A systematic review of literature on Insulin-like growth factor-2-mediated hypoglycaemia in non-islet cell tumours

IF 2.7 Q3 ENDOCRINOLOGY & METABOLISM
Fateen Ata, Hassan Choudry, Adeel Ahmad Khan,  Anum, Ibrahim Khamees, Anas Al-sadi, Abdelaziz Mohamed, Lujain Malkawi, Esra'a Aljaloudi
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引用次数: 0

Abstract

Introduction

Insulin-like growth factor-2 (IGF-2)-mediated hypoglycemia is a rare yet clinically significant entity with considerable morbidity and mortality. Existing literature is limited and fails to offer a comprehensive understanding of its clinical trajectory, management and prognostication.

Methods

Systematic review of English-language articles reporting primary patient data on IMH was searched using electronic databases (PubMed, Scopus and Embase) from any date up to 21 December 2022. Data were analysed in STATA-16.

Results

The systematic review contains 172 studies, including 1 Randomised controlled trial, 1 prospective observational study, 5 retrospective observational studies, 150 case reports, 11 case series and 4 conference abstracts. A total of 233 patients were analysed, averaging 60.6 ± 17.1 years in age, with comparable proportions of males and females. The commonest tumours associated with Insulin-like Growth Factor-2-mediated hypoglycaemia were fibrous tumours (N = 124, 53.2%), followed by non-fibrous tumours originating from the liver (N = 21, 9%), hemangiopericytomas (N = 20, 8.5%) and mesotheliomas (N = 11, 4.7%). Hypoglycaemia was the presenting feature of NICT in 42% of cases. Predominant clinical features included loss of consciousness (26.7%) and confusion (21%). The mean IGF-2 and IGF-1 levels were 882.3 ± 630.6 ng/dL and 41.8 ± 47.8, respectively, with no significant correlation between these levels and patient outcomes. Surgical removal was the most employed treatment modality (47.2%), followed by medication therapy. The recovery rate was 77%, with chronic liver disease (CLD) significantly associated with a poor outcome (OR: 7.23, P: 0.03). Tumours originating from fibrous tissues were significantly associated with recovery (p < .001). In the logistic regression model, CLD remained a significant predictor of poor outcomes.

Conclusion

This systematic review highlights that most non-islet-cell tumour-hypoglycaemia (NICTH) is due to fibrous tumours. NICTs demonstrate a variable prognosis, which is fair if originating from fibrous tissue. Management such as octreotide, corticosteroids, diazoxide, embolization, radiotherapy and surgical resection have disparate success rates.

Abstract Image

关于非胰岛细胞肿瘤中胰岛素样生长因子-2介导的低血糖症的系统性文献综述。
导言:胰岛素样生长因子-2(IGF-2)介导的低血糖症是一种罕见但临床意义重大的疾病,具有相当高的发病率和死亡率。现有文献有限,无法全面了解其临床轨迹、管理和预后:方法:使用电子数据库(PubMed、Scopus 和 Embase)对截至 2022 年 12 月 21 日报告 IMH 主要患者数据的英文文章进行系统性检索。数据用 STATA-16 进行分析:系统综述包含 172 项研究,其中包括 1 项随机对照试验、1 项前瞻性观察研究、5 项回顾性观察研究、150 篇病例报告、11 篇系列病例和 4 篇会议摘要。共分析了 233 名患者,平均年龄(60.6 ± 17.1)岁,男女比例相当。与胰岛素样生长因子-2介导的低血糖相关的最常见肿瘤是纤维性肿瘤(124例,53.2%),其次是源自肝脏的非纤维性肿瘤(21例,9%)、血管瘤(20例,8.5%)和间皮瘤(11例,4.7%)。42%的病例以低血糖为主要特征。主要临床特征包括意识丧失(26.7%)和意识模糊(21%)。IGF-2和IGF-1的平均水平分别为882.3 ± 630.6 ng/dL和41.8 ± 47.8,这些水平与患者的预后无显著相关性。手术切除是最常用的治疗方式(47.2%),其次是药物治疗。痊愈率为 77%,慢性肝病(CLD)与不良预后有显著相关性(OR:7.23,P:0.03)。来源于纤维组织的肿瘤与痊愈显著相关(P 结论:本系统综述强调,大多数非胰岛细胞肿瘤性低血糖症(NICTH)是由纤维性肿瘤引起的。非胰岛细胞瘤的预后不一,如果来自纤维组织,预后尚可。奥曲肽、皮质类固醇、双氮卓、栓塞、放疗和手术切除等治疗方法的成功率各不相同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Endocrinology, Diabetes and Metabolism
Endocrinology, Diabetes and Metabolism Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
5.00
自引率
0.00%
发文量
66
审稿时长
6 weeks
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