Clinical Profile and Treatment Outcomes in Patient with Acromegaly Using 14th Acromegaly Consensus Criteria.

Jyoti Sharma, Rajeev Kasaliwal, Puneet Shivnani, Utkarsh Balani, Payal Bargujar, Pankaj Gupta, Bhawani S Sharma, Vineet Mishra, Akash Mishra, Surendra K Sharma
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引用次数: 0

Abstract

Introduction: 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.

Methods: 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.

Results: 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.

Conclusions: 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.

肢端肥大症患者的临床概况和治疗结果采用第14肢端肥大症共识标准。
肢端肥大症是一种以生长激素(GH)和胰岛素样生长因子1 (IGF-1)分泌过多为特征的慢性全身性疾病。本研究回顾了我们在肢端肥大症患者的内镜下经蝶窦手术(TSS)的经验,重点是根据2023年共识标准的缓解率。方法:在2020年1月至2024年6月期间,我们进行了一项以医院为基础的回顾性研究,涉及42名诊断为肢端肥大症并接受内窥镜TSS治疗的患者。分析临床和激素概况、合并症和结局数据。术后3个月年龄调整后的IGF-1水平定义为缓解。结果:平均诊断年龄36.43±10.70岁。最常见的两种症状是头痛(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%)。术前激素评估显示继发性性腺功能减退41.66%,其次为甲状腺功能减退(23.81%)和皮质醇缺乏(21.43%)。42例患者中有18例(42.85%)达到生化缓解,包括所有5例微腺瘤患者和35.13%的大腺瘤患者。虽然Knosp分级、最大肿瘤直径和术前葡萄糖生长激素水平在单变量分析中显示出显著相关性,但调整后这些相关性不显著。在多变量分析中,术后第2天GH水平(≤2.75 ng/ml)成为缓解的重要预测因子。结论:本研究根据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预后进行了全面的回顾。值得注意的是,术后第2天GH低于2.75 ng/ml是预后的重要预测因子。
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来源期刊
Indian Journal of Endocrinology and Metabolism
Indian Journal of Endocrinology and Metabolism Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.10
自引率
0.00%
发文量
75
期刊介绍: The Indian Journal of Endocrinology and Metabolism (IJEM) aims to function as the global face of Indian endocrinology research. It aims to act as a bridge between global and national advances in this field. The journal publishes thought-provoking editorials, comprehensive reviews, cutting-edge original research, focused brief communications and insightful letters to editor. The journal encourages authors to submit articles addressing aspects of science related to Endocrinology and Metabolism in particular Diabetology. Articles related to Clinical and Tropical endocrinology are especially encouraged. Sub-topic based Supplements are published regularly. This allows the journal to highlight issues relevant to Endocrine practitioners working in India as well as other countries. IJEM is free access in the true sense of the word, (it charges neither authors nor readers) and this enhances its global appeal.
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