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  • Open Access

Genetic epidemiology: Giant cell arteritis and polymyalgia rheumatica

Arthritis Research & Therapy20013:154

https://doi.org/10.1186/ar293

©  BioMed Central Ltd 2001

  • Received: 16 January 2001
  • Accepted: 8 February 2001
  • Published:

Abstract

Giant cell arteritis (GCA) (temporal arteritis) and polymyalgia rheumatica (PMR) are common, frequently related conditions in people generally over 50 years of age. Most studies have shown an association of GCA with HLA-DRB1*04 alleles. As regards isolated PMR, however, the HLA class II genetic susceptibility varies from one population to another. Besides associations with HLA, tumor necrosis factor appears to influence susceptibility to both conditions. Genetic polymorphisms have also been considered to be important candidates as factors of susceptibility to GCA and PMR. In this regard, gene polymorphisms for ICAM-1 (intercellular adhesion molecule 1), RANTES (regulated upon activation, normal T cell expressed, and presumably secreted), and interleukin (IL)-1 receptor antagonist seem to play a role in the pathogenesis of GCA and PMR in some populations. However, additional studies are required to clarify the genetic influence on susceptibility to these conditions.

Keywords

  • disease susceptibility
  • genetic polymorphisms
  • giant cell arteritis
  • HLA-DRB1
  • polymyalgia rheumatica
  • TNF alpha

Introduction

Giant cell arteritis (GCA) (temporal arteritis) constitutes a common vasculitic syndrome in European and North American countries that affects large and middle-sized blood vessels, with a predisposition to the cranial arteries, in people generally over 50 years of age [1].

Polymyalgia rheumatica (PMR) is also a common syndrome in people over the age of 50. The symptoms are pain, aching, and morning stiffness involving the neck, the shoulder girdle, and the hip girdle, which are generally associated with an elevated erythrocyte sedimentation rate [2]. PMR and GCA are related diseases, as PMR may be the presenting manifestation of GCA and is found in up to 50% of patients with GCA [2]. However, PMR is sometimes an isolated condition unrelated to GCA. The possibility of a genetic influence on susceptibility to GCA was initially supported by reports of cases of GCA among first-degree relatives.

Human leukocyte antigens in susceptibility to GCA and PMR

Human leukocyte antigen class II genes

GCA is the best example of an association between vasculitis and genes that lie within the HLA class II region [3]. Most studies have shown an association with HLA-DRB1*04 alleles [4]. In addition, the risk of visual complications is also associated with HLA-DRB1*04 alleles [1]. Unlike PMR in the context of GCA, which is mostly associated with HLA-DRB1*04, the susceptibility to isolated PMR associated with HLA class II genes varies from one population to another [4]. Relapses of PMR, however, have been found to be significantly more common in patients who have the HLA-DRB1*04 allele, and particularly in those carrying the HLA-DRB1*0401 allele [5]. A lack of homozygosity of the shared epitope in GCA has been reported in northwestern Spain [4] and Rochester, Minnesota [6]. This finding contrasts with observations regarding rheumatoid arthritis (RA), where homozygosity of the shared epitope is generally associated with additional risk of a more severe disease. These findings suggest that the pathology seen in GCA may be due to antigenic cross-reactivity or hypersensitivity after exposure and response to an infectious agent [4]. This mechanism would be consistent with some epidemiological data and the observed seasonal variation in disease onset. However, other, unknown, predisposing factors in the elderly may be implicated in the pathogenesis of these conditions.

Role of TNF in susceptibility to GCA and PMR

Apart from HLA-class II genes, it is likely that other genetic factors may contribute to the susceptibility to these conditions, particularly those factors involved in inflammation. GCA and PMR share evidence of an inflammatory process. However, concentrations of tumor necrosis factor (TNF)-α have not been found to be elevated in either condition. In northwestern Spain, GCA and PMR are associated with different TNF microsatellite polymorphisms. GCA is strongly associated with the allele encoding the TNF-a2 microsatellite. This association is largely independent of the association of GCA with HLA class II genes. A negative association with TNF-a10 was also found. In contrast, in patients with isolated PMR, there is a positive association with TNF-b3, which is also independent of the HLA class II association with isolated PMR, and a negative association with TNF-d4 [7]. Thus, TNF and HLA associations appear to be able to influence susceptibility to these conditions independently of each other.

