SAA1 ?/? alleles in amyloidosis
Özet
Background: Amyloidosis, mainly AA type, is one of the common diseases in nepbrology clinics in Turkey. AA type amyloidosis is a complication of various chronic infections or inflammatory diseases such as familial Mediterranean fever (FMF), rheumatoid arthritis (RA), tuberculosis and bronchiectasis. A controversy exists in the literature regarding the relationship between SAA1 genotypes and AA type amyloidosis. This study aimed to investigate SAA1 gene polymorphism in different patient groups: 1) amyloidosis, 2) FMF and 3) healthy controls. Methods: Eighty-two patients from the three groups were included in the study: 1) amyloidosis, 2) FMF without amyloidosis, and 3) healthy controls. SAA1 genotypes were studied by the polymerase chain reaction/restriction fragment length polymorphism (PCR-RFLP) method. Results: The homozygous ?/? genotype is the most common SAA1 genotype among patient groups with amyloidosis, and the ?/? genotype frequency is significantly higher than in healthy controls (68 vs. 38%, p<0.05). Conclusions: The SAA1 ?/? genotype is a risk factor for AA type amyloidosis in Caucasoid populations and more studies are needed to investigate why the ?/? genotype is associated with AA type amyloidosis Japan. © Società Italiana di Nefrologia.
