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Unlabelled: Coexposure to air pollution and tobacco smoke may influence early-life growth, but few studies have investigated their joint effects. We examined the interaction between fetal exposure to maternal smoking and ozone (O) or fine particulate matter (PM) on birth weight, neonatal adiposity, and body mass index (BMI) trajectories through age 3 years.
Methods: Participants were 526 mother-child pairs, born ≥37 weeks. Cotinine was measured at ~27 weeks gestation. Whole pregnancy and trimester-specific O and PM were estimated via. inverse-distance weighted interpolation from stationary monitors. Neonatal adiposity (fat mass percentage) was measured via. air displacement plethysmography. Child weight and length/height were abstracted from medical records. Interaction was assessed by introducing cotinine (<31.5 vs. ≥31.5 ng/mL [indicating active smoking]), O/PM (low [tertiles 1-2] vs. high [tertile 3]), and their product term in linear regression models for birth weight and neonatal adiposity and mixed-effects models for BMI trajectories.
Results: The rate of BMI growth among offspring jointly exposed to maternal smoking and high PM (between 8.1 and 12.7 μg/m) in the third trimester was more rapid than would be expected due to the individual exposures alone (0.8 kg/m per square root year; 95% CI = 0.1, 1.5; for interaction = 0.03). We did not detect interactions between maternal smoking and O or PM at any other time on birth weight, neonatal adiposity, or BMI trajectories.
Conclusions: Although PM was generally below the EPA annual air quality standards of 12.0 μg/m, exposure during the third trimester may influence BMI trajectories when combined with maternal smoking.
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http://dx.doi.org/10.1097/EE9.0000000000000142 | DOI Listing |
Ultrasound Obstet Gynecol
August 2025
Division of Endocrinology and Metabolism, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Objective: Amniotic fluid volume, measured in terms of the amniotic fluid index (AFI), is used widely in prenatal care to assess fetal health and development. We investigated whether distinct longitudinal AFI trajectories exist during pregnancy and their association with fetal growth.
Methods: This secondary analysis of a randomized controlled trial included singleton pregnancies without pre-existing or gestational diabetes mellitus that received prenatal care at National Taiwan University Hospital in Taipei and its Hsin-Chu Branch in Hsinchu, Taiwan.
Diagnostics (Basel)
August 2025
Department of Clinical Analyses, Federal University of Santa Catarina (UFSC), Florianópolis 88036-800, Brazil.
To investigate the association between prenatal ultrasonographic markers of macrossomia and C-peptide, a neonatal hyperinsulinemia marker, in pregnancies complicated by gestational diabetes mellitus (GDM), with a focus on fetal adipose tissue thickness, liver length, and interventricular septal thickness. : This prospective cohort study included 223 pregnant women followed from 28 to 36 weeks of gestation in two referral centers in Brazil. The GDM group and matched controls underwent serial ultrasound assessments of fetal biometry, including thigh, abdominal, and subscapular skinfolds, fetal liver length, and interventricular septum thickness.
View Article and Find Full Text PDFJ Lipid Res
August 2025
Department of Developmental Biology and Genetics, Indian Institute of Science, Bengaluru, Karnataka, 560012, India.
Mitochondria are fundamental in energy homeostasis and undergo dynamic changes in brown and beige fat. Mitochondrial dysfunctions impair thermogenic capacity and cause obesity-associated metabolic diseases. The phospholipid composition is crucial for maintaining mitochondrial function and fission-fusion processes.
View Article and Find Full Text PDFStem Cell Res Ther
August 2025
Institute of Advanced Biomedical Engineering and Science, Tokyo Women's Medical University, 8-1 Kawada-cho, Shinjuku-ku, Tokyo, 162-8666, Japan.
Background: The optimal timing for mesenchymal stem cell (MSC) therapy in Duchenne muscular dystrophy (DMD) remains unclear.
Methods: Neonatal DMD rats received intraperitoneal adipose-derived MSCs according to three schedules: early (postnatal days 1 and 14), continuous (days 1, 14, 28, and 42), or late (days 28 and 42). Wild-type rats and untreated DMD rats served as controls.
Clin Ophthalmol
August 2025
Department of Ophthalmology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, 430022, People's Republic of China.
Background: Gestational diabetes mellitus (GDM) affects 5.8% to 25.1% of pregnant women and is associated with a range of adverse perinatal outcomes, including intrauterine growth restriction, prematurity, neonatal respiratory distress, and adiposity.
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