癌症及其与冠状动脉钙化发展的关系:多种族动脉粥样硬化研究》的评估。

Matthew C Whitlock, Joseph Yeboah, Gregory L Burke, Haiying Chen, Heidi D Klepin, W Gregory Hundley
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引用次数: 0

摘要

背景:尽管癌症及其相应疗法与缺血性心脏病的增加有关,但癌症与冠状动脉钙化(CAC)(亚临床动脉粥样硬化的标志物)发展之间的时间关系尚不清楚:在 "多种族动脉粥样硬化研究"(Multi-Ethnic Study of Atherosclerosis)试验的 3122 名无心血管疾病和癌症的男性和女性中,分别在基线期(2000-2002 年)和随访期(2010-2012 年)进行了 CAC 评分。在这 10 年间,85 名男性(年龄为 63.6±8.3 岁)和 50 名女性(年龄为 62.1±9.8 岁)被诊断出患有癌症(女性主要是乳腺癌、肺癌或子宫癌 [52%],男性主要是前列腺癌或结直肠癌 [78%])。其他 2987 名受试者(男性年龄为 59.6±9.2岁,女性年龄为 59.7±9.4岁)仍未罹患癌症。新的 CAC(基线 Agatston 评分为零,转换为可检测到的 CAC)发病率通过相对风险回归进行建模,并对癌症与未患癌症进行比较。利用对数转换 CAC 的线性回归,比较了这些组中原有 CAC 的增加情况。CAC的发病率与癌症史独立相关(女性和男性的相对风险分别为1.32[P=0.04]和1.29[P=0.01])。在基线有 CAC 的参与者中,未观察到癌症和非癌症参与者之间有明显的 CAC 进展差异(女性 P=0.6,男性 P=0.2):结论:即使考虑了动脉粥样硬化风险因素,癌症诊断仍与 CAC 的发展相关。结论:即使考虑了动脉粥样硬化风险因素,癌症诊断仍与 CAC 的发展有关。然而,对于已有 CAC 的人来说,癌症的存在是否会随着时间的推移而加速 CAC 的发展尚不清楚。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cancer and Its Association With the Development of Coronary Artery Calcification: An Assessment From the Multi-Ethnic Study of Atherosclerosis.

Background: Although cancer and its corresponding therapies are associated with increased ischemic heart disease, the temporal relationship between cancer and the development of coronary artery calcium (CAC), a marker of subclinical atherosclerosis, is unknown.

Methods and results: Among 3122 men and women free of cardiovascular disease and cancer in the Multi-Ethnic Study of Atherosclerosis trial, CAC scoring was performed at baseline (2000-2002) and at follow-up (2010-2012). Over this 10-year period, 85 men (age 63.6±8.3 years) and 50 women (age 62.1±9.8 years) were diagnosed with cancer (predominantly breast, lung, or uterine [52%] in women and prostate or colorectal [78%] in men). The other 2987 subjects (age 59.6±9.2 years for men, 59.7±9.4 years for women) remained cancer free. The incidence of new CAC (baseline Agatston score of zero converting to detectable CAC) was modeled with relative risk regression and compared for cancer versus no cancer. Increase in pre-existing CAC was compared in these groups using linear regression of log transformed CAC. The incidence of CAC was independently associated with cancer history (relative risk 1.32 [P=0.04] and 1.29 [P=0.01] for women and men, respectively). In participants with CAC at baseline, a clear difference of CAC progression was not observed between cancer and noncancer participants (P=0.6 for women, P=0.2 for men).

Conclusions: A diagnosis of cancer is associated with the development of CAC even after accounting for atherosclerotic risk factors. However, in individuals with pre-existing CAC, it is not clear whether the presence of cancer accelerates CAC over time.

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