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儿童时期接受急性淋巴细胞白血病治疗的患者存在身高缺陷和 GH/IGF-1 轴受损。

Height deficit and impairment of the GH/IGF-1 axis in patients treated for acute lymphoblastic leukemia during childhood.

机构信息

Hospital das Clínicas, Universidade Federal de Goiás, Goiânia, Brazil.

出版信息

Horm Res Paediatr. 2013;79(1):9-16. doi: 10.1159/000343936. Epub 2013 Jan 10.

Abstract

BACKGROUND

Endocrine complications after acute lymphoblastic leukemia (ALL) are common.

METHODS

Final height, GH/IGF-1 axis, and body mass index were analyzed after 13.7 (7.0-20.7) years from diagnosis in 34 boys aged <12 years at diagnosis and 41 girls <10 years at diagnosis. A modified German BFM-83 ALL protocol included (n = 42) or did not include (n = 33) prophylactic cranial irradiation. In 27 patients, GH after insulin tolerance test, IGF-1, cortisol, free T(4) and estradiol/testosterone were determined.

RESULTS

Final height was significantly reduced (mean Z-score for height between final height and diagnosis, ΔHAZ = -0.61, p = 0.0001). At that point, 3 patients were obese (4%) and 17 were overweight (22.7%). Patients aged ≤ 4 years at diagnosis and those irradiated had a greater loss in final height (p = 0.001 and p = 0.008, respectively). Abnormalities in GH/IGF-1 axis were observed in 4 patients: 3 had a GH peak <6 ng/ml and 1 had a serum IGF-1 concentration <25 ng/ml. Growth deficit was significantly higher in patients with hormonal deficiency (p = 0.006).

CONCLUSIONS

Treatment of ALL during childhood is associated with final height deficit. Young age at diagnosis and radiotherapy were the major risk factors. GH/IGF-1 deficiency was found particularly in irradiated patients, even though it was detected in 1 non-irradiated patient.

摘要

背景

急性淋巴细胞白血病(ALL)后发生内分泌并发症较为常见。

方法

对 34 名诊断时年龄<12 岁的男孩和 41 名诊断时年龄<10 岁的女孩,在诊断后 13.7(7.0-20.7)年时,分析其最终身高、GH/IGF-1 轴和体重指数。采用改良的德国 BFM-83 ALL 方案(n = 42)或不包括预防性颅照射(n = 33)。在 27 例患者中,测定胰岛素耐量试验后的 GH、IGF-1、皮质醇、游离 T(4)和雌二醇/睾酮。

结果

最终身高明显降低(最终身高与诊断时身高 Z 评分差值ΔHAZ = -0.61,p = 0.0001)。此时,3 例患者肥胖(4%),17 例超重(22.7%)。诊断时年龄≤4 岁和接受照射的患者最终身高损失更大(p = 0.001 和 p = 0.008)。4 例患者 GH/IGF-1 轴异常:3 例 GH 峰值<6ng/ml,1 例血清 IGF-1 浓度<25ng/ml。有激素缺乏的患者生长不足明显更高(p = 0.006)。

结论

儿童期 ALL 治疗与最终身高缺陷相关。诊断时年龄小和放疗是主要的危险因素。特别是在接受放疗的患者中发现 GH/IGF-1 缺乏,尽管在 1 例未接受放疗的患者中也发现了这种情况。

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