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Serum amyloid A serum concentrations and genotype do not explain low incidence of amyloidosis in Hyper-IgD syndrome
Authors:JCH van der Hilst  JPH Drenth  EJ Bodar  J Bijzet  JWM van der Meer  A Simon
Affiliation:1. Department of General Internal Medicinej.vanderhilst@aig.umcn.nl;3. Department of Gastroenterology, UMC St. Radboud, Nijmegen, The Netherlands;4. Department of General Internal Medicine;5. Department of Rheumatology, University Hospital Groningen, Groningen, The Netherlands
Abstract:
Background.?Hyper-IgD and periodic fever syndrome (HIDS) is an autosomal recessively inherited disorder characterized by recurrent episodes of fever and inflammation. Unlike other chronic inflammatory conditions, amyloidosis is very rare in HIDS. For deposition of amyloid of the AA type, high concentrations of SAA are a prerequisite, together with certain SAA1 gene polymorphisms. The SAA1.1 genotype predisposes for amyloidosis, while SAA1.5 genotype exerts a protective effect.

Aim of the study.?To determine if SAA concentrations and SAA1 gene polymorphisms could explain the virtual absence of amyloidosis in HIDS patients.

Methods.?We measured SAA and CRP concentrations in serum of 20 HIDS patients during an attack and during the asymptomatic phase. Genotype of SAA1 gene was determined in 60 HIDS patients.

Results.?SAA serum concentrations during attacks were very high (median 205?mg/l; range 75–520?mg/l, normal?p?=?0.32).

Conclusion.?Patients with HIDS have high SAA during attacks and show sub-clinical inflammation when asymptomatic. The low incidence of amyloidosis cannot be explained by a predominance of non amyloidogenic SAA related genotypes.
Keywords:Periodic fever  Hyper-IgD syndrome  serum amyloid A  amyloidosis  SAA1 genotype
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