Coppola John-Anthony, Shrubsole Martha J, Cai Qiuyin, Smalley Walter E, Dai Qi, Ness Reid M, Fazio Sergio, Zheng Wei, Murff Harvey J
Florida State University College of Medicine, Tallahassee, FL, USA.
Cancer Causes Control. 2015 Apr;26(4):635-43. doi: 10.1007/s10552-015-0555-y. Epub 2015 Mar 12.
Abnormalities in lipid levels have been associated with colorectal neoplasm risk; however, few studies have adjusted for use of cholesterol-lowering medications. The objective of this study was to determine the association of plasma lipid levels with adenoma risk while accounting for statin medication use.
We included 254 subjects with advanced adenoma, 246 with single small adenoma, 179 with multiple small adenoma cases, and 403 control participants in the Tennessee Colorectal Polyp Study who also had plasma lipid measurements performed. Data on the use of statin medications were available for 83.4% of these participants. The association between plasma lipids and adenoma risk was evaluated using logistic regression models.
Participants in the highest quartile of HDL cholesterol (range 52-106 mg/dl) had an adjusted odds ratio of 0.49 (95% CI 0.23, 1.07), 0.35 (95% CI 0.13, 0.91), and 0.22 (95% CI 0.09, 0.54) for single small, multiple small, and advanced adenomas compared to the lowest quartile (range 12-34 mg/dl), respectively. Participants with the highest quartile of triglyceride levels (range 178-721 mg/dl) had an adjusted odds ratio of 2.40 (95% CI 1.26, 4.55), 1.67 (95% CI 0.66, 4.23), and 2.79 (95% CI 1.25, 6.23) for single small, multiple small, and advanced adenoma, respectively, compared to the lowest quartile (range 40-84 mg/dl). When restricted to individuals with known statin medication use, adjusting for statin use did not appreciably affect these results.
We found a direct association between triglyceride plasma levels and an inverse association between plasma HDL cholesterol levels and adenoma risk. Both effects were not appreciably changed when accounting for the regular use of statin medication.
血脂水平异常与结直肠肿瘤风险相关;然而,很少有研究对使用降胆固醇药物进行校正。本研究的目的是在考虑他汀类药物使用情况的同时,确定血浆脂质水平与腺瘤风险之间的关联。
我们纳入了田纳西结直肠息肉研究中的254例进展性腺瘤患者、246例单发小腺瘤患者、179例多发小腺瘤患者以及403例对照参与者,这些参与者均进行了血浆脂质检测。83.4%的参与者有他汀类药物使用数据。使用逻辑回归模型评估血浆脂质与腺瘤风险之间的关联。
高密度脂蛋白胆固醇处于最高四分位数(范围52 - 106mg/dl)的参与者,与最低四分位数(范围12 - 34mg/dl)相比,单发小腺瘤、多发小腺瘤和进展性腺瘤的校正比值比分别为0.49(95%CI 0.23, 1.07)、0.35(95%CI 0.13, 0.91)和0.22(95%CI 0.09, 0.54)。甘油三酯水平处于最高四分位数(范围178 - 721mg/dl)的参与者,与最低四分位数(范围40 - 84mg/dl)相比,单发小腺瘤、多发小腺瘤和进展性腺瘤的校正比值比分别为2.40(95%CI 1.26, 4.55)、1.67(95%CI 0.66, 4.23)和2.79(95%CI 1.25, 6.23)。当仅限于已知使用他汀类药物的个体时,校正他汀类药物的使用对这些结果没有明显影响。
我们发现血浆甘油三酯水平与腺瘤风险呈正相关,血浆高密度脂蛋白胆固醇水平与腺瘤风险呈负相关。在考虑他汀类药物的常规使用时,这两种效应均无明显变化。