Darzy Ken H, Thorner Michael O, Shalet Stephen M
Department of Endocrinology, Christie Hospital, Manchester, UK.
Clin Endocrinol (Oxf). 2009 Feb;70(2):287-93. doi: 10.1111/j.1365-2265.2008.03359.x. Epub 2008 Jul 31.
We have previously demonstrated that spontaneous (physiological) GH secretion was entirely normal in cranially irradiated patients who had normal individual peak GH responses to the insulin tolerance test (ITT) but reduced maximal somatotroph reserve as indicated by substantially reduced group GH responses to the GHRH + arginine stimulation test (AST). The normality of spontaneous GH secretion was attributed to a compensatory increase in hypothalamic stimulatory input within a partially damaged hypothalamic-pituitary (h-p) axis. It is unknown, however, if such compensatory stimulation can also maintain normality of GH secretion in those who fail the ITT but pass the GHRH + AST. STUDY SUBJECTS AND DESIGN: We studied 24-h spontaneous GH secretion by 20-min sampling both in the fed state (n = 11) and in the last 24 h of a 33-h fast (n = 9) in adult cancer survivors with subnormal peak GH responses to the ITT but either normal or relatively less attenuated peak GH responses to the GHRH + AST. The study was conducted 8.3 +/- 1.8 (range 2-23) years after cranial irradiation for nonpituitary brain tumours (n = 9) or leukaemia/lymphoma (n = 2) in comparison with 30 normal controls (fasting, 14).
Previously published diagnostic thresholds for the ITT, GHRH + AST and spontaneous GH secretion were used to characterize GH secretion. Four of the 11 patients with impaired stimulated responses to both tests showed only minor discordancies between stimulated and spontaneous GH secretion. Two of the remaining seven patients had subnormal spontaneous GH secretion. However, spontaneous GH secretion, both individually and as a group, was entirely normal in the remaining five patients who had impaired GH responses to the ITT but normal individual responses to the GHRH + AST; in these five patients, IGF-I standard deviation scores (SDS; -2.7 to -0.8) were significantly reduced to a moderate degree compared with normals.
In cranially irradiated adult cancer survivors, it cannot be assumed that failure to pass the ITT in isolation reflects severe GH deficiency (GHD). It appears that in some patients near-maximal compensatory overdrive of the partially damaged somatotroph axis may result in near-normal quantitative restoration of spontaneous GH secretion, thus limiting further stimulation with the ITT to the extent that impaired GH responses can be seen even before spontaneous GH secretion starts to decline in adults. However, IGF-I status continues to provide useful information about the adequacy of the compensatory process and therefore the degree of normality of GH secretion.
我们之前已经证明,对于胰岛素耐量试验(ITT)中个体生长激素(GH)峰值反应正常,但生长激素释放激素(GHRH)+精氨酸刺激试验(AST)中群体GH反应显著降低表明生长激素储备减少的颅脑照射患者,其自发性(生理性)GH分泌完全正常。自发性GH分泌正常归因于部分受损的下丘脑 - 垂体(h - p)轴内下丘脑刺激输入的代偿性增加。然而,尚不清楚这种代偿性刺激能否在未通过ITT但通过GHRH + AST的患者中维持GH分泌的正常性。
我们对成年癌症幸存者进行了研究,这些患者对ITT的峰值GH反应低于正常水平,但对GHRH + AST的峰值GH反应正常或相对减弱程度较小。在进食状态下(n = 11)和33小时禁食的最后24小时(n = 9),通过20分钟采样研究24小时自发性GH分泌。该研究在因非垂体脑肿瘤(n = 9)或白血病/淋巴瘤(n = 2)接受颅脑照射后8.3±1.8(范围2 - 23)年进行,并与30名正常对照者(禁食,14名)进行比较。
使用先前公布的ITT、GHRH + AST和自发性GH分泌的诊断阈值来表征GH分泌。在两项试验中刺激反应受损的11名患者中有4名在刺激和自发性GH分泌之间仅表现出轻微不一致。其余7名患者中有2名自发性GH分泌低于正常水平。然而,在其余5名对ITT的GH反应受损但对GHRH + AST的个体反应正常的患者中,自发性GH分泌无论是个体还是群体均完全正常;与正常对照相比,这5名患者的胰岛素样生长因子 - I标准差分数(SDS; - 2.7至 - 0.8)显著降低至中等程度。
在接受颅脑照射的成年癌症幸存者中,不能认为单独未通过ITT就反映严重的生长激素缺乏(GHD)。似乎在一些患者中,部分受损的生长激素轴的近乎最大程度的代偿性过度驱动可能导致自发性GH分泌在数量上近乎正常恢复,从而限制了ITT的进一步刺激,以至于在成年人中甚至在自发性GH分泌开始下降之前就能看到GH反应受损。然而,胰岛素样生长因子 - I状态继续提供有关代偿过程充分性以及因此GH分泌正常程度的有用信息。