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首页> 外文期刊>Annals of epidemiology >Multiple metabolic risk factors and mammographic breast density
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Multiple metabolic risk factors and mammographic breast density

机译:多种代谢危险因素和乳房X线照片

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Purpose: We examined whether obesity and a history of diabetes, hypertension, and elevated cholesterol, individually and in combination, are associated with breast density, a strong risk factor for breast cancer. Methods: We measured percent density and dense area using a computer-assisted method (n = 191; age range = 40-61 years). We used linear regression models to examine the associations of each metabolic condition and the number of metabolic conditions (zero, one, two, and three or four conditions) with breast density. Results: Among individual metabolic conditions, only high blood cholesterol was inversely associated with percent density (β = -5.4, 95% confidence interval [CI]: -8.5, -2.2) and dense area (β = -6.7, 95% CI = -11.1, -2.4). Having multiple metabolic conditions was also associated with lower breast density, with two conditions and three or four conditions versus zero conditions associated with 6.4% (95% CI: -11.2, -1.6) and 7.4% (95% CI: -12.9, -1.9) reduction in percent density and with 6.5 cm2 (95% CI: -13.1, -0.1) and 9.5 cm2 (95% CI: -17.1, -1.9) decrease in dense area. Conclusions: A history of high blood cholesterol and multiple metabolic conditions were associated with lower relative and absolute measures of breast density. The positive association between metabolic abnormalities and breast cancer risk may be driven by pathways unrelated to mammographic breast density.
机译:目的:我们检查了肥胖和糖尿病史,高血压,胆固醇升高是否单独或组合与乳房密度有关,乳房密度是乳腺癌的重要危险因素。方法:我们使用计算机辅助方法(n = 191;年龄范围= 40-61岁)测量了密度和密集区域的百分比。我们使用线性回归模型来检查每种代谢状况以及代谢状况的数量(零,一,二,三或四个状况)与乳房密度的关联。结果:在个体代谢状况中,只有高血胆固醇与百分比密度(β= -5.4,95%置信区间[CI]:-8.5,-2.2)和致密区域(β= -6.7,95%CI = -11.1,-2.4)。具有多种代谢状况也与较低的乳腺密度有关,其中两种状况和三或四种状况与零状况相关,分别为6.4%(95%CI:-11.2,-1.6)和7.4%(95%CI:-12.9,- 1.9)的百分比密度降低,密集区域的面积减少6.5 cm2(95%CI:-13.1,-0.1)和9.5 cm2(95%CI:-17.1,-1.9)。结论:高胆固醇血症和多种代谢状况的病史与较低的相对和绝对的乳房密度测量值相关。代谢异常与乳腺癌风险之间的正相关可能是由与乳腺X线密度无关的途径驱动的。

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