# The Impact of Exogenous Vitamin D on Pituitary Effects of Metformin in Postmenopausal Women with Subclinical Hypothyroidism and Normal Vitamin D Status: A Pilot Study

**Authors:** Robert Krysiak, Karolina Kowalcze, Johannes Ott, Simona Zaami, Giuseppe Gullo, Bogusław Okopień

PMC · DOI: 10.3390/nu18050838 · Nutrients · 2026-03-05

## TL;DR

This pilot study shows that adding vitamin D to metformin treatment enhances its effects on pituitary hormones in postmenopausal women with subclinical hypothyroidism.

## Contribution

The study is the first to investigate the interaction between metformin and exogenous vitamin D at the pituitary level in individuals with normal vitamin D status.

## Key findings

- Metformin/vitamin D combination therapy reduced LH and prolactin levels, unlike metformin alone.
- The pituitary hormone-lowering effects of metformin were more pronounced when combined with vitamin D.
- Vitamin D monotherapy only modestly improved insulin sensitivity and increased vitamin D levels.

## Abstract

Background/Objectives: Low vitamin D status was found to attenuate the impact of metformin on circulating levels of anterior pituitary hormones, but this inhibitory effect was absent in vitamin D-repleted subjects. No previous study investigated the interaction between metformin and exogenous vitamin D at the pituitary levels in individuals with normal vitamin D status. Methods: Our pilot, single-center, prospective, matched-cohort study enrolled 59 postmenopausal women with subclinical hypothyroidism and 25-hydroxyvitamin D levels in the range between 75 and 150 nmol/L. For the following six months, all the participants were treated with either metformin/vitamin D combination therapy (group 1, n = 27) or metformin alone (group 2, n = 32). The outcomes of interest included 25-hydroxyvitamin D, fasting glucose, HOMA-IR, HbA1c, TSH, FSH, LH, prolactin, ACTH, free thyroid hormones, estradiol and IGF-1. A parallel study investigated the impact of vitamin D monotherapy on the outcome measures in insulin-resistant women meeting the remaining inclusion criteria. Results: No differences in baseline biomarker values were observed between groups 1 and 2. Ninety-three percent of the patients completed the study. The increase in 25-hydroxyvitamin D levels was observed exclusively in group 1. Although glucose homeostasis markers and post-treatment levels of TSH and FSH were lower at the end of the study than at baseline in both groups, the effect of treatment was more pronounced in group 1 than in group 2. Metformin/vitamin D combination therapy, but not metformin alone, reduced LH and prolactin levels. In both groups, the TSH- and gonadotropin-lowering effects of metformin correlated with baseline levels of these pituitary hormones. Levels of ACTH, free thyroxine, free triiodothyronine, estradiol and IGF-1 remained stable throughout the study. The effects of vitamin D monotherapy were confined to an increase in plasma 25-hydroxyvitamin D concentrations and a modest enhancement in insulin sensitivity. Conclusions: Exogenous vitamin D potentiates the pituitary effects of metformin in postmenopausal women with subclinical hypothyroidism.

## Linked entities

- **Chemicals:** metformin (PubChem CID 4091), 25-hydroxyvitamin D (PubChem CID 5353325), glucose (PubChem CID 5793), TSH (PubChem CID 1150), LH (PubChem CID 341684), prolactin (PubChem CID 168266256), ACTH (PubChem CID 16129617), estradiol (PubChem CID 450)

## Full-text entities

- **Genes:** IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, PRL (prolactin) [NCBI Gene 5617] {aka GHA1, pPRL}, POMC (proopiomelanocortin) [NCBI Gene 5443] {aka ACTH, CLIP, LPH, MSH, NPP, OBAIRH}
- **Diseases:** insulin-resistant (MESH:D007333), Hypothyroidism (MESH:D007037)
- **Chemicals:** 25-hydroxyvitamin D (MESH:C104450), Vitamin D (MESH:D014807), Metformin (MESH:D008687), glucose (MESH:D005947), LH (MESH:D007986), estradiol (MESH:D004958), triiodothyronine (MESH:D014284), thyroxine (MESH:D013974)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12987131/full.md

## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12987131/full.md

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Source: https://tomesphere.com/paper/PMC12987131