scholarly journals A combined cohort analysis of prenatal exposure to phthalate mixtures and childhood asthma

2020 ◽  
Vol 143 ◽  
pp. 105970
Author(s):  
Margaret A. Adgent ◽  
Kecia N. Carroll ◽  
Marnie F. Hazlehurst ◽  
Christine T. Loftus ◽  
Adam A. Szpiro ◽  
...  
2020 ◽  
Vol 27 (23) ◽  
pp. 29280-29290 ◽  
Author(s):  
Wu Yan ◽  
Xu Wang ◽  
Tianyu Dong ◽  
Mengqi Sun ◽  
Mingzhi Zhang ◽  
...  

2022 ◽  
Author(s):  
Shmuel Goldberg ◽  
Elie Picard ◽  
Leon Joseph ◽  
Ron Kedem ◽  
Adir Sommer ◽  
...  

2012 ◽  
Vol 35 (10) ◽  
pp. 1190-1198 ◽  
Author(s):  
A. B. T. Andersen ◽  
R. Erichsen ◽  
D. K. Farkas ◽  
F. Mehnert ◽  
V. Ehrenstein ◽  
...  

2020 ◽  
Vol 9 (5) ◽  
pp. 1271 ◽  
Author(s):  
Eliel Kedar Sade ◽  
Tamar Wainstock ◽  
Erez Tsumi ◽  
Eyal Sheiner

The aim of this population-based study was to evaluate whether prenatal exposure to preeclampsia poses a risk for long-term ophthalmic morbidity. A population-based cohort analysis compared the risk of long-term ophthalmic morbidity among children who were prenatally exposed to preeclampsia and those who were not. The study population was composed of children who were born between the years 1991 and 2014 at a single tertiary medical center. Total ophthalmic hospitalization and time-to-event were both evaluated. A Kaplan–Meier survival curve was conducted to compare cumulative ophthalmic hospitalization incidence based on the severity of preeclampsia. Confounders were controlled using a Cox regression model. A total of 242,342 deliveries met the inclusion criteria, of which 7279 (3%) were diagnosed with mild preeclampsia and 2222 (0.92%) with severe preeclampsia or eclampsia. A significant association was found between severe preeclampsia or eclampsia and the risk of long-term vascular-associated ophthalmic morbidity in the offspring (no preeclampsia 0.3%, mild preeclampsia 0.2% and severe preeclampsia or eclampsia 0.5%, p = 0.008). This association persisted after controlling for maternal age and ethnicity (adjusted hazard ratio (HR) 1.861, 95% CI 1.051–3.295). In conclusion, within our population, prenatal exposure to severe preeclampsia or eclampsia was found to be a risk factor for long-term vascular-associated ophthalmic morbidity in the offspring.


2016 ◽  
Vol 2016 (1) ◽  
Author(s):  
Maria Alexaki ◽  
Marina Vafeiadi* ◽  
Theano Roumeliotaki ◽  
Vaggelis Vittorakis ◽  
Georgia Chalkiadaki ◽  
...  

Author(s):  
Lacey B. Robinson ◽  
Anna Arroyo ◽  
Ruth J. Geller ◽  
Ashley F. Sullivan ◽  
Carlos Camargo Jr

In conclusion, in a cohort of children with a history of severe bronchiolitis those exposed to ASM prenatally are not at increased risk of developing food or environmental allergen sensitization by early childhood. The mechanism by which ASM exposure increases risk of childhood asthma remains unclear, but alterations in the gut microbiome merit consideration.


2019 ◽  
Vol 53 (5) ◽  
pp. 1801090 ◽  
Author(s):  
Seif O. Shaheen ◽  
Cecilia Lundholm ◽  
Bronwyn K. Brew ◽  
Catarina Almqvist

Many epidemiological studies have reported a positive association between prenatal exposure to paracetamol and childhood wheezing and asthma. We investigated whether the link between prenatal analgesic exposure and asthma/wheeze is specific to paracetamol, and whether it is causal or confounded.Using linked Swedish health register data we investigated the relation between various prescribed analgesics in pregnancy and the risk of childhood asthma/wheeze in a population of 492 999, and used negative paternal control and sibling comparison approaches to explore unmeasured confounding.After controlling for potential confounders, prescribed opioids, antimigraine drugs and paracetamol were all positively associated with childhood asthma/wheeze risk at all ages (e.g. for asthma/wheeze at age 4 years: adjusted OR 1.39 (95% CI 1.30–1.49), 1.19 (95% CI 1.01–1.40) and 1.47 (95% CI 1.36–1.59) for opioids, antimigraine drugs and paracetamol, respectively). The results of the paternal control analysis did not suggest the presence of unmeasured confounding by genetics or shared environment. However, the sibling control analysis broadly suggested that associations between prenatal exposure to the analgesics and asthma/wheeze were confounded by specific maternal factors (e.g. for asthma/wheeze at age 4 years: adjusted OR 0.91 (95% CI 0.62–1.31), 0.50 (95% CI 0.17–1.45) and 0.80 (95% CI 0.50–1.29) for opioids, antimigraine drugs and paracetamol, respectively).We propose that analgesic use in pregnancy does not cause childhood asthma/wheeze and that the association is confounded by unmeasured factors that are intrinsic to the mother, such as chronic pain or anxiety.


2015 ◽  
Vol 25 (2) ◽  
pp. 188-195 ◽  
Author(s):  
Xiaoqin Liu ◽  
Zeyan Liew ◽  
Jørn Olsen ◽  
Lars Henning Pedersen ◽  
Bodil Hammer Bech ◽  
...  

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