| Literature DB >> 23343014 |
Ulrike Gehring1, Maribel Casas, Bert Brunekreef, Anna Bergström, Jens Peter Bonde, Jérémie Botton, Cecile Chévrier, Sylvaine Cordier, Joachim Heinrich, Cynthia Hohmann, Thomas Keil, Jordi Sunyer, Christina G Tischer, Gunnar Toft, Magnus Wickman, Martine Vrijheid, Mark Nieuwenhuijsen.
Abstract
Environmental exposures during pregnancy and early life may have adverse health effects. Single birth cohort studies often lack statistical power to tease out such effects reliably. To improve the use of existing data and to facilitate collaboration among these studies, an inventory of the environmental exposure and health data in these studies was made as part of the ENRIECO (Environmental Health Risks in European Birth Cohorts) project. The focus with regard to exposure was on outdoor air pollution, water contamination, allergens and biological organisms, metals, pesticides, smoking and second hand tobacco smoke (SHS), persistent organic pollutants (POPs), noise, radiation, and occupational exposures. The review lists methods and data on environmental exposures in 37 European birth cohort studies. Most data is currently available for smoking and SHS (N=37 cohorts), occupational exposures (N=33), outdoor air pollution, and allergens and microbial agents (N=27). Exposure modeling is increasingly used for long-term air pollution exposure assessment; biomonitoring is used for assessment of exposure to metals, POPs and other chemicals; and environmental monitoring for house dust mite exposure assessment. Collaborative analyses with data from several birth cohorts have already been performed successfully for outdoor air pollution, water contamination, allergens, biological contaminants, molds, POPs and SHS. Key success factors for collaborative analyses are common definitions of main exposure and health variables. Our review emphasizes that such common definitions need ideally be arrived at in the study design phase. However, careful comparison of methods used in existing studies also offers excellent opportunities for collaborative analyses. Investigators can use this review to evaluate the potential for future collaborative analyses with respect to data availability and methods used in the different cohorts and to identify potential partners for a specific research question.Entities:
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Year: 2013 PMID: 23343014 PMCID: PMC3564791 DOI: 10.1186/1476-069X-12-8
Source DB: PubMed Journal: Environ Health ISSN: 1476-069X Impact factor: 5.984
Description of exposure assessment in the birth cohorts by exposure topic
| Outdoor air pollution | 27 | ·Many cohorts assessed outdoor air pollution exposure (27 cohorts). |
| ·Air pollution modeling is becoming increasingly the method of choice: land-use regression modeling (18 cohorts) and dispersion modeling (10 cohorts). | ||
| ·Sixteen cohorts are currently participating in the collaborative EU-funded ESCAPE project that adds land-use regression modeling of nitrogen oxides, particulate matter, soot and particle composition to existing cohort studies using a standardized protocol. | ||
| | | ·Most cohorts currently have data on exposure during pregnancy and/or early life. |
| Water contamination | 13 | ·Disinfection by-products were studied most. |
| ·Exposure assessment usually by means of a combination of questionnaires | ||
| ·Validation by means of biomonitoring in a small number of subjects (3 cohorts). | ||
| | | ·Most studies assessed exposure during pregnancy. |
| Allergens & microbial agents | 27 | ·Exposure to cat and dog allergen was assessed by means of questionnaires in all cohorts and by means of measurements in house dust samples in 9 and 4 cohorts, respectively. |
| ·Mite allergen levels were measured in settled house dust samples in 10 cohorts. | ||
| ·Mold exposure was mainly assessed by means of questionnaires. | ||
| | | ·Exposure was assessed during infancy and/or early childhood in most studies. |
| Metals | 20 | ·Most cohorts have analyzed the effects of low-level environmental exposure to mercury (Hg; 15 cohorts) and lead (Pb; 16 cohorts); little attention to other metals. |
| ·Exposure was mainly assessed by means of biomonitoring. Five cohorts used questionnaires, two of them in addition to biomonitoring, | ||
