# Semaglutide Plus Low-Dose Metformin Combination Therapy for the Treatment of Obesity and Prediabetes in a Woman with Partial Deletion of the X Chromosome Long Arm

**Authors:** Vincenzo Marzolla, Stefania Gorini, Massimiliano Caprio, Marco Infante

PMC · DOI: 10.3390/reports9010075 · Reports - Clinical Practice and Surgical Cases · 2026-02-28

## TL;DR

A 65-year-old woman with a partial X chromosome deletion and obesity showed significant weight loss and metabolic improvements using semaglutide and metformin.

## Contribution

This is the first documented case of semaglutide plus metformin therapy in a patient with a partial Xq deletion and obesity.

## Key findings

- The patient lost 20.95% of her total body weight and improved from obesity to overweight status.
- Metabolic markers like HbA1c, insulin resistance, and liver steatosis improved significantly.
- Body composition analysis showed a 74.6% reduction in fat mass and improved fat-free mass percentage.

## Abstract

Background and Clinical Significance: Over the last two decades, glucagon-like peptide-1 (GLP-1) receptor agonists have dramatically improved the management of type 2 diabetes mellitus and obesity. Currently, little is known about the use of semaglutide (a second-generation GLP-1 receptor agonist) in patients with X chromosome abnormalities. Herein, we describe the therapeutic use of semaglutide in a woman with a partial deletion of the X chromosome long arm (partial Xq deletion) and comorbid obesity. We also conducted a narrative mini-review on overweight, obesity and common metabolic derangements in patients with partial Xq deletions and Turner syndrome. Case Presentation: A 65-year-old Italian woman with a partial Xq deletion, class 1 obesity, insulin resistance, prediabetes, hypercholesterolemia and metabolic dysfunction-associated steatotic liver disease (MASLD) was referred to our Institution for persistent difficulty in managing excess body weight despite regular adherence to different structured physical activity programs and hypocaloric diets. Therefore, we prescribed a combination therapy based on low-dose metformin (500 mg/day) and once-weekly subcutaneous semaglutide (as an adjunct to lifestyle intervention). At 5 months after initiation of the combination therapy, blood tests showed metabolic improvements, including improvement of prediabetes (0.3-percentage-point reduction in glycated hemoglobin [HbA1c] values) and normalization of markers of insulin sensitivity and insulin resistance (QUICKI, HOMA-IR and TyG index). At 8 months, the patient showed substantial weight loss, which amounted to 13.8 kg (percent total body weight loss: 20.95%), and was accompanied by a notable reduction in waist circumference (−14.1 cm). Moreover, body mass index (BMI)-based weight status improved from class 1 obesity to overweight: BMI value of 25.1 kg/m2 at 8 months vs. 31.8 kg/m2 at baseline (near-normalization of BMI values). Bioelectrical impedance analysis (BIA) revealed that the patient’s overall weight loss consisted of 74.6% fat mass (FM) loss (−10.3 kg) and 25.4% fat-free mass (FFM) loss (−3.5 kg). Despite the expected FFM reduction in absolute terms, percent FFM increased at 8 months (+9.6%). This increase in percent FFM was accompanied by a reduction in percent FM at 8 months (−9.6%), indicating an overall improvement in body composition. Normalization of percent FM and FFM values (28.6% and 71.4%, respectively) was also achieved at 8 months. These body composition changes are in line with those observed in clinical trials investigating the use of semaglutide in patients with overweight or obesity. At 6 months, an abdominal ultrasound also showed the disappearance of the sonographic characteristics suggestive of mild-to-moderate hepatic steatosis. Low-dose metformin (500 mg/day) and subcutaneous semaglutide (up to a weekly dose of 1.7 mg) were well tolerated by the patient. Conclusions: To the best of our knowledge, this is the first case documenting the effective use of once-weekly subcutaneous semaglutide plus low-dose metformin combination therapy for the treatment of obesity and prediabetes in a woman with a partial Xq deletion. Large prospective cohort studies are warranted to better investigate the safety and efficacy profile of semaglutide (alone or in combination with metformin) in patients with numerical and structural X chromosome abnormalities, comorbid overweight/obesity and related metabolic disorders.

