OBJECTIVE: To analyse FN gene polymorphisms in type II mixed cryoglobulinemic syndrome (MCsn), an immune-complex mediated systemic vasculitis linked to hepatitis C virus (HCV) infection and characterized by rheumatoid factor (RF) positive B-cell proliferation at high risk for the progression into non Hogkin's lymphoma (NHL).METHODS: Samples from eighty-one patients, with MCsn (type II serum cryoglobulins and clinical signs of vasculitis were studied. Sixty-five (65/81, 80.3%) patients were HCV-positive. Twenty-one (25.9%) patients had developed a B-cell NHL during the course of MCsn. Seventy-two patients with HCV-negative and MC-unrelated NHL and 110 healthy blood donors (HBDs) were taken as controls. HaeIIIb and MspI FN gene polymorphisms were analysed by ELISA, whenever possible.RESULTS: HaeIIIb and MspI allele and genotypic frequencies did not differ between MCsn patients and HBDs. Of note, the DD-MspI allele and genotype frequencies did not differ between MCsn patients and HBDs. Of note, the DD-MspI (OR = 5.56; DI = 1.67-18.51, p = 0.0046) and the AA-HaeIIIb (OR = 5.54, CI = 1.64- 18.76, p = 0.0066) homozygosis appeared significantly and independently associated with the development of B-cell NHL in MCsn patients, with the HaeIIIbA allele possibly conferring an increased risk of NHL in the general population (OR = 1.72, CI = 1.128-2.635, p = 0.0133). In contrast, the major vasculitic manifestations, such as peripheral neuropathy, skin ulcers and glomerulonephritis tended to be associated with the counterpart MspI C allele. No association between FN plasma levels and FN genotypes was found.CONCLUSION: Genotyping for MspI and HaeIIIb FN gene polymorphisms may be clinically relevant to define the predisposition to the major clinical manifestations in MCsn
[Fibronectin gene polymorphisms and clinical manifestations of mixed cryoglobulinemic syndrome: increased risk of lymphoma associated to MspI DD and HaeIII AA genotypes] / Fabris, M; Quartuccio, L; DE RE, V; Pozzato, G; Mazzaro, C; Tavoni, A; Ferri, Clodoveo; Salvin, S; Lerussi, A; Fabro, C; Bombardieri, S; DE VITA, S.. - In: REUMATISMO. - ISSN 0048-7449. - STAMPA. - 60(2008), pp. 28-34.
Data di pubblicazione: | 2008 |
Titolo: | [Fibronectin gene polymorphisms and clinical manifestations of mixed cryoglobulinemic syndrome: increased risk of lymphoma associated to MspI DD and HaeIII AA genotypes] |
Autore/i: | Fabris, M; Quartuccio, L; DE RE, V; Pozzato, G; Mazzaro, C; Tavoni, A; Ferri, Clodoveo; Salvin, S; Lerussi, A; Fabro, C; Bombardieri, S; DE VITA, S. |
Autore/i UNIMORE: | |
Rivista: | |
Volume: | 60 |
Pagina iniziale: | 28 |
Pagina finale: | 34 |
Codice identificativo Scopus: | 2-s2.0-57149136510 |
Codice identificativo Pubmed: | 18810851 |
Citazione: | [Fibronectin gene polymorphisms and clinical manifestations of mixed cryoglobulinemic syndrome: increased risk of lymphoma associated to MspI DD and HaeIII AA genotypes] / Fabris, M; Quartuccio, L; DE RE, V; Pozzato, G; Mazzaro, C; Tavoni, A; Ferri, Clodoveo; Salvin, S; Lerussi, A; Fabro, C; Bombardieri, S; DE VITA, S.. - In: REUMATISMO. - ISSN 0048-7449. - STAMPA. - 60(2008), pp. 28-34. |
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