Serum Amyloid A Level in Egyptian Children with Familial Mediterranean Fever
Author(s) -
Hala M. Lofty,
Huda Marzouk,
Yomna Farag,
Mohamed Nabih,
Iman Khalifa,
Noha Mostafa,
Ahmed Salah,
Laila Ahmed Rashed,
Kamal El-Garf
Publication year - 2016
Publication title -
international journal of rheumatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.8
H-Index - 33
eISSN - 1687-9279
pISSN - 1687-9260
DOI - 10.1155/2016/7354018
Subject(s) - familial mediterranean fever , serum amyloid a , medicine , subclinical infection , amyloidosis , serum amyloid a protein , gastroenterology , acute phase protein , aa amyloidosis , colchicine , inflammation , disease
Background and Objectives . SAA is an acute-phase reactant detected during an FMF attack or other inflammatory conditions. High SAA levels may increase the risk of amyloidosis. The aim of the study is to measure the serum amyloid A (SAA) level in a group of Egyptian children with familial Mediterranean fever (FMF) and study its various correlates, if any. Methods . The study enrolled seventy-one children with FMF. Results . SAA level was high in 78.9% of the studied patients with a mean of 81.62 ± 31.6 mg/L, and CRP was positive in 31% of patients. There was no significant releation between SAA level and any demographic or clinical manifestation. High SAA was more frequent in V726A allele (16.9%) followed by M694V allele (12.3%). Elevated SAA levels were more frequent in patients on low colchicine doses. Forty-five percent (45%) of patients have low adherence to colchicine therapy. Interpretation and Conclusion . High SAA levels were detected two weeks after last FMF attack in a large percentage of Egyptian FMF children. This indicates that subclinical inflammation continues during attack-free periods, and SAA could be used as a marker of it.
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