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. 2019 May 28;14(4):445–454. doi: 10.1093/ecco-jcc/jjz106

Table 2.

Demographic and phenotypic features at time of diagnosis with paediatric-onset Crohn’s disease. Comparisons are made between younger [A1a] and older [A1b] children as defined by Paris classification and between those with arbitrarily designated very-early-onset IBD [VEO-IBD] and others in A1a cohort.

Overall cohort A1 [2 to <17y] [n = 698] A1a <10y [n = 117] A1b [10 to <17y] [n = 581] p-value [A1a vs A1b] VEO-IBD [<6y] [n = 19] >6 to <10y [n = 98] p-value [<6y vs 6-10y]
Age in yearsa 12.9 [10.9, 14.8] 8.4 [7.1, 9.2] 13.7 [11.9, 15.1] <0.001 4.9 [3.8, 5.3] 8.8 [7.7, 9.3] <0.001
Gender [% male] 59% 61% 59% 0.60 58% 61% 0.79
Disease activity as presentation
wPCDAIa 55 [35,75] 50 [30,72] 55 [35,75] 0.43 53 [36,67] 50 [30,73] 0.75
PGA mild 26% 33% 24% 0.61 28% 34% 0.24
PGA moderate 44% 44% 44% 61% 41%
PGA severe 30% 23% 32% 11% 25%
Disease location
 L1 20% 12%* 21% 0.002 6% 13% 0.25
 L2 23% 36%* 20% 53% 33%
 L3 57% 52% 56% 41% 54%
 Any L4ab/L4bb 27% 33% 26% 0.18 Unknownc 33% -
Perianal fistulising disease 16% 12% 17% 0.08 6% 13% 0.69
Disease behaviour
Inflammatory [B1] 87% 96% 85% 0.001 94% 97% 0.58
Stricturing [B2] 9% 3% 11% 6% 2%
Penetrating [B3] 1% 0% 3% 0% 1%
Stricturing and penetrating [B2B3] 3% 1% 1% 0% 0%
Endoscopic severityd
Mild [SES-CD 3–6] 22% 24% 21% 0.75 23% 24% 0.48
Moderate [SES-CD 7–15] 35% 33% 36% 46% 30%
Severe [SES-CD ≥ 16] 43% 43% 43% 31% 46%
Linear growth at presentation
Height z score [mean ± SD] -0.3 ± 1.23 -0.04 ± 1.03 -0.28 ± 1.27 0.32 -0.15 ± 0.87 -0.44 ± 1.05 0.27
Initial induction therapy
EEN 35% 30% 36% 0.27 21% 32% 0.36
Corticosteroids 31% 37% 30% 0.14 42% 35% 0.60
Anti-TNFα 13% 9% 14% 0.06 5% 9% 0.58
5-ASA/SASP 10% 14% 9% 0.12 26% 12% 0.05
Other 11% 10% 11% 0.89 6% 12% 0.43

wPCDAI, Weighted Paediatric Crohn’s Disease Activity Index; PGA, Physician’s Global Assessment; SES-CD, Simplified Endoscopic Severity Score for CD; SD, standard deviation; EEN, exclusive enteral nutrition; anti-TNFα, anti-tumour necrosis factor alpha; 5-ASA/SASP,5-aminosalicylic acid or sulphasalazine; MRE, magnetic resonance enterography..

aValues are presented as median [interquartile range].

b11% of CD cohort did not undergo MRE; small bowel disease proximal to distal ileum [L4b] therefore not evaluated.

cMRE not performed among any children aged <6 years.

dSES-CD data missing in 4%.