Plasma fetuin-A concentration, genetic variation in the AHSG gene and risk of colorectal cancer

被引:22
|
作者
Nimptsch, Katharina [1 ,2 ]
Aleksandrova, Krasimira [3 ]
Boeing, Heiner [3 ]
Janke, Juergen [1 ]
Lee, Young-Ae [4 ]
Jenab, Mazda [5 ]
Kong, So Yeon [5 ]
Tsilidis, Konstantinos K. [6 ,7 ]
Weiderpass, Elisabete [8 ,9 ,10 ,11 ]
Bueno-de-Mesquita, H. B [12 ,13 ,14 ]
Siersema, Peter D. [13 ]
Jansen, Eugene H. J. M. [15 ]
Trichopoulou, Antonia [16 ,17 ]
Tjonneland, Anne [18 ]
Olsen, Anja [18 ]
Wu, Chunsen [19 ]
Overvad, Kim [19 ]
Boutron-Ruault, Marie-Christine [20 ,21 ,22 ]
Racine, Antoine [20 ,21 ,22 ]
Freisling, Heinz [5 ]
Katzke, Verena [23 ]
Kaaks, Rudolf [23 ]
Lagiou, Pagona [16 ,24 ,25 ]
Trichopoulos, Dimitrios [16 ,17 ,25 ]
Severi, Gianluca [26 ]
Naccarati, Alessio [26 ]
Mattiello, Amalia [27 ]
Palli, Domenico [28 ]
Grioni, Sara [29 ]
Tumino, Rosario [30 ]
Peeters, Petra H. [31 ]
Ljuslinder, Ingrid [32 ]
Nystrom, Hanna [33 ]
Brandstedt, Jenny [34 ]
Sanchez, Maria-Jose [35 ,36 ]
Gurrea, Aurelio Barricarte [36 ,37 ]
Bonet, Catalina Bonet [38 ]
Chirlaque, Maria-Dolores [36 ,39 ]
Dorronsoro, Miren [40 ]
Quiros, Jose Ramon [41 ]
Travis, Ruth C. [42 ]
Khaw, Kay-Tee [43 ]
Wareham, Nick [44 ]
Riboli, Elio [45 ]
Gunter, Marc J. [45 ]
Pischon, Tobias [1 ]
机构
[1] Max Delbruck Ctr Mol Med MDC, Mol Epidemiol Res Grp, D-13125 Berlin, Germany
[2] Harvard Univ, Sch Publ Hlth, Dept Nutr, Boston, MA 02115 USA
[3] German Inst Human Nutr Potsdam Rehbrucke, Dept Epidemiol, Potsdam, Nuthetal, Germany
[4] Max Delbruck Ctr Mol Med MDC, Genet Allerg Dis Res Grp, Berlin, Germany
[5] Int Agcy Res Canc IARC WHO, Lyon, France
[6] Univ Oxford, Nuffield Dept Clin Med, Canc Epidemiol Unit, Oxford, England
[7] Univ Ioannina, Sch Med, Dept Hyg & Epidemiol, GR-45110 Ioannina, Greece
[8] Arctic Univ Norway, Univ Tromso, Fac Hlth Sci, Dept Community Med, Tromso, Norway
[9] Canc Registry Norway, Dept Res, Oslo, Norway
[10] Karolinska Inst, Dept Med Epidemiol & Biostat, Stockholm, Sweden
[11] Samfundet Folkhalsan, Helsinki, Finland
[12] Natl Inst Publ Hlth & Environm RIVM, Bilthoven, Netherlands
[13] Univ Med Ctr, Dept Gastroenterol & Hepatol, Utrecht, Netherlands
[14] Univ London Imperial Coll Sci Technol & Med, Fac Med, Sch Publ Hlth, Dept Epidemiol & Biostat, London, England
[15] Natl Inst Publ Hlth & Environm, Ctr Hlth Protect, NL-3720 BA Bilthoven, Netherlands
[16] Hellen Hlth Fdn, Athens, Greece
[17] Acad Athens, Bur Epidemiol Res, Athens, Greece
[18] Danish Canc Soc Res Ctr, Copenhagen, Denmark
[19] Aarhus Univ, Dept Publ Hlth, Epidemiol Sect, Aarhus, Denmark
[20] Ctr Res Epidemiol & Populat Hlth CESP, INSERM, U1018, Nutr Hormones & Womens Hlth Team, Villejuif, France
[21] Univ Paris 11, UMRS 1018, Villejuif, France
[22] Inst Gustave Roussy, Villejuif, France
[23] German Canc Res Ctr, Div Canc Epidemiol, Heidelberg, Germany
[24] Univ Athens, Sch Med, Dept Hyg Epidemiol & Med Stat, GR-11527 Athens, Greece
[25] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[26] Human Genet Fdn HuGeF, Turin, Italy
[27] Univ Naples Federico II, Dipartimento Med Clin & Chirurg, Naples, Italy
[28] Canc Res & Prevent Inst ISPO, Mol & Nutr Epidemiol Unit, Florence, Italy
[29] Fdn IRCCS Ist Nazl Tumori, Epidemiol & Prevent Unit, Milan, Italy
