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自身免疫性艾迪生病中的残余皮质类固醇生成。

Residual Corticosteroid Production in Autoimmune Addison Disease.

机构信息

Department of Clinical Science, University of Bergen, Norway.

K.G. Jebsen Center for Autoimmune Disorders, University of Bergen, Bergen, Norway.

出版信息

J Clin Endocrinol Metab. 2020 Jul 1;105(7):2430-41. doi: 10.1210/clinem/dgaa256.

Abstract

CONTEXT

Contrary to current dogma, growing evidence suggests that some patients with autoimmune Addison disease (AAD) produce corticosteroids even years after diagnosis.

OBJECTIVE

To determine frequencies and clinical features of residual corticosteroid production in patients with AAD.

DESIGN

Two-staged, cross-sectional clinical study in 17 centers (Norway, Sweden, and Germany). Residual glucocorticoid (GC) production was defined as quantifiable serum cortisol and 11-deoxycortisol and residual mineralocorticoid (MC) production as quantifiable serum aldosterone and corticosterone after > 18 hours of medication fasting. Corticosteroids were analyzed by liquid chromatography-tandem mass spectrometry. Clinical variables included frequency of adrenal crises and quality of life. Peak cortisol response was evaluated by a standard 250 µg cosyntropin test.

RESULTS

Fifty-eight (30.2%) of 192 patients had residual GC production, more common in men (n = 33; P < 0.002) and in shorter disease duration (median 6 [0-44] vs 13 [0-53] years; P < 0.001). Residual MC production was found in 26 (13.5%) patients and associated with shorter disease duration (median 5.5 [0.5-26.0] vs 13 [0-53] years; P < 0.004), lower fludrocortisone replacement dosage (median 0.075 [0.050-0.120] vs 0.100 [0.028-0.300] mg; P < 0.005), and higher plasma renin concentration (median 179 [22-915] vs 47.5 [0.6-658.0] mU/L; P < 0.001). There was no significant association between residual production and frequency of adrenal crises or quality of life. None had a normal cosyntropin response, but peak cortisol strongly correlated with unstimulated cortisol (r = 0.989; P < 0.001) and plasma adrenocorticotropic hormone (ACTH; r = -0.487; P < 0.001).

CONCLUSION

In established AAD, one-third of the patients still produce GCs even decades after diagnosis. Residual production is more common in men and in patients with shorter disease duration but is not associated with adrenal crises or quality of life.

摘要

背景

与当前的教条相反,越来越多的证据表明,一些自身免疫性艾迪生病(AAD)患者在诊断后数年仍会产生皮质类固醇。

目的

确定 AAD 患者中皮质类固醇残留产生的频率和临床特征。

设计

在 17 个中心(挪威、瑞典和德国)进行的两阶段、横断面临床研究。残留糖皮质激素(GC)的产生被定义为可定量的血清皮质醇和 11-脱氧皮质醇,而残留盐皮质激素(MC)的产生则被定义为在禁食超过 18 小时后可定量的血清醛固酮和皮质酮。皮质类固醇通过液相色谱-串联质谱法进行分析。临床变量包括肾上腺危象的频率和生活质量。通过标准的 250μg 促皮质素兴奋试验评估皮质醇峰值反应。

结果

在 192 名患者中,有 58 名(30.2%)患者存在 GC 残留产生,男性中更为常见(n=33;P<0.002),疾病持续时间较短(中位数 6[0-44]岁 vs 13[0-53]岁;P<0.001)。26 名(13.5%)患者存在 MC 残留产生,与疾病持续时间较短相关(中位数 5.5[0.5-26.0]岁 vs 13[0-53]岁;P<0.004),氟氢可的松替代剂量较低(中位数 0.075[0.050-0.120]mg vs 0.100[0.028-0.300]mg;P<0.005),血浆肾素浓度较高(中位数 179[22-915]mU/L vs 47.5[0.6-658.0]mU/L;P<0.001)。残留产生与肾上腺危象的频率或生活质量之间没有显著关联。没有患者有正常的促皮质素兴奋反应,但皮质醇峰值与未刺激的皮质醇(r=0.989;P<0.001)和血浆促肾上腺皮质激素(ACTH;r=-0.487;P<0.001)强烈相关。

结论

在已确诊的 AAD 中,即使在诊断后数十年,仍有三分之一的患者会产生 GC。残留产生在男性和疾病持续时间较短的患者中更为常见,但与肾上腺危象或生活质量无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e97/7274491/e492bf2cf76f/dgaa256f0001.jpg

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