Evidence map›Paper›PMID 41724795›Full record

ArticleScientific reports2026

Effects of dietary vitamin D supplementation on bone microarchitecture, mineralization, and mechanical properties in Wistar rat animal model.

Cezary Osiak-Wicha, Siemowit Muszyński, Katarzyna Kras, Ewa Tomaszewska, Beata Szymczyk, Maria Oczkowicz, Małgorzata Świątkiewicz, Dariusz Wiącek, Daniel Kamiński, Marcin B Arciszewski

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

10 authors.

Cezary Osiak-WichaDepartment of Animal Anatomy and Histology, Faculty of Veterinary Medicine, University of Life Sciences in Lublin, Akademicka 12, 20-950, Lublin, Poland.
Siemowit MuszyńskiDepartment of Biophysics, Faculty of Environmental Biology, University of Life Sciences in Lublin, Akademicka 13, 20-950, Lublin, Poland.
Katarzyna KrasDepartment of Animal Anatomy and Histology, Faculty of Veterinary Medicine, University of Life Sciences in Lublin, Akademicka 12, 20-950, Lublin, Poland. katarzyna.kras@up.lublin.pl.
Ewa TomaszewskaDepartment of Animal Physiology, Faculty of Veterinary Medicine, University of Life Sciences in Lublin, Akademicka 12, 20-950, Lublin, Poland.
Beata SzymczykDepartment of Animal Nutrition and Feed Science, National Research Institute of Animal Production, Krakowska 1, 32-083, Balice, Poland.
Maria OczkowiczDepartment of Animal Molecular Biology, National Research Institute of Animal Production, Krakowska 1, 32-083, Balice, Poland.
Małgorzata ŚwiątkiewiczDepartment of Animal Nutrition and Feed Science, National Research Institute of Animal Production, Krakowska 1, 32-083, Balice, Poland.
Dariusz WiącekBohdan Dobrzański Institute of Agrophysics of the Polish Academy of Sciences, Doświadczalna 4, 20-290, Lublin, Poland.
Daniel KamińskiDepartment of Organic and Crystallochemistry, Institute of Chemical Sciences, Faculty of Chemistry, Maria Curie-Sklodowska University, M. Curie-Sklodowskiej 3, 20-031, Lublin, Poland.
Marcin B ArciszewskiDepartment of Animal Anatomy and Histology, Faculty of Veterinary Medicine, University of Life Sciences in Lublin, Akademicka 12, 20-950, Lublin, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vitamin D is essential for proper skeletal development, yet the specific dose-dependent effects of its dietary supplementation during the transition from late adolescence through young adulthood remain unclear. Because the standard diet already supplies 1,000 IU/kg vitamin D₃ and is widely regarded as adequate for growing rats, poorer skeletal outcomes at 0 IU/kg and favorable outcomes at 1,000 IU/kg are expected. The studies objective was therefore to quantify the magnitude and map which dimensions of bone quality respond to vitamin D across the adolescent-to-young-adult transition, and to test whether a supraphysiological intake (5,000 IU/kg) confers additional benefit and we hypothesized that moderate vitamin D would improve bone outcomes versus deficiency, whereas a high dose would offer no added advantage. Male and female Wistar rats (≈ 7 weeks old; n = 6/sex/group) were fed for 12 weeks diets containing 0, 1000, or 5000 IU/kg vitamin D. The right femur was assessed by DXA (BMD), three-point bending (strength, energy absorption, stiffness), growth-plate morphometry, elemental composition, and X-ray diffraction of hydroxyapatite; RANKL/OC/VEGF immunoexpression and serum 25(OH)D were measured. Diets produced graded systemic exposure: 25(OH)D increased with dose in both sexes. Across outcomes, sex showed a strong main effect (males larger/stronger), while dose effects were selective. Compared with 0 IU/kg, 1000 IU/kg increased BMD and several mechanical endpoints (e.g., maximum force/energy) primarily in males, and improved material behavior (post-yield strain) without altering elastic modulus. Growth plate effects were limited: the hypertrophic (Zone IV) thickness was lower with deficiency and greater with supplementation, with sex- and dose-specific patterns; other zones showed minimal dose effects. The 5000 IU/kg diet raised 25(OH)D but did not consistently outperform 1000 IU/kg and showed no broad detriments across measured variables. During late growth, moderate vitamin D (1000 IU/kg) improves femoral mass and selected mechanical/biomechanical properties relative to deficiency, with sex-specific magnitudes of effect. A higher dose (5000 IU/kg) increases circulating vitamin D metabolite, but provides no clear additional skeletal benefit. These data support moderate supplementation as optimal in this model.

Indexed as

Bone and BonesCalcification, PhysiologicDietary SupplementsVitamin DAnimalsBiomechanical PhenomenaBone DensityFemaleFemurMaleRatsRats, WistarVitamin DBone markersBone metabolismBone remodelingGrowth plateMineral homeostasis

Identifiers

PMID41724795
PMCPMC13022431

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LicenceCC BY
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Registered trials

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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.