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Endocrine Abstracts (2025) 110 EP1096 | DOI: 10.1530/endoabs.110.EP1096

1Ege University, Endocrinology, İzmir, Türkiye; 2Ege University, Internal Medicine, İzmir, Türkiye; 3Ege University, Faculty of Medicine, İzmir, Türkiye; 4Ege University, Medical Biochemistry, İzmir, Türkiye; 5Ege University, Biostatistics and Medical Informatics, İzmir, Türkiye; 6Ege University, Medical Biology, İzmir, Türkiye


JOINT1141

Introduction: Acromegaly is a disorder characterized by excessive secretion of growth hormone (GH), leading to increased insulin-like growth factor-1 (IGF-1) levels. Nonalcoholic fatty liver disease (NAFLD), a significant global health concern, is considered the hepatic manifestation of metabolic syndrome and may progress to fibrosis, cirrhosis, or hepatocellular carcinoma. The noninvasive test fibrosis-4 (FIB-4) score are the commonly used and recommended hepatic fibrosis scores for screening liver fibrosis. FIB-4 upper cut-off of < 1.3 suggests better diagnostic accuracy for predicting NAFLD. Nuclear factor kappa B (NF-κB) activation may contribute to insulin resistance and metabolic syndrome-related pathologies, including hepatic steatosis in acromegalic patients. This study aims to investigate the inflammatory processes in acromegalic patients with hepatosteatosis and controls to determine NF-κB levels in both conditions.

Methods: A total of thirty participants, including sixteen acromegalic patients and fourteen controls, will be included. We obtained demographic data, hormonal and metabolic parameters, and abdomen ultrasonography (USG) reports. NF-κB levels were measured using ELISA.

Results: The median age and gender distribution of the study participants were similar across groups (P >0.05). Among the clinical parameters, there were significant differences in the mean values of fasting insulin (P = 0.002), GH (P = 0.049), IGF-1 (P <0.001), and FIB-4 (P = 0.001), with higher values observed in acromegaly patients. In univariate logistic regression analysis, fasting insulin was found to increase the risk of acromegaly (O r = 2.76; 95% CI [1.032-7.380]), and FIB-4 was also identified as a risk factor (P = 0.009). In the multivariate analysis, FIB-4 remained a significant risk factor (P = 0.009). ROC analysis for distinguishing between acromegaly and control group revealed that fasting insulin had an AUC of 0.833 (sensitivity=68%, specificity=92%), while FIB-4 had an AUC of 0.821 (sensitivity=76%, specificity=93%). In sensitivity analyses, the acromegaly group was evaluated as controlled and uncontrolled. When comparing the mean FIB-4 values among the three groups, a significant difference was observed (P = 0.005). Post-hoc comparisons revealed significant differences between the healthy and controlled acromegaly groups (P <0.001) as well as between the healthy and uncontrolled acromegaly groups (P <0.001). The median NFKB levels were similar between the healthy and acromegaly groups (P = 0.339). No significant difference was detected when comparing NFKB medians among the three groups (P = 0.539).

Conclusion: This study is the first study to investigate NF-κB levels in acromegalic patients with hepatosteatosis, highlighting its potential role in metabolic dysfunction and hepatic inflammation. FIB-4 was identified as a risk factor to increase the risk of acromegaly. No significant difference was detected when comparing NFKB.

Volume 110

Joint Congress of the European Society for Paediatric Endocrinology (ESPE) and the European Society of Endocrinology (ESE) 2025: Connecting Endocrinology Across the Life Course

European Society of Endocrinology 
European Society for Paediatric Endocrinology 

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