Aimaretti Gianluca, Baldelli Roberto, Corneli Ginevra, Croce Chiara, Rovere Silvia, Baffoni Claudia, Bellone Simonetta, Gasco SValentina, Granata Riccarda, Grottoli Silvia, Ghigo Ezio
Division of Endocrinology and Metabolism, Department of Internal Medicine, University of Turin, Turin, Italy.
Endocr Dev. 2005;9:76-88. doi: 10.1159/000085758.
In the current guidelines for the diagnosis of adult GH deficiency (GHD) it is stated that, within the appropriate clinical context, it has to be shown by provocative tests only. But the diagnostic value of measuring IGF-I levels has been recently revisited. It has been confirmed that normal IGF-I levels do not rule out severe GHD in adults. However, it has also been emphasized that very low IGF-I levels in patients highly suspected for GHD (and without malnutrition, liver disease or hypothyroidism) could be considered definite evidence for severe GHD. This assumption particularly applies to patients with childhood-onset, severe GHD or with multiple hypopituitarism acquired in adulthood. The value of measuring IGF-I levels for monitoring the efficacy and the adequacy of rhGH replacement remains definitely accepted.
在当前成人生长激素缺乏症(GHD)的诊断指南中指出,在适当的临床背景下,必须仅通过激发试验来证实。但最近对测量胰岛素样生长因子-I(IGF-I)水平的诊断价值进行了重新审视。已证实正常的IGF-I水平不能排除成人严重GHD。然而,也有人强调,在高度怀疑患有GHD(且无营养不良、肝病或甲状腺功能减退)的患者中,极低的IGF-I水平可被视为严重GHD的确切证据。这一假设尤其适用于儿童期发病的严重GHD患者或成年后获得性多发性垂体功能减退患者。测量IGF-I水平对于监测重组人生长激素(rhGH)替代治疗的疗效和充分性的价值仍然得到明确认可。