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. 2018 Dec 12;3(2):67–73. doi: 10.1093/jcag/gwy067

Table 1.

Demographic characteristics: n = 122

Variable Statistics
Age, y, median (minimum, maximum) 11 (1, 18)
Gender, n (%)
Male 44 (36.1)
Female 78 (63.9)
Age diagnosed with CD, y, median (minimum, maximum) 7.0 (0.75, 16)
Time since start of the GFD, months, median (minimum, maximum) 32 (3, 208)
Perceived severity of diagnosis, n (%)
None 21 (17.2)
Mild 22 (18.0)
Moderate 38 (31.2)
Severe 41 (33.6)
Symptom onset prior to diagnosis, n, (%)
Less than one year 56 (46.3)
1–3 years 34 (28.1)
Over 3 years 23 (19.7)
No symptoms/NA 8 (6.6)
Co-morbidities, n, (%)
Autoimmune Thyroid Disease 5 (4.1)
Type 1 Diabetes 17 (13.9)
Down Syndrome 3 (2.5)
Selective IgA Deficiency 1 (0.8)
Reported Current total family income, n, (%)
<$29,252 2 (1.7)
$29,252–$49,999 3 (2.6)
$50,000–$69,999 9 (7.7)
$70,000–$89,999 14 (12.0)
Over $ 90,000 89 (76.1)
Member of Canadian Celiac Association, n, (%) 38 (31.4)
Education resources were provided at diagnosis, n, (%) 115 (94.3)
Family member with CD diagnosis, n, (%) 50 (41.3)
Ability to identify gluten-free food items, n, (%) 119 (97.5)
Requests more education on the gluten-free diet, n, (%) 55 (45.1)
Symptoms experienced if gluten is ingested, n, (%)
No 33 (8.0)
Yes 81 (68.6)
Unknown 4 (3.4)

Abbreviations: SD, Standard Deviation