Reduced amyloid-A-degrading activity in serum in amyloidosis associated with rheumatoid arthritis.
نویسندگان
چکیده
The ability to degrade amyloid A fibrils was studied in the serum of 31 patients with amyloidosis associated with rheumatoid arthritis, 33 patients with rheumatoid arthritis without amyloidosis, and 47 healthy controls. Fibrillar amyloid A protein and the radial diffusion method were used. The mean degrading activity in serum was significantly lower in patients with rheumatoid arthritis complicated by amyloidosis (58 +/- 19% SD of the activity in a pooled sample of sera from 100 healthy blood donors used as standard) than in patients with rheumatoid arthritis alone (78 +/- 14%; p less than 0.001) or controls (99 +/- 19%; p less than 0.001). Alpha 1-antitrypsin, concentrations of which were raised in both groups of patients, inhibited the degrading activity in serum even in low concentrations. A negative correlation between degrading activity and alpha 1-antitrypsin concentrations was observed. These findings suggest that reduced amyloid-A-degrading activity is due to inhibition rather than to deficiency of enzyme.
منابع مشابه
تعیین شیوع آمیلوئیدوز در بیماران مبتلا به آرتریت روماتوئید طول کشیده با روش آسپیراسیون نسج چربی
Background & Aim: Secondary amyloidosis(reactive) is an important late complication in chronic imflammatory disorder such as rheumatoid arthritis. The present study was undertaken to determine the prevalence of secondary amyloidosis in rheumatology patients with rheumatoid arthritis(RA) and assess associated clinical and laboratory characteristics. Patients & Methods: In this cross-sectiona...
متن کاملSerum amyloid protein levels in south american children with rheumatoid arthritis: a co-operative study.
Serum amyloid protein (SAA) levels were determined by radioimmunoassay in 90 children with juvenile rheumatoid arthritis (JRA). Significantly higher levels of SAA were present in children with the polyarticular and systemic forms of the disease. SAA levels correlate with disease activity, increasing during acute exacerbations, decreasing during remission and in patients having prednisone therap...
متن کاملDiarrhea, nephrotic syndrome and hidradenitis suppurativa: an unusual case.
In contrast to AL amyloidosis, where clonal plasma cells in bone marrow produce immunoglobulins that are amyloidogenic, and familial amyloidoses in which a mutant protein forms amyloid fibrils, the incidence of AA amyloidoses has been reduced since the treatment of infectious diseases and rheumatoid arthritis improved. AA amyloidoses are due to amyloid formed from serum amyloid A, an acute phas...
متن کاملTherapeutic Strategies in Amyloid A Amyloidosis Secondary to Rheumatoid Arthritis
Amyloidosis is a disorder of protein conformation and metabolism that results in the depo‐ sition of insoluble amyloid fibrils in tissues, which causes organ dysfunction; systemic amy‐ loidosis is characterized by failure of multiple organs and the presence of amyloid precursor protein in the serum [1-3]. Reactive amyloid A (AA) amyloidosis is one of the most severe complications of several chr...
متن کاملAmyloid Goiter Associated with Amyloidosis Secondary to Rheumatoid Arthritis
Amyloidosis refers to a variety of conditions in which amyloid proteins are abnormally deposited in organs and/or tissues. The most common forms of systemic amyloidosis are primary amyloidosis (PA) of light chains and secondary amyloidosis (SA) caused by chronic inflammatory diseases such as rheumatoid arthritis (RA). Although involvement of the thyroid gland by amyloid is a relatively common p...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- British medical journal
دوره 284 6316 شماره
صفحات -
تاریخ انتشار 1982