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Reduced irisin levels in patients with acromegaly

  • Suleyman Nahit Sendur ORCID logo EMAIL logo , Gokhan Baykal , Busra Firlatan , Busra Aydin , Incilay Lay ORCID logo , Selcuk Dagdelen , Mehmet Alikasifoglu and Tomris Erbas
Published/Copyright: July 19, 2022

Abstract

Objectives

Several metabolic disturbances are seen in acromegaly however, data regarding the contribution of irisin to these disturbances is currently insufficient. In a cohort of patients with acromegaly, we measured serum irisin levels in active and controlled cases and determined independent factors that effect serum irisin including fibronectin type III domain-containing protein 5 (FNDC5) genotyping.

Methods

A cross-sectional case-control study including 46 patients with acromegaly (28 F/18 M, age: 50.3 ± 12.1 year, BMI: 30.7 ± 5.1 kg/m2) and 81 age-, gender-, body mass index- and body composition-matched healthy controls was conducted. 15 acromegalic patients (33%) had active disease. Irisin levels were measured by enzyme-linked immunosorbent assay. Three different regions (rs3480, rs1746661, and rs16835198) of FNDC5 were subjected to polymorphism analyses.

Results

Both groups were overweight and had similar body composition. Irisin levels were lower in patients with acromegaly than controls (median [IQR]: 44.8 [41.7–46.7] ng/mL vs. 51.7 [45.5–60.1] ng/mL, p≤0.001, respectively). Active and controlled patients had similar irisin levels. Irisin was not correlated with growth hormone (GH), insulin-like growth factor 1 (IGF-1), and IGF-1 index. In multiple linear regression model, somatostatin receptor ligand use (β=−20.30, 95% CI [−34]–[−6], p=0.006) was determined as the only independent factor that affect serum irisin.

Conclusions

Serum irisin levels are low in patients with acromegaly who are on somatostatin receptor ligand therapy. Single nucleotide polymorphisms (SNPs) of FNDC5 have no independent effects on circulating irisin levels under somatostatin ligand action. Endocrine muscle functions also seem to be regulated by somatostatin action, which requires further studies.


Corresponding author: Suleyman Nahit Sendur, Department of Endocrinology and Metabolism, Hacettepe University School of Medicine, 06100, Sihhiye, Ankara, Turkey, Phone: +90 312 305 1148, Fax: +90 312 305 2302, E-mail:

Funding source: Hacettepe University

Award Identifier / Grant number: THD-2018-16966

  1. Research funding: The research was supported by Hacettepe University by the project ID THD-2018-16966. The funder only had a role for material supply. The funder had no role in study design, data collection, analysis or interpretation as well as manuscript preparation and the decision to submit for publication.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: Authors state no conflict of interest.

  4. Informed consent: Informed consent was obtained from all individuals included in this study.

  5. Ethical approval: The study was approved by the institutional noninterventional clinical research ethics board (project ID: GO 17/853). All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.

  6. Data availability: Some or all datasets generated during and/or analysed during the current study are not publicly available but are available from the corresponding author on reasonable request.

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Received: 2022-01-19
Accepted: 2022-06-30
Published Online: 2022-07-19

© 2022 Walter de Gruyter GmbH, Berlin/Boston

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