首页> 外文期刊>Obstetrics and Gynecology: Journal of the American College of Obstetricians and Gynecologists >Hormonal Add-Back Therapy for Females Treated With Gonadotropin-Releasing Hormone Agonist for Endometriosis A Randomized Controlled Trial
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Hormonal Add-Back Therapy for Females Treated With Gonadotropin-Releasing Hormone Agonist for Endometriosis A Randomized Controlled Trial

机译:促性腺激素释放激素激动剂治疗子宫内膜异位症的女性激素加回疗法随机对照试验

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OBJECTIVE:To assess whether add-back therapy with norethindrone acetate or norethindrone acetate plus conjugated equine estrogens is superior to maintain bone health in adolescents and young women using gonadotropin-releasing hormone agonists for endometriosis. Gonadotropin-releasing hormone agonists are associated with deleterious effects on bone. Hormonal add-back may mitigate these effects.METHODS:Adolescents and young women (n=51) received a random, double-blind assignment to add-back with norethindrone acetate (5 mg/day) plus conjugated equine estrogens (0.625 mg/day) or norethindrone acetate plus placebo for 12 months. Body composition, bone mineral content, and bone mineral density (BMD) were obtained by dual-energy X-ray absorptiometry every 6 months. Quality-of-life measures were collected every 3 months. Intention-to-treat comparison of outcomes was conducted by repeated-measures analysis of variance.RESULTS:Thirty-four adolescents and young women completed the trial; dropouts did not differ from those who completed the trial. Bone mineral density was normal at baseline. At 12 months, total body bone mineral content and BMD had increased in the norethindrone acetate plus conjugated equine estrogens group (bone mineral content +37 g, P<.001 and BMD +0.012 g/cm(2), P=.05), but not in those receiving norethindrone acetate plus placebo (bone mineral content P=.19 and BMD P=.95). Lean mass increased only in those receiving conjugated equine estrogens (+1.4 kg, P=.001). Improvements in physical functioning domains of quality-of-life assessments were greater with norethindrone acetate plus conjugated equine estrogens (P=.005). No differences were seen at the hip or lumbar spine by dual-energy X-ray absorptiometry. No significant adverse events occurred.CONCLUSION:Hormonal add-back successfully preserved bone health and improved quality of life for adolescents and young women with endometriosis during 12 months of gonadotropin-releasing hormone agonist therapy. Combination norethindrone acetate plus conjugated equine estrogens add-back appears to be more effective for increasing total body bone mineral content, areal BMD, and lean mass than norethindrone acetate monotherapy.CLINICAL TRIAL REGISTRATION:ClinicalTrials.gov; www.clinicaltrials.gov, NCT00474851.LEVEL OF EVIDENCE:I
机译:目的:评估使用乙酸炔诺酮或乙酸炔诺酮加缀合的马雌激素的补充疗法,对于使用促性腺激素释放激素激动剂治疗子宫内膜异位症的青少年和年轻女性,在维持骨骼健康方面是否更好。促性腺激素释放激素激动剂与对骨骼的有害作用有关。激素补充可能减轻这些影响。方法:青少年(51岁)和年轻妇女随机,双盲分配醋酸乙酸炔诺酮(5毫克/天)和缀合的马雌激素(0.625毫克/天)。 )或醋酸炔诺酮加安慰剂治疗12个月。每6个月通过双能X射线吸收法获得身体成分,骨矿物质含量和骨矿物质密度(BMD)。每3个月收集一次生活质量评估。结果:对意向性治疗结果进行比较,采用重复测量方差分析。结果:34名青少年和年轻妇女完成了该试验。辍学人数与完成审判的人没有什么不同。基线时骨矿物质密度正常。在第12个月时,乙酸炔诺酮和结合的马雌激素组的总骨矿物质含量和BMD升高(骨矿物质含量+37 g,P <.001和BMD +0.012 g / cm(2),P = .05) ,但接受醋酸炔诺酮和安慰剂的患者则不然(骨矿物质含量P = .19和BMD P = .95)。瘦体重仅在接受共轭马雌激素的人群中增加(+1.4 kg,P = .001)。醋酸炔诺酮加马雌激素结合物对生活质量评估的身体机能域的改善更大(P = .005)。双能X线骨密度仪在臀部或腰椎没有发现差异。结论:在促性腺激素释放激素激动剂治疗的12个月内,激素补充成功地维护了青少年和子宫内膜异位症的年轻女性的骨骼健康并改善了其生活质量。与醋酸炔诺酮单药相比,醋酸炔诺酮和马雌激素结合剂的添加似乎更有效地增加了全身骨矿物质含量,面积骨密度和瘦体重。临床试验注册:ClinicalTrials.gov; www.clinicaltrials.gov,NCT00474851。证据级别:I

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