| ·There are well-standardized protocols for most of the metals. | ||
| ·Inductively coupled plasma mass spectrometry (ICP-MS) and atomic absorption spectroscopy (AAS) were used most. | ||
| | | ·Most measurements were performed in cord blood; other non-invasive matrices such as hair and urine are gaining attention. |
| Pesticides a | 18 | ·Many studies assessed household use (16 cohorts); and occupational exposure (13 cohorts), fewer cohorts assessed dietary exposure (6 cohorts) or residence proximity to crops (2 cohorts). |
| | | ·Exposures via household use, occupational exposure and diet, were mainly assessed by means of questionnaires. |
| Persistent organic pollutants | 19 | ·Exposure assessment by means of high performance liquid chromatography (HPLC) measurements in biological samples with adjustment for lipid content. |
| ·Variation between studies with regard to sampling medium, timing of sample collection and lipid adjustment. | ||
| | | Most data available for polychlorinated biphenyl (PCB) and dichlorodiphenyltrichloroethane (DDT). |
| Other chemical exposures b | 17 | ·Few cohorts have measured these contaminants (13 cohorts), but this is a rapidly developing field and more cohorts are planning to assess exposure to other chemicals (7 cohorts). |
| ·Exposure was mainly assessed by means of biomonitoring. | ||
| | | There is heterogeneity with regard to the type of biological media used and the timing of the exposure measurement. |
| Radiation | 12 | |
| ·Mainly assessed by questionnaire: maternal occupational exposures (3 cohorts), prenatal medical ionizing radiation exposures (6 cohorts); 2 cohorts currently plan to ask questions about medical radiation exposures in children. | ||
| ·1 cohort is planning to assess residential radon exposure using geographical methods. | ||
| ·No standardized questionnaires or protocols in this field. | ||
| ·Only six cohorts are collecting UV-related data through questionnaire questions on sunburn in children, use of sun beds during pregnancy, and time spent outdoors. | ||
| ·None of the cohorts collect data on maternal and child skin type, sunscreen use, or clothing. | ||
| ·Standard questionnaires are not available. | ||
| ·Very few cohorts assess exposure to non-ionizing radiation: 2 cohorts include occupational electromagnetic field (EMF) exposure in their questionnaires, 2 cohorts assess extreme low frequency (ELF) exposure to overhead high-voltage power lines through geographical information from electricity companies, 2 cohorts include questions about mobile phone use of the mother during pregnancy and 4 on children’s mobile phone use. | ||
| ·A few cohorts have started using base-station maps combined with information from home appliances and personal radio frequency (RF) exposimeters, in order to estimate whole body RF/ELF-EMF exposure. | ||
| | | ·There are no standardized or validated questionnaires, models or protocols in use at this moment. |
| Smoking and second hand tobacco smoke | 37 | ·All cohorts have information about exposure during pregnancy and 29 cohorts in addition assessed exposure at different periods during infancy and childhood. |
| | | Assessment mainly by questionnaire; cotinine measurements in biological samples (mainly urine) in 14 cohorts. |
| Noise | 14 | ·All cohorts used questionnaire assessments, mainly about noise annoyance. |
| ·5 cohorts used noise propagation modeling or noise maps. | ||
| ·Traffic is the source of noise that has been studied most. | ||
| | | ·Most cohorts assessed exposure during pregnancy. |
| Occupational exposures | 33 | ·All cohorts have information on maternal occupation and most cohorts (n=26) have information on paternal occupation for at least one point in time. |
| ·Data mainly collected by means of questionnaires (most often job title; sometimes checklist occupation or occupational exposures). | ||
| ·Coding of maternal job title (n=17) or use of Job Exposure Matrices (JEM) (n=8) planned/done in a number of studies. |
* N = Number of cohorts with exposure assessment, counting the cohorts of the Faroes, the old INMA cohorts and the new INMA cohorts as one cohort each; a Organochlorine pesticides are under persistent organic pollutants; b brominated flame retardants, perfluorinated compounds phthalates and phenols.