Influence of genetic polymorphisms in the susceptibility to GCA and PMR

ICAM-1 biallelic polymorphisms

Genetic polymorphisms in endothelial-cell adhesion molecules have also been considered to be important candidate susceptibility factors for GCA and PMR. The intercellular adhesion molecule (ICAM-1) is a member of the immunoglobulin-like superfamily group of adhesion molecules and is a ligand for β2 integrins present on leukocytes. It plays an important role in interactions between endothelial cells and leukocytes during inflammation. Expression of ICAM-1 on vascular endothelial cells can be significantly increased in the presence of mediators, which include lipopolysaccharide and cytokines such as interleukin-1 (IL-1), TNFα, and interferon-γ. In biopsies of temporal arteries from GCA patients, ICAM-1 is highly expressed in the adventitial microvessels and neovessels within inflammatory infiltrates [8], and changes in concentrations of circulating soluble ICAM-1 have been correlated with disease activity in GCA [9]. Two polymorphisms of the coding region have been identified for ICAM-1: G or R at codon 241 (exon 4) and K or E at codon 469 (exon 6) [10]. In Italian patients with PMR and GCA, a higher frequency of the allele R at codon 241 of ICAM-1 has recently been reported [11]. In these patients, an association between polymorphism at codon 241 and an increased risk of relapses in PMR was also observed. However, unlike the findings in most series, GCA was not associated with HLA-DRB1*04 in that particular region of northern Italy. In northwestern Spain, in contrast, where susceptibility to GCA has been associated with HLA-DRB1*04 [4], no evidence was found of an interaction between HLA-DRB1*04 and polymorphisms of ICAM-1. Thus, in that particular region, ICAM-1 polymorphisms are not genetic risk factors affecting the susceptibility and severity of GCA [12].

Polymorphism in the human RANTES gene promoter

The cytokine RANTES is a potent chemotactic factor for monocytes, CD45RO+ memory T cells, basophils, eosinophils, and mast cells. Increased serum levels of this CC chemokine have been found in untreated PMR [13]. Hajeer et al have recently reported a novel polymorphism (G or A) in the human RANTES gene promoter at position –403 [14]. Because of this finding, an analysis of the polymorphism at this position was performed in patients with isolated PMR and with biopsy-proven GCA unassociated with PMR. The frequency of allele A was significantly higher in patients with PMR – but not in patients with GCA – than in controls [15]. This observation suggests that the presence of the RANTES allele A at position –403 may make a person susceptible to the development of PMR.

CCR5 polymorphism

RANTES is secreted by T lymphocytes, platelets, and synovial fibroblasts. After interaction with the CC chemokine receptor 5 (CCR5), it activates memory T cells and monocytes, which are the predominant cells in the synovial tissue of patients with PMR [16]. The chemokine receptor CCR5 is encoded by the CMKBR5 gene located on the p21.3 region of human chromosome 3, and is the major coreceptor for the macrophage-tropic strains of HIV-1. A 32-nucleotide deletion (Δ32) in one or both alleles of the CCR5 gene has been observed [17,18]. This 32-bp deletion within the coding region results in a frame shift, because of which this gene variant yields a protein product – a nonfunctional receptor – that is biologically inactive [17,18]. In patients homozygous for CCR5Δ32, the concentration of RANTES secreted by their lymphocytes is 5–10 times that found in patients homozygous for CCR5 [19]. Chemokines are suggested to be critical for establishment of inflammatory processes in autoimmune diseases such as RA. In a series of 673 patients with RA, none had the homozygous CCR5Δ32 genotype, compared with a frequency of 0.009 in a group of 815 controls [20]. However, two other studies have not confirmed the association of CCR5 with RA [21,22]. To assess whether this 32-bp deletion might play a role in PMR, Salvarani et al examined the CCR5 genotype in 88 patients with PMR in whom RA was excluded, and in 87 controls [23]. Those workers found that the allele and genotype frequencies of CCR5Δ32 in patients with PMR and healthy controls did not differ significantly. They also found that the 32-bp deletion from the CCR5 receptor was not associated with any particular feature of the disease or with a different frequency of relapses. Thus, the 32-bp deletion of the CCR5 receptor does not seem to be implicated in the pathogenesis of PMR.

