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Adrenal Incidentaloma: A New Cause of the Metabolic Syndrome?

医学 内科学 内分泌学 亚临床感染 偶发瘤 体质指数 腺瘤 甲状腺机能正常 肾上腺腺瘤 胰岛素耐受试验 地塞米松抑制试验 糖耐量受损 胰岛素 胰岛素抵抗 甲状腺 地塞米松 胰岛素敏感性
作者
Massimo Terzolo,Anna Pia,Anna Alı̀,G. Osella,Giuseppe Reimondo,Silvia Bovio,Fulvia Daffara,Massimo Procopio,P. Paccotti,Giorgio Borretta,Alberto Angeli
出处
期刊:The Journal of Clinical Endocrinology and Metabolism [Oxford University Press]
卷期号:87 (3): 998-1003 被引量:324
标识
DOI:10.1210/jcem.87.3.8277
摘要

A number of patients with adrenal incidentaloma are exposed to a slight degree of cortisol excess resulting from functional autonomy of the adrenal mass (usually a cortical adenoma). At present, there are only scant data on the unwanted effects of this endocrine condition referred to as subclinical Cushing’s syndrome. The aim of the present study was to look for some features of the metabolic syndrome in patients with incidental adrenal adenoma. Forty-one patients (9 men and 32 women) bearing adrenal incidentaloma with typical computed tomography features of cortical adenoma were studied. For both patients and controls, exclusion criteria were age equal to 70 yr or greater, previous history of fasting hyperglycemia, or impaired glucose tolerance (IGT), severe hypertension, current use of medication or concomitant relevant illnesses, and body mass index (BMI) equal to 30 kg/m2 or greater. Forty-one patients with euthyroid multinodular goiter accurately matched for sex, age, and BMI served for a 1:1 case-control analysis. The study design included an oral glucose tolerance test (75 g) and an endocrine workup aimed at the study of the hypothalamic-pituitary-adrenal axis. Age and BMI were fully comparable between patients (54.0 ± 10.7 yr, 23.8 ± 2.4 kg/m2) and controls (52.2 ± 11.6 yr, 23.5 ± 2.8 kg/m2). Fasting glucose and fasting insulin levels were not different between the two groups (4.96 ± 0.61 mmol/liter vs. 4.88 ± 0.58 mmol/liter; 67 ± 34 pmol/liter vs. 59 ± 32 pmol/liter), but the 2-h postchallenge glucose was significantly higher in patients than in controls (7.43 ± 2.49 mmol/liter vs. 6.10 ± 1.44 mmol/liter, P = 0.01). Fifteen patients (36%) reached the World Health Organization criteria for IGT and two other patients (5%) reached those for diabetes, and 14% of the controls qualified for IGT (P = 0.01). No difference in the lipid pattern was seen between the two groups, but either systolic or diastolic blood pressure were higher in patients (135.4 ± 15.5 mm Hg vs. 125.0 ± 15.6 mm Hg, P = 0.003; 82.9 ± 9.1 mm Hg vs. 75.3 ± 6.6 mm Hg, P < 0.0001). We calculated the whole-body insulin sensitivity index derived from the oral glucose tolerance test that was significantly reduced in the patients (4.3 ± 1.7 vs. 5.7 ± 2.5, P = 0.01). In a multiple regression analysis, 2-h glucose was associated with BMI and midnight cortisol values (r2 = 0.36, P = 0.002). The comparison of the patients with nonfunctioning adenoma (n = 29) with those with subclinical Cushing’s syndrome (n = 12) yielded significant differences as to 2-h glucose and triglyceride levels, which were significantly higher in the second group (7.02 ± 1.76 mmol/liter vs. 8.72 ± 3.17 mmol/liter, P = 0.03; 1.06 ± 0.4 mmol/liter vs. 1.73 ± 0.96 mmol/liter, P = 0.002), but the insulin sensitivity index was conversely reduced (5.2 ± 1.4 vs. 2.9 ± 1.2, P < 0.0001). In conclusion, many patients with incidental adrenal adenoma display altered glucose tolerance, that may be explained by reduced insulin sensitivity, and increased blood pressure levels in comparison with carefully age- and BMI-matched controls. The slight hypercortisolism observed in some such patients may significantly contribute to this state of insulin resistance. Midnight serum cortisol appears as a sensitive marker of the metabolic effects of subclinical Cushing’s syndrome.

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