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首页> 外文期刊>Journal of the American Academy of Dermatology >Correlates of low bone mass in children with generalized forms of epidermolysis bullosa.
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Correlates of low bone mass in children with generalized forms of epidermolysis bullosa.

机译:小儿广泛性大疱性表皮松解症儿童低骨质的相关性。

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BACKGROUND: Epidermolysis bullosa (EB) is a family of rare, heterogeneous, genetic disorders characterized by fragility of the skin and mucous membranes. Reduced bone mass and fractures have been recognized as complications of generalized forms of EB. OBJECTIVES: We sought to describe the range and to estimate the prevalence of low bone mass in children with generalized EB, and to identify correlates of low bone mass in this population. METHODS: This was a prospective, observational study of 24 patients with generalized EB. Each patient completed a history, physical examination, laboratory studies, bone age, and x-rays of the lumbar spine. Those aged 6 years and older underwent dual energy x-ray absorptiometry scans of the lumbar spine. Primary outcomes were areal bone mineral density (aBMD) based on chronologic age, bone age, and adjusted for height Z-score. Descriptive statistics were used to summarize results, and linear regression was used to determine factors associated with low aBMD. RESULTS: Mean lumbar spine aBMD Z-scores +/- SD were: -2.6 +/- 1.4 for chronologic age, -1.7 +/- 1.3 for bone age, and -1.0 +/- 1.2 after adjusting for height Z-score. aBMD Z-scores were less than or equal to -2 in 64% for chronologic age, 50% for bone age, and 28% after adjusting for height Z-score. aBMD correlated with height Z-score, weight Z-score, extensive blistering, immobility, albumin, hemoglobin, iron, erythrocyte sedimentation rate, and c-reactive protein values. LIMITATIONS: Small sample size was a limitation. CONCLUSIONS: Children with severe, generalized recessive dystrophic EB have low aBMD for age. Deficits in aBMD were reduced after adjusting for delayed skeletal maturation and small body size.
机译:背景:大疱表皮松解症(EB)是一类罕见的,异质性,遗传性疾病,其特征是皮肤和粘膜易碎。骨量减少和骨折已被认为是全身性EB的并发症。目的:我们试图描述广泛性EB患儿的低骨量范围并估计其患病率,并确定该人群中低骨量的相关性。方法:这是一项对24例全身性EB患者的前瞻性观察研究。每位患者均完成了病史,体格检查,实验室研究,骨龄和腰椎X线检查。年龄在6岁及以上的患者接受了腰椎的双能X线骨密度仪扫描。主要结局是根据年龄,骨骼年龄并根据Z值高度调整后的面骨矿物质密度(aBMD)。描述性统计用于总结结果,线性回归用于确定与低aBMD相关的因素。结果:腰椎aBMD平均Z评分+/- SD为:按年龄排序为-2.6 +/- 1.4,按年龄分类的为-1.7 +/- 1.3,针对高度Z评分调整后为-1.0 +/- 1.2。按年龄排序,aBMD Z得分小于或等于-2,在年龄上为64%,在骨骼年龄为50%,在调整高度Z得分后为28%。 aBMD与身高Z分数,体重Z分数,广泛的水疱,固定性,白蛋白,血红蛋白,铁,红细胞沉降率和c反应蛋白值相关。局限性:小样本量是一个局限。结论:患有严重,全身性隐性营养不良性EB的儿童的年龄aBMD低。在为延迟骨骼成熟和小体型进行调整后,aBMD的缺陷得以减少。

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