Department of Endocrinology, Erciyes University Medical School, Kayseri, Turkey.
Clin Endocrinol (Oxf). 2007 Dec;67(6):931-7. doi: 10.1111/j.1365-2265.2007.02989.x. Epub 2007 Jul 30.
Recent investigations have provided evidence for a high prevalence of pituitary dysfunction in patients with subarachnoid haemorrhage (SAH). However, apart from one study, all of the previous data were obtained from retrospective studies. To our knowledge there is no previously reported study in which pituitary function was investigated in the same patients immediately after SAH and 12 months later. The aim of this study was to understand the prevalence and progression of anterior pituitary hormone deficiencies both in the acute phase of SAH and 12 months after the event.
Twenty-two SAH patients (11 men, 11 women) were included in the study. Pituitary function was evaluated in the early acute phase (within 24 h of admission) and after 12 months.
Pituitary hormone deficiencies in the acute phase were as follows: 31.8% had gonadotrophin, 22.7% had ACTH and 22.7% had GH deficiencies. At 12 months after SAH: 0.0% had gonadotrophin, 13.6% had ACTH and 36.4% had GH deficiencies. Overall, after 12 months, pituitary hormone deficiencies recovered in 15 (68.2%) patients and new-onset pituitary hormone deficiencies were present in nine (40.9%) patients.
GH deficiency (GHD) was the most common pituitary deficit at 12 months after SAH and the majority of the patients (87.5%) had isolated GHD. During the 12-month follow-up, pituitary function was found to either improve or worsen in a considerable number of patients.
最近的研究证据表明,蛛网膜下腔出血(SAH)患者的垂体功能障碍发生率较高。然而,除了一项研究外,之前所有的数据都是从回顾性研究中获得的。据我们所知,目前还没有之前报道过的研究在 SAH 后立即和 12 个月后对同一患者的垂体功能进行调查。本研究旨在了解急性 SAH 期和事件后 12 个月时,垂体前叶激素缺乏的发生率和进展情况。
研究纳入 22 例 SAH 患者(男 11 例,女 11 例)。在早期急性阶段(入院后 24 小时内)和 12 个月后评估垂体功能。
急性期垂体激素缺乏症如下:促性腺激素缺乏 31.8%,ACTH 缺乏 22.7%,GH 缺乏 22.7%。SAH 后 12 个月:促性腺激素缺乏 0.0%,ACTH 缺乏 13.6%,GH 缺乏 36.4%。总体而言,12 个月后,15 例(68.2%)患者的垂体激素缺乏症得到恢复,9 例(40.9%)患者出现新的垂体激素缺乏症。
GH 缺乏症(GHD)是 SAH 后 12 个月时最常见的垂体缺陷,大多数患者(87.5%)存在孤立性 GHD。在 12 个月的随访期间,相当数量的患者发现垂体功能要么改善,要么恶化。