Plasma phytoestrogens are not altered by probiotic consumption in postmenopausal women with and without a history of breast cancer

被引:53
作者
Nettleton, JA
Greany, KA
Thomas, W
Wangen, KE
Adlercreutz, H
Kurzer, MS [1 ]
机构
[1] Univ Minnesota, Dept Food Sci & Nutr, St Paul, MN 55108 USA
[2] Univ Minnesota, Div Biostat, Minneapolis, MN 55407 USA
[3] Univ Helsinki, Folkhalsan Res Ctr, FIN-00014 Helsinki, Finland
[4] Univ Helsinki, Div Clin Chem, Biomedicum, FIN-00014 Helsinki, Finland
关键词
soy; probiotic; plasma isoflavones;
D O I
10.1093/jn/134.8.1998
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Soy phytoestrogens were suggested to reduce the risk of a number of diseases including breast cancer. Given that these compounds are metabolized by bacteria, alteration of intestinal bacteria and enzymes may affect phytoestrogen metabolism. We hypothesized that probiotics, when consumed with soy protein, would increase plasma isoflavones, as well as equol producer frequency, in postmenopausal women. We further hypothesized that these effects would differ between women who have had breast cancer and women who have not. To test these hypotheses, 20 breast cancer survivors and 20 controls completed four 6-wk treatments in a randomized, crossover design: supplementation with soy protein (S) (26.6 +/- 4.5 g protein, 44.4 +/- 7.5 mg isoflavones/d); soy + probiotics (S+P) (10(9) colony-forming units Lactobacillus acidophilus DDS + 1 and Bifidobacterium longum, 15-30 mg fructooligosaccharide/d); milk protein (M) (215.6 +/- 4.5 g protein/d); and milk + probiotics (M + P). Plasma phytoestrogen concentrations did not differ between controls and survivors, although genistein tended to be lower in survivors at baseline (P = 0.15), and during soy (P = 0.16) and milk protein (P = 0.16) consumption. As expected, soy consumption increased plasma phytoestrogen concentrations (P < 0.0001). Plasma phytoestrogen concentrations and the number of equol producers did not differ between the S and S+P diets. At the same time, plasma equol concentrations as well as urinary equol excretion in 2 subjects were more than 7-fold different between the 2 diets. These results indicate that this particular probiotic supplement does not generally affect plasma isoflavones, although the large differences between plasma and urinary equol in some subjects suggest that equol producer status may be modifiable in some individuals.
引用
收藏
页码:1998 / 2003
页数:6
相关论文
共 51 条
[1]  
ADLERCREUTZ H, 1982, LANCET, V2, P1295
[2]   URINARY-EXCRETION OF LIGNANS AND ISOFLAVONOID PHYTOESTROGENS IN JAPANESE MEN AND WOMEN CONSUMING A TRADITIONAL JAPANESE DIET [J].
ADLERCREUTZ, H ;
HONJO, H ;
HIGASHI, A ;
FOTSIS, T ;
HAMALAINEN, E ;
HASEGAWA, T ;
OKADA, H .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1991, 54 (06) :1093-1100
[3]   Time-resolved fluoroimmunoassay for plasma enterolactone [J].
Adlercreutz, H ;
Wang, GJJ ;
Lapcík, O ;
Hampl, R ;
Wähälä, K ;
Mäkelä, T ;
Lusa, K ;
Talme, M ;
Mikola, H .
ANALYTICAL BIOCHEMISTRY, 1998, 265 (02) :208-215
[4]   In vitro incubation of human feces with daidzein and antibiotics suggests interindividual differences in the bacteria responsible for equol production [J].
Atkinson, C ;
Berman, S ;
Humbert, O ;
Lampe, JW .
JOURNAL OF NUTRITION, 2004, 134 (03) :596-599
[5]   SOYA - A DIETARY SOURCE OF THE NON-STEROIDAL ESTROGEN EQUOL IN MAN AND ANIMALS [J].
AXELSON, M ;
SJOVALL, J ;
GUSTAFSSON, BE ;
SETCHELL, KDR .
JOURNAL OF ENDOCRINOLOGY, 1984, 102 (01) :49-56
[6]   Metabolism of isoflavones and lignans by the gut microflora: a study in germ-free and human flora associated rats [J].
Bowey, E ;
Adlercreutz, H ;
Rowland, I .
FOOD AND CHEMICAL TOXICOLOGY, 2003, 41 (05) :631-636
[7]   Time-resolved fluoroimmunoassay for equol in plasma and urine [J].
Brouwers, E ;
L'homme, R ;
Al-Maharik, N ;
Lapcík, O ;
Hampl, R ;
Wähälä, K ;
Mikola, H ;
Adlercreutz, H .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2003, 84 (05) :577-588
[8]   Metabolism of daidzein and genistein by intestinal bacteria [J].
Chang, YC ;
Nair, MG .
JOURNAL OF NATURAL PRODUCTS, 1995, 58 (12) :1892-1896
[9]  
Cole C. B., 1989, Microbial Ecology in Health and Disease, V2, P223
[10]  
Dai Q, 2002, CANCER EPIDEM BIOMAR, V11, P815