Effect of human placental extract on menopausal symptoms, fatigue, and risk factors for cardiovascular disease in middle-aged Korean women

被引:44
作者
Kong, Mi-Hee [1 ]
Lee, Eun-Ju [2 ]
Lee, Soon-Yong [3 ]
Cho, Seong-Jin [4 ]
Hong, Young-Sun [5 ]
Park, Sat-Byul [1 ]
机构
[1] Ajou Univ, Coll Med, Dept Family Practice, Suwon 441749, South Korea
[2] Ajou Univ, Coll Med, Dept Radiol, Suwon 441749, South Korea
[3] Ajou Univ, Coll Med, Dept Prevent Med, Suwon 441749, South Korea
[4] Hallym Univ, Coll Med, Dept Pathol, Seoul, South Korea
[5] Ewha Womans Univ, Coll Med, Dept Internal Med, Seoul, South Korea
来源
MENOPAUSE-THE JOURNAL OF THE NORTH AMERICAN MENOPAUSE SOCIETY | 2008年 / 15卷 / 02期
关键词
human placental extract; menopausal symptoms; fatigue;
D O I
10.1097/gme.0b013e3181405b74
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: In Korea, human placental extract (HPE) has recently been used to treat various diseases (chronic liver diseases, menopause syndrome, chronic fatigue, skin pigment diseases, etc.), but evidence-based studies are not yet sufficient. The aim of this study was to examine the effects of HPE on menopausal symptoms, fatigue, and risk factors for cardiovascular disease in middle-aged Korean women in a randomized controlled trial. Design: Korean women, aged 40 to 64 years, with menopausal symptoms and fatigue were recruited as participants. The women were randomly assigned to a placebo group or an HPE group. The HPE group received subcutaneous injections of HPE in the abdomen for 8 weeks, whereas the placebo group received normal saline. Then, the Menopause Rating Scale, and Fatigue Severity Scale, and Visual Analog Scale were administered, and risk factors for cardiovascular disease were assessed. Results: The Menopause Rating Scale total baseline score was not different between the two groups; however, the score of the HPE group decreased significantly at 8 weeks compared with that of the placebo group (P = 0.033). Fatigue Severity Scale and Visual Analog Scale scores of the placebo group did not change, whereas the scores of the HPE group decreased significantly during the study period (Fatigue Severity Scale, P = 0.002; Visual Analog Scale, P = 0.001). The baseline 17 beta-estradiol level was not significantly different between the two groups, but the 17 beta-estradiol level of the HPE group was significantly increased at 8 weeks compared with that of the placebo group (P = 0.031). No changes in risk factors for cardiovascular disease were observed in either group. Conclusions: Menopausal symptoms and fatigue in middle-aged Korean women improved after 8 weeks of HPE treatment, whereas risk factors for cardiovascular disease did not change during the study period.
引用
收藏
页码:296 / 303
页数:8
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