Kalantaridou Sophia N, Vanderhoof Vien H, Calis Karim A, Corrigan Emily C, Troendle James F, Nelson Lawrence M
Integrative Reproductive Medicine Unit, Reproductive Biology and Medicine Branch, Intramural Research Program, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA.
Fertil Steril. 2008 Nov;90(5):1805-11. doi: 10.1016/j.fertnstert.2007.08.040. Epub 2007 Oct 25.
To assess sexual function in women with spontaneous 46,XX primary ovarian insufficiency after at least 3 months of a standardized hormone replacement regimen.
Cross-sectional cohort, controlled.
National Institutes of Health Clinical Research Center.
PATIENT(S): Women with primary ovarian insufficiency (n = 143) and regularly menstruating controls (n = 70).
INTERVENTION(S): Self-administered questionnaires, 100 microg/day E(2) patch, oral medroxyprogesterone acetate 10 mg for 12 days each month for patients.
MAIN OUTCOME MEASURE(S): Derogatis Interview for Sexual Function Self-Report (DISF-SR).
RESULT(S): Women with primary ovarian insufficiency had significantly lower DISF-SR composite scores compared with control women. Their serum total testosterone levels were significantly correlated with DISF-SR composite score, although this accounted for only 4% of the variance in this measure. Patients with testosterone levels below normal tended to have lower DISF-SR composite scores. Of patients with primary ovarian insufficiency, 9 of 127 (7%) scored below the second percentile on the composite sexual function score, compared with 1 of 49 control women (2%).
CONCLUSION(S): As assessed by the DISF-SR, sexual function is in the normal range for most young women with 46,XX spontaneous primary ovarian insufficiency who are receiving physiologic E(2) replacement. However, as a group, these young women score significantly lower on this sexual function scale than control women.
评估在接受至少3个月标准化激素替代治疗方案后,46,XX型原发性卵巢功能不全女性的性功能。
横断面队列研究,有对照。
国立卫生研究院临床研究中心。
原发性卵巢功能不全女性(n = 143)和月经规律的对照女性(n = 70)。
自行填写问卷,患者使用100微克/天的雌二醇贴片,每月口服醋酸甲羟孕酮10毫克,共12天。
性功能自我报告的德罗加蒂斯访谈(DISF-SR)。
与对照女性相比,原发性卵巢功能不全女性的DISF-SR综合评分显著更低。她们的血清总睾酮水平与DISF-SR综合评分显著相关,尽管这仅占该指标方差的4%。睾酮水平低于正常的患者往往有更低的DISF-SR综合评分。在原发性卵巢功能不全患者中,127人中有9人(7%)的综合性功能评分低于第2百分位数,而49名对照女性中有1人(2%)。
通过DISF-SR评估,对于大多数接受生理性雌二醇替代治疗的46,XX型原发性卵巢功能不全年轻女性,其性功能处于正常范围。然而,作为一个群体,这些年轻女性在该性功能量表上的得分显著低于对照女性。