 is associated with join destruction in RA. Arthritis Rheum 41:S60 van der Laan MH, Slagboom PE, Meulenbelt I et al (1998) A functional polymorphism in the promotor of plasminogen activator inhibitor-1 is associated with join destruction in RA. Arthritis Rheum 41:S60
11.
go back to reference Tàssies D, Espinosa G, Muñoz-Rodríguez FJ et al (2000) The 4G/5G polymorphism of the type-1 plasminogen activators inhibitor gene and thrombosis in patients with antiphospholipid syndrome. Arthritis Rheum 43:2349–2358PubMedCrossRef Tàssies D, Espinosa G, Muñoz-Rodríguez FJ et al (2000) The 4G/5G polymorphism of the type-1 plasminogen activators inhibitor gene and thrombosis in patients with antiphospholipid syndrome. Arthritis Rheum 43:2349–2358PubMedCrossRef
12.
go back to reference McCormack LJ, Nagi DK, Stickland MH et al (1996) Promoter (4G/5G) plasminogen activator inhibitor-1 genotype in Pima Indians: relationship to plasminogen activator inhibitor-1 levels and features of the insulin resistance syndrome. Diabetologia 39:1512–1518PubMedCrossRef McCormack LJ, Nagi DK, Stickland MH et al (1996) Promoter (4G/5G) plasminogen activator inhibitor-1 genotype in Pima Indians: relationship to plasminogen activator inhibitor-1 levels and features of the insulin resistance syndrome. Diabetologia 39:1512–1518PubMedCrossRef
13.
go back to reference Cardiel MH, Abello-Banfi M, Ruiz-Mercado R et al (1993) How the measure health status in rheumatoid arthritis in non-English speaking patients: validation of a Spanish version of the Health Assessment Questionnaire Disability Index (Spanish HAQ-DI). Clin Exp Rheumatol 11:117–121PubMed Cardiel MH, Abello-Banfi M, Ruiz-Mercado R et al (1993) How the measure health status in rheumatoid arthritis in non-English speaking patients: validation of a Spanish version of the Health Assessment Questionnaire Disability Index (Spanish HAQ-DI). Clin Exp Rheumatol 11:117–121PubMed
14.
go back to reference Prevoo ML, van ‘t Hof MA, Kuper HH et al (1995) Modified disease activity scores that include twenty-eight-joint counts. Development and validation in a prospective longitudinal study of patients with rheumatoid arthritis. Arthritis Rheum 38:44–48PubMedCrossRef Prevoo ML, van ‘t Hof MA, Kuper HH et al (1995) Modified disease activity scores that include twenty-eight-joint counts. Development and validation in a prospective longitudinal study of patients with rheumatoid arthritis. Arthritis Rheum 38:44–48PubMedCrossRef
15.
go back to reference Miller SA, Dykes DD, Polesky HF (1988) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 16:1215PubMedCrossRef Miller SA, Dykes DD, Polesky HF (1988) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 16:1215PubMedCrossRef
16.
go back to reference Margaglione M, Grandone E, Cappucci G et al (1997) An alternative method for PAI-1 promoter polymorphism (4G/5G) typing. Thromb Haemost 77:605–606PubMed Margaglione M, Grandone E, Cappucci G et al (1997) An alternative method for PAI-1 promoter polymorphism (4G/5G) typing. Thromb Haemost 77:605–606PubMed
17.
go back to reference Muñoz-Valle JF, Vázquez-Del Mercado M, García-Iglesias T et al (2003) T(H)1/T(H)2 cytokine profile, metalloprotease-9 activity and hormonal status in pregnant rheumatoid arthritis and systemic lupus erythematosus patients. Clin Exp Immunol 131:377–384PubMedCrossRef Muñoz-Valle JF, Vázquez-Del Mercado M, García-Iglesias T et al (2003) T(H)1/T(H)2 cytokine profile, metalloprotease-9 activity and hormonal status in pregnant rheumatoid arthritis and systemic lupus erythematosus patients. Clin Exp Immunol 131:377–384PubMedCrossRef
18.
go back to reference Ruiz-Quezada S, Vázquez-Del Mercado M, Parra-Rojas I et al (2004) Genotype and allele frequency of PAI-1 promoter polymorphism in healthy subjects from the west of Mexico. Association with biochemical and hematological parameters. Ann Genet 47:155–162PubMedCrossRef Ruiz-Quezada S, Vázquez-Del Mercado M, Parra-Rojas I et al (2004) Genotype and allele frequency of PAI-1 promoter polymorphism in healthy subjects from the west of Mexico. Association with biochemical and hematological parameters. Ann Genet 47:155–162PubMedCrossRef
19.
go back to reference Lisker R, Ramírez E, González-Villalpando C et al (1995) Racial admixture in a mestizo population from Mexico City. Am J Hum Biol 7:213–216CrossRef Lisker R, Ramírez E, González-Villalpando C et al (1995) Racial admixture in a mestizo population from Mexico City. Am J Hum Biol 7:213–216CrossRef
20.
go back to reference Rangel-Villalobos H, Muñoz-Valle JF, González-Martín A et al (2008) Genetic admixture, relatedness, and structure patterns among Mexican populations revealed by the Y-chromosome. Am J Phys Anthropol 135:448–461PubMedCrossRef Rangel-Villalobos H, Muñoz-Valle JF, González-Martín A et al (2008) Genetic admixture, relatedness, and structure patterns among Mexican populations revealed by the Y-chromosome. Am J Phys Anthropol 135:448–461PubMedCrossRef
21.
go back to reference Nuño-Arana I, Páez-Riberos LA, Sando-val-Ramírez L et al (2005) High prevalence of 5G allele in Amerindian tribes and Mestizos from Mexico at 4G/5G PAI-I gene promoter polymorphism. Thromb Haemost 93:1005–1007PubMed Nuño-Arana I, Páez-Riberos LA, Sando-val-Ramírez L et al (2005) High prevalence of 5G allele in Amerindian tribes and Mestizos from Mexico at 4G/5G PAI-I gene promoter polymorphism. Thromb Haemost 93:1005–1007PubMed
22.
go back to reference Torres-Carrillo N, Magdalena Torres-Carrillo N, Vázquez-Del Mercado M et al (2008) Distribution of–844 G/A and Hind III C/G PAI-1 polymorphisms and plasma PAI-1 levels in Mexican subjects: comparison of frequencies between populations. Clin Appl Thromb Hemost 14:220–226PubMedCrossRef Torres-Carrillo N, Magdalena Torres-Carrillo N, Vázquez-Del Mercado M et al (2008) Distribution of–844 G/A and Hind III C/G PAI-1 polymorphisms and plasma PAI-1 levels in Mexican subjects: comparison of frequencies between populations. Clin Appl Thromb Hemost 14:220–226PubMedCrossRef
Metadata
Title
PAI-1 mRNA expression and plasma level in rheumatoid arthritis: relationship with 4G/5G PAI-1 polymorphism
Authors
José Francisco Muñoz-Valle
Sandra Luz Ruiz-Quezada
Edith Oregón-Romero
Rosa Elena Navarro-Hernández
Eduardo Castañeda-Saucedo
Ulises De la Cruz-Mosso
Berenice Illades-Aguiar
Marco Antonio Leyva-Vázquez
Natividad Castro-Alarcón
Isela Parra-Rojas
Publication date
01-12-2012
Publisher
Springer-Verlag
Published in
Rheumatology International / Issue 12/2012
Print ISSN: 0172-8172
Electronic ISSN: 1437-160X
DOI
https://doi.org/10.1007/s00296-011-2279-y

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