In the LifeLines Cohort Study, a recruitment strategy was adopted that aimed to include three generations of participants. Firstly, all GPs in the three northern provinces of the Netherlands were invited to participate and asked to invite their registered patients aged 25–49 years. Patients who were unable to read Dutch or who had limited life expectancy due to severe illness were excluded by the GP and not invited for participation. Participants who gave written informed consent were included as the “index population”. Subsequently, all persons in the index population were asked to indicate whether family members (partner, parents, parents-in-law, and children) could be invited and to provide their contact details. Family members were invited by LifeLines; those who gave their informed consent were included in the study as “family member”. Furthermore, persons aged 18 years and older could participate in this study through “self-registration” via the LifeLines website. These self-registrants were also asked to invite family members as outlined above. LifeLines aimed to include three generations of participants, but individuals who had no family member participating in the study were not excluded. Although the inclusion started in 2006 and ended in 2013, most participants (57%) were included in the last two years.
All participants aged 18 years and older were asked to complete a comprehensive questionnaire covering the occurrence of diseases, general health, lifestyle, diet, physical activity, personality, social support, medication use and more. In addition, all participants aged 18 years and older were invited to one of the 10 research sites within the region where a number of measurements were performed covering anthropometry, blood pressure, pulmonary function, heart function (electrocardiogram) and cognition [2 ,9 ]. In addition, a fasting blood sample was taken, 24 hour urine was collected, and psychiatric disorders were assessed in an interview with one of the research nurses [2 ,10 (link)].
All participants signed an informed consent form before they received an invitation for the physical examination. The LifeLines Cohort Study is conducted according to the principles of the Declaration of Helsinki and in accordance with research code University Medical Center Groningen (UMCG). The LifeLines study is approved by the medical ethical committee of the UMCG, the Netherlands. For a comprehensive overview of the data collection, please visit the LifeLines catalogue atwww.LifeLines.net .
All participants aged 18 years and older were asked to complete a comprehensive questionnaire covering the occurrence of diseases, general health, lifestyle, diet, physical activity, personality, social support, medication use and more. In addition, all participants aged 18 years and older were invited to one of the 10 research sites within the region where a number of measurements were performed covering anthropometry, blood pressure, pulmonary function, heart function (electrocardiogram) and cognition [2 ,9 ]. In addition, a fasting blood sample was taken, 24 hour urine was collected, and psychiatric disorders were assessed in an interview with one of the research nurses [2 ,10 (link)].
All participants signed an informed consent form before they received an invitation for the physical examination. The LifeLines Cohort Study is conducted according to the principles of the Declaration of Helsinki and in accordance with research code University Medical Center Groningen (UMCG). The LifeLines study is approved by the medical ethical committee of the UMCG, the Netherlands. For a comprehensive overview of the data collection, please visit the LifeLines catalogue at
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