[30] Civ MP Arezzo Hosp, Canc Registry & Histopathol Unit, Asp Ragusa, Italy
[31] Univ Med Ctr Utrecht, Dept Epidemiol, Julius Ctr Hlth Sci & Primary Care, Utrecht, Netherlands
[32] Umea Univ, Oncol, Dept Radio Sci, Umea, Sweden
[33] Umea Univ, Dept Surg, Dept Surg & Perioperat Sci, Umea, Sweden
[34] Lund Univ, Lund Oncol & Pathol, Dept Clin Sci, Skane Univ Hosp, Lund, Sweden
[35] Inst Invest Biosanitaria Granada Granada Ibs, Escuela Andaluza Salud Publ, Granada, Spain
[36] CIBERESP, Consortium Biomed Res Epidemiol & Publ Hlth, Barcelona, Spain
[37] Navarre Publ Hlth Inst, Pamplona, Spain
[38] Catalan Inst Oncol ICO, Canc Epidemiol Res Program, Barcelona, Spain
[39] Murcia Reg Hlth Author, Dept Epidemiol, Murcia, Spain
[40] Publ Hlth Direct & Biodonostia Ciberesp, Basque Reg Hlth Dept, San Sebastian, Spain
[41] Publ Hlth Directorate, Asturias, Spain
[42] Univ Oxford, Nuffield Dept Populat Hlth, Canc Epidemiol Unit, Oxford, England
[43] Univ Cambridge, Addenbrookes Hosp, Sch Clin Med, Clin Gerontol,Dept Publ Hlth & Primary Care, Cambridge CB2 2QQ, England
[44] Univ Cambridge, MRC, Epidemiol Unit, Cambridge, England
[45] Univ London Imperial Coll Sci Technol & Med, Div Epidemiol Publ Hlth & Primary Care, London, England
基金
英国医学研究理事会;
关键词
fetuin-A; AHSG; colorectal cancer; INSULIN-RESISTANCE; MENDELIAN RANDOMIZATION; TYROSINE KINASE; RECTAL-CANCER; RECEPTOR; COLON; INSTRUMENTS; EXPRESSION; REGRESSION; INHIBITOR;
D O I
10.1002/ijc.29448
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Fetuin-A, also referred to as alpha 2-Heremans-Schmid glycoprotein (AHSG), is a liver protein known to inhibit insulin actions. Hyperinsulinemia is a possible risk factor for colorectal cancer; however, the role of fetuin-A in the development of colorectal cancer is unclear. We investigated the association between circulating fetuin-A and colorectal cancer risk in a nested case-control study within the European Prospective Investigation into Cancer and Nutrition. Fetuin-A concentrations were measured in prediagnostic plasma samples from 1,367 colorectal cancer cases and 1,367 matched controls. In conditional logistic regression models adjusted for potential confounders, the estimated relative risk (95% confidence interval) of colorectal cancer per 40 mg/mL higher fetuin-A concentrations (approximately one standard deviation) was 1.13 (1.02-1.24) overall, 1.21 (1.05-1.39) in men, 1.06 (0.93-1.22) in women, 1.13 (1.00-1.27) for colon cancer and 1.12 (0.94-1.32) for rectal cancer. To improve causal inference in a Mendelian Randomization approach, five tagging single nucleotide polymorphisms of the AHSG gene were genotyped in a subset of 456 case-control pairs. The AHSG allele-score explained 21% of the interindividual variation in plasma fetuin-A concentrations. In instrumental variable analysis, genetically raised fetuin-A was not associated with colorectal cancer risk (relative risk per 40 mg/mL genetically determined higher fetuin-A was 0.98, 95% confidence interval: 0.73-1.33). The findings of our study indicate a modest linear association between fetuin-A concentrations and risk of colorectal cancer but suggest that fetuin-A may not be causally related to colorectal cancer development.
引用
收藏
页码:911 / 920
页数:10
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