# Combined Glucagon-Like Peptide-1 Receptor Agonist (GLP-1RA) and Sodium-Glucose Cotransporter 2 Inhibitor (SGLT2i) Therapy to Restore Fertility in Patients With Obesity, Polycystic Ovary Syndrome, and Incident Type 2 Diabetes

**Authors:** Mainak Banerjee, Sujoy Dasgupta

PMC · DOI: 10.7759/cureus.102358 · Cureus · 2026-01-26

## TL;DR

Combining GLP-1RA and SGLT2i therapies helped two obese women with PCOS and T2D achieve weight loss and spontaneous pregnancies.

## Contribution

This is the first report of combined GLP-1RA and SGLT2i therapy restoring fertility in PCOS patients with obesity and T2D.

## Key findings

- Two patients achieved significant weight loss and menstrual normalization within seven months.
- Both patients had successful spontaneous pregnancies after treatment.
- Pregnancies were uncomplicated and resulted in healthy live births.

## Abstract

Obesity and type 2 diabetes (T2D) frequently complicate polycystic ovary syndrome (PCOS), exacerbating subfertility. We report two cases of obese women with newly diagnosed T2D and PCOS-related subfertility successfully treated with a combination of a glucagon-like peptide-1 receptor agonist (GLP-1RA) and a sodium-glucose co-transporter 2 inhibitor (SGLT2i). Both patients achieved rapid, substantial weight loss (23% and 10.2%, respectively), leading to menstrual normalization and accidental spontaneous conception within seven months. Medications were discontinued upon confirmation of pregnancy. Both pregnancies were uncomplicated, resulting in healthy live births. Early combination therapy with GLP-1RA and SGLT2i may offer a potent approach to expedite spontaneous conception in this high-risk population. While inadvertent early pregnancy exposure shows no major teratogenic concern based on emerging preliminary studies, immediate discontinuation with transitioning to metformin and/or insulin prior to planning pregnancy remains the clinical standard until robust safety profiles regarding embryotoxicity are established.

## Linked entities

- **Chemicals:** metformin (PubChem CID 4091), insulin (PubChem CID 70678557)
- **Diseases:** obesity (MONDO:0011122), type 2 diabetes (MONDO:0005148), polycystic ovary syndrome (MONDO:0008487)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, SHBG (sex hormone binding globulin) [NCBI Gene 6462] {aka ABP, SBP, TEBG}, SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}
- **Diseases:** MASLD (MESH:D008107), inflammation (MESH:D007249), congenital malformations (OMIM:163000), fetal macrosomia (MESH:D005320), oligomenorrhea (MESH:D009839), fatty liver (MESH:D005234), weight gain (MESH:D015430), Obesity (MESH:D009765), glycosuria (MESH:D006029), caloric deficit (MESH:D009461), metabolic (MESH:D008659), renal pelvis dilatation (MESH:C531743), acanthosis (MESH:D000052), anovulation (MESH:D000858), grade 2 (MESH:D008224), hyperandrogenism (MESH:D017588), PCOS (MESH:D011085), hypothyroidism (MESH:D007037), malnutrition (MESH:D044342), infertility (MESH:D007246), weight loss (MESH:D015431), dizziness (MESH:D004244), insulin resistance (MESH:D007333), T2D (MESH:D003924), OSA (MESH:D020181)
- **Chemicals:** clomiphene (MESH:D002996), Metformin (MESH:D008687), testosterone (MESH:D013739), blood glucose (MESH:D001786), insulin (MESH:D007328), FBG (-), letrozole (MESH:D000077289), dapagliflozin (MESH:C529054), glucose (MESH:D005947)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12936452/full.md

## References

12 references — full list in the complete paper: https://tomesphere.com/paper/PMC12936452/full.md

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Source: https://tomesphere.com/paper/PMC12936452