Sharma Jyoti, Kasaliwal Rajeev, Shivnani Puneet, Balani Utkarsh, Bargujar Payal, Gupta Pankaj, Sharma Bhawani S, Mishra Vineet, Mishra Akash, Sharma Surendra K
Department of Endocrinology, Mahatma Gandhi Medical College and Hospital, Jaipur, Rajasthan, India.
Department of Neurosurgery, Mahatma Gandhi Medical College and Hospital, Jaipur, Rajasthan, India.
Indian J Endocrinol Metab. 2025 Mar-Apr;29(2):195-201. doi: 10.4103/ijem.ijem_522_24. Epub 2025 Apr 29.
Acromegaly is a chronic systemic disease characterized by excessive secretion of growth hormone (GH) and insulin-like growth factor 1 (IGF-1). This study reviews our experience with endoscopic transsphenoidal surgery (TSS) in acromegaly patients, focusing on remission rates according to the 2023 consensus criteria.
We conducted a hospital based, retrospective study involving 42 patients diagnosed with acromegaly who underwent endoscopic TSS, between January 2020 and June 2024. Clinical and hormonal profiles, comorbidities and outcome data were analysed. Remission was defined as age-adjusted IGF-1 levels 3 months post-surgery.
Mean age at diagnosis was 36.43 ± 10.70 years. The two most frequent presenting symptoms were headache (64.28%) and visual deficits (47.61%). Common comorbidities included diabetes mellitus (23.8%) and hypertension (28.57%). Pre-operative hormonal evaluation revealed secondary hypogonadism in 41.66% of patients, followed by hypothyroidism (23.81%) and cortisol deficiency (21.43%). Biochemical remission was achieved in 18 out of 42 patients (42.85%), including all five patients with microadenomas and 35.13% of those with macroadenomas. Although Knosp grade, maximum tumour diameter and pre-operative post glucose growth hormone levels showed significant associations in univariate analyses, these associations were not significant after adjustment. On multivariate analysis, post-operative day 2 GH levels (≤2.75 ng/ml) emerged as a significant predictor of remission.
This study provides the comprehensive review of clinical presentations and outcomes of patients with acromegaly based on the latest acromegaly consensus guidelines. Notably, a post-operative day 2 GH less than 2.75 ng/ml emerged as a significant predictor of outcome.
肢端肥大症是一种慢性全身性疾病,其特征是生长激素(GH)和胰岛素样生长因子1(IGF-1)分泌过多。本研究回顾了我们在内镜经蝶窦手术(TSS)治疗肢端肥大症患者方面的经验,重点关注根据2023年共识标准的缓解率。
我们进行了一项基于医院的回顾性研究,纳入了2020年1月至2024年6月期间42例诊断为肢端肥大症并接受内镜TSS的患者。分析了临床和激素特征、合并症及结局数据。缓解定义为术后3个月年龄校正的IGF-1水平。
诊断时的平均年龄为36.43±10.70岁。最常见的两个症状是头痛(64.28%)和视力障碍(47.61%)。常见合并症包括糖尿病(23.8%)和高血压(28.57%)。术前激素评估显示,41.66%的患者存在继发性性腺功能减退,其次是甲状腺功能减退(23.81%)和皮质醇缺乏(21.43%)。42例患者中有18例(42.85%)实现了生化缓解,其中包括所有5例微腺瘤患者和35.13%的大腺瘤患者。尽管在单因素分析中,Knosp分级、最大肿瘤直径和术前葡萄糖负荷后生长激素水平显示出显著相关性,但调整后这些相关性并不显著。多因素分析显示,术后第2天的GH水平(≤2.75 ng/ml)是缓解的显著预测因素。
本研究基于最新的肢端肥大症共识指南,对肢端肥大症患者的临床表现和结局进行了全面回顾。值得注意的是,术后第2天GH低于2.75 ng/ml是结局的显著预测因素。