Gullu Sevim, Keles Hatice, Delibasi Tuncay, Tonyukuk Vedia, Kamel Nuri, Erdogan Gurbuz
Department of Endocrinology and Metabolic Diseases, School of Medicine, Ankara University, 06100 Ankara, Turkey.
Eur J Endocrinol. 2004 Apr;150(4):465-71. doi: 10.1530/eje.0.1500465.
The aim was to evaluate the validity of current remission criteria in acromegaly, a random GH level of <2.5 microg/l, a glucose-suppressed GH level of <1 microg/l and a normal IGF-I level.
In forty-one patients treated for acromegaly (23 males and 18 females, 20-69 years) and 94 healthy subjects (50 males and 44 females, 20-78 years), basal GH and IGF-I levels and nadir GH levels after 75 g oral glucose were evaluated in decade blocks; these were assayed by sensitive immunoradiometric assays.
Basal GH levels varied widely from 0.022 to 10.4 in healthy subjects and were >2.5 microg/l in 19%. The mean post-glucose GH nadir was 0.067+/-0.009 microg/l (range 0.003-0.4 microg/l) and the upper limit of the GH nadir was 0.26 microg/l (means+2 S.D.) in healthy subjects. Thirty-five patients with acromegaly had high-for-age IGF-I levels in relation to our healthy subjects. In this group, 15 (42.9%) patients had basal GH levels of <2.5 microg/l, 14 (40%) patients had nadir GH levels of <1 microg/l, and three (8.6%) patients had GH suppression to <0.26 microg/l which was defined as normal GH suppression in our healthy subjects. Only six patients with acromegaly had normal-for-age IGF-I levels and all of these patients had basal GH levels of <2.5 microg/l and all but one had nadir GH levels of <0.26 microg/l.
A basal or random GH level of <2.5 microg/l is not a reliable criterion for remission in acromegaly and the currently accepted normal upper limit of 1 microg/l for post-glucose GH suppression is too high. Post-glucose nadir GH levels, measured with sensitive assays, can be <1.0 microg/l in 40% and basal GH levels can be <2.5 microg/l in 43% of the active acromegalic patients. IGF-I levels appeared to correlate better with a nadir GH cut-off of 0.26 microg/l rather than 1 microg/l in the determination of disease activity.
旨在评估当前肢端肥大症缓解标准的有效性,即随机生长激素(GH)水平<2.5微克/升、葡萄糖抑制后GH水平<1微克/升以及胰岛素样生长因子-I(IGF-I)水平正常。
对41例接受肢端肥大症治疗的患者(23例男性和18例女性,年龄20 - 69岁)和94名健康受试者(50例男性和44例女性,年龄20 - 78岁),按十年年龄段分组评估基础GH和IGF-I水平以及口服75克葡萄糖后GH的最低点水平;这些指标通过灵敏的免疫放射分析测定。
健康受试者的基础GH水平差异很大,范围为0.022至10.4,19%的人>2.5微克/升。健康受试者葡萄糖负荷后GH最低点的平均值为0.067±0.009微克/升(范围0.003 - 0.4微克/升),GH最低点的上限为0.26微克/升(均值 + 2标准差)。35例肢端肥大症患者的IGF-I水平相对于我们的健康受试者处于同年龄组偏高状态。在该组中,15例(42.9%)患者的基础GH水平<2.5微克/升,14例(40%)患者的GH最低点水平<1微克/升,3例(8.6%)患者的GH抑制至<0.26微克/升,而在我们的健康受试者中这被定义为正常的GH抑制。只有6例肢端肥大症患者的IGF-I水平处于同年龄组正常范围,所有这些患者的基础GH水平<2.5微克/升,除1例之外所有患者的GH最低点水平<0.26微克/升。
基础或随机GH水平<2.5微克/升并非肢端肥大症缓解的可靠标准,目前所接受的葡萄糖负荷后GH抑制正常上限1微克/升过高。采用灵敏检测方法测得的葡萄糖负荷后GH最低点水平,在40%的活动期肢端肥大症患者中可<1.0微克/升,基础GH水平在43%的患者中可<2.5微克/升。在疾病活动度的判定中,IGF-I水平与GH最低点截断值0.26微克/升的相关性似乎优于与1微克/升的相关性。