## Linked entities

- **Chemicals:** semaglutide (PubChem CID 56843331), metformin (PubChem CID 4091)
- **Diseases:** obesity (MONDO:0011122), prediabetes (MONDO:0006920), metabolic dysfunction-associated steatotic liver disease (MONDO:0013209)

## Full-text entities

- **Genes:** DPP4 (dipeptidyl peptidase 4) [NCBI Gene 1803] {aka ADABP, ADCP2, CD26, DPPIV, TP103}, PIK3C2A (phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha) [NCBI Gene 5286] {aka CPK, OCSKD, PI3-K-C2(ALPHA), PI3-K-C2A, PI3K-C2-alpha, PI3K-C2alpha}, TG (thyroglobulin) [NCBI Gene 7038] {aka AITD3, TGN}, TPO (thyroid peroxidase) [NCBI Gene 7173] {aka MSA, TDH2A, TPX}, GIP (gastric inhibitory polypeptide) [NCBI Gene 2695], INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, GGT1 (gamma-glutamyltransferase 1) [NCBI Gene 2678] {aka CD224, D22S672, D22S732, GGT, GGT 1, GGTD}, GGTLC4P (gamma-glutamyltransferase light chain 4 pseudogene) [NCBI Gene 729838] {aka GGT}, CALCA (calcitonin related polypeptide alpha) [NCBI Gene 796] {aka CALC1, CGRP, CGRP-I, CGRP-alpha, CGRP1, CT}
- **Diseases:** weight (MESH:D015431), Overweight (MESH:D050177), hypoglycemic (MESH:C000721848), myopathic facies (MESH:D019066), premature (MESH:C536271), autoimmune disorders (MESH:D001327), metabolic defect (MESH:D008659), X chromosome abnormalities (MESH:D002869), Primary ovarian insufficiency (MESH:D016649), premature menopause (MESH:D008594), FFM (MESH:C536030), fracture (MESH:D050723), MASH (MESH:D005234), obstructive sleep apnea (MESH:D020181), short stature (MESH:D006130), inflammation (MESH:D007249), kidney failure (MESH:D051437), allergies (MESH:D004342), vomiting (MESH:D014839), ischemic heart disease (MESH:D017202), visceral (MESH:D007418), CKD (MESH:D051436), ovarian insufficiency (MESH:D010051), prominent (MESH:C000721290), congenital heart defects (MESH:D006330), lean mass (MESH:D013851), narrow palate (MESH:D016893), metabolic syndrome (MESH:D024821), lumbar degenerative disk disease (MESH:D055959), adenoid hypertrophy (MESH:D006984), hypertension (MESH:D006973), Xq deletion (MESH:C536732), sunburn (MESH:D013471), esotropia (MESH:D004948), shield chest (MESH:D013898), MASLD (MESH:D008107), diarrhea (MESH:D003967), breast cancer (MESH:D001943), hypotensive (MESH:D007022), Obesity (MESH:D009765), T2D (MESH:D003924), death (MESH:D003643), appendicitis (MESH:D001064), kidney disease (MESH:D007674), renal malformations (MESH:D006030), constipation (MESH:D003248), uterine atrophy (MESH:D001284), vitamin B12 deficiency (MESH:D014806), sarcopenia (MESH:D055948), nausea (MESH:D009325), hypovitaminosis D (MESH:D014808), GERD (MESH:D005764), insulin resistance (MESH:D007333), developmental delay (MESH:D002658), dysesthesia (MESH:D010292), thyroid nodules (MESH:D016606), injury to (MESH:D014947), folate deficiency (MESH:C562799), X chromosome monosomy (MESH:C537814), excess (MESH:D006970)
- **Chemicals:** blood glucose (MESH:D001786), folate (MESH:D005492), MMA (MESH:D008764), glucose (MESH:D005947), homocysteine (MESH:D006710), water (MESH:D014867), simvastatin (MESH:D019821), carbohydrate (MESH:D002241), Metformin (MESH:D008687), vitamin D (MESH:D014807), vitamin B12 (MESH:D014805), oxygen (MESH:D010100), cholesterol (MESH:D002784), 25(OH)D (-), cholecalciferol (MESH:D002762), calcium (MESH:D002118), lipid (MESH:D008055), triglyceride (MESH:D014280), omeprazole (MESH:D009853), 25-hydroxyvitamin D (MESH:C104450), alcohol (MESH:D000438), ezetimibe (MESH:D000069438), RA (MESH:D011883)
- **Species:** gut metagenome (species) [taxon 749906], Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

109 references — full list in the complete paper: https://tomesphere.com/paper/PMC13030616/full.md

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Source: https://tomesphere.com/paper/PMC13030616