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. 2022 Apr 19;66(2):229–236. doi: 10.20945/2359-3997000000457

Table 1. Sample description.

N = 94
Gender, n (%)
Female 49 (52,1%)
Male 45 (47,9%)
Age (years)
Mean 5,96
SD/Min-Max 3,811/1-18
Age at T1D diagnosis (years)
Mean 5,94
SD/Min-Max 2,57/1,08-10,75
Follow-up of T1D (years)
Mean 4,57
SD/Min-Max 2,94; 0,08 10,08
PH of AID n (%) 3 (3,2%)
AIT 3 (100%)
FH of AID n (%) 14 (14,9%)
T1D 6 (42,86%)
SLE 3 (21,43%)
CD 2 (14,29%)
Psoríase e and T1D 1 (7,14%)
AIT 2 (14,29%)
HLA screening, n (%)
Negative 8 (15,4%)
Positive 44 (84,6%)
IgA deficiency, n (%) 1 (1,1%)
Antibodies IgA/IgG at diagnosis, n (%)
Negative 90 (95,7%)
Positive 4 (4,3%)
Antibodies IgA/ IgG (2 years) n (%)
Not applicable 15 (16,7%)
Negative 75 (83,3%)
Antibodies IgA/IgG (5 years) n (%)
Not applicable 28 (31,1%)
Negative 62 (68,9%)
Biopsy histology n (%)
Number of biopsies 4 (4,3%)
Positive 4 (100%)
CD diagnosis n (%)
Negative 90 (95,7%)
Positive 4 (4,3%)

AID: autoimmune disease; AIT: autoimmune thyroiditis; CD: celiac disease; FH: family history; PH: past history; SLE: systemic lupus erythematosus.