Department of Medicine, Oregon Health & Science University, 3303 SW Bond Avenue, Portland, OR 97239, USA.
Pituitary. 2012 Dec;15(4):562-70. doi: 10.1007/s11102-011-0369-1.
New criteria that define acromegaly remission are more stringent: normal (age/sex-adjusted) insulin-like growth factor type 1 (IGF-1), growth hormone (GH) random (GHr) <1 μg/L, and a GH nadir (GHn) during oral glucose tolerance test (OGTT) of <0.4 μg/L. Discordance between GH and IGF-1 values is often attributed to somatostatin receptor ligands (SRLs) or radiation. The purpose of this study was to evaluate rates of discordant IGF-1 and GH levels in patients with GH secreting adenomas (after pituitary surgery), who were naïve to any other treatment. We retrospectively analyzed data over a 5 year time period (2006-2010), in post-surgery acromegaly patients who had elevated IGF-1 but normal GH levels (per the new cure criteria). Symptoms of acromegaly were scored according to a 4-point scale. Fifty-four patients had post-operative GHr and IGF-1 measurements, 28 patients had GHn during OGTT, and 16 patients had 5-point 2-h GH day curve tests. Thirteen of 54 (24%) patients were found to have intermittent persistent discordant values; high IGF-1 and normal GH at final evaluation (77% of these patients were women). Patients had a median number of IGF-1 evaluations of 7.5 (range: 2-15) over a median of 22 months (range: 3-47 months). Mean elevated IGF-1 in the discordant population was 1.25 × upper limit of normal (ULN) ± 0.17 (range: 1.01-1.6 × ULN). Twelve of the 13 (92%) patients had macroadenomas; 10 of the 13 (69%) patients had mammosomatotroph, mixed lacto/somatotroph tumors or prolactin staining. No patient in the discordant population was on estrogen replacement therapy or had overt cardiac disease. When the relatively asymptomatic discordant population was compared with 35 patients from the concordant population (six were excluded because of preoperative medical treatment for acromegaly), no significant difference between age, gender distribution, body mass index (BMI), presence of diabetes mellitus (DM) or glucose intolerance and adrenal insufficiency between groups was noted. In our study of postoperative patients with acromegaly naïve to both SRLs and radiation, using new GH cut-off levels, 24% had intermittent or persistent discordant values. Our results highlight that relying on IGF-1 or GH measurements alone is not adequate for assessing disease control in surgically treated acromegaly patients. Management of such patients needs to be individualized and long-term studies evaluating morbidity and mortality incorporated into treatment decisions. Further studies with larger patient populations and longer follow-up are required to determine the long-term implications of discordant GH and IGF-1 value patterns.
正常(年龄/性别调整)胰岛素样生长因子 1(IGF-1),生长激素(GH)随机(GHr)<1μg/L,口服葡萄糖耐量试验(OGTT)时 GH 最低点(GHn)<0.4μg/L。GH 和 IGF-1 值之间的差异通常归因于生长抑素受体配体(SRL)或放射治疗。本研究的目的是评估 GH 分泌腺瘤(垂体手术后)患者中 GH 和 IGF-1 水平不一致的发生率,这些患者尚未接受任何其他治疗。我们回顾性分析了 5 年时间(2006-2010 年)的数据,在术后肢端肥大症患者中,IGF-1 升高但 GH 水平正常(根据新的治愈标准)。肢端肥大症的症状根据 4 分制进行评分。54 例患者有术后 GHr 和 IGF-1 测量值,28 例患者有 OGTT 时的 GHn,16 例患者有 5 点 2 小时 GH 日曲线试验。54 例患者中有 13 例(24%)被发现存在间歇性持续不一致的数值;最终评估时 IGF-1 高,GH 正常(这些患者中有 77%为女性)。患者中位 IGF-1 评估次数为 7.5(范围:2-15),中位随访时间为 22 个月(范围:3-47 个月)。不一致人群中平均升高的 IGF-1 为正常值上限(ULN)的 1.25×±0.17(范围:1.01-1.6×ULN)。13 例患者中有 12 例(92%)为大腺瘤;13 例中有 10 例(69%)为乳促混合生长激素瘤或催乳素染色。不一致人群中没有患者接受雌激素替代治疗或有明显的心脏病。当将相对无症状的不一致人群与来自一致人群的 35 例患者(因术前治疗肢端肥大症而排除 6 例)进行比较时,两组间年龄、性别分布、体重指数(BMI)、糖尿病(DM)或葡萄糖耐量和肾上腺功能不全的存在均无显著差异。在我们对术后肢端肥大症患者的研究中,这些患者既未接受 SRL 治疗,也未接受放射治疗,使用新的 GH 截止值,24%的患者存在间歇性或持续性不一致的数值。我们的结果表明,仅依靠 IGF-1 或 GH 测量不足以评估手术治疗的肢端肥大症患者的疾病控制情况。此类患者的管理需要个体化,并且需要将评估发病率和死亡率的长期研究纳入治疗决策中。需要进一步的研究,包括更大的患者人群和更长的随访时间,以确定不一致的 GH 和 IGF-1 值模式的长期影响。