Matsushita Masaki, Kitoh Hiroshi, Mishima Kenichi, Kadono Izumi, Sugiura Hiroshi, Hasegawa Sachi, Nishida Yoshihiro, Ishiguro Naoki
Department of Orthopaedic Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Pediatr Int. 2016 Aug;58(8):705-8. doi: 10.1111/ped.12890. Epub 2016 Apr 5.
Achondroplasia (ACH) and hypochondroplasia (HCH) are the most common form of short-limb skeletal dysplasias caused by activated fibroblast growth factor receptor 3 (FGFR3) signaling. Although decreased bone mass was reported in gain-of-function mutation in Fgfr3 mice, both disorders have never been described as osteoporotic. In the present study, we evaluated bone mineral density (BMD) in ACH and HCH patients.
We measured spinal BMD (L1-L4) in 18 ACH and four HCH patients with an average age of 19.8 ± 7.5 years (range, 10-33 years). BMD Z-score in each individual was calculated for normalizing age and gender. Correlation between body mass index (BMI) and BMD was analyzed. Moreover, BMD and Z-score were compared between ACH patients and HCH patients.
The average BMD of ACH/HCH patients was 0.805 ± 0.141 g/cm(2) (range, 0.554-1.056 g/cm(2) ), resulting in an average Z-score of -1.1 ± 0.8 (range, -2.4 to 0.6) of the standard value. A slightly positive correlation was observed between BMI and BMD (r = 0.45; P = 0.13). There was no significant difference in BMD and Z-score between ACH and HCH patients.
Spinal BMD was reduced in ACH/HCH patients, and was mildly correlated with individual BMI. We should carefully monitor BMD and examine osteoporosis-related symptoms in adolescent and adult ACH/HCH patients. © 2016 Japan Pediatric Society.
软骨发育不全(ACH)和低软骨发育不全(HCH)是由激活的成纤维细胞生长因子受体3(FGFR3)信号传导引起的最常见的短肢骨骼发育不良形式。尽管在Fgfr3小鼠的功能获得性突变中报告了骨量减少,但这两种疾病从未被描述为骨质疏松症。在本研究中,我们评估了ACH和HCH患者的骨密度(BMD)。
我们测量了18例ACH患者和4例HCH患者的脊柱骨密度(L1-L4),这些患者的平均年龄为19.8±7.5岁(范围为10-33岁)。计算每个个体的BMD Z评分以对年龄和性别进行标准化。分析体重指数(BMI)与BMD之间的相关性。此外,比较了ACH患者和HCH患者之间的BMD和Z评分。
ACH/HCH患者的平均BMD为0.805±0.141 g/cm²(范围为0.554-1.056 g/cm²),导致标准值的平均Z评分为-1.1±0.8(范围为-2.4至0.6)。观察到BMI与BMD之间存在轻微的正相关(r = 0.45;P = 0.13)。ACH和HCH患者之间的BMD和Z评分没有显著差异。
ACH/HCH患者的脊柱骨密度降低,并且与个体BMI轻度相关。我们应该仔细监测青少年和成年ACH/HCH患者的BMD并检查骨质疏松相关症状。©2016日本儿科学会。