Obesity in patients with craniopharyngioma in the South Asian region – A distinct phenotype

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引用次数: 0

Abstract

Background

Craniopharyngiomas are rare benign tumors located in the sellar and suprasellar region, with an incidence of 0.5–2 cases per million as reported in Western studies. Post-treatment, including surgery and/or radiotherapy, many patients develop significant obesity, primarily due to hypothalamic damage and associated complications such as hypopituitarism. In the South Asian population, genetic predisposition to obesity at lower BMIs, coupled with a carbohydrate-rich diet, may exacerbate obesity in craniopharyngioma patients, presenting a unique challenge.

Methods

This submission is a commentary based on a comprehensive literature review. The authors conducted the review using PubMed to focus on English-language articles covering hypothalamic obesity, craniopharyngioma and obesity in the South Asian population from 1939 to the present.

Results

The literature review revealed that 50–60 % of patients treated for craniopharyngioma develop obesity, predominantly linked to hypothalamic damage, although these data are mainly derived from Western studies. Hypopituitarism was frequently observed, further contributing to the obesity. Despite a caloric intake appropriate for the age and gender, these patients exhibited reduced physical activity as measured by wrist accelerometers. Patients with hypothalamic obesity due to craniopharyngioma are at risk for metabolic syndrome and cardiovascular morbidity. Additionally, visual impairment was common, leading to a decreased quality of life. The South Asian population, genetically predisposed to visceral obesity and a carbohydrate-rich diet, may display a distinct phenotype. Although multiple treatment modalities have been tried, there is no definite treatment modality available to counteract this condition at present.

Conclusion

South Asian phenotype of craniopharyngioma-related obesity is characterized by significant metabolic and hormonal dysregulation, influenced by both dietary and genetic factors. Nevertheless, there may be a lot to be still understood about this devastating, rapid, relentless hypothalamic obesity syndrome. Also, a higher morbidity rate within this population, underscores the need for further research to develop targeted interventions.
南亚地区颅咽管瘤患者的肥胖症--一种独特的表型
背景颅咽管瘤是一种罕见的良性肿瘤,位于蝶鞍和鞍上区,据西方研究报告,其发病率为 0.5-2 例/百万人。在接受手术和/或放疗等治疗后,许多患者会出现明显肥胖,这主要是由于下丘脑受损和相关并发症(如垂体功能减退症)所致。在南亚人群中,较低体重指数的遗传易导致肥胖,再加上富含碳水化合物的饮食习惯,可能会加重颅咽管瘤患者的肥胖,从而带来独特的挑战。作者使用 PubMed 进行了综述,重点关注从 1939 年至今有关下丘脑肥胖症、颅咽管瘤和南亚人群肥胖症的英文文章。结果文献综述显示,50%-60% 接受过颅咽管瘤治疗的患者会出现肥胖症,主要与下丘脑损伤有关,尽管这些数据主要来自西方研究。垂体功能减退症也经常出现,这进一步加剧了肥胖。尽管这些患者摄入的热量与年龄和性别相符,但根据腕部加速度计的测量,他们的体力活动却有所减少。颅咽管瘤导致的下丘脑肥胖症患者有代谢综合征和心血管疾病的风险。此外,视力受损也很常见,导致生活质量下降。南亚人在遗传上易患内脏肥胖症,饮食中富含碳水化合物,因此可能表现出独特的表型。结论南亚人的颅咽管瘤相关肥胖症表型的特点是受饮食和遗传因素的影响,代谢和内分泌严重失调。尽管如此,人们对这种破坏性的、快速的、无情的下丘脑肥胖综合征仍有很多不了解之处。此外,这一人群的发病率较高,这也凸显了进一步研究开发针对性干预措施的必要性。
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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