ArticleJournal of the Endocrine Society2026
Exploratory assessment of preconception phthalate exposure on pregnancy and offspring health outcomes in mice.
Article in Journal of the Endocrine Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Prenatal Dibutyl Phthalate Exposure Dysregulates Fetal-Placental Vascular Function and Placental Vasculature-Specific Lipid Metabolism.bioRxiv : the preprint server for biology · 2026Article
- Exploratory assessment of preconception phthalate exposure on pregnancy and offspring health outcomes in mice.Journal of the Endocrine Society · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Understanding how endocrine-disrupting chemicals influence reproductive success requires attention to sensitive windows beyond gestation, including the understudied preconception period. In this exploratory pilot study, female CD-1 mice were exposed to a human-relevant phthalate mixture (200 µg/kg/day) for 30 days prior to mating. Although implantation and litter size were unaffected, exposed dams exhibited nonsignificant shifts in estrus cyclicity, spending more time in proestrus and less in metestrus. Maternal liver transcriptomics revealed persistent changes more than a month after exposure ceased, with differential expression of genes involved in mitochondrial metabolism, oxidative phosphorylation, and xenobiotic processing, suggesting long-term metabolic reprograming in the absence of overt toxicity. Maternal effects coincided with developmental alterations at mid-gestation. At E14.5, fetuses from exposed dams were heavier, and placentas displayed expansion of the junctional zone, a region critical for endocrine function. This early growth enhancement reversed later in life, as exposed male offspring exhibited reduced adult body weight, consistent with altered developmental programing. Transcriptomic profiling revealed pronounced sex-specific placental responses: female placentas exhibited extensive reprograming across immune, metabolic, and extracellular matrix pathways (518 differentially expressed genes [DEGs]), whereas male placentas showed minimal differential expression (9 DEGs), despite enrichment for RNA processing and mitochondrial pathways. Adult offspring livers also displayed sex-specific transcriptional signatures, with exposed females downregulating metabolic and immune-regulatory genes and exposed males upregulating inflammatory pathways. Collectively, these hypothesis-generating findings provide early evidence that preconception exposures can shape maternal physiology, placental development, and long-term offspring health, highlighting the preconception period as a critical yet understudied window of susceptibility.
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Registered trials
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