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Early life phthalate exposure and atopic disorders in children: a prospective birth cohort study
I-Jen Wang1, Ching-Chun Lin, Yen-Ju Lin
1Department of Pediatrics, Taipei Hospital, Ministry of Health and Welfare, Taipei, Taiwan; China Medical University, Taichung, Taiwan; College of Medicine, National Yang-Ming University, Taipei, Taiwan.
Insights
Early life exposure to certain phthalates, like mono-(2-ethylhexyl) phthalate (MEHP), may increase children's risk of allergic sensitization and atopic dermatitis (AD). Higher MEHP levels at age 2 correlated with elevated immunoglobulin E (IgE) in boys.
Area of Science:
- Environmental Health
- Immunology
- Pediatrics
Background:
- The impact of phthalate exposure on immune system development and atopic disorders is not fully understood.
- Phthalates are common endocrine-disrupting chemicals found in many consumer products.
Purpose of the Study:
- To investigate the association between prenatal and early postnatal phthalate exposure and immunoglobulin E (IgE) levels and atopic dermatitis (AD) in children.
- To utilize objective biomarkers for assessing phthalate exposure and allergic outcomes.
Main Methods:
- A prospective cohort study of 483 mother/infant pairs (Taiwan Birth Panel study).
- Urine samples collected during the 3rd trimester of pregnancy and at ages 2 and 5 years.
- Analysis of phthalate metabolites (MEP, MBP, MBzP, MEHP) using ultra-performance liquid chromatography-tandem mass spectrometry.
- Assessment of serum total IgE levels and diagnosis of AD at ages 2 and 5 years.
- Statistical analysis using multivariate linear and logistic regression.
Main Results:
- Phthalate metabolite levels were highest at age 2.
- Mono-(2-ethylhexyl) phthalate (MEHP) levels at age 2 showed a positive correlation with serum IgE, particularly in boys.
- Monobenzyl phthalate (MBzP) levels at age 2 were significantly associated with the development of AD.
- No significant associations were found for other phthalate metabolites with IgE or AD.
Conclusions:
- Early-life exposure to specific phthalates, such as MEHP and MBzP, may contribute to an increased risk of allergic sensitization and atopic disorders in children.
- Gender differences may influence the relationship between phthalate exposure and allergic outcomes.
Abstract:
The role of phthalate exposure at different stages in the immune system and atopic disorders is not well-known. This study aims to evaluate the effects of prenatal and postnatal phthalate exposures on immunoglobulin E (IgE) levels and atopic dermatitis (AD) in children by objective biomarkers. We conducted a prospective Taiwan Birth Panel cohort study with 483 mother/infant pairs. Finally, 161 urine specimens at 3rd trimester of pregnancy, 219 urine specimens from children at age 2, and 192 urine specimens at age 5 were analyzed after excluding missing data and loss to follow-up. Urine monoethyl phthalate (MEP), monobutyl phthalate (MBP), monobenzyl phthalate (MBzP), and mono-(2-ethylhexyl) phthalate (MEHP) at 3rd trimester of pregnancy and at ages 2 and 5 were measured by ultra-performance liquid chromatography coupled with tandem mass spectrometry. At ages 2 and 5, information on the development of AD and serum total IgE was collected. The association between urine phthalate metabolite levels at different stages and serum IgE and AD was evaluated by multivariate linear regression and logistic regression. Urine phthalate metabolite levels were higher at age 2 than those at pregnancy and age 5. At each period, urine MBP levels were higher than MEP, MEHP, and MBzP. MEHP levels at age 2 positively correlated with serum IgE levels (per ln-unit: β=0.191, p=0.02). Analyses stratified by gender revealed that MEHP levels positively correlated with serum IgE levels only in boys (per ln-unit: β=0.256, p=0.03). When dividing into quartiles, urine MBzP levels at age 2 had a significant association with AD. We found no statistically significant association of other phthalate metabolites with IgE and AD. Early life phthalate exposure may increase the risk of allergic sensitization and atopic disorders.
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