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Male Sex Coupled with Articular Manifestations Cause a 4-fold Increase in Susceptibility to Amyloidosis in Patients with Familial Mediterranean Fever Homozygous for the M694V-MEFV Mutation
RUTH GERSHONI-BARUCH, RIVA BRIK, MERAV LIDAR, MARWAN SHINAWI, and AVI LIVNEH
ABSTRACT. Methods. A total of 124 patients with FMF who were all homozygous for the M694V mutation, including 47 patients with nephropathic amyloidosis, were identified. A detailed chart review and physical examination were undertaken to determine demographic characteristics, history, clinical manifestations, and treatment, and we calculated the disease severity score from the Tel-Hashomer key. Results. A preponderance of male patients was documented (73:51; 1.4). The overall male:female ratio was significantly higher among patients with amyloidosis (32:15; 2.1) compared to patients without amyloidosis (41:36; 1.1). FMF severity scores, independently calculated for male and female patients, were equally high (9.5 ± 3.0 and 9.7 ± 2.8, respectively). The frequency of arthritic attacks, significantly higher in women than men (p = 0.015), remained notably higher in male FMF patients with amyloidosis compared to male FMF patients without amyloidosis (p = 0.002). Significant correlation between arthritis attacks and amyloidosis was found (R > 0.285, p < 0.001). Conclusion. Susceptibility to renal amyloidosis is influenced both by sex and the occurrence of joint attacks, acting as 2 MEFV independent factors (OR 2.37, 95% CI 1.06-5.26 and OR 3.27, 95% CI 1.23-8.68, respectively). (J Rheumatol 2003;30:308-12) Key Indexing Terms:
FAMILIAL MEDITERRANEAN FEVER
From the Departments of Human Genetics and Pediatrics, Rambam Medical Center; Bruce Rappoport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa; Heller Institute of Medical Research, Sheba Medical Center, Tel-Hashomer; and Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel. R. Gershoni-Baruch, MD, Senior Lecturer and Chief, Department of Medical Genetics; R. Brik, MD, Senior Lecturer, Chief, Department of Pediatrics; M. Lidar, MD, Department of Internal Medicine; M. Shinawi, MD, Department of Pediatrics; A. Livneh, MD, Professor of Medicine/Rheumatology, Chief, Department of Internal Medicine. Address reprint requests to Dr. R. Gershoni-Baruch, Department of Medical Genetics, Rambam Medical Center, Haifa, Israel. E-mail: rgershoni@rambam.health.gov.il Submitted February 12, 2002; revision accepted June 6, 2002. |