# Evaluation of the Effect of IL‐1 Antagonists on Pituitary Function

**Authors:** Fadime Aktas Koc, Baris Sariakcali, Ali Sahin

PMC · DOI: 10.1155/ije/8796993 · International Journal of Endocrinology · 2026-01-11

## TL;DR

This study examines how IL-1 inhibitors affect pituitary function in patients with Familial Mediterranean Fever.

## Contribution

The study provides new insights into the impact of IL-1 antagonists on pituitary hormone levels in FMF patients.

## Key findings

- No significant differences were found in TSH, ACTH, cortisol, LH, estradiol, IGF-1, or PRL levels between groups.
- Differences were observed in FSH, total testosterone, and GH levels between the IL-1 inhibitor and control groups.
- No significant adrenal or pituitary insufficiencies were observed in patients using IL-1 inhibitors.

## Abstract

Familial Mediterranean fever (FMF) is a hereditary autoinflammatory disease frequently observed in populations along the Eastern Mediterranean coast, characterized by recurrent fever, abdominal pain, and joint inflammation. The disease results from mutations in the MEFV gene, which plays a critical role in regulating IL‐1β secretion. Mutations in pyrin lead to uncontrolled IL‐1β release, driving FMF’s inflammatory symptoms. IL‐1 inhibitors, such as anakinra, rilonacept, and canakinumab, have been introduced as adjunctive treatments. This paper aims to investigate the effects of IL‐1 inhibitors on pituitary functions in FMF patients.

The study was conducted at Sivas Cumhuriyet University Hospital and included patients who had been using IL‐1 inhibitors for at least 6 months. The control group consisted of patients receiving colchicine treatment only. Blood samples were collected to measure various pituitary and endocrine hormones. Patients with conditions like corticosteroid use, cancer, or hemodialysis were excluded. Hormonal levels were analyzed, and cortisol‐deficient patients underwent a Synacthen test.

No significant differences were found in TSH, ACTH, cortisol, LH, estradiol, IGF‐1, or PRL levels between the groups. However, differences were noted in FSH, total testosterone, and GH levels, with higher FSH and GH in the control group and higher testosterone in the experimental group.

Although IL‐1 plays a role in hormone secretion pathways, further studies are needed to better understand the effect of IL‐1 antagonists on pituitary function, as no significant adrenal or pituitary insufficiencies were observed.

## Linked entities

- **Genes:** MEFV (MEFV innate immunity regulator, pyrin) [NCBI Gene 4210]
- **Proteins:** IL1B (interleukin 1 beta), Mefv (Mediterranean fever)
- **Chemicals:** colchicine (PubChem CID 2833), cortisol (PubChem CID 5754), TSH (PubChem CID 1150), ACTH (PubChem CID 16129617), LH (PubChem CID 341684), estradiol (PubChem CID 450), PRL (PubChem CID 7099), testosterone (PubChem CID 6013), GH (PubChem CID 7023107)
- **Diseases:** Familial Mediterranean fever (MONDO:0009572), FMF (MONDO:0009572)

## Full-text entities

- **Genes:** PRL (prolactin) [NCBI Gene 5617] {aka GHA1, pPRL}, MEFV (MEFV innate immunity regulator, pyrin) [NCBI Gene 4210] {aka FMF, MEF, PAAND, TRIM20}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, POMC (proopiomelanocortin) [NCBI Gene 5443] {aka ACTH, CLIP, LPH, MSH, NPP, OBAIRH}, GGH (gamma-glutamyl hydrolase) [NCBI Gene 8836] {aka GATD10, GH}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}
- **Diseases:** fever (MESH:D005334), adrenal or pituitary insufficiencies (MESH:D000309), inflammatory (MESH:D007249), abdominal pain (MESH:D015746), cancer (MESH:D009369), hereditary autoinflammatory disease (MESH:D056660), FMF (MESH:D010505)
- **Chemicals:** colchicine (MESH:D003078), testosterone (MESH:D013739), LH (MESH:D007986), estradiol (MESH:D004958), canakinumab (MESH:C541220), cortisol (MESH:D006854)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12791021/full.md

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Source: https://tomesphere.com/paper/PMC12791021