Chatzittofis Andreas, Boström Adrian E, Öberg Katarina Görts, Flanagan John N, Schiöth Helgi B, Arver Stefan, Jokinen Jussi
Department of Clinical Sciences/Psychiatry, Umeå University, Umeå, Sweden; Medical School, University of Cyprus, Nicosia, Cyprus.
Department of Neuroscience, Uppsala University, Uppsala, Sweden.
Sex Med. 2020 Jun;8(2):243-250. doi: 10.1016/j.esxm.2020.02.005. Epub 2020 Mar 12.
Hypersexual disorder as suggested to be included in the Diagnostic and Statistical Manual of Mental Disorders-5 integrates aspects of sexual desire deregulation, impulsivity, and compulsivity. However, it is unknown how it affects gonadal activity and the function of the hypothalamus-pituitary-gonadal (HPG) axis.
The aim of this study was to investigate testosterone and luteinizing hormone (LH) levels in hypersexual men compared with healthy controls. Furthermore, we investigated associations between epigenetic markers and hormone levels.
Basal morning plasma levels of testosterone, LH, and sex hormone-binding globulin (SHBG) were assessed in 67 hypersexual men (mean age: 39.2 years) compared with 39 age-matched healthy controls (mean age: 37.5 years). The Sexual Compulsivity Scale and the Hypersexual Disorder: Current Assessment Scale were used for assessing hypersexual behavior, the Montgomery-Åsberg Depression Scale-self rating was used for depression severity, and the Childhood Trauma Questionnaire (CTQ) was used for assessing history of childhood adversity. The genome-wide methylation pattern of more than 850 K CpG sites was measured in whole blood using the Illumina Infinium Methylation EPIC BeadChip. CpG sites located within 2,000 bp of the transcriptional start site of hypothalamus pituitary adrenal (HPA) and HPG axis-coupled genes were included.
Testosterone and LH plasma levels in association with clinical rating and a secondary outcome was the epigenetic profile of HPA and HPG axis-coupled CpG sites with testosterone and LH levels.
LH plasma levels were significantly higher in patients with hypersexual disorder than in healthy volunteers. No significant differences in plasma testosterone, follicle stimulating hormone, prolactin, and SHBG levels were found between the groups. There were no significant associations between DNA methylation of HPA and HPG axis-coupled genes and plasma testosterone or LH levels after multiple testing corrections.
Subtle dysregulation of the HPG axis, with increased LH plasma levels but no difference in testosterone levels may be present in hypersexual men. Chatzittofis A, Boström AE, Öberg KG, et al. Normal Testosterone but Higher Luteinizing Hormone Plasma Levels in Men With Hypersexual Disorder. Sex Med 2020;8:243-250.
建议纳入《精神疾病诊断与统计手册》第5版的性欲亢进障碍整合了性欲失调、冲动性和强迫性等方面。然而,尚不清楚它如何影响性腺活动以及下丘脑-垂体-性腺(HPG)轴的功能。
本研究旨在比较性欲亢进男性与健康对照者的睾酮和黄体生成素(LH)水平。此外,我们还研究了表观遗传标记与激素水平之间的关联。
评估了67名性欲亢进男性(平均年龄:39.2岁)与39名年龄匹配的健康对照者(平均年龄:37.5岁)清晨基础血浆中的睾酮、LH和性激素结合球蛋白(SHBG)水平。使用性强迫量表和性欲亢进障碍:当前评估量表评估性欲亢进行为,使用蒙哥马利-阿斯伯格抑郁量表自评评估抑郁严重程度,使用儿童创伤问卷(CTQ)评估童年逆境史。使用Illumina Infinium甲基化EPIC芯片在全血中测量超过85万个CpG位点的全基因组甲基化模式。纳入位于下丘脑-垂体-肾上腺(HPA)和HPG轴相关基因转录起始位点2000 bp内的CpG位点。
睾酮和LH血浆水平与临床评分的关联,次要观察指标是HPA和HPG轴相关CpG位点的表观遗传谱与睾酮和LH水平的关联。
性欲亢进障碍患者的LH血浆水平显著高于健康志愿者。两组之间的血浆睾酮、促卵泡激素、催乳素和SHBG水平无显著差异。经过多次检验校正后,HPA和HPG轴相关基因的DNA甲基化与血浆睾酮或LH水平之间无显著关联。
性欲亢进男性可能存在HPG轴的细微失调,表现为LH血浆水平升高但睾酮水平无差异。查齐托菲斯A、博斯特罗姆AE、奥伯格KG等。性欲亢进男性睾酮水平正常但黄体生成素血浆水平较高。《性医学》2020年;8:243 - 250。