Circulating Fatty Acids and Prostate Cancer Risk: Individual Participant Meta-Analysis of Prospective Studies

被引:44
|
作者
Crowe, Francesca L. [1 ]
Appleby, Paul N. [1 ]
Travis, Ruth C. [1 ]
Barnett, Matt [2 ]
Brasky, Theodore M. [3 ]
Bueno-de-Mesquita, H. Bas [4 ,5 ,6 ]
Chajes, Veronique [7 ,8 ]
Chavarro, Jorge E. [9 ,10 ,11 ,12 ,13 ]
Chirlaque, Maria-Dolores [14 ,15 ]
English, Dallas R. [16 ,17 ]
Gibson, Robert A. [18 ]
Giles, Graham G. [16 ,17 ]
Goodman, Gary E. [2 ]
Henning, Susanne M. [19 ]
Kaaks, Rudolf [20 ]
King, Irena B. [2 ,21 ]
Kolonel, Lawrence N. [22 ]
Kristal, Alan R. [23 ]
Neuhouser, Marian L. [2 ]
Park, Song-Yi [22 ]
Severi, Gianluca [16 ,17 ]
Siddiq, Afshan [24 ]
Stampfer, Meir J. [9 ,10 ,11 ,12 ,13 ]
Stattin, Paer [25 ]
Tangen, Catherine M. [23 ]
Tjonneland, Anne [26 ]
Trichopoulos, Dimitrios [10 ,27 ,28 ]
Tumino, Rosario [29 ]
Wilkens, Lynne R. [22 ]
Key, Timothy J. [1 ]
Allen, Naomi E. [30 ,31 ]
机构
[1] Univ Oxford, Nuffield Dept Populat Hlth, Canc Epidemiol Unit, Oxford OX3 7LF, England
[2] Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Seattle, WA 98104 USA
[3] Ohio State Univ, Coll Med, Dept Internal Med, Div Canc Prevent & Control, Columbus, OH 43210 USA
[4] Natl Inst Publ Hlth & Environm RIVM, Bilthoven, Netherlands
[5] Univ Med Ctr, Dept Gastroenterol & Hepatol, Utrecht, Netherlands
[6] Univ London Imperial Coll Sci Technol & Med, Sch Publ Hlth, London, England
[7] Int Agcy Res Canc, Nutr & Metab Sect, F-69372 Lyon, France
[8] Int Agcy Res Canc, Nutr Epidemiol Grp, F-69372 Lyon, France
[9] Harvard Univ, Sch Publ Hlth, Dept Nutr, Boston, MA 02115 USA
[10] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[11] Channing Div Network Med, Boston, MA USA
[12] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[13] Harvard Univ, Sch Med, Boston, MA USA
[14] Murcia Reg Hlth Author, Dept Epidemiol, Murcia, Spain
[15] CIBER Epidemiol & Publ Hlth CIBERESP, Madrid, Spain
[16] Canc Council Victoria, Canc Epidemiol Ctr, Carlton, Vic, Australia
[17] Univ Melbourne, Sch Populat Hlth, Ctr Mol Environm Genet & Analyt Epidemiol, Melbourne, Vic 3010, Australia
[18] Univ Adelaide, FOODplus Res Ctr, Glen Osmond, SA, Australia
[19] Univ Calif Los Angeles, David Geffen Sch Med, Ctr Human Nutr, Los Angeles, CA 90095 USA
[20] German Canc Res Ctr, Dept Canc Epidemiol, Heidelberg, Germany
[21] Univ New Mexico, Dept Internal Med, Albuquerque, NM 87131 USA
[22] Univ Hawaii, Ctr Canc, Canc Epidemiol Program, Honolulu, HI 96822 USA
[23] Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Canc Prevent Program, Seattle, WA 98104 USA
[24] Univ London Imperial Coll Sci Technol & Med, Sch Publ Hlth, Dept Genom Common Dis, London, England
[25] Umea Univ, Dept Surg & Perioperat Sci Urol & Androl, Umea, Sweden
[26] Danish Canc Soc, Res Ctr, Copenhagen, Denmark
[27] Acad Athens, Bur Epidemiol Res, Athens, Greece
[28] Hellen Hlth Fdn, Athens, Greece
[29] Civ & MP Arezzo Hosp, Canc Registry & Histopathol Unit, Asp Ragusa, Italy
[30] Univ Oxford, Nuffield Dept Populat Hlth, Clin Trial Serv Unit, Oxford, England
[31] Univ Oxford, Nuffield Dept Populat Hlth, Epidemiol Studies Unit, Oxford, England
来源
基金
美国国家卫生研究院;
关键词
C-REACTIVE PROTEIN; PLASMA PHOSPHOLIPIDS; MORTALITY; BLOOD; TRIAL; PROGRESSION; BIOMARKERS; HORMONES; INSULIN; SMOKERS;
D O I
10.1093/jnci/dju240
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Individual studies have suggested that some circulating fatty acids are associated with prostate cancer risk, but have not been large enough to provide precise estimates of associations, particularly by stage and grade of disease. Methods Principal investigators of prospective studies on circulating fatty acids and prostate cancer were invited to collaborate. Investigators provided individual participant data on circulating fatty acids (weight percent) and other characteristics of prostate cancer cases and controls. Prostate cancer risk by study-specific fifths of 14 fatty acids was estimated using multivariable-adjusted conditional logistic regression. All statistical tests were two-sided. Results Five thousand and ninety-eight case patients and 6649 control patients from seven studies with an average follow-up of 5.1 (SD = 3.3) years were included. Stearic acid (18: 0) was inversely associated with total prostate cancer (odds ratio [OR] Q5 vs Q1 = 0.88, 95% confidence interval [CI] = 0.78 to 1.00, P-trend = .043). Prostate cancer risk was, respectively, 14% and 16% greater in the highest fifth of eicosapentaenoic acid (20:5n-3) (OR = 1.14, 95% CI = 1.01 to 1.29, P-trend = .001) and docosapentaenoic acid (22: 5n-3) (OR = 1.16, 95% CI = 1.02 to 1.33, P-trend = .003), but in each case there was heterogeneity between studies (P = .022 and P < .001, respectively). There was heterogeneity in the association between docosapentaenoic acid and prostate cancer by grade of disease (P = .006); the association was statistically significant for low-grade disease but not high-grade disease. The remaining 11 fatty acids were not statistically associated with total prostate cancer risk. Conclusion There was no strong evidence that circulating fatty acids are important predictors of prostate cancer risk. It is not clear whether the modest associations of stearic, eicosapentaenoic, and docosapentaenoic acid are causal.
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页数:10
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