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他莫昔芬在经前期乳房痛妇女黄体中期使用并不改变血清抑制素 A 和 B 水平。

Toremifene use does not alter serum inhibin A and B levels during mid-luteal phase in women with premenstrual mastalgia.

机构信息

Department of Obstetrics and Gynecology, Satakunta Central Hospital, Pori, Finland.

出版信息

Gynecol Endocrinol. 2010 Feb;26(2):114-7. doi: 10.3109/09513590903215441.

Abstract

AIMS

To find out if there is any link between the therapeutic effect of toremifene on premenstrual mastalgia and luteal phase serum inhibin A and/or B levels.

METHODS

Forty-eight patients participating in a randomized cross-over trial on toremifene vs. placebo for premenstrual mastalgia gave three blood samples during the luteal phase of the menstrual cycle: the first at baseline, the second during the third toremifene/placebo cycle, and the third during the third placebo/toremifene cycle, respectively. The blood samples were analyzed for inhibin A and B with respective specific two-site enzyme-linked immunosorbent assays. Toremifene (20 mg/d) and placebo were administered during the luteal phase only.

RESULTS

When all the toremifene-treated cycles were compared with all the placebo cycles and with the baseline, the median inhibin A levels were 42, 38, and 40 pg/ml, respectively (baseline versus toremifene, p = 0.638; baseline versus placebo, p = 0.468; and toremifene versus placebo, p = 0.365). The median inhibin B levels were at baseline 19 ng/l, during placebo 20 ng/l, and during toremifene 17 ng/l (baseline versus toremifene, p = 0.983; baseline versus placebo, p = 0.519; and toremifene versus placebo, p = 0.880).

CONCLUSION

A luteal administration of toremifene does not seem to result in any changes in mid-luteal concentrations of inhibin A or B in serum.

摘要

目的

探究托瑞米芬治疗经前期乳房痛的疗效与黄体期血清抑制素 A 和/或 B 水平之间是否存在关联。

方法

48 例参与托瑞米芬与安慰剂治疗经前期乳房痛的随机交叉试验的患者在月经周期的黄体期分别采集 3 份血样:第 1 份在基础期,第 2 份在第 3 个托瑞米芬/安慰剂周期,第 3 份在第 3 个安慰剂/托瑞米芬周期。采用特定的双位点酶联免疫吸附试验分析抑制素 A 和 B。仅在黄体期给予托瑞米芬(20 mg/d)和安慰剂。

结果

将所有托瑞米芬治疗周期与所有安慰剂周期以及基础期进行比较,抑制素 A 中位数水平分别为 42、38 和 40 pg/ml(基础期与托瑞米芬比较,p=0.638;基础期与安慰剂比较,p=0.468;托瑞米芬与安慰剂比较,p=0.365)。抑制素 B 中位数水平基础期为 19 ng/l,安慰剂期为 20 ng/l,托瑞米芬期为 17 ng/l(基础期与托瑞米芬比较,p=0.983;基础期与安慰剂比较,p=0.519;托瑞米芬与安慰剂比较,p=0.880)。

结论

黄体期给予托瑞米芬似乎不会导致血清中抑制素 A 或 B 的中黄体期浓度发生任何变化。

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