Influence of the IL-1 receptor antagonist gene

The IL-1 receptor antagonist (IL-1 RN) gene is located on chromosome 2, in close proximity to the IL-1A and IL-1B genes. Several polymorphic sites have been described for this gene, including a variable number of 86-base-pair tandem repeats within its second intron [24]. Allele 2 of this polymorphism was associated with increased production of IL-1 RN by monocytes and with higher plasma concentrations. It has also been associated with severity of the disease in systemic lupus erythematosus, ulcerative colitis, and alopecia areata. Boiardi and colleagues recently reported a significant association between susceptibility to PMR and the IL-1 RN*2 allele, particularly in the homozygous state [25]. However, they found no associations between IL-1 RN biallelic gene polymorphism and relapses of the disease or duration of corticosteroid therapy.

Conclusion

Although a genetic influence in the pathogenesis of GCA and PMR does exist, additional studies in different populations are required to clarify the pathogenesis of these common and frequently associated conditions. Moreover, it will be clinically useful to search for genetic markers that may predict the severity of disease in both conditions.

Abbreviations

bp: 

base pair

CC: 

CC-chemokine

CCR5: 

CC_chemokine receptor 5

GCA: 

giant cell arteritis

HLA: 

human leukocyte antigen

ICAM: 

intercellular adhesion molecule

IL: 

interleukin

IL-1 RN: 

IL-1 receptor antagonist

PMR: 

polymyalgia rheumatica

RA: 

rheumatoid arthritis

RANTES: 

regulated upon activation; normal T cell expressed and presumably secreted

TNF: 

tumor necrosis factor.

