Research Article

Clinical Characteristics of EGPA Patients in Comparison to GPA Subgroup with Increased Blood Eosinophilia from POLVAS Registry

Table 2

Demographic and clinical characteristics of EGPA patients diagnosed before and after the 2012 year.

Variable≤2012 (n = 70)>2012 (n = 41)p-Value

Demographic characteristics

Age at diagnosis, years41.3 (33.1–52.4)49.17 (40.3–58.4)<0.01
Female gender, number (%)51 (72.86)26 (63.41)0.30
Smoking in the past, number (%)4 (5.71)8 (19.51)0.97

Clinical manifestations

Constitutional symptoms65 (92.86)34 (82.93)0.23
Musculoskeletal31 (44.29)24 (58.54)0.11
Cutaneous37 (52.86)21 (51.22)0.96
Ocular3 (4.29)4 (9.76)0.25
ENT64 (91.43)28 (68.29)<0.01
Respiratory69 (98.57)38 (92.68)0.62
Cardiovascular35 (50.00)12 (29.27)
Gastrointestinal20 (28.57)12 (29.27)0.89
Renal20 (28.57)10 (24.39)0.64
Central nervous system6 (8.57)5 (12.20)0.52
Neurological36 (51.43)17 (41.46)0.36
Flare-ups, number3 (1–3)0 (0–1)<0.01
Flare-ups, number/time of observation, years0.28 (0.18–0.35)0.00 (0.00–0.33)
Patients with flare-ups requiring hospital admission, number15 (21.43)12 (29.27)0.26

Remission induction therapy

Oral glucocorticosteroids69 (98.57)34 (82.93)α<0.01
Glucocorticosteroid pulses56 (80.00)18 (43.90)<0.01
Cyclophosphamide31 (44.29)18 (43.90)0.75
Azathioprine11 (15.71)3 (7.32)0.25
Methotrexate8 (11.43)13 (31.71)<0.01
Mycophenolate mofetil0 (0.00)5 (12.20)<0.01
The cumulative time of glucocorticosteroid treatment, years7.00 (5.00–10.00)2.00 (1.00–4.00)<0.01
The cumulative dose of intravenous glucocorticosteroids (g)4.20 (0.00–8.60)1.45 (0.00–6.00)0.37

Maintenance therapy

Oral glucocorticosteroids37 (52.86)32 (78.05)0.08
Azathioprine19 (27.14)15 (36.59)0.36
Methotrexate9 (12.86)19 (46.34)<0.01
Mycophenolate mofetil5 (7.14)11 (26.83)0.09

Laboratory parameters

Blood eosinophilia (/μl)β4,946 (2,400–8,253)3,200 (358–5,800)<0.01
Max. CRP at diagnosis (mg/l)23.9 (10.0–58.0)22.7 (10.0–60.0)0.91
ANCA-positive, n (%)23 (32.86)22 (53.66)0.11

Categorical variables are presented as numbers (percentages), continuous variables as median, and 0.25–0.75 interquartile range. αAmong seven cases that did not receive oral GCs in the remission induction phase, all but one were administered intravenous GCs and the remaining one cyclophosphamide; in the maintenance therapy, all received oral GCs. βData available in 55 (78.57.%) and 26 (63.41%) EGPA patients in the first and second subgroups, respectively. Statistically significant differences are highlighted with an asterisk. Abbreviations: ANCA, anti-neutrophil cytoplasmic antibodies; CRP, C-reactive protein; EGPA, eosinophilic granulomatosis with polyangiitis; and ENT, ear/nose/throat.