Colin Catherine, Schott Anne-Marie, Valette Pierre-Jean
Radiology Unit, Lyon Sud Hospital, Lyon 1 University, Hospices Civils de Lyon, 69495, Pierre Bénite Cedex, France,
Eur Radiol. 2014 Oct;24(10):2412-6. doi: 10.1007/s00330-014-3278-7. Epub 2014 Jun 28.
Numerous studies established high mammographic density (MD) as a significant breast cancer risk. By adopting both radiological and epidemiological perspectives, we analysed the capacity of this radiological parameter to express an individual level of risk and the methods for assessing the relationship between MD categories and risk. MD is unable to identify individual underlying anatomical and physiological components. Many factors affect accurate and reproducible measurements and consequently classifications of MD. Significant relative risks were found by comparing the MD categories in the tails of distribution (i.e. the group of women with the lowest MD to that with the highest MD), which represent <10 % of women in each group: the majority of the population was ignored. When a relevant threshold of MD was applied to compare another group and the entire population was included to compare the two groups, some studies showed no significant or only moderate relative risk (RR) between women with readings above and those below the threshold. Sensitivity and specificity remain unknown. MD cannot be considered a worthwhile test by which to categorically identify high-risk women in screening. Key points • Unknown individual anatomical and physiological components do not express the risk level.• The epidemiological conditions are not relevant to distinguish a high-risk category.• The most relevant studies show no or moderate risks.
众多研究已证实乳腺钼靶高密度(MD)是乳腺癌的一项重要风险因素。通过采用放射学和流行病学的视角,我们分析了这一放射学参数表达个体风险水平的能力以及评估MD类别与风险之间关系的方法。MD无法识别个体潜在的解剖学和生理学组成部分。许多因素会影响MD测量的准确性和可重复性,进而影响MD的分类。通过比较分布两端的MD类别(即MD最低的女性群体与MD最高的女性群体)发现了显著的相对风险,而每组中处于两端的女性占比均不到10%:大多数人群被忽视了。当应用一个相关的MD阈值来比较另一组人群并纳入全体人群进行两组比较时,一些研究表明,MD读数高于阈值和低于阈值的女性之间没有显著的相对风险,或仅有中度相对风险(RR)。敏感性和特异性仍然未知。在筛查中,MD不能被视为一种能够明确识别高危女性的有效检测方法。要点•未知的个体解剖学和生理学组成部分无法表达风险水平。•流行病学条件与区分高危类别无关。•最相关的研究显示无风险或仅有中度风险。