Management policy for postoperative acromegaly patients with normal IGF-1 and high GH levels on oral glucose tests.

IF 3.3 2区 医学 Q2 ENDOCRINOLOGY & METABOLISM Pituitary Pub Date : 2024-12-26 DOI:10.1007/s11102-024-01487-9
Yasuyuki Kinoshita, Akira Taguchi, Fumiyuki Yamasaki, Shumpei Onishi, Atsushi Tominaga, Nobutaka Horie
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Abstract

Purpose: Acromegaly patients occasionally achieve either of the remission criterion of IGF-1 or GH level postoperatively; however, treatment for patients with discordant IGF-1 and GH levels remains unclear. This study aimed to clarify the clinical courses and features of postoperative patients with normal IGF-1 and high GH levels and support their management.

Methods: Overall, 110 acromegaly patients underwent initial surgery and a 75-g oral glucose tolerance test (OGTT) 3 months postoperatively. Of the 110, 23 patients with normal IGF-1 and nadir GH levels of ≥ 0.4 µg/L on OGTT (high-GH group) were categorized into three subtypes based on their repeated examinations thereafter: late-remission type (nadir GH level on OGTT of < 0.4 µg/L later), recurrence type (elevated IGF-1 and GH levels later), and persistent type (normal IGF-1 levels and constantly high nadir GH levels on OGTTs).

Results: Proportion of patients in the high-GH group was 23.6%, and they were distributed as follows: late-remission type (n = 10), recurrence type (n = 5), and persistent type (n = 8). There were significantly more women (P = 0.0178) than men in the late-remission type, and patients in the persistent type had significantly larger tumors (P = 0.0110) and higher preoperative GH levels (P = 0.0018) than those that achieved complete remission 3 months postoperatively.

Conclusion: Careful monitoring without additional medications is recommended at first in acromegaly patients with normal IGF-1 and high GH levels considering the possibility of recurrence in the future.

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IGF-1正常、口服血糖GH高的肢端肥大症术后患者的管理策略
目的:肢端肥大症患者术后IGF-1或GH缓解标准偶有达到;然而,对于IGF-1和GH水平不一致的患者的治疗仍不清楚。本研究旨在阐明IGF-1正常和GH水平高的术后患者的临床病程和特点,并为其治疗提供支持。方法:总共有110例肢端肥大症患者接受了初始手术,并在术后3个月进行了75 g口服葡萄糖耐量试验(OGTT)。110例患者中,IGF-1正常,OGTT最低GH水平≥0.4µg/L的23例(高GH组),根据此后的反复检查将其分为三种亚型:晚期缓解型(OGTT最低GH水平)。结果:高GH组患者比例为23.6%,分布如下:晚期缓解型(n = 10),复发型(n = 5)和持续性(n = 8)。晚期缓解型患者中女性明显多于男性(P = 0.0178),持续型患者术后3个月肿瘤较大(P = 0.0110),术前GH水平明显高于完全缓解型患者(P = 0.0018)。结论:考虑到未来复发的可能性,建议对IGF-1正常且生长激素水平高的肢端肥大症患者在开始时进行仔细监测,而不需要额外的药物治疗。
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来源期刊
Pituitary
Pituitary 医学-内分泌学与代谢
CiteScore
7.10
自引率
7.90%
发文量
90
审稿时长
6 months
期刊介绍: Pituitary is an international publication devoted to basic and clinical aspects of the pituitary gland. It is designed to publish original, high quality research in both basic and pituitary function as well as clinical pituitary disease. The journal considers: Biology of Pituitary Tumors Mechanisms of Pituitary Hormone Secretion Regulation of Pituitary Function Prospective Clinical Studies of Pituitary Disease Critical Basic and Clinical Reviews Pituitary is directed at basic investigators, physiologists, clinical adult and pediatric endocrinologists, neurosurgeons and reproductive endocrinologists interested in the broad field of the pituitary and its disorders. The Editorial Board has been drawn from international experts in basic and clinical endocrinology. The journal offers a rapid turnaround time for review of manuscripts, and the high standard of the journal is maintained by a selective peer-review process which aims to publish only the highest quality manuscripts. Pituitary will foster the publication of creative scholarship as it pertains to the pituitary and will provide a forum for basic scientists and clinicians to publish their high quality pituitary-related work.
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