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接受抗雄激素和雌激素治疗的男变女变性者的血清和尿液组织激肽释放酶浓度。

Serum and urine tissue kallikrein concentrations in male-to-female transsexuals treated with antiandrogens and estrogens.

作者信息

Slagter Margrita H, Gooren Louis J G, de Ronde Willem, Soosaipillai Antoninus, Scorilas Andreas, Giltay Erik J, Paliouras Miltiadis, Diamandis Eleftherios P

机构信息

Department of Endocrinology, VU University Medical Centre, Amsterdam, The Netherlands.

出版信息

Clin Chem. 2006 Jul;52(7):1356-65. doi: 10.1373/clinchem.2006.068932. Epub 2006 Apr 27.

Abstract

BACKGROUND

The expression of human tissue kallikrein genes is regulated by steroid hormones, but most studies have been conducted with cancer cell lines. Our purpose was to examine serum and urinary tissue kallikrein concentration changes in male-to-female transsexuals before and after treatment with antiandrogens and estrogens.

METHODS

Thirty-five male-to-female transsexuals receiving cyproterone acetate and estrogens (orally or transdermally) were included in this study. Serum and urine samples were collected before initiation of therapy and 4 and 12 months post therapy. ELISAs were used to measure multiple kallikreins in serum and urine.

RESULTS

After antiandrogen and estrogen therapy, serum testosterone concentrations decreased dramatically, as did serum and urinary concentrations of human glandular kallikrein (hK2) and prostate-specific antigen (PSA; hK3). Statistically significant but relatively small changes in serum and urinary concentrations of many other kallikreins were also seen. Kallikreins in serum and urine were correlated before and after treatment.

CONCLUSIONS

The concentrations of hK2 and hK3, but not of any other kallikreins, decrease dramatically after combined antiandrogen and estrogen treatment in male-to-female transsexuals. The smaller responses of the other kallikreins presumably reflect their expression in multiple tissues.

摘要

背景

人类组织激肽释放酶基因的表达受类固醇激素调节,但大多数研究是在癌细胞系中进行的。我们的目的是检测接受抗雄激素和雌激素治疗前后的男变女变性者血清和尿液中组织激肽释放酶浓度的变化。

方法

本研究纳入了35名接受醋酸环丙孕酮和雌激素(口服或经皮给药)治疗的男变女变性者。在治疗开始前以及治疗后4个月和12个月采集血清和尿液样本。采用酶联免疫吸附测定法(ELISA)检测血清和尿液中的多种激肽释放酶。

结果

抗雄激素和雌激素治疗后,血清睾酮浓度显著降低,人腺体激肽释放酶(hK2)和前列腺特异性抗原(PSA;hK3)的血清和尿液浓度也显著降低。许多其他激肽释放酶的血清和尿液浓度也出现了具有统计学意义但相对较小的变化。治疗前后血清和尿液中的激肽释放酶存在相关性。

结论

在男变女变性者中,联合抗雄激素和雌激素治疗后,hK2和hK3的浓度显著降低,但其他激肽释放酶的浓度未出现显著变化。其他激肽释放酶反应较小可能反映了它们在多种组织中的表达情况。

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