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非典型乳糜泻患者(无论有无生长激素缺乏)的生长及成人身高

Growth and adult height in atypical coeliac patients, with or without growth hormone deficiency.

作者信息

Salardi Silvana, Cacciari Emanuele, Volta Umberto, Santoni Roberta, Ragni Luca, Elleri Daniela, Cicognani Alessandro, Vaira Dino

机构信息

Department of Pediatrics, University of Bologna, Bologna, Italy.

出版信息

J Pediatr Endocrinol Metab. 2005 Aug;18(8):769-75. doi: 10.1515/jpem.2005.18.8.769.

Abstract

OBJECTIVE

To evaluate the effect of a gluten-free diet on growth and adult height, when available, in coeliac children without gastrointestinal symptoms.

PATIENTS AND METHODS

Sixty-one coeliac children without gastro-intestinal symptoms were included in the study. The age at diagnosis was 9.50 +/- 3.3 years. Thirty-eight had short stature at diagnosis (< 10th percentile) and 23 had normal stature. Thirty-seven reached adult height.

RESULTS

After beginning the diet an increase in growth velocity was seen in 30 patients (responders) (20 with initial short stature), while in 31 patients (18 with short stature) there was no catch-up growth (non-responders). Bone age at diagnosis was significantly more delayed in the responders than in the non-responders. Target height was significantly higher in children with normal stature at diagnosis than those with short stature. Growth hormone (GH) deficiency was found and confirmed after 6-12 months of diet in 12 of the 38 patients (32%) with short stature. In the group of the 30 'short' patients who attained final height, target height was attained or improved in 12 patients (40%): in eight of the 16 (50%) responders and in four of the 14 (29%) non-responders; in eight (all responders) out of 22 (36%) without GH deficiency, and in four out of eight (50%) patients with GH deficiency treated with GH (all non-responders).

CONCLUSIONS

In children in whom coeliac disease is diagnosed because of short stature, a gluten-free diet will be successful if at diagnosis there is a delay of bone age and in the first year of diet there is an evident catch-up growth. When this does not occur, i.e. in half of the patients (18 out of 38), it may be because of an associated and transient GH deficiency. In these patients a period of GH replacement therapy as well as a gluten-free diet may improve their final height.

摘要

目的

评估无麸质饮食对无症状腹腔疾病患儿生长及成人身高(如适用)的影响。

患者与方法

61名无症状腹腔疾病患儿纳入本研究。诊断时年龄为9.50±3.3岁。38名患儿诊断时身材矮小(低于第10百分位数),23名患儿身材正常。37名患儿达到成人身高。

结果

开始饮食后,30名患者(反应者)(20名初始身材矮小)生长速度加快,而31名患者(18名身材矮小)未出现追赶生长(无反应者)。反应者诊断时的骨龄明显比无反应者延迟。诊断时身材正常的儿童目标身高显著高于身材矮小的儿童。38名身材矮小的患者中,12名(32%)在饮食6 - 12个月后发现并确诊生长激素(GH)缺乏。在30名达到最终身高的“矮小”患者组中,12名患者(40%)达到或改善了目标身高:16名反应者中的8名(50%)和14名无反应者中的4名(29%);22名无GH缺乏患者中的8名(36%)(均为反应者),以及8名接受GH治疗的GH缺乏患者中的4名(50%)(均为无反应者)。

结论

对于因身材矮小而诊断为腹腔疾病的儿童,如果诊断时骨龄延迟且饮食第一年有明显的追赶生长,无麸质饮食将会成功。如果未出现这种情况,即一半的患者(38名中的18名),可能是由于存在相关的短暂性GH缺乏。对于这些患者,一段时间的GH替代治疗以及无麸质饮食可能会改善他们的最终身高。

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