Plasma total cholesterol concentration and risk of higher-grade prostate cancer: A nested case-control study and a dose-response meta-analysisopen access
- Authors
- Liu, Hui; Shui, Irene M.; Keum, NaNa; Shen, Xudan; Wu, Kana; Clinton, Steven K.; Cao, Yin; Song, Mingyang; Zhang, Xuehong; Platz, Elizabeth A.; Giovannucci, Edward L.
- Issue Date
- Oct-2023
- Publisher
- WILEY
- Keywords
- dose-response meta-analysis; nested case-control study; prostate cancer; total cholesterol
- Citation
- International Journal of Cancer, v.153, no.7, pp 1337 - 1346
- Pages
- 10
- Indexed
- SCIE
SCOPUS
- Journal Title
- International Journal of Cancer
- Volume
- 153
- Number
- 7
- Start Page
- 1337
- End Page
- 1346
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/21160
- DOI
- 10.1002/ijc.34621
- ISSN
- 0020-7136
1097-0215
- Abstract
- Our 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.
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Collections - College of Life Science and Biotechnology > Department of Food Science & Biotechnology > 1. Journal Articles

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