Skip to main content
. 2018 Oct 12;6(1):34–37. doi: 10.5152/eurjrheum.2018.18115

Table 2.

Summary of the demographic and clinical features of the patients

Group 1 (Patients with exon 2 mutations)
n:82
Group 2 (Patients with exon 10 mutations)
n:1304
Group 3 (Patients with exon 2 and 10 mutations)
n:140
p Bonferroni’s correction (post hoc test)
Sex [M n (%)] 28 (34.1) 630 (48.3) 80 (57.1) 0.001 1–2: p=0.016
1–3: p=0.012
2–3: p=0.05
Age at baseline clinical visit [Median (%25–%75)] 26.5 (19.75–37) 24 (18–34) 27.5 (21.25–37.75) 0.114
Age at onset of symptoms [Median (%25–%75)] 20 (13–26) 14 (8–21) 19 (13–25) <0.001 2–3: <0.001
2–1: <0.001
1–3: 0.931
Fever 71 (86.6) 1196 (91.7) 128 (91.4) 0.274
Peritonitis 78 (95.1) 1232 (94.5) 131 (93.6) 0.871
Pleuritis 37 (45.1) 653 (50.1) 68 (48.6) 0.660
ELE* 3 (3.7) 351 (26.9) 24 (17.1) <0.001 1–2: <0.001
1–3: 0.003
2–3: 0.01
Arthritis 22 (26.8) 594 (45.6) 45 (32.1) <0.0001 1–2: 0.01
1–3: 0.45
2–3: 0.002
Myalgia 12 (14.6) 199 (15.3) 19 (13.6) 0.863
Vasculitis 2 (2.4) 100 (7.7) 5 (3.6) 0.490
Amyloidosis 3 (3.7) 133 (10.2) 6 (4.3) 0.014 1–2: 0.02
1–3: 1
2–3: 0.05
CRF** 1 (1.2) 69 (5.3) 3 (2.1) 0.75
Family history of FMF 32 (39) 780 (59.8) 73 (52.1) <0.001 1–2: <0.001
1–3: 0.07
2–3: 0.08
Family history of amyloidosis 5 (6.1) 267 (20.5) 25 (17.9) 0.005 1–2: 0.01
1–3: 0.01
2–3: 0.51
Family history of CRF 3 (3.7) 79 (6.1) 7 (5) 0.606

Data are given as n (%);

*

ELE: erysipel-like erythema;

**

CRF: chronic renal failure