J. Markowitz et al., GROWTH FAILURE IN PEDIATRIC INFLAMMATORY BOWEL-DISEASE, Journal of pediatric gastroenterology and nutrition, 16(4), 1993, pp. 373-380
To assess whether children with inflammatory bowel disease (IBD) devel
op permanent impairment of linear growth, we analyzed records from 48
young adults who had IBD during childhood or early adolescence (Tanner
I-III; 11.8 +/- 2.4 years old at diagnosis). All were fully grown (Ta
nner V; 21.1 +/- 3.0 years) at last examination. Adult heights were pr
edicted from data obtained at or shortly after the diagnosis of IBD by
three methods: height for age percentile, the Bailey-Pinneau (BP), an
d Roche-Wainer-Thissen (RWT) methods. Predicted adult heights were the
n compared with the actual ultimate height of each subject. Permanent
growth failure occurred in 19-35% of subjects, depending upon the meth
od used to assess growth. Overall, 31% (15 of 48) of the subjects had
deficits of adult height identified by two or more methods, including
14 of 38 (37%) of those with Crohn's disease but only one of 10 with u
lcerative colitis. Age at diagnosis of IBD, age at last examination, a
ge at cessation of linear growth, and site of IBD did not differ betwe
en impaired and normal growth groups. Duration of corticosteroid use w
as longer (p < 0.05) in growth-impaired subjects. In addition, althoug
h 60% of all subjects had periods of poor growth that put them in heig
ht-for-age percentiles two or more major growth channels below previou
s percentiles, only 19% remained at these levels upon achieving their
final adult heights. Permanent impairment of linear growth leading to
clinically meaningful deficits of ultimate adult height is common in p
atients with IBD in childhood or early adolescence. New therapeutic ap
proaches are needed to address this problem.