# Statins for polycystic ovary syndrome in varying resource settings: a phenome-wide association study and evidence synthesis

**Authors:** Laura A. Zahn, Taylor D. Budine, Jana K. Shirey-Rice, Meghan M. Joly, Robert S. Wallis, Gordon R. Bernard, Kenneth J. Holroyd, Jill M. Pulley, Rebecca N. Jerome

PMC · DOI: 10.3389/fphar.2025.1562587 · Frontiers in Pharmacology · 2025-08-13

## TL;DR

This study explores using simvastatin, a common cholesterol drug, to treat polycystic ovary syndrome (PCOS), showing it may be safe and effective, especially in low-resource areas.

## Contribution

The study identifies a novel therapeutic use of simvastatin for PCOS through a PheWAS and evidence synthesis.

## Key findings

- A PheWAS identified a novel signal linking HMGCR variants to ovarian disease, including PCOS.
- Literature review supports the use of statins to improve PCOS symptoms with a favorable safety profile.
- Simvastatin is proposed as a cost-effective treatment option for PCOS in resource-limited settings.

## Abstract

There are many diseases prevalent around the globe that lack accessible and safe treatment options. Through Vanderbilt University Medical Center’s and Repurposing Essential Medicines Internationally program (Project Remedi), we aim to identify novel therapeutic uses for medications already approved and on the World Health Organization’s (WHO) Essential Medicines List (EML). We explored additional uses for simvastatin, an oral 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitor that is on the EML and may have additional therapeutic use outside of hypercholesterolemia.

We conducted a phenome wide association study (PheWAS) of a 3-hydroxy-3-methylglutaryl-CoA reductase (HMGCR) gene single nucleotide polymorphism (SNP) Ile638Val in 35,000 patient samples to identify novel uses for simvastatin. We then assessed biologic rationale and existing clinical evidence base related to novel phenotypes for simvastatin use for key PheWAS results.

PheWAS of HMGCR variants identified a novel signal related to ovarian disease, in addition to a validating signal related to lipid dysfunction. Review of the literature substantiated involvement of HMG-CoA reductase signaling in hormone synthesis and posited involvement of dysfunction in this pathway in the development of polycystic ovary syndrome (PCOS). Synthesis of the literature regarding use of statins supported the role of these agents in improvement of symptoms and quality of life in women affected by PCOS who are not pregnant or trying to conceive, with a safety profile similar to this agent’s use in hyperlipidemia.

Given the evidence supporting safety and efficacy of simvastatin for PCOS management, the widespread availability on the EML and affordability worldwide, simvastatin is a promising therapeutic avenue for PCOS. A large-scale efficacy trial would be valuable in further substantiating this use. Repurposing simvastatin, a widely available medicine, can provide clinicians and patients with an additional strategy for PCOS, especially in areas where medical care is limited.

## Linked entities

- **Genes:** HMGCR (3-hydroxy-3-methylglutaryl-CoA reductase) [NCBI Gene 3156]
- **Chemicals:** simvastatin (PubChem CID 54454), 3-hydroxy-3-methylglutaryl-coenzyme A (PubChem CID 445127), HMG-CoA (PubChem CID 445127)
- **Diseases:** polycystic ovary syndrome (MONDO:0008487), hyperlipidemia (MONDO:0021187)

## Full-text entities

- **Genes:** VCAM1 (vascular cell adhesion molecule 1) [NCBI Gene 7412] {aka CD106, INCAM-100}, CYP19A1 (cytochrome P450 family 19 subfamily A member 1) [NCBI Gene 1588] {aka ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, SHBG (sex hormone binding globulin) [NCBI Gene 6462] {aka ABP, SBP, TEBG}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, HMGCR (3-hydroxy-3-methylglutaryl-CoA reductase) [NCBI Gene 3156] {aka LDLCQ3, LGMDR28, MYPLG}
- **Diseases:** insulin resistance (MESH:D007333), hyperlipidemia (MESH:D006949), Obesity (MESH:D009765), lipid dysfunction (MESH:D052439), Dyslipidemia (MESH:D050171), alopecia (MESH:D000505), TB (MESH:D014390), diabetes (MESH:D003920), metabolic syndrome (MESH:D024821), acanthosis nigricans (MESH:D000052), acne (MESH:D000152), lipoprotein disorders (MESH:C563618), muscle damage (MESH:D009133), hypertension (MESH:D006973), infertility (MESH:D007246), disorders of reproduction and metabolism (MESH:D060737), cysts (MESH:D003560), hirsutism (MESH:D006628), myalgia (MESH:D063806), hypercholesterolemia (MESH:D006937), polycystic (MESH:D007690), venous thromboembolism (MESH:D054556), cardiovascular disease (MESH:D002318), EML (MESH:D020329), endocrinopathy (MESH:C567425), pelvic pain (MESH:D017699), metabolic dysfunctions (MESH:D008659), rhabdomyolysis (MESH:D012206), ovarian cysts (MESH:D010048), PCOS (MESH:D011085), hyperandrogenism (MESH:D017588), ovarian disease (MESH:D010049), type II diabetes (MESH:D003924), miscarriage (MESH:D000022), abnormal menstruation (MESH:D008599), depression (MESH:D003866), malnutrition (MESH:D044342), impaired glucose tolerance (MESH:D018149), coronary atherosclerosis (MESH:D003324)
- **Chemicals:** PheWAS (-), mevalonate (MESH:D008798), triglyceride (MESH:D014280), testosterone (MESH:D013739), flutamide (MESH:D005485), TG (MESH:D013866), cholesterol (MESH:D002784), lipid (MESH:D008055), HMG-CoA (MESH:C008047), Atorvastatin (MESH:D000069059), DHEA (MESH:D003687), estradiol (MESH:D004958), ezetimibe (MESH:D000069438), T (MESH:D014316), Metformin (MESH:D008687), TC (MESH:D013667), Simvastatin (MESH:D019821), glucose (MESH:D005947), steroid (MESH:D013256), androstenedione (MESH:D000735), dehydroepiandrosterone sulfate (MESH:D019314), pitavastatin (MESH:C108475), blood glucose (MESH:D001786), fluvastatin (MESH:D000077340), rosuvastatin (MESH:D000068718), pravastatin (MESH:D017035), lovastatin (MESH:D008148)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** 75356374-A-G

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## References

78 references — full list in the complete paper: https://tomesphere.com/paper/PMC12345606/full.md

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Source: https://tomesphere.com/paper/PMC12345606