Division of Adolescent Medicine, Children's Hospital Boston, Boston, MA 02115, USA.
Metabolism. 2012 Jul;61(7):1010-20. doi: 10.1016/j.metabol.2011.11.016. Epub 2012 Jan 16.
Anorexia nervosa (AN) is characterized by subnormal estrogen and dehydroepiandrosterone (DHEA) levels. We sought to determine whether the combination of DHEA + estrogen/progestin is superior to placebo in preserving skeletal health over 18 months in AN. Females with AN, aged 13 to 27 years, were recruited for participation in this double-blind, placebo-controlled, randomized trial. Ninety-four subjects were randomized, of whom 80 completed baseline assessments and received either study drug (oral micronized DHEA 50 mg + 20 µg ethinyl estradiol/0.1 mg levonorgestrel combined oral contraceptive pill [COC] daily; n = 43) or placebo (n = 37). Serial measurements of areal bone mineral density (aBMD), bone turnover markers, and serum hormone concentrations were obtained. Sixty subjects completed the 18-month trial. Spinal and whole-body aBMD z scores were preserved in the DHEA + COC group, but decreased in the placebo group (comparing trends, P = .008 and P = .001, respectively). Bone turnover markers initially declined in subjects receiving DHEA + COC and then returned to baseline. No differences in body composition, adverse effects of therapy, or alterations in biochemical safety parameters were observed. Combined therapy with DHEA + COC appears to be safe and effective for preventing bone loss in young women with AN, whereas placebo led to decreases in aBMD. Dehydroepiandrosterone + COC may be safely used to preserve bone mass as efforts to reverse the nutritional, psychological, and other hormonal components of AN are implemented.
神经性厌食症(AN)的特征是雌激素和脱氢表雄酮(DHEA)水平低于正常水平。我们试图确定 DHEA+雌激素/孕激素联合治疗是否优于安慰剂,以在 18 个月内改善 AN 患者的骨骼健康。招募了年龄在 13 至 27 岁之间的 AN 女性参与这项双盲、安慰剂对照、随机试验。94 名受试者被随机分组,其中 80 名完成了基线评估并接受了研究药物(口服微粒化 DHEA 50mg+20µg 炔雌醇/0.1mg 左炔诺孕酮联合口服避孕药[COC],每日一次;n=43)或安慰剂(n=37)。定期测量骨矿物质密度(aBMD)、骨转换标志物和血清激素浓度。60 名受试者完成了 18 个月的试验。DHEA+COC 组的脊柱和全身 aBMD z 评分保持不变,但安慰剂组的 aBMD z 评分下降(比较趋势,P=0.008 和 P=0.001)。DHEA+COC 组的骨转换标志物最初下降,然后恢复到基线。未观察到身体成分、治疗的不良反应或生化安全性参数的改变。联合 DHEA+COC 治疗似乎安全有效,可预防年轻 AN 女性的骨丢失,而安慰剂则导致 aBMD 下降。DHEA+COC 可安全用于维持骨量,同时努力逆转 AN 的营养、心理和其他激素成分。