Al Kindi Manal K, Al Essry Faiza S, Al Essry Fatma S, Mula-Abed Waad-Allah S
Department of Chemical Pathology, Royal Hospital, Muscat, Sultanate of Oman.
Oman Med J. 2012 Nov;27(6):471-4. doi: 10.5001/omj.2012.112.
There are technical limitations for the currently available methods of measuring serum total and free testosterone in females. The study objectives were to evaluate the usefulness of serum total testosterone, sex hormone-binding globulin (SHBG), free androgen index (FAI), and calculated free testosterone (CFT) in the assessment of androgen status in women investigated for suspected hyperandrogenism.
This is a case control study that was conducted during the period from 1(st) May 2011 to 31(st) October 2011 on 122 patients aged (18-45 years) whom were referred to the Clinical Biochemistry Laboratory from the Endocrinology and Gynecology Clinics, Royal Hospital, Oman. Women with no clinical feature or laboratory data indicative of hormonal dysfunction and with midluteal progesterone >30 nmol/L were selected as controls (group 1; n=18). The patients were divided into subgroups based on the clinical/laboratory diagnosis of polycystic ovary syndrome (PCOS [group 2; n=19), hirsutism (group 3; n=18), menstrual disturbances (irregularities) or infertility (group 4; n=49), as well as combination of PCOS or hirsutism and menstrual disturbances or infertility (group 5; n=18). Serum total testosterone and SHBG were measured, FAI was calculated as percentage ratio of total testosterone to SHBG values, and CFT was calculated according to Vermeulen equation.
There was a statistically significant difference in the mean levels of testosterone, FAI and CFT in each patient group compared with the control group. For diagnosing hyperandrogenism, each indicator was selected at the recommended cut-off: testosterone >3.0 nmol/L, SHBG <30 nmol/L, FAI >5%, and CFT >32 pmol/L. In group 2, 89.5% and 94.7% of the patients had increased FAI and CFT, respectively; compared with 36.4% for increased testosterone. In group 3, 88.9% and 88.9% of the patients had similarly increased FAI and CFT, respectively; compared with 66.7% for testosterone. In group 4, patients had 63.3% and 73.5% elevated FAI and CFT, respectively; compared with 53.1% for testosterone, while in group 5, patients had 83.3% and 88.9% elevated FAI and CFT, respectively, compared with 61.1% for testosterone.
The diagnosis of hyperandrogenism was most obvious when using CFT or FAI than testosterone alone. It is thus recommended to include these calculated parameters (CFT and/or FAI) in the routine investigation and assessment of women with disorders related to clinical or biochemical hyperandrogenism.
目前用于测量女性血清总睾酮和游离睾酮的方法存在技术局限性。本研究的目的是评估血清总睾酮、性激素结合球蛋白(SHBG)、游离雄激素指数(FAI)和计算游离睾酮(CFT)在评估疑似高雄激素血症女性雄激素状态中的作用。
这是一项病例对照研究,于2011年5月1日至2011年10月31日期间对122名年龄在18至45岁之间、从阿曼皇家医院内分泌科和妇科诊所转诊至临床生物化学实验室的患者进行。选择无临床特征或实验室数据表明激素功能障碍且黄体中期孕酮>30 nmol/L的女性作为对照组(第1组;n = 18)。根据多囊卵巢综合征(PCOS [第2组;n = 19])、多毛症(第3组;n = 18)、月经紊乱(不规律)或不孕(第4组;n = 49)以及PCOS或多毛症与月经紊乱或不孕的组合(第5组;n = 18)的临床/实验室诊断将患者分为亚组。测量血清总睾酮和SHBG,计算FAI作为总睾酮与SHBG值的百分比比值,并根据Vermeulen方程计算CFT。
与对照组相比,各患者组的睾酮、FAI和CFT平均水平存在统计学显著差异。为诊断高雄激素血症,每个指标均选择推荐的临界值:睾酮>3.0 nmol/L,SHBG <30 nmol/L,FAI >5%,CFT >32 pmol/L。在第2组中,分别有89.5%和94.7%的患者FAI和CFT升高;相比之下,睾酮升高的患者为36.4%。在第3组中,分别有88.9%和88.9%的患者FAI和CFT同样升高;相比之下,睾酮升高的患者为66.7%。在第4组中,患者的FAI和CFT分别升高63.3%和73.5%;相比之下,睾酮升高的患者为53.1%,而在第5组中,患者的FAI和CFT分别升高83.3%和88.9%,相比之下,睾酮升高的患者为61.1%。
使用CFT或FAI诊断高雄激素血症比单独使用睾酮更为明显。因此,建议在对临床或生化高雄激素血症相关疾病的女性进行常规检查和评估时纳入这些计算参数(CFT和/或FAI)。