ab214016

Role of A-SAA in monitoring subclinical inflammation and in colchicine dosage in familial Mediterranean fever

A. Duzova, A. Bakkaloglu, N. Besbas, R. Topaloglu, S. Ozen, F. Ozaltin, Y. Bassoy, E. Yilmaz¹

Department of Pediatrics, Pediatric Nephrology and Rheumatology Unit; ¹Department of Medical Biology, Hacettepe University Faculty of Medicine, Ankara, Turkey

ABSTRACT
Objectives
1) To compare the sensitivity of serum amyloid A protein (A-SAA) and other acute phase proteins (APPs) in determining subclinical inflammation in patients with familial Mediterranean fever (FMF) during an attack-free period; 2) to define those clinical, laboratory features that may modify the A-SAA level; and 3) to evaluate the effect of an increase in the colchicine dose on the A-SAA level.

Methods
A-SAA, CRP, ESR, fibrinogen and ferritin levels were measured in 183 patients [88 F, 95 M; median age 11.0 years (1.0-20.0)] with FMF during an attack-free period. Mutational analysis was available in 157 patients. The colchicine dose was increased in 26 randomly chosen patients with no attacks within the last year; laboratory studies were repeated at the end of the second month.

Results
During an attack-free period, the median A-SAA level was 74 (6-1,500) mg/L; other APPs were within normal ranges in 49-93% of the patients. Age, gender, age at onset, age at diagnosis, the duration of treatment and the frequency of attacks had no significant effect on the A-SAA level. Homozygous and compound heterozygous patients had higher A-SAA levels than heterozygous patients [129 mg/L (8-1,500) versus 29 mg/L (6-216); p < 0.005]. There was a dramatic decrease in the A-SAA level [from 244 mg/L (16-1,400) to 35.5 mg/L (8-1,120); p < 0.001] and an increase in the hemoglobin (1.89 ± 0.10 mmol/L to 1.98 ± 0.19 mmol/L; p < 0.005) after the increase in colchicine dose in 26 patients.

Conclusion
Subclinical inflammation continues during an attack-free period in FMF patients. A-SAA was the best marker of subclinical inflammation. Patients who are homozygous or compound heterozygotes of MEFV mutations had higher A-SAA levels. An increase in the colchicine dose resulted in a dramatic decrease in A-SAA and an increase in hemoglobin level. These findings favor the use of A-SAA in drug monitoring.

Key words
Familial Mediterranean fever, serum amyloid A protein, C-reactive protein, erythrocyte sedimentation rate, acute phase proteins, subclinical inflammation, colchicine.

Please address correspondence to: Ali Duzova, MD, Department of Pediatrics, Pediatric Nephrology and Rheumatology Unit, Hacettepe University Faculty of Medicine, 06100, Ankara, Turkey.
E-mail: aduzova@hacettepe.edu.tr