Levine Arie, Shamir Raanan, Wine Eytan, Weiss Batya, Karban Amir, Shaoul Ron R, Reif Shimon S, Yakir Benjamin, Friedlander Marcello, Kaniel Yael, Leshinsky-Silver Esther
Pediatric Gastroenterology and Nutrition Unit, E. Wolfson Medical Center, Holon, Israel.
Am J Gastroenterol. 2005 Jul;100(7):1598-604. doi: 10.1111/j.1572-0241.2005.41737.x.
Delayed growth is common in pediatric Crohn's disease (CD). Multiple factors have been shown to affect growth in this situation, the most prominent being the presence and severity of inflammation and inadequate nutritional intake. Inflammation, anorexia, and weight loss are all manifestations of circulating TNF-alpha, which is elevated in CD. The ability to secrete TNF-alpha may be affected by polymorphisms in the TNF-alpha promoter. The aim of our study was to determine whether growth retardation and disease severity in pediatric onset CD are affected by TNF promoter genotype.
Genotyping for TNF-alpha and NOD2/CARD15 single nucleotide polymorphisms was performed in 87 patients with detailed growth records. Parameters including disease location and disease severity were recorded, and the effect of these polymorphisms on Z-scores for height and weight at disease onset and during follow-up were analyzed.
Lower age of onset was linked to more height retardation, while the presence of colonic disease and the absence of ileal disease were more likely to predict the absence of growth retardation. The presence of two polymorphisms thought to decrease circulating TNF-alpha was associated with higher mean Z-scores for height and a trend toward less growth retardation. Two other polymorphisms were modestly associated with disease severity.
Polymorphisms in the TNF-alpha promoter may independently modulate growth and disease severity in pediatric onset CD. The effect of these polymorphisms does not appear to be mediated via weight loss, and is relatively modest.
生长发育迟缓在儿童克罗恩病(CD)中很常见。多种因素已被证明会影响这种情况下的生长发育,其中最突出的是炎症的存在和严重程度以及营养摄入不足。炎症、厌食和体重减轻都是循环肿瘤坏死因子-α(TNF-α)的表现,而在CD中该因子水平会升高。TNF-α启动子的多态性可能会影响其分泌能力。我们研究的目的是确定儿童期发病的CD中生长发育迟缓及疾病严重程度是否受TNF启动子基因型影响。
对87例有详细生长记录的患者进行TNF-α和NOD2/CARD15单核苷酸多态性基因分型。记录包括疾病部位和疾病严重程度等参数,并分析这些多态性对疾病发作时及随访期间身高和体重Z值的影响。
发病年龄较小与更严重的身高发育迟缓有关,而结肠疾病的存在及回肠疾病的缺失更有可能预示无生长发育迟缓。两种被认为会降低循环TNF-α水平的多态性与更高的平均身高Z值及生长发育迟缓减轻的趋势相关。另外两种多态性与疾病严重程度有一定关联。
TNF-α启动子的多态性可能独立调节儿童期发病的CD的生长发育及疾病严重程度。这些多态性的影响似乎并非通过体重减轻介导,且相对较小。