Article Text

other Versions

Fibronectin gene polymorphisms are associated with the development of B-cell lymphoma in type II mixed cryoglobulinemia.
  1. Martina Fabris (martina.fabris{at}
  1. Clinic of Rheumatology, University of Udine, Italy
    1. Luca Quartuccio (lucaquartuccio{at}
    1. Clinic of Rheumatology, University of Udine, Italy
      1. Valli De Re (vdere{at}
      1. IRCCS-National Cancer Institute, Aviano, Pordenone, Italy
        1. Gabriele Pozzato (g.pozzato{at}
        1. Division of Internal Medicine, U.C.O., University of Trieste, Italy
          1. Cesare Mazzaro (mazzaro{at}
          1. Division of Internal Medicine 2, S. Maria degli Angeli Hospital, Pordenone, Italy
            1. Clodoveo Ferri (clferri{at}
            1. Clinic of Rheumatology, University of Modena, Italy
              1. Chiara Baldini (a.tavoni{at}
              1. Clinic of Rheumatology, University of Pisa, Italy
                1. Sara Salvin (coxiella80{at}
                1. Clinic of Rheumatology, University of Udine, Italy
                  1. Salvatore De Vita (salvatore.devita{at}
                  1. Clinic of Rheumatology, University of Udine, Italy


                    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 Hodgkin’s lymphoma (NHL).

                    Methods. Samples from seventy-four patients, with MCsn (type II serum cryoglobulins and clinical signs of vasculitis) were studied. Fifty-eight (78.4%) patients were HCV-positive. Twenty-one (28.4%) 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 PCR and specific restriction enzyme digestions, following reported procedures. Plasma FN levels were analysed by ELISA, whenever possible.

                    Results. HaeIIIb and MspI allele and genotype frequencies did not differ between MCsn patients and HBDs. Of note, the DD-MspI (OR=5.99;CI=1.77-20.261, p=0.0039) and the AA-HaeIIIb (OR=4.82, CI=1.42-16.39, p=0.0176) homozygosis appeared significantly associated with the development of B-cell NHL in MCsn patients, with the HaeIIIb A allele possibly conferring an increased risk of NHL in the general population (OR=1.72, CI=1.128-2.635, p=0.0133). None of the other MCsn-related clinical manifestations were significantly associated with a particular genetic pattern. 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 risk of lymphoma development in MCsn.

                    • NHL
                    • cryoglobulinemic syndrome
                    • fibronectin
                    • gene polymorphism
                    • risk factor

                    Statistics from

                    Request Permissions

                    If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.