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首页> 外文期刊>The Journal of rheumatology >Linear growth and final height in patients with systemic juvenile idiopathic arthritis treated with longterm glucocorticoids.
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Linear growth and final height in patients with systemic juvenile idiopathic arthritis treated with longterm glucocorticoids.

机译:长期糖皮质激素治疗的系统性幼年特发性关节炎患者的线性生长和最终身高。

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OBJECTIVE: To assess linear growth and final height in patients given glucocorticoids during childhood for systemic juvenile idiopathic arthritis (JIA). METHODS: Heights throughout followup for JIA and final height were recorded in 24 patients. Height data were expressed as the height standard deviation score for chronological age (HSDS/CA). Final height was compared to reference values for the French population and to target height. RESULTS: During glucocorticoid therapy, mean loss of HSDS/CA was -2.7 +/- 1.5 and was positively correlated with prednisone therapy duration (p < 0.01). After prednisone discontinuation, 17 patients (70%) had catch-up growth and 7 (30%) continued to experience slow linear growth. Mean final height was -2.0 +/- 1.8 HSDS and was correlated with mean height at prednisone discontinuation (p < 0.0001). Mean final height was significantly greater in the patients with catch-up growth at prednisone discontinuation (-1.5 +/- 1.6 vs -3.6 +/- 1.2 HSDS), and 87% of patients had a final height below their target height. CONCLUSION: These data suggest that chronic inflammation and prednisone therapy may adversely affect growth in patients with JIA, and that final height may be closely dependent both on the severity of growth retardation during the active phase of the disease and on linear growth after remission. Thus treatments like growth hormone presently under investigation to improve final height may be most effective when given early after disease onset and/or at remission.
机译:目的:评估儿童期全身性幼年特发性关节炎(JIA)接受糖皮质激素治疗的患者的线性生长和最终身高。方法:记录了JIA整个随访期间的身高和最终身高,其中24例患者。身高数据表示为按年龄划分的身高标准偏差评分(HSDS / CA)。将最终身高与法国人口的参考值和目标身高进行比较。结果:在糖皮质激素治疗期间,HSDS / CA的平均损失为-2.7 +/- 1.5,与泼尼松治疗时间呈正相关(p <0.01)。泼尼松停药后,有17名患者(70%)出现了追赶性生长,而7名患者(30%)继续出现缓慢的线性增长。平均最终身高为-2.0 +/- 1.8 HSDS,与泼尼松停药时的平均身高相关(p <0.0001)。泼尼松停药后有追赶性生长的患者的平均最终身高明显更高(-1.5 +/- 1.6 vs -3.6 +/- 1.2 HSDS),并且87%的患者的最终身高低于目标身高。结论:这些数据表明,慢性炎症和泼尼松治疗可能会对JIA患者的生长产生不利影响,最终高度可能与疾病活动期生长迟缓的严重程度以及缓解后的线性生长密切相关。因此,目前正在研究中以改善最终身高为目标的诸如生长激素的治疗​​,在疾病发作后和/或缓解后尽早使用可能是最有效的。

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