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库辛综合征中生长激素缺乏:关于诊断和管理的最新情况
1Neuroendocrine Unit and Neuroendocrine and Pituitary Tumor Clinical Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
Expert review of endocrinology & metabolism
|September 13, 2025
概括
增长激素缺乏症 (GHD) 在缓解期的库辛综合征 (CS) 患者中很常见. 增长激素替代疗法可以改善儿童和成人的结果,但需要仔细监测.
科学领域:
- 内分泌学 在内分泌学.
- 代谢障碍 代谢障碍 代谢障碍
背景情况:
- 内源性库辛综合征 (CS) 会导致严重的健康问题和死亡率.
- 生长激素缺乏症 (GHD) 是CS患者常见的并发症,即使在缓解后也持续存在.
研究的目的:
- 审查CS缓解期患者GHD的流行病学,机制和临床方面.
- 讨论GHD诊断以及生长激素替代疗法的有效性和安全性.
主要方法:
- 系统的电子文献搜索 (PubMed) 到2025年7月.
- 审查的重点是患有库辛病 (垂体CS) 的患者.
主要成果:
- 在活跃的CS中,GHD普遍存在,并且可以在缓解中持续存在.
- 在儿童中,GHD会导致线性生长下降. 在成年人中,GHD与心脏代谢负担增加,肌肉强度降低,骨密度降低和骨折率更高有关.
- 在儿童中,生长激素的替代疗法可以改善成人身高;在成人中,它可以提高生活质量,骨密度,肌肉强度和脂质概况,并有高血糖症的风险.
结论:
- 对于缓解的CS患者来说,GHD是一个重要的关注点.
- 增长激素替代疗法对缓解期的儿科和成人患者都有好处,需要仔细监测潜在的副作用,如高血糖症.
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