Decensi A, Robertson C, Ballardini B, Paggi D, Guerrieri-Gonzaga A, Bonanni B, Manetti L, Johansson H, Barreca A, Bettega D, Costa A
FIRC Chemoprevention Unit, European Institute of Oncology, Milan, Italy.
Eur J Cancer. 1999 Apr;35(4):596-600. doi: 10.1016/s0959-8049(98)00428-6.
Studies in breast cancer patients have shown that tamoxifen decreases circulating levels of lipoprotein(a) (Lp(a)), an independent risk factor for premature coronary heart disease, and insulin-like growth factor-I (IGF-I), a promising surrogate biomarker for breast cancer. Since a common hormone regulatory pathway has been suggested for both biomarkers, we measured Lp(a) levels for 6 months in 68 healthy women participating in a chemoprevention trial of tamoxifen and correlated its changes with IGF-I. After 1 month, mean Lp(a) levels decreased by 23% with tamoxifen and increased by 6% with placebo (P = 0.033). No further change was observed after 2 and 6 months. Women with abnormal values at baseline (i.e. > 30 mg/dl) showed the highest reduction. The mean levels of IGF-I decreased by 23.5% with tamoxifen and remained stable with placebo, but the changes induced by tamoxifen in Lp(a) and IGF-I levels were uncorrelated. Our results support the observation that tamoxifen may be a suitable preventive option for women with multiple disease risk factors.
对乳腺癌患者的研究表明,他莫昔芬可降低循环中的脂蛋白(a) [Lp(a),冠心病早发的独立危险因素]以及胰岛素样生长因子-I(IGF-I,一种很有前景的乳腺癌替代生物标志物)的水平。由于已有人提出这两种生物标志物存在共同的激素调节途径,我们对68名参与他莫昔芬化学预防试验的健康女性的Lp(a)水平进行了6个月的测量,并将其变化与IGF-I进行关联分析。1个月后,他莫昔芬组的Lp(a)平均水平下降了23%,而安慰剂组则上升了6%(P = 0.033)。2个月和6个月后未观察到进一步变化。基线值异常(即> 30 mg/dl)的女性下降幅度最大。他莫昔芬使IGF-I的平均水平下降了23.5%,而安慰剂组保持稳定,但他莫昔芬引起的Lp(a)和IGF-I水平变化不相关。我们的结果支持以下观点:对于具有多种疾病危险因素的女性,他莫昔芬可能是一种合适的预防选择。