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生长激素和胃饥饿素对神经性厌食症少女和对照组口服葡萄糖负荷的反应。

Growth hormone and ghrelin responses to an oral glucose load in adolescent girls with anorexia nervosa and controls.

作者信息

Misra Madhusmita, Miller Karen K, Herzog David B, Ramaswamy Kavitha, Aggarwal Avichal, Almazan Cecilia, Neubauer Gregory, Breu Jeffrey, Klibanski Anne

机构信息

Neuroendocrine Unit, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02114, USA.

出版信息

J Clin Endocrinol Metab. 2004 Apr;89(4):1605-12. doi: 10.1210/jc.2003-031861.

Abstract

Anorexia nervosa (AN) is associated with high levels of GH and low levels of IGF-I suggestive of a nutritionally acquired lack of GH action or GH resistance. The suppression of GH levels after administration of inhibitors of GH secretion such as oral glucose is the definitive test to distinguish normal from pathological states of GH excess, such as acromegaly. However, suppression of GH by glucose has not been well characterized in states of adaptive GH excess, such as AN, especially in a younger adolescent population with relatively higher GH levels, compared with adults. In this study, we investigated GH suppression after a 100-g oral glucose load over a 1-h period in 19 adolescent girls with AN and 20 healthy controls of similar chronologic and bone age. We also compared nocturnal GH secretion characteristics by deconvolutional analysis in both groups to determine differences in secretory patterns between adolescents whose GH values suppressed vs. those whose values did not after oral glucose. Fasting levels of ghrelin, a GH secretagogue, and suppression of ghrelin with oral glucose were also determined to assess whether GH suppression or nonsuppression could be related to ghrelin values at respective time points. At 0 min (0') of the oral glucose tolerance test, girls with AN had significantly lower levels of glucose (P = 0.009) and higher levels of GH (P = 0.04) than controls. Nadir GH values were higher in AN than in controls (2.0 +/- 1.8 vs. 0.5 +/- 0.5 ng/ml, P = 0.001). Only 31.6% of girls with AN suppressed their GH values to 1 ng/ml or less vs. 85.0% of healthy adolescents (P = 0.0005). All healthy controls had nadir postglucose GH values of 2 ng/ml or less. Nadir GH concentrations during the oral glucose tolerance test correlated directly with all measures of GH secretion [basal (r = 0.37, P = 0.02), pulsatile (r = 0.56, P = 0.0002), and total (r = 0.57, P = 0.0002)]. Adolescent girls who did not suppress their GH values to 1 ng/ml or less had significantly higher levels of ghrelin at 0', 30', and 60' (P = 0.02, 0.004, and 0.008), significantly higher GH at 0' (P = 0.001), and higher nocturnal basal (P = 0.002), pulsatile (P = 0.05), and total GH secretion (P = 0.03) than those who did suppress below this level. Ghrelin values were higher in AN than in controls at each time point (P = 0.02, 0.0002, and 0.01 at 0', 30', and 60') but did not predict GH values at these time points. Adolescent girls with AN fail to adequately suppress their GH values after a 100-g oral glucose load. This lack of suppression may be related to the higher GH secretion seen in adolescents with this disorder. In contrast, all healthy adolescents suppress their GH values to 2 ng/ml or less but not 1 ng/ml or less after a glucose load. Although ghrelin values are higher in AN than in controls, we could not demonstrate a relationship between ghrelin and GH values. The inability of healthy girls to uniformly suppress GH levels to 1 ng/ml or less, a normal level defined for adults, may be related to higher GH secretion in the pubertal years, compared with adult life. Further studies are needed to define GH suppression in an adolescent population.

摘要

神经性厌食症(AN)与高水平的生长激素(GH)和低水平的胰岛素样生长因子-I(IGF-I)相关,提示营养性获得性GH作用缺乏或GH抵抗。给予GH分泌抑制剂(如口服葡萄糖)后GH水平的抑制是区分GH分泌正常状态与病理性GH分泌过多状态(如肢端肥大症)的决定性试验。然而,在适应性GH分泌过多状态(如AN)中,葡萄糖对GH的抑制作用尚未得到很好的描述,尤其是在与成年人相比GH水平相对较高的年轻青少年人群中。在本研究中,我们调查了19名患有AN的青春期女孩和20名年龄和骨龄相似的健康对照者在1小时内口服100克葡萄糖负荷后GH的抑制情况。我们还通过去卷积分析比较了两组的夜间GH分泌特征,以确定口服葡萄糖后GH值被抑制的青少年与未被抑制的青少年之间分泌模式的差异。还测定了胃饥饿素(一种GH促分泌素)的空腹水平以及口服葡萄糖后胃饥饿素的抑制情况,以评估GH抑制或未抑制是否与各个时间点的胃饥饿素值相关。在口服葡萄糖耐量试验的0分钟(0')时,患有AN的女孩的葡萄糖水平显著低于对照组(P = 0.009),而GH水平显著高于对照组(P = 0.04)。AN组的最低GH值高于对照组(2.0±1.8 vs. 0.5±0.5 ng/ml,P = 0.001)。只有31.6%的患有AN的女孩将其GH值抑制到1 ng/ml或更低,而健康青少年的这一比例为85.0%(P = 0.0005)。所有健康对照者口服葡萄糖后的最低GH值均为2 ng/ml或更低。口服葡萄糖耐量试验期间的最低GH浓度与GH分泌的所有指标直接相关[基础值(r = 0.37,P = 0.02)、脉冲值(r = 0.56,P = 0.0002)和总值(r = 0.57,P = 0.0002)]。GH值未抑制到1 ng/ml或更低的青春期女孩在0'、30'和60'时的胃饥饿素水平显著更高(P = 0.02、0.004和0.008),在0'时的GH水平显著更高(P = 0.001),夜间基础GH分泌(P = 0.002)、脉冲GH分泌(P = 0.05)和总GH分泌(P = 0.03)也更高,高于那些GH值抑制到该水平以下的女孩。在每个时间点,AN组的胃饥饿素值均高于对照组(0'、30'和60'时分别为P = 0.02、0.0002和0.01),但不能预测这些时间点的GH值。患有AN的青春期女孩在口服100克葡萄糖负荷后未能充分抑制其GH值。这种抑制缺乏可能与该疾病青少年中较高的GH分泌有关。相比之下,所有健康青少年在葡萄糖负荷后将其GH值抑制到2 ng/ml或更低,但未抑制到1 ng/ml或更低。尽管AN组的胃饥饿素值高于对照组,但我们未能证明胃饥饿素与GH值之间的关系。健康女孩无法将GH水平一致地抑制到1 ng/ml或更低(这是为成年人定义的正常水平),可能与青春期相比成年期较高的GH分泌有关。需要进一步研究来确定青少年人群中的GH抑制情况。

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