Plasma total cholesterol concentration and risk of higher‐grade prostate cancer: A nested case‐control study and a dose‐response meta‐analysis

Author:

Liu Hui12ORCID,Shui Irene M.3,Keum NaNa4,Shen Xudan5,Wu Kana2,Clinton Steven K.6,Cao Yin78,Song Mingyang9,Zhang Xuehong210ORCID,Platz Elizabeth A.11ORCID,Giovannucci Edward L.212

Affiliation:

1. Central Lab, Sir Run Run Shaw Hospital, School of Medicine Zhejiang University Hangzhou China

2. Department of Nutrition Harvard School of Public Health Boston Massachusetts USA

3. Merck & Co., Inc. Rahway New Jersey USA

4. Department of Food Science and Biotechnology Dongguk University Goyang South Korea

5. Institute of Drug Metabolism and Pharmaceutical Analysis, Zhejiang Province Key Laboratory of Anti‐Cancer Drug Research Zhejiang University Hangzhou China

6. Division of Public Health Sciences, Division of Medical Oncology The James Cancer Hospital and The Ohio State University Comprehensive Cancer Center Columbus Ohio USA

7. Department of Surgery Washington University School of Medicine St Louis Missouri USA

8. Alvin J. Siteman Cancer Center Washington University School of Medicine St. Louis Missouri USA

9. Clinical and Translational Epidemiology Unit, Massachusetts General Hospital Harvard Medical School Boston Massachusetts USA

10. Channing Division of Network Medicine, Department of Medicine Brigham and Women's Hospital and Harvard Medical School Boston Massachusetts USA

11. Department of Epidemiology Johns Hopkins Bloomberg School of Public Health, and the Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins Baltimore Maryland USA

12. Department of Epidemiology Harvard School of Public Health Boston Massachusetts USA

Abstract

AbstractOur previous publication found an increased risk of higher‐grade (Gleason sum ≥7) prostate cancer for men with high total cholesterol concentration (≥200 mg/dl) in the Health Professionals Follow‐up Study (HPFS). With additional 568 prostate cancer cases, we are now able to investigate this association in more detail. For the nested case‐control study, we included 1260 men newly diagnosed with prostate cancer between 1993 and 2004, and 1328 controls. For the meta‐analyses, 23 articles studied the relationship between total cholesterol level and prostate cancer incidence were included. Logistic regression models and dose‐response meta‐analysis were performed. An increased risk of higher‐grade (Gleason sum ≥4 + 3) prostate cancer for high vs low quartile of total cholesterol level was observed in the HPFS (ORmultivariable = 1.56; 95% CI = 1.01‐2.40). This finding was compatible with the association noted in the meta‐analysis of highest vs lowest group of total cholesterol level, which suggested a moderately increased risk of higher‐grade prostate cancer (Pooled RR =1.21; 95%CI: 1.11‐1.32). Moreover, the dose‐response meta‐analysis indicated that an increased risk of higher‐grade prostate cancer occurred primarily at total cholesterol levels ≥200 mg/dl, where the RR was 1.04 (95%CI: 1.01‐1.08) per 20 mg/dl increase in total cholesterol level. However, total cholesterol concentration was not associated with the risk of prostate cancer overall either in the HPFS or in the meta‐analysis. Our primary finding, as well as the result of the meta‐analysis suggested a modest increased risk of higher‐grade prostate cancer, at total cholesterol concentrations exceeding 200 mg/dl.

Funder

National Cancer Institute

National Heart, Lung, and Blood Institute

Publisher

Wiley

Subject

Cancer Research,Oncology

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