肾上腺形态作为典型21-羟化酶缺乏症成人长期疾病控制的指标

Endocrinology and metabolism (Seoul, Korea) Pub Date : 2022-02-01 Epub Date: 2022-02-08 DOI:10.3803/EnM.2021.1278
Taek Min Kim, Jung Hee Kim, Han Na Jang, Man Ho Choi, Jeong Yeon Cho, Sang Youn Kim
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引用次数: 4

摘要

背景:由于临床和实验室环境的变化,监测典型21-羟化酶缺乏症(21OHD)的成人具有挑战性。此外,21OHD的肾上腺成像指南尚未出台。我们评估了典型21OHD患者肾上腺形态与疾病控制状况的关系。方法:本回顾性横断面研究纳入90例成年21OHD患者和270例年龄和性别匹配的健康对照。我们使用腹部计算机断层扫描评估肾上腺体积、宽度和肿瘤的存在,并评估肾上腺体积和宽度与激素状态的相关性。我们研究了肾上腺体积和宽度在21OHD患者(17α-羟基孕酮[17-OHP])中识别控制良好状态的诊断价值。结果:21OHD患者的肾上腺形态表现为肥大(45.6%)、大小正常(42.2%)和萎缩(12.2%)。肾上腺肿瘤12例(13.3%)。21OHD患者肾上腺体积和宽度明显大于对照组(18.2±12.2 mL vs. 7.1±2.0 mL, 4.7±1.9 mm vs. 3.3±0.5 mm)。结论:肾上腺体积和宽度可作为监测经典21OHD患者的可靠定量参数。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Adrenal Morphology as an Indicator of Long-Term Disease Control in Adults with Classic 21-Hydroxylase Deficiency.

Adrenal Morphology as an Indicator of Long-Term Disease Control in Adults with Classic 21-Hydroxylase Deficiency.

Adrenal Morphology as an Indicator of Long-Term Disease Control in Adults with Classic 21-Hydroxylase Deficiency.

Adrenal Morphology as an Indicator of Long-Term Disease Control in Adults with Classic 21-Hydroxylase Deficiency.
Background Monitoring adults with classical 21-hydroxylase deficiency (21OHD) is challenging due to variation in clinical and laboratory settings. Moreover, guidelines for adrenal imaging in 21OHD are not yet available. We evaluated the relationship between adrenal morphology and disease control status in classical 21OHD. Methods This retrospective, cross-sectional study included 90 adult 21OHD patients and 270 age- and sex-matched healthy controls. We assessed adrenal volume, width, and tumor presence using abdominal computed tomography and evaluated correlations of adrenal volume and width with hormonal status. We investigated the diagnostic performance of adrenal volume and width for identifying well-controlled status in 21OHD patients (17α-hydroxyprogesterone [17-OHP] <10 ng/mL). Results The adrenal morphology of 21OHD patients showed hypertrophy (45.6%), normal size (42.2%), and hypotrophy (12.2%). Adrenal tumors were detected in 12 patients (13.3%). The adrenal volume and width of 21OHD patients were significantly larger than those of controls (18.2±12.2 mL vs. 7.1±2.0 mL, 4.7±1.9 mm vs. 3.3±0.5 mm, P<0.001 for both). The 17-OHP and androstenedione levels were highest in patients with adrenal hypertrophy, followed by those with normal adrenal glands and adrenal hypotrophy (P<0.05 for both). Adrenal volume and width correlated positively with adrenocorticotropic hormone, 17-OHP, 11β-hydroxytestosterone, progesterone sulfate, and dehydroepiandrosterone sulfate in both sexes (r=0.33–0.95, P<0.05 for all). For identifying well-controlled patients, the optimal cut-off values of adrenal volume and width were 10.7 mL and 4 mm, respectively (area under the curve, 0.82–0.88; P<0.001 for both). Conclusion Adrenal volume and width may be reliable quantitative parameters for monitoring patients with classical 21OHD.
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