Evidence map›Paper›PMID 40362671›Full record

ArticleInternational journal of molecular sciences2025

Maternal Serum 25-Hydroxyvitamin D as a Possible Modulator of Fetal Adiposity: A Prospective Longitudinal Study.

Keisuke Akita, Satoru Ikenoue, Junko Tamai, Toshimitsu Otani, Marie Fukutake, Yoshifumi Kasuga, Mamoru Tanaka

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Keisuke AkitaDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Shinanomachi, Shinjuku-ku 160-8582, Tokyo, Japan.
Satoru IkenoueDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Shinanomachi, Shinjuku-ku 160-8582, Tokyo, Japan.ORCID 0000-0003-3652-5389
Junko TamaiDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Shinanomachi, Shinjuku-ku 160-8582, Tokyo, Japan.ORCID 0009-0002-8974-6898
Toshimitsu OtaniDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Shinanomachi, Shinjuku-ku 160-8582, Tokyo, Japan.
Marie FukutakeDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Shinanomachi, Shinjuku-ku 160-8582, Tokyo, Japan.
Yoshifumi KasugaDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Shinanomachi, Shinjuku-ku 160-8582, Tokyo, Japan.ORCID 0000-0003-2395-9591
Mamoru TanakaDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Shinanomachi, Shinjuku-ku 160-8582, Tokyo, Japan.

Funding

JAMW Ogyaa Donation Foundation NAJapan Society for the Promotion of Science 19K09761, 22K16864
6 · The paper itself

Abstract

25-hydroxyvitamin D (25(OH)D) regulates lipid metabolism, and its decrease is proposed as a pathogenesis of metabolic syndrome, gestational diabetes mellitus (GDM), and eventually fetal adiposity. Decreased 25(OH)D is also linked with the development of gestational diabetes mellitus (GDM), which is associated with increased fetal adiposity. Fetuses are dependent on the supply of 25(OH)D from maternal circulation. However, the influence of maternal serum 25(OH)D on fetal adiposity remains unclear. This study aimed to investigate the association between maternal serum 25(OH)D and fetal adiposity. A prospective longitudinal study was conducted in a cohort of 89 (including 21 GDM) singleton pregnancies. Maternal blood samples were obtained at 10, 24, 30, and 36 weeks, and fetal ultrasonography was performed at 24, 30, and 36 weeks of gestation. Estimated fetal adiposity (EFA) was calculated as the average z-score of cross-sectional arm and thigh percentage fat area and anterior abdominal wall thickness as previously reported. The multiple linear regression analyses indicated that maternal 25(OH)D levels across gestation were not associated with EFA at 24 and 30 weeks, while maternal 25(OH)D at 24 weeks was inversely correlated with EFA at 36 weeks. Particularly, in the GDM group, maternal 25(OH)D levels at 10, 24, 30, and 36 weeks all showed a significant negative correlation with EFA at 36 weeks. Decreased maternal serum 25(OH)D level could be an early biomarker of increased fetal adiposity in late gestation, especially in diabetic pregnancies.

Indexed as

AdiposityDiabetes, GestationalFetusVitamin DAdultFemaleHumansLongitudinal StudiesPregnancyProspective StudiesUltrasonography, Prenatal25-hydroxyvitamin DVitamin D25-hydroxyvitamin Dfetal adiposityfetal ultrasonographygestational diabetes mellitus

Identifiers

PMID40362671
PMCPMC12073073

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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 OpenQuestion graph.