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总血清胆固醇与胰腺癌:巢式病例对照研究。

Total Serum Cholesterol and Pancreatic Cancer: A Nested Case-Control Study.

机构信息

Department of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.

Center for Clinical Epidemiology and Biostatistics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.

出版信息

Cancer Epidemiol Biomarkers Prev. 2019 Feb;28(2):363-369. doi: 10.1158/1055-9965.EPI-18-0421. Epub 2018 Oct 17.

Abstract

BACKGROUND

Pancreatic cancer is the third leading cause of cancer-related death in the United States. Total serum cholesterol (TSC) may predict cancer risk, although its role independent of statins remains elusive. We examined the association between TSC and pancreatic cancer risk independent of statins.

METHODS

A nested case-control analysis was conducted among statin-naïve patients within The Health Improvement Network (THIN), a United Kingdom-based general practice database. Cases were >40 years old and diagnosed with pancreatic cancer after at least 6 months of follow-up. Controls were selected by incidence density sampling and matched by age, sex, practice site, and follow-up. Primary exposure was TSC (mmol/L) prior to index date. Conditional logistic regression estimated ORs for pancreatic cancer risk associated with TSC. Sensitivity analyses were conducted among nondiabetics.

RESULTS

Among 1,241 cases and 3,307 matched controls, an average 8% reduction was observed in pancreatic cancer risk per mmol/L increase in TSC [OR 0.92, 95% confidence interval (CI): 0.85-1.00; nondiabetics: OR 0.91, 95% CI: 0.83-0.99]. When TSC was measured at 12-month intervals prior to diagnosis, the OR between TSC and pancreatic cancer was 0.88 at 0 to 12 months (95% CI: 0.77-1.00; nondiabetics: OR 0.81, 95% CI: 0.68-0.96). No significant association was seen at subsequent discrete intervals before index date.

CONCLUSIONS

TSC is a significant predictor of short-term risk for pancreatic cancer. This risk increase associated with lower TSC was independent of statins.

IMPACT

TSC could serve as a biomarker for risk stratification, screening, and early diagnosis of pancreatic cancer in future clinical prediction models.

摘要

背景

在美国,胰腺癌是导致癌症相关死亡的第三大原因。总血清胆固醇(TSC)可能预测癌症风险,尽管其独立于他汀类药物的作用仍不清楚。我们研究了 TSC 与独立于他汀类药物的胰腺癌风险之间的关系。

方法

在英国基于一般实践数据库的健康改善网络(THIN)中,对他汀类药物初治患者进行了嵌套病例对照分析。病例为年龄>40 岁,并在至少 6 个月的随访后被诊断为胰腺癌。对照通过发病率密度抽样选择,并按年龄、性别、就诊地点和随访进行匹配。主要暴露是索引日期前的 TSC(mmol/L)。条件逻辑回归估计了 TSC 与胰腺癌风险相关的比值比(OR)。在非糖尿病患者中进行了敏感性分析。

结果

在 1241 例病例和 3307 例匹配对照中,TSC 每增加 1mmol/L,胰腺癌风险平均降低 8%[OR 0.92,95%置信区间(CI):0.85-1.00;非糖尿病患者:OR 0.91,95% CI:0.83-0.99]。当 TSC 在诊断前 12 个月内以 12 个月的间隔测量时,TSC 与胰腺癌之间的 OR 为 0 至 12 个月时为 0.88(95%CI:0.77-1.00;非糖尿病患者:OR 0.81,95%CI:0.68-0.96)。在索引日期之前的随后离散间隔内未发现明显关联。

结论

TSC 是胰腺癌短期风险的重要预测指标。这种与较低 TSC 相关的风险增加独立于他汀类药物。

意义

TSC 可作为未来临床预测模型中胰腺癌风险分层、筛查和早期诊断的生物标志物。

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