Tehran environmental and neurodevelopmental disorders (TEND) cohort study: Phase I, feasibility assessment

Purpose To advance knowledge about childhood neurodevelopmental disorders and study their environmental determinants, we conducted a study in Tehran, Iran to assess the feasibility of prospective birth cohort study. Methods We evaluated participation of pregnant women, feasibility of sampling biolog...

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Published inJournal of environmental health science and engineering Vol. 18; no. 2; pp. 733 - 742
Main Authors Shamsipour, Mansour, Pirjani, Reihaneh, Jeddi, Maryam Zare, Effatpanah, Mohammad, Rastkari, Noushin, Kashani, Homa, Shirazi, Mahboobeh, Hassanvand, Mohammad Sadegh, NinoKünzli, Shariat, Mamak, Javadi, Fatemeh Sadat, Shariatpanahi, Ghazal, Hassanpour, Gholamreza, Peykarporsan, Zahra, Jamal, Akram, Ardestani, Mina Ebad, Hoseini, Fatemeh Sadat, Dalili, Hosein, Nayeri, Fatemeh Sadat, Mesdaghinia, Alireza, Naddafi, Kazem, Shahtaheri, Seyed Jamaleddin, Nasseri, Simin, Yunesian, Farzad, Rezaeizadeh, Golnaz, Amini, Heresh, Yokoyama, Kazuhito, Vigeh, Mohsen, Yunesian, Masud
Format Journal Article
LanguageEnglish
Published Cham Springer International Publishing 01.12.2020
BioMed Central Ltd
Nature Publishing Group
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Summary:Purpose To advance knowledge about childhood neurodevelopmental disorders and study their environmental determinants, we conducted a study in Tehran, Iran to assess the feasibility of prospective birth cohort study. Methods We evaluated participation of pregnant women, feasibility of sampling biological material, and health care services availability in Tehran in four steps: (1) first trimester of pregnancy; (2) third trimester of pregnancy; (3) at delivery; and (4) two to three months after delivery. We collected related data through questionnaires, also various biological samples were obtained from mothers (blood, urine, milk and nails—hands and feet) and newborns (umbilical cord blood, meconium, and urine samples) from February 2016 to October 2017. Results overall 838 eligible pregnant women were approached. The participation rate was 206(25%) in our study and about 185(90%) of subjects were recruited in hospitals. Out of 206 participants in the first trimester, blood, urine, hand nail, and foot nail samples were collected from 206(100%),193(93%), 205(99%), and 205(99%), respectively. These values dropped to 65(54%), 83(69%), 84(70%), and 84(70%) for the remaining participants 120(58%) in the third trimester, respectively. Also, we gathered milk samples from 125(60%) of mothers at two to three months after delivery. Conclusion Our findings suggest that hospitals were better places for recruitment of subjects in a birth cohort in Tehran. We further concluded that birth cohort study recruitment can be improved by choosing appropriate gestational ages. Obtaining the newborn’s urine, meconium, and umbilical cord blood were challenging procedures and require good collaboration between hospital staff and researchers.
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ISSN:2052-336X
2052-336X
DOI:10.1007/s40201-020-00499-4