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童年接受颅脊髓放射治疗的年轻成年人的生长激素释放激素加精氨酸刺激试验

Growth hormone releasing hormone plus arginine stimulation testing in young adults treated in childhood with cranio-spinal radiation therapy.

作者信息

Ham J Nina, Ginsberg Jill P, Hendell Christine D, Moshang Thomas

机构信息

Division of Endocrinology and Diabetes, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

出版信息

Clin Endocrinol (Oxf). 2005 May;62(5):628-32. doi: 10.1111/j.1365-2265.2005.02272.x.

Abstract

OBJECTIVE

Growth hormone deficiency (GHD) secondary to cranio-spinal radiation therapy (CSRT) is a complication seen in medulloblastoma survivors. The standard for diagnosis of adult GHD is a peak GH < 3 microg/l by the insulin tolerance test (ITT). However, insulin tolerance testing exposes patients to the risks of hypoglycaemia. Recent studies suggest that the GH releasing hormone + arginine (GHRH + ARG) test can identify GHD in cranially irradiated patients at longer time intervals after radiation. We evaluated the GHRH + ARG stimulation test compared to the ITT in young adults diagnosed with medulloblastoma during childhood.

PATIENTS

We evaluated 10 young adult patients (age range 17-26 years) who were treated with CSRT during childhood for medulloblastoma, and who had resultant childhood-onset GHD.

MEASUREMENTS

Subjects underwent GH provocative testing with the ITT and the GHRH + ARG test. IGF-I and IGFBP3 levels were also measured at baseline.

RESULTS

Insulin tolerance testing and GHRH + arginine stimulation were performed at a mean +/- SD 14 +/- 4.4 years after cranial radiation. All patients failed the ITT with median peak GH 0.40 microg/l (range < 0.05-2.2). GHRH + arginine gave higher peak GH levels with a mean of 7.9 +/- 5.7 microg/l (P = 0.003). Four patients had peak GH > 9 microg/l and were between 7.8 and 19.6 years from cranial radiation. There was no correlation of peak GH levels with time interval since CSRT. Thirty-three per cent of subjects had normal IGF-I; neither IGF-I nor IGFBP3 standard deviation scores (SDS) correlated with ITT results.

CONCLUSIONS

Using a GHRH + arginine cut-off for GHD of 9 microg/l, four patients would have been misclassified as GH sufficient, despite being > 7 years (with two patients being nearly 20 years) out from CSRT. These findings suggest that the pituitary GH-producing cells of young adults continue to maintain responsiveness to GHRH + arginine more than 5-10 years after cranial irradiation.

摘要

目的

颅脊髓放射治疗(CSRT)继发的生长激素缺乏(GHD)是髓母细胞瘤幸存者中出现的一种并发症。成人GHD的诊断标准是胰岛素耐量试验(ITT)中生长激素峰值<3μg/L。然而,胰岛素耐量试验会使患者面临低血糖风险。最近的研究表明,生长激素释放激素+精氨酸(GHRH+ARG)试验可以在放疗后的较长时间间隔内识别接受过颅脑照射的患者是否存在GHD。我们比较了GHRH+ARG刺激试验与ITT在儿童期被诊断为髓母细胞瘤的年轻成年人中的效果。

患者

我们评估了10名年轻成年患者(年龄范围17 - 26岁),他们在儿童期因髓母细胞瘤接受了CSRT治疗,并因此导致儿童期起病的GHD。

测量

受试者接受了ITT和GHRH+ARG试验的生长激素激发试验。同时在基线时测量了胰岛素样生长因子-I(IGF-I)和胰岛素样生长因子结合蛋白3(IGFBP3)水平。

结果

在颅脑放疗后平均±标准差14±4.4年进行了胰岛素耐量试验和GHRH+精氨酸刺激试验。所有患者的ITT均未通过,生长激素峰值中位数为0.40μg/L(范围<0.05 - 2.2)。GHRH+精氨酸试验产生的生长激素峰值水平更高,平均为7.9±5.7μg/L(P = 0.003)。4名患者的生长激素峰值>9μg/L,且距离颅脑放疗已有7.8至19.6年。生长激素峰值水平与自CSRT后的时间间隔无相关性。33%的受试者IGF-I水平正常;IGF-I和IGFBP3标准差评分(SDS)均与ITT结果无关。

结论

使用9μg/L的GHRH+精氨酸作为GHD的临界值,4名患者会被误分类为生长激素充足,尽管他们距离CSRT已超过7年(其中两名患者接近20年)。这些发现表明,年轻成年人的垂体生长激素分泌细胞在颅脑照射后5 - 10年以上仍继续保持对GHRH+精氨酸的反应性。

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