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The
authors studied the role of NOD2 genotype on disease location
and severity and on growth retardation. Genotyping for 3 NOD2
single nucleotide polymorphism was performed in 93 patients who had
detailed growth records and disease assessments. Effects on z scores
for height and weight were assessed. NOD2 mutations were found
in 35% of patients; these mutations correlated with an ileal location
of the illness. Height retardation, both at the onset and at follow
up, was also associated with an ileal localization of the disease.
Use of steroids and immunosuppressant therapy also affected growth.
However the degree of disease severity was the strongest association
with impaired growth, height and weight failure odd ratios were 6.12
and 4.5 respectively. NOD2 genotype was not correlated with
growth retardation.
Wine
E, Reif SS, Leshinsky-Silver E, et al. Pediatric Crohn’s
disease and growth retardation: the role of genotype, phenotype and
disease severity. Pediatrics 2004;114:1281-6.
Editor’s
Comment: The first disease associated mutations for Crohn’s
disease were found in the NOD2/CARD15 gene located in the paracentric
region of chromosome 16.1-3 There were 3 loci identified
as independent risk factors for the development of the illness. These
mutations were not directly correlated with the presence of growth
retardation, a manifestation of Crohn’s disease that affect up
to one-third of the patients. NOD2 mutations were related to disease
location, and they were present in 43% of patients who had ileal
involvement. These children had height retardation when the disease
was diagnosed and it persisted during follow-up. Other studies have
also implicated NOD2 mutations with growth retardation.4
Short stature and poor growth in Crohn’s disease is known to be
primarily the result of inadequate nutrition due to anorexia and
postprandial pain leading to poor intake, compounded by malabsorption
and by other factors such as steroid treatment. Improvement usually
follows nutritional rehabilitation. The genotype may affect growth
through NOD2 mutations which determine the disease location and
severity.
Fima Lifshitz, MD
References - (linked to )
- Hugot JP, Chamaillard M, Zouali H, et al. Nature
2001;411:599-603.
- Ogura Y, Bonen DK, Inohara N, et al. Nature 2001;411:603-6.
- Hampe J, Cuthbert A, Croucher PJ, et al. Lancet
2001;357:1925-8.
- Lesage S, Zouali H, Cezard JP, et al. Am J Hum Genet
2002;70:845-57.
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