Recommendations for methods, evaluations of collaboration with existing data, and areas of interest for future work including new data/new methods by exposure topic
| Outdoor air pollution | ·Exposure modeling is currently the state-of the art method | ·Within the ESCAPE project, a standardized exposure assessment is being added to a number of birth cohort studies and will soon be linked to existing health data in these cohorts; pooled analyses will be performed for a number of health endpoints | ·Assessment of long-term exposure to ultrafine particles, which are currently not being assessed within cohort studies. |
| | ·Few studies so far compared land-use regression models with dispersion models; results are inconsistent | | |
| | ·Residential mobility, time-activity pattern, and exposure at non-residential addresses should be evaluated in exposure assessment | | |
| | ·Assessment of long-term validity (i.e. stability) of land-use regression models which are based on one measurement campaign | | |
| | ·There is currently little validation of modeled exposures against personal exposure measurements | | |
| Water contamination | ·Best method for exposure assessment is to combine information of water-related behaviors obtained by questionnaire with newly or routinely collected water contaminant measurements | ·Further opportunity to study exposure to water pollutants in cohorts without water exposure assessment; routinely collected water pollutants are often available | ·Assessment of exposure to substances such as pharmaceuticals, Perfluorooctanesulfonic acid (PFOS)/Perfluorooctanoic Acid (PFOA), and (other) endocrine disrupters |
| | ·Validation of questionnaires against biomonitoring since it has been conducted in only a few subjects | ·Consideration of source of water as an exposure indicator (ground water versus surface water) | |
| | ·Assessment of variability and measurement error of questionnaires by repeated assessments | ·Data pooling currently being done in the HIWATE project | |
| | | ·Access to publicly collected data should be increased and European databases should be made available to researchers | |
| Allergens & microbial agents | ·Measurements in house dust or air samples are recommended | ·Meta-analyses in the framework of the GA2LEN (allergens) and AIRALLERG projects (allergens and biocontaminants) and ENRIECO case study on mold and dampness | ·Use of newly developed analysis techniques such as molecular methods or DNA fingerprinting |
| | ·Use of questionnaires is inexpensive, but questionnaires were found to have a low sensitivity | | |
| | ·Exposure at non-residential locations and timing of exposure should be taken into account | | |
| Metals | ·Human biological monitoring is the state of the art method for estimation of total dose. | ·Data pooling and/or meta-analysis of the data available in the European birth cohorts can overcome this problem if conversion models can be developed to transfer between different biological media (hair, cord blood, urine, etc.). | ·Validation of questionnaire data against human biological monitoring is needed. |
| | ·Inductively coupled plasma mass spectrometry (ICP-MS) is more sensitive and faster than Atomic absorption spectroscopy (AAS) | | |
| | ·In general labs are using well standardized protocols. It is recommended to validate the analytical technique in each lab including a sample with known concentration of metal/s every X number of samples. This will be useful to validate both the pre-treatment and the analytic process. | | |
| | ·Some studies compared Mercury levels in biological samples with fish/shellfish consumption assessed through validated food frequency questionnaires with encouraging results. More studies are needed to confirm these findings. For other metals, validation of other exposure assessment methods must be further explored. | | |
| Pesticides | ·There are multiple pesticides and multiple pathways of exposure conducing to varying exposure assessment | ·Since few cohorts assessed exposure to pesticides there is a large scope of doing more work on pesticide exposure within the European birth cohorts, particularly by analyzing available biological samples | ·Include validation studies in exposure assessment |
| | ·Biomonitoring hardly feasible for large cohorts, but recommended on sub-populations for validation purposes and identification of main exposure sources | ·Use of Geographic Information System (GIS) technologies with existing European data on soil occupancy and satellite imagings/maps of crops to assess bystander exposure due to agricultural activities | ·Assessment of time-activity pattern and exposure at non-residential locations |
| | ·There is a need for harmonization of exposure assessment by biomonitoring (choice of molecules of interest, biological matrices, sampling and storage conditions, chemical analyses controlled by international comparison programs, etc.) between studies | | |
| | ·Validation of questionnaires needed | | |
| | ·Inclusion of exposure at non-residential locations may improve exposure assessment | | |
| Persistent organic pollutants | ·High-performance liquid chromatography (HPLC) derived methods are the state of the art for measurements of POPs | ·The possibility to perform a pooled or meta-analysis on the association between exposure to POPs and birth outcomes in the European birth cohorts have been evaluated within a case study that is part of ENRIECO and continued in CHICOS ( | ·There is high degree of variability between studies in study design including timing of sample collection and collection medium. Therefore additional data collection according to a standardized protocol may be needed, especially if the outcomes of interest are hypothesized to be related to exposure at specific time windows during fetal life or early childhood. |
| | ·All analyzing laboratories should participate in inter-laboratory calibration tests. | ·Data pooling is possible for polychlorinated biphenyl (PCB), and dichlorodiphenyltrichloroethane (DDT). For other POPs there is little data or too much heterogeneity with regard to the sampling media or the timing of exposure assessment. | |
| | ·Especially for detecting POPs in low concentrations in small volumes equipment with a high sensitivity is needed. | ·Conversion factors needed to be developed to allow pooling of data. | |
| | ·The persistence of organochlorines makes sample degradation a lesser problem as for other more readily degradable compounds. However, it is recommended to store samples at −80°C at least, if measurements are planned to be performed after several years. | | |
