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成年垂体功能减退患者生长激素替代治疗后中枢性甲状腺功能减退的暴露

Unmasking of central hypothyroidism following growth hormone replacement in adult hypopituitary patients.

作者信息

Agha Amar, Walker Dorothy, Perry Les, Drake William M, Chew Shern L, Jenkins Paul J, Grossman Ashley B, Monson John P

机构信息

William Harvey Research Institute, Queen Mary University of London, London, UK.

出版信息

Clin Endocrinol (Oxf). 2007 Jan;66(1):72-7. doi: 10.1111/j.1365-2265.2006.02688.x.

DOI:10.1111/j.1365-2265.2006.02688.x
PMID:17201804
Abstract

BACKGROUND

The effect of GH replacement on thyroid function in hypopituitary patients has hitherto been studied in small groups of children and adults with conflicting results.

OBJECTIVE

We aimed to define the effect and clinical significance of adult GH replacement on thyroid status in a large cohort of GH-deficient patients.

PATIENTS AND METHOD

We studied 243 patients with severe GH deficiency due to various hypothalamo-pituitary disorders. Before GH treatment, 159 patients had treated central hypothyroidism (treated group) while 84 patients were considered euthyroid (untreated group). GH dose was titrated over 3 months to achieve serum IGF-1 concentration in the upper half of the age-adjusted normal range. Serial measurements of serum T4, T3, TSH and quality of life were made at baseline and at 3 and 6 months after commencing GH replacement.

RESULTS

In the untreated group, we observed a significant reduction in serum T4 concentration without a significant increase in serum T3 or TSH concentration; 30/84 patients (36%) became hypothyroid and needed initiation of T4 therapy. Similar but lesser changes were seen in the treated group, 25 of whom (16%) required an increase in T4 dose. Patients who became hypothyroid after GH replacement had lower baseline serum T4 concentration, were more likely to have multiple pituitary hormone deficiencies and showed less improvement in quality of life compared with patients who remained euthyroid.

CONCLUSION

GH deficiency masks central hypothyroidism in a significant proportion of hypopituitary patients and this is exposed after GH replacement. We recommend that hypopituitary patients with GH deficiency and low normal serum T4 concentration should be considered for T4 replacement prior to commencement of GH in order to provide a robust baseline from which to judge the clinical effects of GH replacement.

摘要

背景

迄今为止,生长激素(GH)替代治疗对垂体功能减退患者甲状腺功能的影响仅在少数儿童和成人中进行了研究,结果相互矛盾。

目的

我们旨在确定在一大群生长激素缺乏患者中,成人GH替代治疗对甲状腺状态的影响及其临床意义。

患者与方法

我们研究了243例因各种下丘脑 - 垂体疾病导致严重生长激素缺乏的患者。在GH治疗前,159例患者患有中枢性甲状腺功能减退并已接受治疗(治疗组),而84例患者甲状腺功能正常(未治疗组)。GH剂量在3个月内进行滴定,以使血清胰岛素样生长因子 - 1(IGF - 1)浓度达到年龄校正后正常范围的上半部分。在基线以及开始GH替代治疗后的3个月和6个月时,对血清甲状腺素(T4)、三碘甲状腺原氨酸(T3)、促甲状腺激素(TSH)和生活质量进行系列测量。

结果

在未治疗组中,我们观察到血清T4浓度显著降低,而血清T3或TSH浓度无显著升高;84例患者中有30例(36%)出现甲状腺功能减退,需要开始T4治疗。治疗组也观察到类似但程度较轻的变化,其中25例(16%)需要增加T4剂量。与甲状腺功能仍正常的患者相比,GH替代治疗后出现甲状腺功能减退的患者基线血清T4浓度较低,更可能存在多种垂体激素缺乏,且生活质量改善较少。

结论

生长激素缺乏在相当比例的垂体功能减退患者中掩盖了中枢性甲状腺功能减退,而在GH替代治疗后这种情况会暴露出来。我们建议,在开始GH治疗之前,应考虑对生长激素缺乏且血清T4浓度略低于正常的垂体功能减退患者进行T4替代治疗,以便提供一个稳定的基线,从而判断GH替代治疗的临床效果。

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