Authors’ Affiliations

(1)
Rheumatology Division, Hospital-Xeral Calde, Lugo, Spain

References

  1. Gonzalez-Gay MA, Garcia-Porrua C, Llorca J, Hajeer AH, Branas F, Dababneh A, Gonzalez-Louzao C, Rodriguez-Gil E, Rodriguez-Ledo P, Ollier WE: Visual manifestations of giant cell arteritis: trends and clinical spectrum in 161 patients. Medicine (Baltimore). 2000, 79: 283-292. 10.1097/00005792-200009000-00001.View ArticleGoogle Scholar
  2. Gonzalez-Gay MA, Garcia-Porrua C, Salvarani C, Hunder GG: Diagnostic approach in a patient presenting with polymyalgia. Clin Exp Rheumatol. 1999, 17: 276-278.PubMedGoogle Scholar
  3. Weyand CM, Hicok KC, Hunder GG, Goronzy JJ: The HLA-DRB1 locus as a genetic component in giant cell arteritis: mapping of a disease-linked sequence motif to the antigen binding site of the HLA-DR molecule. J Clin Invest. 1992, 90: 2355-2361.PubMedPubMed CentralView ArticleGoogle Scholar
  4. Dababneh A, Gonzalez-Gay MA, Garcia-Porrua C, Hajeer A, Thomson W, Ollier W: Giant cell arteritis and polymyalgia rheumatica can be differentiated by distinct patterns of HLA class II association. J Rheumatol. 1998, 25: 2140-2145.PubMedGoogle Scholar
  5. Gonzalez-Gay MA, Garcia-Porrua C, Vazquez-Caruncho M, Dababneh A, Hajeer A, Ollier WE: The spectrum of polymyalgia rheumatica in northwestern Spain: incidence and analysis of variables associated with relapse in a 10-year study. J Rheumatol. 1999, 26: 1326-1332.PubMedGoogle Scholar
  6. Weyand CM, Hunder NNH, Hicock KC, Hunder GG, Goronzy JJ: HLA-DRB1 alleles in polymyalgia rheumatica, giant cell arteritis and rheumatoid arthritis. Arthritis Rheum. 1994, 37: 514-520.PubMedView ArticleGoogle Scholar
  7. Mattey DL, Hajeer AH, Dababneh A, Thomson W, Gonzalez-Gay MA, Garcia-Porrua C, Ollier WE: Association of giant cell arteritis and polymyalgia rheumatica with different tumor necrosis factor microsatellite polymorphisms. Arthritis Rheum. 2000, 43: 1749-1755. 10.1002/1529-0131(200008)43:8<1749::AID-ANR11>3.0.CO;2-K.PubMedView ArticleGoogle Scholar
  8. Cid MC, Cebrian M, Font C, Coll-Vinent B, Hernandez-Rodriguez J, Esparza J, Urbano-Marquez A, Grau JM: Cell adhesion molecules in the development of inflammatory infiltrates in giant cell arteritis: inflammation-induced angiogenesis as the preferential site of leukocyte-endothelial cell interactions. Arthritis Rheum. 2000, 43: 184-194. 10.1002/1529-0131(200001)43:1<184::AID-ANR23>3.0.CO;2-N.PubMedView ArticleGoogle Scholar
  9. Coll-Vinent B, Vilardell C, Font C, Oristrell J, Hernandez-Rodriguez J, Yagüe J, Urbano-Marquez A, Grau JM, Cid MC: Circulating soluble adhesion molecules in patients with giant cell arteritis. Correlation between soluble intercellular adhesion molecule-1 (sICAM-1) concentrations and disease activity. Ann Rheum Dis. 1999, 58: 189-192.PubMedPubMed CentralView ArticleGoogle Scholar
  10. Vora DK, Rosenbloom CL, Beaudet AL, Cottingham RW: Polymorphisms and linkage analysis for ICAM-1 and the selectin gene cluster. Genomics. 1994, 21: 473-477. 10.1006/geno.1994.1303.PubMedView ArticleGoogle Scholar
  11. Salvarani C, Casali B, Boiardi L, Ranzi A, Macchioni P, Nicoli D, Farnetti E, Brini M, Portioli I: Intercellular adhesion molecule 1 gene polymorphisms in polymyalgia rheumatica/giant cell arteritis: association with disease risk and severity. J Rheumatol. 2000, 27: 1215-1221.PubMedGoogle Scholar
  12. Amoli MM, Shelley E, Mattey DL, Garcia-Porrua C, Thomson W, Hajeer AH, Ollier WER, Gonzalez-Gay MA: Lack of association between ICAM-1 gene polymorphisms and giant cell arteritis. J Rheumatol. 2001,Google Scholar