| Other chemical exposures (brominated flame retardants, perfluorinated compounds, phthalates and phenols) | Human biological monitoring is the state of the art method for estimation of total dose | There is currently little published data in the cohorts, but many measurements are ongoing and we recommend cohorts starting to work towards combined and comparison studies. | This is an emerging field and there is a rapidly growing expertise in the cohorts, which would benefit from continued communication and coordination. |
| | ·For non-persistent exposures with very short half-lives (phthalates and phenols), we recommend repeated measurements as standard practice. | ·Conversion factors should be developed to transfer from concentrations in one medium/time point to another in order to compare/combine data from different cohorts. | ·Very little is known about the effects of postnatal exposure to emerging chemicals, and therefore we recommend further evaluation of these new chemicals in children. |
| | ·Issues of contamination from storage materials and lab equipment, and storage conditions are of great importance and need to be addressed in depth. We recommend to closely follow published recommendations on sampling collection and packing, storage, and analysis (see COPHES website: | | ·Active dialogue and partnership among the scientists representing the various disciplines would be essential for selecting new contaminants and setting prioritization for measurement in birth cohort studies. |
| | ·It is recommended to conduct a European evaluation of inter- and intra-laboratory variability. | | |
| | ·Validation of other exposure assessment methods such as questionnaires, occupational Job Exposure Matrices (JEMs), environmental measurements, and/or toxicokinetic models is needed | | |
| Radiation | | | |
| | ·Assessment of medical radiation exposures (X-ray, computer tomography (CT)-scan) by standardized questionnaires | ·Existing data are not sufficient for pooled studies. | ·Assessment of medical radiation exposure |
| | ·Assessment of occupational exposure by means of badge dose information or if not possible by questions on x-ray equipment and protective equipment used | | ·Evaluation of link with other EUROPEAN cohorts of children exposed to CT scans |
| | ·Assessment through job-exposure matrices difficult | | |
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| | ·ENRIECO has developed a set of core questions on sun exposure for different exposure-time windows that is recommended for use in cohort studies | ·Existing data are not sufficient for pooled studies | ·Inclusion of vitamin D and UV exposure related questions in cohort questionnaires. |
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| | ·Use of core set of standardized questions to assess mobile and cordless phone use | ·Comparison studies with existing data comparing questionnaire data between cohorts | ·Integration of standardized questions on use of mobile phones to facilitate future combined analyses of non-cancer effects |
| | ·Validation of questionnaires using information of other types of studies | | ·Collaborative efforts focusing on design of questions related to other RF-EMF sources (e.g. WiFi, new communication technologies, microwave ovens, baby phones) |
| | ·Coordination between cohorts in developing validated exposure models for RF and ELF-EMF | | |
| Smoking and second hand tobacco smoke | ·Questionnaires are most suitable method for larger epidemiological studies and for assessment of long-term exposure | ·Combined analyses on the effects of pre- and postnatal exposure to second hand tobacco smoke have been performed within a case study that is part of ENRIECO | ·Large studies with close monitoring of second-hand tobacco smoke exposure before conception, during trimesters of pregnancy and during the first year of life to disentangle the role of exposure during different periods |
| | ·Relevance of the timing of the exposure (before conception; during pregnancy, infancy, childhood or later in life) is not clear. Large studies can enhance knowledge if exposure is assessed repeatedly during different time periods. | | ·Specific questions recommended for the different exposure periods |
| Noise | ·Objective measures should be in accordance with the European Union’s Environmental Noise Directive (END) guidelines. | ·Few European cohorts currently have data from objective noise assessments that could be combined | ·Inclusion of objective and subjective exposure assessments |
| | ·Noise propagation modeling is recommended for large studies. | | ·Assessment of time-activity pattern |
| | ·Questionnaire- assessments of noise annoyance should be performed in addition to objective measures; standard scales can be recommended. Information on non-residential exposure, time-activity pattern, and insulation of buildings, window opening behavior and the position of bedroom in relation to source of noise should be included in exposure assessment. | | |
| Occupational exposures | ·A number of Job Exposure Matrices (JEMs) have been built in Europe covering different periods of time and different types of exposures. | ·Within the ENRIECO project, the possibility to perform pooled/meta-analyses of the association between adverse health outcomes and selected occupations of mothers and fathers during vulnerable periods has been explored; 14 cohorts are eligible for this analysis, 12 have already expressed their interest. A protocol for the analysis has been developed. | ·For an adequate data collection on occupational exposures job title is not sufficient. In addition, one should collect description of task, type of industry, number of hours per week, and if possible name of company, existence of biomonitoring data. Free text should be kept in the data base for additional details. |
| | ·JEMs need to be validated against objective measures of exposure (work environment, biomarkers) | | ·A good training of coders should be organized for harmonization of occupation coding |
| | ·If JEMs are used, they should be country- and agent-specific since work environments differ between countries and time periods. | | ·Standardized questionnaires for physical load should be published |
| | ·To avoid any influence of birth outcome on the availability of occupational information and on its quality, we recommend that data should be collected before birth. This is mandatory when questionnaires on occupational exposures are used and optional for job title. | | |
| ·The period of interest is around conception and each trimester - or at least one trimester of pregnancy (depending on the health outcome studied) for mothers, and before conception for fathers. |