TY - JOUR
T1 - Human Early Life Exposome (HELIX) study
T2 - a European population-based exposome cohort
AU - Maitre, Lea
AU - de Bont, Jeroen
AU - Casas, Maribel
AU - Robinson, Oliver
AU - Aasvang, Gunn Marit
AU - Agier, Lydiane
AU - Andrusaityte, Sandra
AU - Ballester, Ferran
AU - Basagana, Xavier
AU - Borras, Eva
AU - Brochot, Celine
AU - Bustamante, Mariona
AU - Carracedo, Angel
AU - de Castro, Montserrat
AU - Dedele, Audrius
AU - Donaire-Gonzalez, David
AU - Estivill, Xavier
AU - Evandt, Jorunn
AU - Fossati, Serena
AU - Giorgis-Allemand, Lise
AU - Gonzalez, Juan R.
AU - Granum, Berit
AU - Grazuleviciene, Regina
AU - Gutzkow, Kristine Bjerve
AU - Haug, Line Smastuen
AU - Hernandez-Ferrer, Carles
AU - Heude, Barbara
AU - Ibarluzea, Jesus
AU - Julvez, Jordi
AU - Karachaliou, Marianna
AU - Keun, Hector C.
AU - Krog, Norun Hjertager
AU - Lau, Chung-Ho E.
AU - Leventakou, Vasiliki
AU - Lyon-Caen, Sarah
AU - Manzano, Cyntia
AU - Mason, Dan
AU - McEachan, Rosemary
AU - Meltzer, Helle Margrete
AU - Petraviciene, Inga
AU - Quentin, Joane
AU - Roumeliotaki, Theano
AU - Sabido, Eduard
AU - Saulnier, Pierre-Jean
AU - Siskos, Alexandros P.
AU - Siroux, Valerie
AU - Sunyer, Jordi
AU - Tamayo, Ibon
AU - Urquiza, Jose
AU - Vafeiadi, Marina
AU - van Gent, Diana
AU - Vives-Usano, Marta
AU - Waiblinger, Dagmar
AU - Warembourg, Charline
AU - Chatzi, Leda
AU - Coen, Muireann
AU - van den Hazel, Peter
AU - Nieuwenhuijsen, Mark J.
AU - Slama, Remy
AU - Thomsen, Cathrine
AU - Wright, John
AU - Vrijheid, Martine
PY - 2018/9/1
Y1 - 2018/9/1
N2 - Purpose Essential to exposome research is the collection of data on many environmental exposures from different domains in the same subjects. The aim of the Human Early Life Exposome (HELIX) study was to measure and describe multiple environmental exposures during early life (pregnancy and childhood) in a prospective cohort and associate these exposures with molecular omics signatures and child health outcomes. Here, we describe recruitment, measurements available and baseline data of the HELIX study populations. Participants The HELIX study represents a collaborative project across six established and ongoing longitudinal population-based birth cohort studies in six European countries (France, Greece, Lithuania, Norway, Spain and the UK). HELIX used a multilevel study design with the entire study population totalling 31472 mother-child pairs, recruited during pregnancy, in the six existing cohorts (first level); a subcohort of 1301 mother-child pairs where biomarkers, omics signatures and child health outcomes were measured at age 6-11 years (second level) and repeat-sampling panel studies with around 150 children and 150 pregnant women aimed at collecting personal exposure data (third level). Findings to date Cohort data include urban environment, hazardous substances and lifestyle-related exposures for women during pregnancy and their offspring from birth until 6-11 years. Common, standardised protocols were used to collect biological samples, measure exposure biomarkers and omics signatures and assess child health across the six cohorts. Baseline data of the cohort show substantial variation in health outcomes and determinants between the six countries, for example, in family affluence levels, tobacco smoking, physical activity, dietary habits and prevalence of childhood obesity, asthma, allergies and attention deficit hyperactivity disorder. Future plans HELIX study results will inform on the early life exposome and its association with molecular omics signatures and child health outcomes. Cohort data are accessible for future research involving researchers external to the project.
AB - Purpose Essential to exposome research is the collection of data on many environmental exposures from different domains in the same subjects. The aim of the Human Early Life Exposome (HELIX) study was to measure and describe multiple environmental exposures during early life (pregnancy and childhood) in a prospective cohort and associate these exposures with molecular omics signatures and child health outcomes. Here, we describe recruitment, measurements available and baseline data of the HELIX study populations. Participants The HELIX study represents a collaborative project across six established and ongoing longitudinal population-based birth cohort studies in six European countries (France, Greece, Lithuania, Norway, Spain and the UK). HELIX used a multilevel study design with the entire study population totalling 31472 mother-child pairs, recruited during pregnancy, in the six existing cohorts (first level); a subcohort of 1301 mother-child pairs where biomarkers, omics signatures and child health outcomes were measured at age 6-11 years (second level) and repeat-sampling panel studies with around 150 children and 150 pregnant women aimed at collecting personal exposure data (third level). Findings to date Cohort data include urban environment, hazardous substances and lifestyle-related exposures for women during pregnancy and their offspring from birth until 6-11 years. Common, standardised protocols were used to collect biological samples, measure exposure biomarkers and omics signatures and assess child health across the six cohorts. Baseline data of the cohort show substantial variation in health outcomes and determinants between the six countries, for example, in family affluence levels, tobacco smoking, physical activity, dietary habits and prevalence of childhood obesity, asthma, allergies and attention deficit hyperactivity disorder. Future plans HELIX study results will inform on the early life exposome and its association with molecular omics signatures and child health outcomes. Cohort data are accessible for future research involving researchers external to the project.
KW - birth cohort
KW - exposome
KW - epidemiology
KW - omics
KW - public health
KW - community child health
KW - USE REGRESSION-MODELS
KW - LAND-USE
KW - AIR-POLLUTION
KW - CHILD COHORT
KW - EXPOSURE
KW - PROFILE
KW - HEALTH
KW - PREGNANCY
KW - MOTHER
KW - AREAS
U2 - 10.1136/bmjopen-2017-021311
DO - 10.1136/bmjopen-2017-021311
M3 - Article
C2 - 30206078
SN - 2044-6055
VL - 8
JO - BMJ Open
JF - BMJ Open
IS - 9
M1 - 021311
ER -