Effects of phytoestrogen genistein on cytogenetic biomarkers in postmenopausal women: 1 year randomized, placebo-controlled study

被引:34
作者
Atteritano, Marco
Pernice, Francesco
Mazzaferro, Susanna
Mantuano, Stefania
Frisina, Alessia
D'Anna, Rosario
Cannata, Maria Letizia
Bitto, Alessandra
Squadrito, Francesco
Frisina, Nicola
Buemi, Michele
机构
关键词
genistein; cytogenetic; biomarker; postmenopausal woman; osteopenic; genomic damage;
D O I
10.1016/j.ejphar.2008.04.049
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
To evaluate in a twelve-month, randomized place bo-control led study whether pure administration of phytoestrogen genistein (54 mg/day) might reduce cytogenetic biomarkers in peripheral lymphocytes of postmenopausal women. A total of 57 postmenopausal women met the criteria and were randomly assigned to receive phytoestrogen genistein (n = 30) or placebo (n = 27). There was no significant difference in age, length of time since menopause or body mass index between the two groups. After one year, plasma genistein level was 0.14 +/- 0.01 mu mol/L in the control group and 0.72 +/- 0.08 mu mol/L in the genistein group (P< 0.0001). At baseline, sister chromatid exchange rate was 4.97 +/- 2.17 in the control group and 4.96 +/- 1.83 in the genistein group (P = 0.89). After one year, sister chromatid exchange rate was 4.96 +/- 2.16 in the control group and 3.98 +/- 1.14 in the genistein group (P< 0.05). High frequency cells count was 3% in the genistein group and 5% in the control group (P < 0.05) at the end of the study. Chromosomal aberration frequency was 5.55% in the control group at time 0 and 5.75% in the genistein group; after one year, the figures were 5.86% in the control group and 4.5% in the genistein group (P < 0.05). After one year, there was a negative relationship between sister chromatid exchange rate and plasma levels (r = - 0.43; P < 0.05) in the genistein group. Phytoestrogen genistein has been shown in postmenopausal women to be effective in the reduction of cytogenetic biomarkers. The protective effect on genoma damage appears to be a particularly promising tool in reducing the risk of cancer. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:22 / 26
页数:5
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