In Utero Exposure to Caffeine and Acetaminophen, the Gut Microbiome, and Neurodevelopmental Outcomes: A Prospective Birth Cohort Study

• Published in: International journal of environmental research and public health Vol. 19; no. 15; p. 9357
• Main Authors: Laue, Hannah E, Shen, Yike, Bloomquist, Tessa R, Wu, Haotian, Brennan, Kasey J M, Cassoulet, Raphael, Wilkie, Erin, Gillet, Virginie, Desautels, Anne-Sandrine, Abdelouahab, Nadia, Bellenger, Jean Philippe, Burris, Heather H, Coull, Brent A, Weisskopf, Marc G, Zhang, Wei, Takser, Larissa, Baccarelli, Andrea A
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 30.07.2022; MDPI
• Subjects: Abundance; Acetaminophen; Acetaminophen - adverse effects; Age; Analgesics; Bacteria - genetics; Birth Cohort; Caffeine; Caffeine - adverse effects; Caregivers; Children; Cognitive ability; Cohort analysis; Cohort Studies; Colonization; Digestive system; DNA sequencing; Exposure; Families & family life; Family income; Feces; Female; Gastrointestinal Microbiome; Humans; Intestinal microflora; Intrauterine exposure; Meconium; Metabolism; Metagenomics; Microbiomes; Microbiota; Neurodevelopment; Pregnancy; Prenatal experience; Prenatal exposure; Prospective Studies; Questionnaires; Relative abundance; RNA, Ribosomal, 16S - genetics; acetaminophen; caffeine; children’s health; neurodevelopment; microbiome
• ISSN: 1660-4601; 1661-7827; 1660-4601
• DOI: 10.3390/ijerph19159357

Pregnant individuals are exposed to acetaminophen and caffeine, but it is unknown how these exposures interact with the developing gut microbiome. We aimed to determine whether acetaminophen and/or caffeine relate to the childhood gut microbiome and whether features of the gut microbiome alter the relationship between acetaminophen/caffeine and neurodevelopment. Forty-nine and 85 participants provided meconium and stool samples at 6-7, respectively, for exposure and microbiome assessment. Fecal acetaminophen and caffeine concentrations were quantified, and fecal DNA underwent metagenomic sequencing. Caregivers and study staff assessed the participants' motor and cognitive development using standardized scales. Prenatal exposures had stronger associations with the childhood microbiome than concurrent exposures. Prenatal acetaminophen exposure was associated with a trend of lower gut bacterial diversity in childhood [β = -0.17 Shannon Index, 95% CI: (-0.31, -0.04)] and was marginally associated with differences in the relative abundances of features of the gut microbiome at the phylum (Firmicutes, Actinobacteria) and gene pathway levels. Among the participants with a higher relative abundance of Proteobacteria, prenatal exposure to acetaminophen and caffeine was associated with lower scores on WISC-IV subscales. Acetaminophen during bacterial colonization of the naïve gut is associated with lasting alterations in childhood microbiome composition. Future studies may inform our understanding of downstream health effects.