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肢端肥大症中的肾上腺病变:代谢方面和芳烃受体相互作用蛋白基因是否起作用?在基线和长期随访后的评估。

Adrenal lesions in acromegaly: do metabolic aspects and aryl hydrocarbon receptor interacting protein gene have a role? Evaluation at baseline and after long-term follow-up.

机构信息

Endocrinology Unit, Department of Medical and Surgical Sciences, University of Padova, Padova, Italy.

出版信息

J Endocrinol Invest. 2011 May;34(5):353-60. doi: 10.1007/BF03347459. Epub 2010 Jul 1.

Abstract

BACKGROUND

Adrenal lesions are discovered in acromegaly more frequently than in general population, without relationship with primary disease. Some patients, carriers of aryl hydrocarbon receptor interacting protein (AIP) gene mutations, developed an adrenal neoplasm.

AIM

To evaluate the role of metabolic and genetic aspects and the follow-up of adrenal nodules in acromegaly.

MATERIAL AND METHODS

We studied 69 acromegalic patients (30 male and 39 female, 56 ± 15 yr) who had been referred to the Endocrinology Unit of Padua. In all patients we determined body mass index (BMI) and waist-to-hip ratio (WHR); we performed an oral glucose tolerance test (OGTT) whenever possible. If adrenal computed tomography revealed a lesion, the patient underwent an endocrine and genetic study.

RESULTS

Adrenal lesions were identified in 14 patients and were not related to gender, duration of disease, GH or IGF-I concentrations, basal and after-OGTT glucose and insulin levels, log(HOMA-IR) and Quantitative Insulin Sensitivity Check Index (QUICKI) values, whereas BMI and WHR were higher in patients with adrenal lesions. Baseline endocrine and radiological study revealed benign lesions; during mean 4-yr follow-up none of the patients showed hormone excess, even though some lesions increased in size. We did not find any mutation in AIP gene, except heterozygous silent alteration (T48T).

CONCLUSIONS

The frequency of non-functioning adrenal lesions in acromegaly is not associated with the considered aspects, except BMI and WHR. The prolonged follow-up showed that these lesions have a tendency to increase in size independently of the control of acromegaly, so a morphological follow- up is recommended.

摘要

背景

在肢端肥大症中比在普通人群中更常发现肾上腺病变,与原发性疾病无关。一些患者,携带芳香烃受体相互作用蛋白(AIP)基因突变,发展为肾上腺肿瘤。

目的

评估代谢和遗传因素以及肢端肥大症患者肾上腺结节的随访作用。

材料和方法

我们研究了 69 名肢端肥大症患者(30 名男性和 39 名女性,56±15 岁),他们曾被转介到帕多瓦的内分泌科。在所有患者中,我们确定了体重指数(BMI)和腰臀比(WHR);如果肾上腺计算机断层扫描显示病变,则对患者进行内分泌和遗传研究。

结果

在 14 名患者中发现了肾上腺病变,且与性别、疾病持续时间、GH 或 IGF-I 浓度、基础和口服葡萄糖耐量试验(OGTT)后血糖和胰岛素水平、log(HOMA-IR)和定量胰岛素敏感性检查指数(QUICKI)值无关,而 BMI 和 WHR 在有肾上腺病变的患者中更高。基线内分泌和影像学研究显示良性病变;在平均 4 年的随访期间,尽管一些病变增大,但没有患者出现激素过多。除了杂合子沉默突变(T48T)外,我们没有发现 AIP 基因突变。

结论

除了 BMI 和 WHR 外,肢端肥大症中非功能性肾上腺病变的频率与所考虑的方面无关。延长的随访显示,这些病变有增大的趋势,独立于肢端肥大症的控制,因此建议进行形态学随访。

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