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肢端肥大症患者随访的缓解标准。

Remission criteria for the follow-up of patients with acromegaly.

作者信息

Gullu Sevim, Keles Hatice, Delibasi Tuncay, Tonyukuk Vedia, Kamel Nuri, Erdogan Gurbuz

机构信息

Department of Endocrinology and Metabolic Diseases, School of Medicine, Ankara University, 06100 Ankara, Turkey.

出版信息

Eur J Endocrinol. 2004 Apr;150(4):465-71. doi: 10.1530/eje.0.1500465.

Abstract

OBJECTIVE

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.

DESIGN

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

目的

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。

设计

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。

结果

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。

结论

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。

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