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首页> 外文期刊>Inflammatory bowel diseases >Final adult height of children with inflammatory bowel disease is predicted by parental height and patient minimum height Z-score.
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Final adult height of children with inflammatory bowel disease is predicted by parental height and patient minimum height Z-score.

机译:父母的身高和患者的最低身高Z分数可预测患有炎性肠病的儿童的最终成人身高。

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BACKGROUND: This study was designed to elucidate the contribution of parental height to the stature of children with inflammatory bowel disease (IBD), who often exhibit growth impairment. Accordingly, we compared patients' final adult heights and target heights based on measured parental heights and examined predictors of final adult height in pediatric IBD patients. METHODS: We prospectively analyzed the growth of 295 patients diagnosed between ages 1 and 18 (211 Crohn's disease [CD], 84 ulcerative colitis [UC]) and their family members (283 mothers, 231 fathers, 55 siblings). RESULTS: Twenty-two percent had growth impairment (height for age Z-score <-1.64, equivalent to <5th percentile on growth curve) in more than 1 measurement since diagnosis; most growth-impaired patients had CD (88% CD versus 12% UC). Parents of the growth-impaired group had lower mean height Z-scores compared to parents of nongrowth-impaired patients (-0.67 versus 0.02 for mothers [P < 0.001]; -0.31 versus 0.22 for fathers [P = 0.002]). For 108 patients who reached adult heights and had available parental heights, the growth-impaired group continued to demonstrate lower adult height Z-scores (-1.38 versus 0.07; P < 0.001). Adult heights were within 1 SD of target heights even for the growth-impaired group. Only 11.3% remained persistently growth-impaired in adulthood. Multivariate regression analysis demonstrated lower parental height and minimum patient height Z-score as significant predictors of lower final adult height in IBD. CONCLUSIONS: Parental height is a powerful determinant of linear growth even in the presence of chronic inflammation, and should be an integral part of the evaluation of growth in IBD children.
机译:背景:本研究旨在阐明父母身高对炎症性肠病(IBD)患儿的身材的贡献,这些患儿常表现出生长障碍。因此,我们根据测量的父母身高比较了患者的最终成人身高和目标身高,并检查了小儿IBD患者最终成人身高的预测指标。方法:我们前瞻性分析了295例1到18岁之间的患者(211克罗恩病[CD],84例溃疡性结肠炎[UC])及其家人(283例母亲,231例父亲,55个兄弟姐妹)的生长情况。结果:自诊断以来,有22%的患者有1项以上的生长障碍(Z评分的身高<-1.64,相当于生长曲线上的<5%)。大多数生长受损的患者患有CD(88%CD与12%UC)。与非生长障碍患者的父母相比,生长障碍组的父母的平均身高Z分数较低(母亲为-0.67对0.02(母亲[P <0.001];父亲为-0.31对0.22 [P = 0.002])。对于达到成人身高并有可用父母身高的108例患者,生长障碍组继续显示出较低的成人身高Z值(-1.38对0.07; P <0.001)。即使对于生长受损的人群,成年人的身高都在目标身高的1 SD之内。在成年后,仍然只有11.3%的人持续成长受损。多元回归分析表明,较低的父母身高和最低患者身高Z分数是IBD最终成人身高较低的重要预测指标。结论:即使在慢性炎症的情况下,父母的身高也是线性增长的有力决定因素,并且应成为IBD儿童生长发育评估不可或缺的部分。

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