# The paradoxical GH response at OGTT does not predict Pasireotide efficacy but matters for glucose metabolism

**Authors:** G. Occhi, G. Voltan, S. Chiloiro, A. Bianchi, P. Maffei, F. Dassie, G. Mantovani, G. Del Sindaco, D. Ferone, F. Gatto, M. Losa, S. Cannavò, C. Scaroni, F. Ceccato

PMC · DOI: 10.1007/s40618-025-02534-3 · 2025-01-22

## TL;DR

This study finds that a paradoxical GH response during an oral glucose test does not predict how well pasireotide treats acromegaly but is linked to worse glucose metabolism.

## Contribution

The study clarifies that GH-Par does not predict pasireotide efficacy but is associated with glucose metabolism changes.

## Key findings

- Pasireotide effectively reduced IGF-1 levels in most patients regardless of GH-Par status.
- GH-Par patients had a higher risk of glucose metabolism alterations after pasireotide treatment.
- Pre-existing glucose metabolism issues were more common in GH-Par patients.

## Abstract

A paradoxical increase in GH after oral glucose load (GH-Par) characterizes about one-third of acromegaly patients and is associated with a better response to first-generation somatostatin receptor ligands (fg-SRLs). Pasireotide is typically considered as a second-/third-line treatment. Here, we investigated the predictive role of GH-Par in pasireotide response and adverse event development.

we collected a multicenter Italian retrospective cohort of 59 patients treated with pasireotide for at least 3 months, all having GH profile from OGTT. IGF-1 normalization or at least 30% reduction at the last follow-up visit defined a responder patient.

Considering the entire cohort, median IGF-1 levels before pasireotide (available in 57 patients) were 1.38 times the upper limit of normal (ULN) in patients with large (median size 18 mm) and invasive (82%) adenomas after failure of fg-SRL treatment. After a 40-month median treatment, pasireotide effectively reduced IGF-1 ULN levels in 41 patients, 37 of whom achieving normalization, and 4 with a ≥ 30% reduction. Thirteen patients were classified as GH-Par. The median pasireotide duration, dosage, and efficacy (9/12 responder in the GH-Par group and 32/45 in the GH-NPar) were similar between groups. However, the occurrence of new-onset or worsening glucose metabolism alterations (GMAs) after pasireotide was more frequent in GH-NPar (from 37 to 80%; p < 0.001) compared to GH-Par patients (from 69 to 76%), likely due to the higher prevalence of pre-existing GMAs in the GH-Par group before starting pasireotide (p = 0.038).

The GH-Par does not predict the response to pasireotide in acromegaly but can predict a worse metabolic profile.

## Linked entities

- **Proteins:** GH1 (growth hormone 1), IGF1 (insulin like growth factor 1)
- **Chemicals:** pasireotide (PubChem CID 9941444)
- **Diseases:** acromegaly (MONDO:0019933)

## Full-text entities

- **Genes:** IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, GGH (gamma-glutamyl hydrolase) [NCBI Gene 8836] {aka GATD10, GH}
- **Diseases:** GH-Par (MESH:D015868), adenomas (MESH:D000236), acromegaly (MESH:D000172)
- **Chemicals:** glucose (MESH:D005947), GMAs (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12049373/full.md

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Source: https://tomesphere.com/paper/PMC12049373