GNAS突变与生长激素分泌垂体腺瘤患者手术结果的关系

Endocrinology and metabolism (Seoul, Korea) Pub Date : 2021-04-01 Epub Date: 2021-03-23 DOI:10.3803/EnM.2020.875
Hyein Jung, Kyungwon Kim, Daham Kim, Ju Hyung Moon, Eui Hyun Kim, Se Hoon Kim, Cheol Ryong Ku, Eun Jig Lee
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引用次数: 5

摘要

背景:鸟嘌呤核苷酸结合蛋白α刺激(GNAS)基因与分泌生长激素(GH)的垂体腺瘤有关。我们调查了韩国肢端肥大症患者GNAS突变的患病率,并评估突变状态是否与生化或临床特征相关。方法:对2005年至2014年在Severance医院接受手术治疗的126例肢端肥大症患者进行研究。我们进行了GNAS基因分析,并评估了肿瘤的年龄、性别、激素水平、术后生化缓解和免疫组织化学染色结果。结果:75例(59.5%)患者存在GNAS突变。GNAS突变患者和未突变患者的年龄分布和Knosp分类相似。gnas阴性组和gnas突变组女性患者所占比例分别为76.5%和48.0% (P=0.006)。免疫组化染色显示,gnas突变组垂体肿瘤组织GH表达高于突变阴性组(98.7%比92.2%,P=0.015)。在口服葡萄糖耐量试验中,GNAS突变患者术前胰岛素样生长因子-1水平较高(791.3 ng/mL vs. 697.0 ng/mL, P=0.045),术后即刻基础(0.9 ng/mL vs. 1.0 ng/mL, P=0.191)和最低GH水平较低(0.3 ng/mL vs. 0.6 ng/mL, P=0.012)。最后,gnas突变组在手术切除后1周和6个月的手术缓解率均显著高于突变阴性组(70.7% vs 54.9%, P=0.011;85.3% vs. 82.4%, P=0.007)。结论:GH分泌垂体肿瘤GNAS突变与术前较高的胰岛素样生长因子-1水平和手术缓解率以及术后较低的GH最低点相关。因此,GNAS突变状态可以预测肢端肥大症患者的手术反应性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Associations of GNAS Mutations with Surgical Outcomes in Patients with Growth Hormone-Secreting Pituitary Adenoma.

Associations of GNAS Mutations with Surgical Outcomes in Patients with Growth Hormone-Secreting Pituitary Adenoma.

Background: The guanine nucleotide-binding protein, alpha stimulating (GNAS) gene has been associated with growth hormone (GH)-secreting pituitary adenoma. We investigated the prevalence of GNAS mutations in Korean patients with acromegaly and assessed whether mutation status correlated with biochemical or clinical characteristics.

Methods: We studied 126 patients with acromegaly who underwent surgery between 2005 and 2014 at Severance Hospital. We performed GNAS gene analysis and evaluated age, sex, hormone levels, postoperative biochemical remission, and immunohistochemical staining results of the tumor.

Results: GNAS mutations were present in 75 patients (59.5%). Patients with and without GNAS mutations showed similar age distribution and Knosp classification. The proportion of female patients was 76.5% and 48.0% in the GNAS-negative and GNAS-mutation groups, respectively (P=0.006). In immunohistochemical staining, the GNAS-mutation group showed higher GH expression in pituitary tumor tissues than the mutation-negative group (98.7% vs. 92.2%, P=0.015). Patients with GNAS mutations had higher preoperative insulin-like growth factor-1 levels (791.3 ng/mL vs. 697.0 ng/mL, P=0.045) and lower immediate postoperative basal (0.9 ng/mL vs. 1.0 ng/mL, P=0.191) and nadir GH levels (0.3 ng/mL vs. 0.6 ng/mL, P=0.012) in oral glucose tolerance tests. Finally, the GNAS-mutation group showed significantly higher surgical remission rates than the mutation-negative group, both at 1 week and 6 months after surgical resection (70.7% vs. 54.9%, P=0.011; 85.3% vs. 82.4%, P=0.007, respectively).

Conclusion: GNAS mutations in GH-secreting pituitary tumors are associated with higher preoperative insulin-like growth factor-1 levels and surgical remission rates and lower immediate postoperative nadir GH levels. Thus, GNAS mutation status can predict surgical responsiveness in patients with acromegaly.

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