[特应性骨骼发育迟缓是哮喘患儿身材矮小和胸部畸形的可能原因]。

Kinderarztliche Praxis Pub Date : 1993-10-01
W F Baum, E Klöditz, H H Thiemann
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引用次数: 0

摘要

胸部畸形不仅发生在患有严重哮喘的患者身上,也发生在患有轻度哮喘的患者身上。它也发生在患有特应性皮炎的儿童和不伴有支气管哮喘的特应性家庭成员中。这一观察结果和哮喘儿童倾向于发育低下的事实,促使了对哮喘儿童的生理机能调查。观察哮喘本身还是特应性倾向是造成生长发育障碍的原因是很有趣的。本研究是一项横断面研究,涉及173名年龄在1岁半至18岁之间的哮喘男孩。该方案包括年龄、骨龄、骨成熟度差(骨密度:年龄差减去骨龄)、身高、哮喘类型和严重程度(通过治疗范围测量)。在整个组中,睡眠不足(身高<平均-2 SD)的比率为4.7%。外在哮喘患者的比率上升至6.6%。这相当于正常比率的两到三倍。11.6%的先证者表现出超过2年的骨骼发育迟缓。骨密度的程度与年龄和哮喘类型有显著的相关性,但与病程、严重程度或糖皮质激素治疗无关。因此,骨骼发育迟缓不能被认为是支气管哮喘的直接后果,然而,外源性和内源性哮喘患者骨密度平均值的显著差异表明,骨骼发育迟缓可能是特应性的,因此可能会说骨骼发育迟缓是特应性的。(摘要删节250字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Atopic skeletal retardation as a possible cause for short stature and thoracic deformity in children with asthma].

Deformities of the chest occur not only in asthmatics suffering from severe attacks, but also in those having a mild form of the disease. It also occurs in children with atopic dermatitis and in members of atopic families without concomitant bronchial asthma. This observation and the fact that asthmatic children tend towards hyposomia, has prompted auxological investigations of asthmatic children. It was of interest to see whether asthma itself or the atopic disposition is responsible for disturbances of growth and development. The investigation was carried out as a cross-sectional study involving 173 asthmatic boys aged 1 1/2-18 years. The programme included among other things age, bone age, bone maturity difference (BMD: difference age minus bone age) height, type and severity of asthma (measured by means of scope of therapy). The rate of hyposomia (height < mean -2 SD) amounted in the whole group to 4.7 per cent. It rose in the extrinsic asthmatics to 6.6 per cent. This corresponds with a rise of two or three times the normal rate. 11.6 per cent of the probands showed a skeletal retardation of more than 2 years. The degree of BMD showed a significant dependence on age and type of asthma but not on the duration of the disease, severity or glucocorticoid therapy. Skeletal retardation cannot, therefore, be regarded as a direct consequence of bronchial asthma, whereas the significantly different averages of BMD in extrinsic and intrinsic asthmatics point to an atopic genesis, hence it might be possible to speak of an atopic retardation of the skeleton.(ABSTRACT TRUNCATED AT 250 WORDS)

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