# Twenty-Four-Month rhGH Intervention: Insights into Redox Regulation, Vascular Biomarkers, and Body Composition in Adult GHD Patients

**Authors:** Maria Kościuszko, Angelika Buczyńska, Justyna Hryniewicka, Agnieszka Adamska, Katarzyna Siewko, Marcin Zaniuk, Adam Jacek Krętowski, Anna Popławska-Kita

PMC · DOI: 10.3390/ijms27031451 · International Journal of Molecular Sciences · 2026-01-31

## TL;DR

A 24-month rhGH treatment in adults with growth hormone deficiency improves redox balance, vascular function, and body composition.

## Contribution

This study provides new evidence on the long-term effects of rhGH therapy on redox regulation and vascular biomarkers in GHD patients.

## Key findings

- rhGH therapy significantly increased IGF-1 and improved redox markers like Ox-LDL, Trx, and OGG1.
- Vascular biomarkers E-selectin, ICAM-1, and VCAM-1 decreased, indicating better endothelial function.
- Lean body mass and bone mineral density increased, while lipid profiles remained unchanged.

## Abstract

Adult growth hormone deficiency (GHD) is linked to increased cardiovascular and metabolic risk due to oxidative stress (OS), endothelial dysfunction, and unhealthy body composition. Long-term systemic effects of recombinant human growth hormone (rhGH) therapy remain insufficiently defined. This study assessed the impact of 24-month rhGH replacement on OS, vascular markers, body composition, and bone mineral density (BMD) in adults with severe GHD. Fifteen adults with confirmed GHD received rhGH for 24 months. Serum insulin-like growth factor 1 (IGF-1), oxidized LDL (Ox-LDL), thioredoxin (Trx), 8-oxoguanine DNA glycosylase 1 (OGG1), E-selectin, intercellular adhesion molecule 1 (ICAM-1), and vascular cell adhesion molecule 1 (VCAM-1) were measured at baseline and 12 and 24 months. Body composition and BMD were evaluated by DXA. IGF-1 increased significantly at 12 and 24 months (p < 0.001). Ox-LDL markedly decreased (p < 0.00001), while Trx and OGG1 increased (p < 0.05). Levels of E-selectin, ICAM-1, and VCAM-1 declined, indicating improved endothelial function. Lean body mass and BMD increased, while body fat parameters showed heterogeneous changes. Lipid profiles were unchanged. Significant correlations were observed between vascular markers and adiposity, and between BMD, triglycerides, and IGF-1. A 24-month course of rhGH therapy improves redox balance, vascular function, and body composition in adults with severe GHD, supporting the use of redox and vascular biomarkers to monitor treatment efficacy.

## Linked entities

- **Genes:** IGF1 (insulin like growth factor 1) [NCBI Gene 3479], OGG1 (8-oxoguanine DNA glycosylase) [NCBI Gene 4968]
- **Proteins:** TXN (thioredoxin), Sele (selectin, endothelial cell), ICAM1 (intercellular adhesion molecule 1), VCAM1 (vascular cell adhesion molecule 1)

## Full-text entities

- **Genes:** TXN (thioredoxin) [NCBI Gene 7295] {aka TRDX, TRX, TRX1, TXN1, Trx80}, OGG1 (8-oxoguanine DNA glycosylase) [NCBI Gene 4968] {aka HMMH, HOGG1, MUTM, OGH1}, VCAM1 (vascular cell adhesion molecule 1) [NCBI Gene 7412] {aka CD106, INCAM-100}, SELE (selectin E) [NCBI Gene 6401] {aka CD62E, ELAM, ELAM1, ESEL, LECAM2, selectin-e}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, GH1 (growth hormone 1) [NCBI Gene 2688] {aka GH, GH-N, GHB5, GHN, IGHD1A, IGHD1B}, ICAM1 (intercellular adhesion molecule 1) [NCBI Gene 3383] {aka BB2, CD54, P3.58}
- **Diseases:** GHD (MESH:D004393), Adult growth hormone deficiency (MESH:C537404), endothelial dysfunction (MESH:D014652), adiposity (MESH:D018205)
- **Chemicals:** Lipid (MESH:D008055), triglycerides (MESH:D014280)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

58 references — full list in the complete paper: https://tomesphere.com/paper/PMC12897723/full.md

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Source: https://tomesphere.com/paper/PMC12897723