Division of Metabolism, Endocrinology, and Diabetes, University of Michigan, Ann Arbor, Michigan.
Department of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, Michigan.
J Clin Endocrinol Metab. 2019 Jul 1;104(7):2615-2622. doi: 10.1210/jc.2018-02527.
The ovaries and adrenals are sources of androgens in women. Although dehydroepiandrosterone (DHEA), DHEA sulfate (DHEAS), and testosterone (T) all decline with age, these C19 steroids correlate poorly with parameters of androgen action in postmenopausal women.
To comprehensively compare the androgen profiles of pre- and postmenopausal women.
We quantified 19 steroids-including DHEA; DHEAS; T; androstenedione (A4); and the following adrenal-specific 11-oxygenated C19 steroids (11oxyandrogens): 11β-hydroxytestosterone (11OHT), 11-ketotestosterone (11KT), 11β-hydroxyandrostenedione (11OHA4), and 11-ketoandrostenedione (11KA4)-using liquid chromatography-tandem mass spectrometry in morning serum obtained from 100 premenopausal (age 20 to 40 years) and 100 postmenopausal (age ≥ 60 years) women. Double immunofluorescence of 3β-hydroxysteroid dehydrogenase type 2 (HSD3B2) with cytochrome b5 (CYB5A) or sulfotransferase 2A1 (SULT2A1) was performed in normal adrenal glands obtained from eight premenopausal and eight postmenopausal women.
DHEA, DHEAS, A4, and T were significantly higher in pre- than in postmenopausal women (2.9, 2.8, 2.9, and 1.6-fold, respectively; P < 0.0001). In contrast, the 11-oxyandrogens did not decrease with aging, and the 11OHT/T and 11OHA4/A4 ratios showed strong positive correlations with age (r = 0.5 and 0.8, respectively; P < 0.0001). Double immunofluorescence analysis showed that with the involution of the zona reticularis in the old adrenals, the sharp zonal segregation of HSD3B2 and CYB5A becomes less distinct, and areas of HSD3B2 and CYB5A overlap are observed.
Unlike DHEA, DHEAS, A4, and T, the 11oxyandrogens do not decline in aging women. Structural changes within the adrenal cortex might explain the evolution of androgen profiles in aging women.
卵巢和肾上腺是女性雄激素的来源。虽然脱氢表雄酮(DHEA)、硫酸脱氢表雄酮(DHEAS)和睾酮(T)都随年龄增长而下降,但这些 C19 类固醇与绝经后妇女雄激素作用的参数相关性较差。
全面比较绝经前和绝经后妇女的雄激素谱。
我们使用液相色谱-串联质谱法定量分析了 19 种类固醇,包括 DHEA;DHEAS;T;雄烯二酮(A4);以及以下肾上腺特异性 11-氧化 C19 类固醇(11oxyandrogens):11β-羟睾酮(11OHT)、11-酮睾酮(11KT)、11β-羟基雄烯二酮(11OHA4)和 11-酮雄烯二酮(11KA4),共 100 名绝经前(年龄 20 至 40 岁)和 100 名绝经后(年龄≥60 岁)女性的清晨血清中进行检测。对 8 名绝经前和 8 名绝经后女性的正常肾上腺进行 3β-羟甾脱氢酶 2 型(HSD3B2)与细胞色素 b5(CYB5A)或磺基转移酶 2A1(SULT2A1)的双重免疫荧光染色。
与绝经后妇女相比,绝经前妇女的 DHEA、DHEAS、A4 和 T 明显更高(分别为 2.9、2.8、2.9 和 1.6 倍;P<0.0001)。相比之下,11-氧雄激素并不会随年龄增长而下降,并且 11OHT/T 和 11OHA4/A4 比值与年龄呈强正相关(r=0.5 和 0.8,P<0.0001)。双重免疫荧光分析显示,随着老年肾上腺网状带的萎缩,HSD3B2 和 CYB5A 的明显区域分离变得不那么明显,并且观察到 HSD3B2 和 CYB5A 的重叠区域。
与 DHEA、DHEAS、A4 和 T 不同,11oxyandrogens 在衰老女性中不会下降。肾上腺皮质内的结构变化可能解释了衰老女性雄激素谱的演变。