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儿童大疱性表皮松解症的普遍型的低骨量相关因素。

Correlates of low bone mass in children with generalized forms of epidermolysis bullosa.

机构信息

Department of Dermatology, Stanford University School of Medicine, Stanford, CA 94305-5168, USA.

出版信息

J Am Acad Dermatol. 2011 Nov;65(5):1001-9. doi: 10.1016/j.jaad.2010.08.028. Epub 2011 May 7.

Abstract

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.

摘要

背景

大疱性表皮松解症(EB)是一组罕见的、异质性的遗传性疾病,其特征为皮肤和黏膜脆弱。已认识到骨质减少和骨折是 EB 全身性形式的并发症。

目的

我们旨在描述广泛性 EB 患儿的骨量减少范围,并估计其患病率,并确定该人群中骨量减少的相关因素。

方法

这是一项对 24 例广泛性 EB 患儿进行的前瞻性、观察性研究。每位患者均完成病史、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腰椎双能 X 线吸收法骨密度扫描。主要结局是基于年龄、骨龄和身高 Z 评分调整后的面积骨矿物质密度(aBMD)。使用描述性统计来总结结果,并使用线性回归来确定与低 aBMD 相关的因素。

结果

平均腰椎 aBMD Z 评分±SD 为:年龄为 -2.6±1.4,骨龄为-1.7±1.3,身高 Z 评分调整后为-1.0±1.2。年龄的 aBMD Z 评分小于或等于-2 的占 64%,骨龄为 50%,身高 Z 评分调整后为 28%。aBMD 与身高 Z 评分、体重 Z 评分、广泛水疱、活动受限、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

样本量小是一个局限性。

结论

患有严重、全身性隐性营养不良性 EB 的儿童的年龄相关 aBMD 较低。在调整骨骼成熟延迟和身材矮小后,aBMD 缺陷减少。

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