Geier David A, Geier Mark R
Vice-President of the Institute of Chronic Illnesses, Silver Spring, MD, USA.
Neuro Endocrinol Lett. 2007 Oct;28(5):565-73.
Impairments in social relatedness and communication, repetitive behaviors, abnormal movement patterns, and sensory dysfunction characterize autism spectrum disorders (ASDs). Seventy consecutive patients with an ASD diagnosis (DSM-IV criteria, >/= 6 years-old) who presented to the Genetic Centers of America for outpatient genetic/developmental evaluations from 2005-2007 were examined. Patients were evaluated using CLIA-approved Laboratory Cooperation of America (LabCorp) testing for: serum testosterone, serum free testosterone, % free testosterone, serum/plasma dehydroepiandrosterone (DHEA), androstendione, and follicle-stimulating hormone (FSH). Morning blood samples collected following an overnight fast, compared to the pertinent reference means, showed significantly increased relative mean levels for: serum testosterone (158%), serum free testosterone (214%), percent free testosterone (121%), DHEA (192%), and androstenedione (173%). By contrast, compared to the pertinent reference mean, the relative mean level of FSH (51%) was significantly decreased. Additionally, at least one of the androgen attributes examined exceeded its recognized laboratory age- and sex-specific reference range in 81.4% (57 of 70) of the patients examined. With respect to their age- and sex-specific reference ranges, females had significantly higher overall mean relative testosterone and relative free testosterone levels than males. Increased androgens in patients diagnosed with ASDs may involve cyclical interactions between the androgen and the transsulfuration pathways, particularly following mercury exposure. A review of therapies that have significantly improved clinical outcomes in ASD patients indicates they share commonality in helping lower androgens. Thus, androgens should be routinely clinically measured in patients with an ASD diagnosis and appropriate androgen-lowering therapies considered for those who have significantly elevated levels.
社交关系和沟通障碍、重复行为、异常运动模式以及感觉功能障碍是自闭症谱系障碍(ASD)的特征。对2005年至2007年期间前往美国遗传中心进行门诊遗传/发育评估的70例连续诊断为ASD(符合《精神疾病诊断与统计手册第四版》标准,年龄≥6岁)的患者进行了检查。使用美国临床实验室改进修正案(CLIA)批准的美国实验室合作公司(LabCorp)检测方法对患者进行评估,检测项目包括:血清睾酮、血清游离睾酮、游离睾酮百分比、血清/血浆脱氢表雄酮(DHEA)、雄烯二酮和促卵泡激素(FSH)。与相关参考均值相比,过夜禁食后采集的早晨血样显示,以下各项的相对平均水平显著升高:血清睾酮(158%)、血清游离睾酮(214%)、游离睾酮百分比(121%)、DHEA(192%)和雄烯二酮(173%)。相比之下,与相关参考均值相比,FSH的相对平均水平(51%)显著降低。此外,在接受检查的患者中,81.4%(70例中的57例)的雄激素指标中至少有一项超出其公认的实验室年龄和性别特异性参考范围。就其年龄和性别特异性参考范围而言,女性的总体平均相对睾酮和相对游离睾酮水平显著高于男性。被诊断为ASD的患者雄激素水平升高可能涉及雄激素与转硫途径之间的循环相互作用,尤其是在接触汞之后。对在ASD患者中显著改善临床结果的疗法进行的综述表明,它们在帮助降低雄激素方面具有共性。因此,对于诊断为ASD的患者,应常规进行临床雄激素检测,对于雄激素水平显著升高的患者,应考虑采取适当的降低雄激素疗法。