The Canadian Partnership for Tomorrow Project: a pan-Canadian platform for research on chronic disease prevention

被引:72
作者
Dummer, Trevor J. B. [1 ]
Awadalla, Philip [2 ]
Boileau, Catherine [3 ]
Craig, Camille [4 ]
Fortier, Isabel [4 ]
Goel, Vivek [5 ,6 ]
Hicks, Jason M. T. [7 ]
Jacquemont, Sebastien [8 ]
Knoppers, Bartha Maria [9 ]
Le, Nhu [10 ]
McDonald, Treena [10 ]
McLaughlin, John [11 ]
Mes-Masson, Anne-Marie [12 ]
Nuyt, Anne-Monique [13 ]
Palmer, Lyle J. [14 ]
Parker, Louise [15 ]
Purdue, Mark [16 ]
Robson, Paula J. [17 ]
Spinelli, John J. [18 ]
Thompson, David [7 ]
Vena, Jennifer [17 ]
Zawati, Ma'n [9 ]
机构
[1] Univ British Columbia, Sch Populat & Publ Hlth, Vancouver, BC, Canada
[2] Ontario Inst Canc Res, Montreal, PQ, Canada
[3] CARTaGENE, Montreal, PQ, Canada
[4] McGill Univ, Res Inst, Hlth Ctr, Montreal, PQ, Canada
[5] Univ Toronto, Res & Innovat, Toronto, ON, Canada
[6] Ontario Agcy Hlth Protect & Promot, Halifax, NS, Canada
[7] Dalhousie Univ, Atlantic PATH, Halifax, NS, Canada
[8] Ctr Hosp Univ St Justine, Montreal, PQ, Canada
[9] McGill Univ, Ctr Genom & Policy, Montreal, PQ, Canada
[10] BC Canc Res Ctr, Vancouver, BC, Canada
[11] Publ Hlth Ontario, Toronto, ON, Canada
[12] Univ Montreal, Inst Canc Montreal, Montreal, PQ, Canada
[13] CHU St Justine Res Ctr, Pediat, Montreal, PQ, Canada
[14] Univ Adelaide, Sch Publ Hlth, Adelaide, SA, Australia
[15] Dalhousie Univ, Dept Med, Halifax, NS, Canada
[16] NCI, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
[17] Alberta Hlth Serv, CancerControl Alberta, Edmonton, AB, Canada
[18] BC Canc, Populat Oncol, Vancouver, BC, Canada
关键词
CANCER; COHORT; EPIDEMIOLOGY; NUTRITION; MEDICINE; GENOMICS; BIOBANK; HEALTH; BLOOD;
D O I
10.1503/cmaj.170292
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Understanding the complex interaction of risk factors that increase the likelihood of developing common diseases is challenging. The Canadian Partnership for Tomorrow Project (CPTP) is a prospective cohort study created as a population-health research platform for assessing the effect of genetics, behaviour, family health history and environment (among other factors) on chronic diseases. METHODS: Volunteer participants were recruited from the general Canadian population for a confederation of 5 regional cohorts. Participants were enrolled in the study and core information obtained using 2 approaches: attendance at a study assessment centre for all study measures (questionnaire, venous blood sample and physical measurements) or completion of the core questionnaire (online or paper), with later collection of other study measures where possible. Physical measurements included height, weight, percentage body fat and blood pressure. Participants consented to passive follow-up through linkage with administrative health databases and active follow-up through recontact. All participant data across the 5 regional cohorts were harmonized. RESULTS: A total of 307 017 participants aged 30-74 from 8 provinces were recruited. More than half provided a venous blood sample and/or other biological sample, and 33% completed physical measurements. A total of 709 harmonized variables were created; almost 25% are available for all participants and 60% for at least 220 000 participants. INTERPRETATION: Primary recruitment for the CPTP is complete, and data and biosamples are available to Canadian and international researchers through a data-access process. The CPTP will support research into how modifiable risk factors, genetics and the environment interact to affect the development of cancer and other chronic diseases, ultimately contributing evidence to reduce the global burden of chronic disease.
引用
收藏
页码:E710 / E717
页数:8
相关论文
共 32 条
[1]  
[Anonymous], 2016, TABL CANSIM 105 0501
[2]   Using the Standardized Difference to Compare the Prevalence of a Binary Variable Between Two Groups in Observational Research [J].
Austin, Peter C. .
COMMUNICATIONS IN STATISTICS-SIMULATION AND COMPUTATION, 2009, 38 (06) :1228-1234
[3]   Cohort profile of the CARTaGENE study: Quebec's population-based biobank for public health and personalized genomics [J].
Awadalla, Philip ;
Boileau, Catherine ;
Payette, Yves ;
Idaghdour, Youssef ;
Goulet, Jean-Philippe ;
Knoppers, Bartha ;
Hamet, Pavel ;
Laberge, Claude .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2013, 42 (05) :1285-1299
[4]   Diet and cancer - The European prospective investigation into cancer and nutrition [J].
Bingham, S ;
Riboli, E .
NATURE REVIEWS CANCER, 2004, 4 (03) :206-215
[5]   The Canadian Partnership for Tomorrow Project: building a pan-Canadian research platform for disease prevention [J].
Borugian, Marilyn J. ;
Robson, Paula ;
Fortier, Isabel ;
Parker, Louise ;
McLaughlin, John ;
Knoppers, Bartha Maria ;
Bedard, Karine ;
Gallagher, Richard P. ;
Sinclair, Sandra ;
Ferretti, Vincent ;
Whelan, Heather ;
Hoskin, David ;
Potter, John D. .
CANADIAN MEDICAL ASSOCIATION JOURNAL, 2010, 182 (11) :1197-1201
[6]   Serum Fatty Acid Reference Ranges: Percentiles from a New Zealand National Nutrition Survey [J].
Bradbury, Kathryn E. ;
Skeaff, Clark Murray ;
Crowe, Francesca L. ;
Green, Timothy J. ;
Hodson, Leanne .
NUTRIENTS, 2011, 3 (01) :152-163
[7]   Size matters: just how big is BIG? Quantifying realistic sample size requirements for human genome epidemiology [J].
Burton, Paul R. ;
Hansell, Anna L. ;
Fortier, Isabel ;
Manolio, Teri A. ;
Khoury, Muin J. ;
Little, Julian ;
Elliott, Paul .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2009, 38 (01) :263-273
[8]  
Canadian Cancer Society's Advisory Committee on Cancer Statistics, 2015, CAN CANC STAT 2015
[9]   China Kadoorie Biobank of 0.5 million people: survey methods, baseline characteristics and long-term follow-up [J].
Chen, Zhengming ;
Chen, Junshi ;
Collins, Rory ;
Guo, Yu ;
Peto, Richard ;
Wu, Fan ;
Li, Liming .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2011, 40 (06) :1652-1666
[10]   A New Initiative on Precision Medicine [J].
Collins, Francis S. ;
Varmus, Harold .
NEW ENGLAND JOURNAL OF MEDICINE, 2015, 372 (09) :793-795