Cohort profile: LifeLines DEEP, a prospective, general population cohort study in the northern Netherlands: study design and baseline characteristics

被引:167
作者
Tigchelaar, Ettje F. [1 ,2 ]
Zhernakova, Alexandra [1 ,2 ]
Dekens, Jackie A. M. [1 ,2 ]
Hermes, Gerben [2 ,3 ]
Baranska, Agnieszka [2 ,4 ]
Mujagic, Zlatan [2 ,5 ]
Swertz, Morris A. [1 ,2 ,6 ]
Munoz, Angelica M. [1 ,7 ]
Deelen, Patrick [1 ,6 ]
Cenit, Maria C. [1 ]
Franke, Lude [1 ]
Scholtens, Salome [8 ,9 ]
Stolk, Ronald P. [8 ,9 ]
Wijmenga, Cisca [1 ,2 ]
Feskens, Edith J. M. [2 ,10 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Genet, Groningen, Netherlands
[2] Top Inst Food & Nutr, Wageningen, Netherlands
[3] Wageningen Univ, Microbiol Lab, NL-6700 AP Wageningen, Netherlands
[4] Maastricht Univ, Med Ctr, Dept Toxicol Nutr & Toxicol Res NUTRIM, Maastricht, Netherlands
[5] Maastricht Univ, Med Ctr, Div Gastroenterol Hepatol, Maastricht, Netherlands
[6] Univ Groningen, Univ Med Ctr Groningen, Genom Coordinat Ctr, Groningen, Netherlands
[7] Univ Antioquia, Res Grp Food & Human Nutr, Medellin, Colombia
[8] Univ Groningen, Univ Med Ctr Groningen, LifeLines Cohort Study, Groningen, Netherlands
[9] Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, Groningen, Netherlands
[10] Wageningen Univ, Div Human Nutr, Sect Nutr & Epidemiol, NL-6700 AP Wageningen, Netherlands
关键词
IRRITABLE-BOWEL-SYNDROME; GENOME-WIDE ASSOCIATION; QUALITY-OF-LIFE; CELIAC-DISEASE; EPIDEMIOLOGY; ENVIRONMENT; IMPUTATION; COMMUNITY; COUNTRIES; CATALOG;
D O I
10.1136/bmjopen-2014-006772
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose: There is a critical need for population-based prospective cohort studies because they follow individuals before the onset of disease, allowing for studies that can identify biomarkers and disease-modifying effects, and thereby contributing to systems epidemiology. Participants: This paper describes the design and baseline characteristics of an intensively examined subpopulation of the LifeLines cohort in the Netherlands. In this unique subcohort, LifeLines DEEP, we included 1539 participants aged 18 years and older. Findings to date: We collected additional blood (n= 1387), exhaled air (n= 1425) and faecal samples (n= 1248), and elicited responses to gastrointestinal health questionnaires (n= 1176) for analysis of the genome, epigenome, transcriptome, microbiome, metabolome and other biological levels. Here, we provide an overview of the different data layers in LifeLines DEEP and present baseline characteristics of the study population including food intake and quality of life. We also describe how the LifeLines DEEP cohort allows for the detailed investigation of genetic, genomic and metabolic variation for a wide range of phenotypic outcomes. Finally, we examine the determinants of gastrointestinal health, an area of particular interest to us that can be addressed by LifeLines DEEP. Future plans: We have established a cohort of which multiple data levels allow for the integrative analysis of populations for translation of this information into biomarkers for disease, and which will offer new insights into disease mechanisms and prevention.
引用
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页数:9
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