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首页> 外文期刊>Clinical Endocrinology >ACTH-secreting pituitary microadenomas are associated with a higher prevalence of central hypothyroidism compared to other microadenoma types
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ACTH-secreting pituitary microadenomas are associated with a higher prevalence of central hypothyroidism compared to other microadenoma types

机译:与其他类型的微腺瘤相比,分泌ACTH的垂体微腺瘤与中央甲状腺功能减退的患病率更高

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摘要

Context Unlike pituitary macroadenomas, microadenomas (micros) are not commonly associated with hypopituitarism. In clinical practice, we have observed that patients with ACTH-secreting micros have a higher than expected prevalence of central hypothyroidism (HT), and we speculated that this effect might be because of glucocorticoid-induced suppression of the hypothalamic-pituitary- thyroid axis. Objective To determine whether there is a difference in the prevalence of central HT among ACTH micros compared to other types of microadenoma, and if so, to investigate whether this is directly related to the degree of hypercortisolism. Design, setting and patients Retrospective study of 149 newly diagnosed patients with pituitary micros: 34 ACTH-secreting, 72 prolactin-secreting (PRLomas) and 43 clinically nonfunctioning adenomas (NFAs). Main outcomes measures Prevalence of central HT, correlation between normalized free T4 or TSH vs normalized urinary free cortisol (UFC) or salivary cortisol. Results The prevalence of central HT was significantly higher in the ACTH compared to the non-ACTH adenomas: 18% (ACTH), 1% (PRL) and 0% (NFAs). The mean normalized free T4 was lower in the ACTH micros compared to the non-ACTH micros (1·29 ± 0·06 vs 1·50 ± 0·23, P = 0·0001). There was no correlation between the degree of hypercortisolism, as reflected by 24-h urine free cortisol and salivary cortisol, and free T4 or TSH levels among the ACTH adenomas. Similarly, there were no differences in mean UFC or salivary cortisol between ACTH adenomas with and without central HT. Following transsphenoidal adenomectomy, central HT recovered in three of six patients with ACTH micros. Conclusions These findings suggest that patients with ACTH-secreting microadenomas should always, at a minimum, undergo testing for central HT. However, given the potential for recovery of thyroid function following cure of Cushing disease, we recommend withholding thyroid hormone replacement until after pituitary surgery.
机译:背景与垂体大腺瘤不同,微腺瘤(micros)通常不伴有垂体功能低下。在临床实践中,我们观察到分泌ACTH的微粒体患者的中央甲状腺功能减退症(HT)患病率高于预期,我们推测这种作用可能是由于糖皮质激素抑制了下丘脑-垂体-甲状腺轴。目的确定与其他类型的微腺瘤相比,ACTH显微镜中中央HT的患病率是否存在差异,如果存在,则调查这是否与皮质醇过多症的程度直接相关。设计,背景和患者对149例新诊断的垂体瘤患者的回顾性研究:分泌34种ACTH,分泌72种催乳素(PRLomas)和43种临床上无功能的腺瘤(NFA)。主要结局指标中央HT的患病率,正常游离T4或TSH与正常尿游离皮质醇(UFC)或唾液皮质醇之间的相关性。结果与非ACTH腺瘤相比,ACTH中中心HT的患病率显着更高:18%(ACTH),1%(PRL)和0%(NFA)。与非ACTH显微镜相比,ACTH显微镜中的平均归一化游离T4更低(1·29±0·06与1·50±0·23,P = 0·0001)。 24小时无尿皮质醇和唾液皮质醇所反映的皮质醇过高程度与ACTH腺瘤中游离T4或TSH水平之间没有相关性。同样,有和没有中心HT的ACTH腺瘤之间的平均UFC或唾液皮质醇也没有差异。经蝶窦切除术后,六名ACTH显微镜患者中有三名恢复了中心HT。结论这些发现表明,分泌ACTH的微小腺瘤患者应至少接受中央HT的检查。但是,考虑到库欣病治愈后可能恢复甲状腺功能,我们建议在垂体手术后停止甲状腺激素替代治疗。

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