Department of Medicine, Vagelos College of Physicians and Surgeons, Columbia University, 650 West 168th Street, Rm.1014, New York, NY, 10032, USA.
Department of Neurosurgery, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY, USA.
Pituitary. 2021 Apr;24(2):170-183. doi: 10.1007/s11102-020-01094-4. Epub 2020 Oct 30.
Outcome of acromegaly surgery is assessed by IGF-1 and glucose-suppressed GH, but whether the latter provides additional clinically relevant information when IGF-1 is normal is unclear. The role of GH suppression testing after surgery requires clarification.
We studied 97 acromegaly patients with normal IGF-1 after surgery by measuring GH after oral glucose longitudinally, initially at ≥ 3 months after surgery and repeated one or more times ≥ 1 year later. Nadir GH was categorized as normal or abnormal relative to the 97.5th percentile of nadir GH in 100 healthy subjects, which were ≤ 0.14 µg/L (DSL IRMA) or ≤ 0.15 µg/L(IDS iSYS). Signs and symptoms scores and insulin resistance were followed longitudinally.
Of 68 patients with initial normal GH suppression 63 (93%) remained in remission and of 29 with initial abnormal GH suppression, 9 (31%) recurred. Recurrence was more common in patients with abnormal suppression (P < 0.001). A total of 14 patients recurred, including 5 with normal GH suppression progressing to abnormal and then recurrence. Overall, serial signs and symptoms and insulin resistance assessments did not identify patients with abnormal suppression or recurrence.
Risk of recurrence after surgery is increased for patients with a normal IGF-1 level, but abnormal GH suppression. We newly find, using both our and others' cut-offs, that while normal suppression predicts long-term remission in most patients, some can progress from normal to abnormal suppression and then recurrence after many years of follow up. Nadir GH levels are of prognostic value in acromegaly patients with normal IGF-1 levels after surgery.
生长激素腺瘤患者术后的治疗效果通过 IGF-1 和葡萄糖抑制后 GH 来评估,但 IGF-1 正常时,后者是否提供了额外的临床相关信息尚不清楚。术后 GH 抑制试验的作用尚需明确。
我们通过口服葡萄糖后纵向测量 GH,研究了 97 例术后 IGF-1 正常的肢端肥大症患者,最初在术后≥3 个月进行,并在≥1 年后重复一次或多次。相对于 100 例健康对照者中 GH 最低值的第 97.5 百分位数(DSL IRMA≤0.14µg/L,IDS iSYS≤0.15µg/L),将 GH 最低值分为正常或异常。我们对症状和体征评分及胰岛素抵抗进行了纵向随访。
68 例初始 GH 抑制正常的患者中,有 63 例(93%)持续缓解,而 29 例初始 GH 抑制异常的患者中,有 9 例(31%)复发。抑制异常的患者复发更为常见(P<0.001)。共有 14 例患者复发,其中 5 例 GH 抑制正常的患者进展为异常,然后再次复发。总体而言,连续的症状和体征及胰岛素抵抗评估未能识别出 GH 抑制异常或复发的患者。
对于 IGF-1 水平正常但 GH 抑制异常的患者,术后复发的风险增加。我们新发现,使用我们和其他人的截断值,尽管大多数患者的正常抑制预测长期缓解,但有些患者在多年随访后可从正常抑制进展为异常抑制,然后复发。术后 IGF-1 水平正常的肢端肥大症患者的 GH 最低值具有预后价值。