  13. Pulsatelli L, Meliconi R, Boiardi L, Macchioni P, Salvarani C, Facchini A: Elevated serum concentrations of the chemokine RANTES in patients with polymyalgia rheumatica. Clin Exp Rheumatol. 1998, 16: 263-268.PubMedGoogle Scholar
  14. Hajeer AH, al Sharif F, Ollier WE: A polymorphism at position –403 in the human RANTES promoter. Eur J Immunogenet. 1999, 26: 375-376. 10.1046/j.1365-2370.1999.00163.x.PubMedView ArticleGoogle Scholar
  15. Makki RF, al Sharif F, Gonzalez-Gay MA, Garcia-Porrua C, Ollier WE, Hajeer AH: RANTES gene polymorphism in polymyalgia rheumatica, giant cell arteritis and rheumatoid arthritis. Clin Exp Rheumatol. 2000, 18: 391-393.PubMedGoogle Scholar
  16. Meliconi R, Pulsatelli L, Uguccioni M, Salvarani C, Macchioni P, Melchiorri C, Focherini MC, Frizziero L, Facchini A: Leukocyte infiltration in synovial tissue from the shoulder of patients with polymyalgia rheumatica: quantitative analysis and influence of corticosteroid treatment. Arthritis Rheum. 1996, 39: 1199-1207.PubMedView ArticleGoogle Scholar
  17. Samson M, Libert F, Doranz BJ, Rucker J, Liesnard C, Farber CM, Saragosti S, Lapoumeroulie C, Cognaux J, Forceille C, Muyldermans G, Verhofstede C, Burtonboy G, Georges M, Imai T, Rana S, Yi Y, Smyth RJ, Collman RG, Doms RW, Vassart G, Parmentier M: Resistance to HIV-1 infection in caucasian individuals bearing mutant alleles of the CCR-5 chemokine receptor gene. Nature. 1996, 382: 722-725. 10.1038/382722a0.PubMedView ArticleGoogle Scholar
  18. Liu R, Paxton WA, Choe S, Ceradini D, Martin SR, Horuk R, Mac-Donald ME, Stuhlmann H, Koup RA, Landau NR: Homozygous defect in HIV-1 coreceptor accounts for resistance of some multiply-exposed individuals to HIV-1 infection. Cell. 1996, 86: 367-377.PubMedView ArticleGoogle Scholar
  19. Paxton WA, Kang S: Chemokine receptor allelic polymorphisms: relationships to HIV resistance and disease progression. Semin Immunol. 1998, 10: 187-194. 10.1006/smim.1998.0132.PubMedView ArticleGoogle Scholar
  20. Gomez-Reino JJ, Pablos JL, Carreira PE, Santiago B, Serrano L, Vicario JL, Balsa A, Figueroa M, de Juan MD: Association of rheumatoid arthritis with a functional chemokine receptor, CCR5. Arthritis Rheum. 1999, 42: 989-992. 10.1002/1529-0131(199905)42:5<989::AID-ANR18>3.0.CO;2-U.PubMedView ArticleGoogle Scholar
  21. Garred P, Madsen HO, Petersen J, Marquart H, Hansen TM, Freiesleben Sorensen S, Volck B, Svejgaard A, Andersen V: CC chemokine receptor 5 polymorphism in rheumatoid arthritis. J Rheumatol. 1998, 25: 1462-1465.PubMedGoogle Scholar
  22. Cooke SP, Forrest G, Venables PJ, Hajeer A: The delta32 deletion of CCR5 receptor in rheumatoid arthritis. Arthritis Rheum. 1998, 41: 1135-1136. 10.1002/1529-0131(199806)41:6<1135::AID-ART24>3.0.CO;2-N.PubMedView ArticleGoogle Scholar
  23. Salvarani C, Boiardi L, Timms JM, Silvestri T, Ranzi A, Macchioni PL, Pulsatelli L, di Giovine FS: Absence of the association with CC chemokine receptor 5 polymorphism in polymyalgia rheumatica. Clin Exp Rheumatol. 2000, 18: 591-595.PubMedGoogle Scholar
  24. Tarlow JK, Blakemore AI, Lennard A, Solari R, Hughes HN, Steinkasserer A, Duff GW: Polymorphism in human IL-1 receptor antagonist gene intron 2 is caused by variable numbers of an 86-bp tandem repeat. Hum Genet. 1993, 91: 403-404.PubMedView ArticleGoogle Scholar
  25. Boiardi L, Salvarani C, Timms JM, Silvestri T, Macchioni PL, Pulsatelli L, di Giovine FS: Interleukin-1 cluster and tumor necrosis factor-α gene polymorphisms in polymyalgia rheumatica. Clin Exp Rheumatol. 2000, 18: 675-681.PubMedGoogle Scholar

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© BioMed Central Ltd 2001

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