ReviewJournal of Korean medical science2026
Maternal Diabetes Mellitus and Child Neurodevelopmental Disorders: Rethinking Causality in Light of Environmental Pollutants.
Review in Journal of Korean medical science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Numerous epidemiological studies have linked maternal diabetes mellitus (DM) to neurodevelopmental disorders in offspring, such as autism spectrum disorder and attention-deficit/hyperactivity disorder. However, recent evidence challenges a direct causal relationship: sibling-matched analyses show similar risks regardless of gestational DM status, and glycemic control during pregnancy does not consistently predict neurodevelopmental outcomes. We propose that exposure to environmental pollutants-rather than DM itself-may underlie these associations. Although usually examined separately, many pollutants both increase DM risk and disrupt fetal brain development, providing a biologically plausible basis for the observed epidemiological patterns. Because fetuses encounter these pollutants via placental transfer from maternal blood, understanding what determines maternal circulating pollutant levels is essential. Two major sources contribute: (1) ongoing external exposure through food, air, water, and consumer products, and (2) the release of previously accumulated lipophilic pollutants stored in adipose tissue. Often overlooked, adipose tissue serves as an important reservoir, and lipolysis mobilizes these compounds into circulation. Importantly, key pathophysiological features of DM-insulin resistance and insulin deficiency-accelerate lipolysis, increasing circulating pollutant levels. These pollutant-related mechanisms may also account for associations observed with other maternal conditions, such as obesity, eating disorders, psychological stress, and intrahepatic cholestasis of pregnancy, all of which may also be linked to elevated pollutant levels in maternal circulation. These insights suggest that maternal risk factors should be reconsidered in light of toxicokinetic dynamics, particularly the mobilization of lipophilic pollutants stored in fat. This perspective may offer a unifying explanation for otherwise disparate epidemiological findings and help guide more effective prevention strategies.
Indexed as
Identifiers
What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.