Cagnoli Michele, Richter Roland, Böhm Peter, Knye Kathrin, Empting Susann, Mohnike Klaus
Otto-von-Guericke-University Magdeburg. Dept. of Paediatrics, University Magdeburg Universitätsplatz 2, 39106 Magdeburg, Germany.
Otto-von-Guericke-University Magdeburg. Dept. of Paediatrics, University Magdeburg Universitätsplatz 2, 39106 Magdeburg, Germany, E-mail:
Pediatr Endocrinol Rev. 2017 Nov;15(Suppl 1):119-122. doi: 10.17458/per.vol15.2017.crb.spontaneousgrowtheffect.
Whereas nutritional vitamin D deficient rickets affects many people world-wide, X-linked hypophosphatemic rickets (XLH, MIM 307800) has a prevalence of only 1:25.000. Like other rare diseases burden of disease in XLH and the effect of the current standard of care are inadequately described. Only few height data of untreated patients with XLH have been published. Here we report on height before start of therapy of 127 patients with XLH from 49 centres. One investigator collected all data from patient files documented at regular visits by treating physicians. Height standard deviation score (HSDS) was calculated and the geometrical mean was analysed. At birth all patients had a documented height within the healthy reference population. In this cross-sectional analysis of documented height at time of diagnosis decelerates until a mean age of 4.3 years to a nadir, i.e. lowest HSDS of -3.2 HSDS. Afterwards a spontaneous catch-up growth of +1.3 HSDS occurs until start of puberty. To assess the impact of calcitriol and phosphate supplementation on growth we analysed from a cohort of 18 patients treated at the Dept. of Paediatrics at O.-v.-Guericke-University Magdeburg. In this subgroup, size at birth and all time lowest HSDS (r=0.56 p=0.002) are correlated as well as all time low HSDS and last height during puberty (r=0.62 p=0.001). 10 of 18 patients were treated before age 18 months. Within this group the mean HSDS decelerates to -2.2 SDS at age 4.4 y. and increased to -1.4 SDS at age 9.9 years. Adult height, i.e. mean age 17.6 years was -2.4 HSDS. In conclusion, untreated children with XLR are characterized by normal length at birth, diminished growth rate compared to reference children until 4.3 years and spontaneous catch-up growth of 1.3 HSDS until start of puberty. Improved growth rate in XLR children occured by combined phosphate and calcitriol treatment before 18 months.
尽管营养性维生素D缺乏性佝偻病在全球影响着许多人,但X连锁低磷血症性佝偻病(XLH,MIM 307800)的患病率仅为1:25000。与其他罕见病一样,XLH的疾病负担以及当前治疗标准的效果描述不足。关于未经治疗的XLH患者的身高数据仅有少量发表。在此,我们报告了来自49个中心的127例XLH患者治疗开始前的身高情况。由一名研究人员从治疗医生定期记录的患者档案中收集所有数据。计算身高标准差评分(HSDS)并分析几何平均数。所有患者出生时的身高记录均在健康参考人群范围内。在本次对诊断时记录身高的横断面分析中,身高增长速度在平均年龄4.3岁之前逐渐减缓至最低点,即最低HSDS为 -3.2 HSDS。之后,在青春期开始前会出现1.3 HSDS的自发追赶生长。为评估骨化三醇和补充磷酸盐对生长的影响,我们分析了马格德堡奥托 - 冯 - 格里克大学儿科治疗的18例患者队列。在这个亚组中,出生时的身高与所有时间的最低HSDS(r = 0.56,p = 0.002)相关,所有时间的低HSDS与青春期的最终身高也相关(r = 0.62,p = 0.001)。18例患者中有10例在18个月龄前接受治疗。在该组中,平均HSDS在4.4岁时降至 -2.2 SDS,在9.9岁时升至 -1.4 SDS。成人身高,即平均年龄17.6岁时为 -2.4 HSDS。总之,未经治疗的XLH儿童的特点是出生时身长正常,与参考儿童相比在4.3岁之前生长速度减慢,在青春期开始前有1.3 HSDS的自发追赶生长。18个月龄前联合磷酸盐和骨化三醇治疗可使XLH儿童的生长速度加快。