Martin Varga
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Martin Varga has a total of 29 co-authors. Here are the top co-authors by number of shared publications:
- Barbara Kofler
Research Program for Receptor Biochemistry and Tumor Metabolism, Department of Pediatrics, University Hospital of the Paracelsus Medical University, Salzburg, Austria
3 shared publications - Karl Sotlar
Department of Pathology, University Hospital of the Paracelsus Medical Private University, 5020 Salzburg, Austria
3 shared publications - René Günther Feichtinger
Department of Pediatrics, University Hospital of the Paracelsus Medical Private University, 5020 Salzburg, Austria
3 shared publications - Sara Huber
Research Program for Receptor Biochemistry and Tumor Metabolism, Department of Pediatrics, University Hospital of the Paracelsus Medical University, Salzburg, Austria
3 shared publications - Theo F. J. Kraus
Institute of Pathology, University Hospital Salzburg, Paracelsus Medical University, Müllner Hauptstr. 48, A-5020 Salzburg, Austria
3 shared publications - Klaus Emmanuel
Department of Surgery, Paracelsus Medical University Salzburg, 5020 Salzburg, Austria
2 shared publications
Latest Publications
- Open Access
- 30 August 2026
- Published by MDPI AG in Diagnostics
- Vol. 16 (17) , 2792
Preoperative Bioelectrical Impedance Analysis Identifies Altered Body Composition, Which Is Associated with Severe Postoperative Complications in Major Hepatopancreaticobiliary Surgery
Background: Altered body composition is common in patients undergoing major hepatopancreaticobiliary (HPB) surgery and may be associated with increased postoperative morbidity. Conventional markers such as body mass index (BMI) and serum albumin have limited sensitivity for detecting early nutritional changes. Bioelectrical impedance analysis (BIA) provides an objective assessment of body composition, and phase angle (PA) may serve as a proxy for cellular status. Methods: This single-center retrospective observational cohort study included 73 patients undergoing major HPB surgery. Preoperative BIA-derived variables included resistance (R), reactance (Xc), PA, fat-free mass index (FFMI), fat mass index (FMI), and the Body Composition Chart (BCC). Nutritional Risk Screening 2002 (NRS 2002), serum albumin, and prealbumin were assessed preoperatively. BIA-derived data were compared with published healthy reference data. Postoperative complications were graded according to the Clavien–Dindo classification. Results: Patients demonstrated significant alterations in BIA-derived variables compared with healthy controls. Xc and PA were significantly reduced across all analyzable/matched sex and BMI strata (all p < 0.05). The median PA in the surgical cohort was 4.3° and significantly lower than reference values for both female and male patients (p < 0.001). FFMI and FMI distributions indicated a high prevalence of adverse body composition phenotypes, including low fat-free mass and increased adiposity. In multivariable Firth penalized logistic regression, a BCC classification outside the green reference zone (odds ratio (OR) 3.32, 95% confidence interval (CI) 1.04–12.87, p = 0.043) and higher Eastern Cooperative Oncology Group (ECOG) performance status (OR 2.07, 95% CI 1.08–4.24, p = 0.028) were independently associated with severe postoperative complications. Conclusions: Patients undergoing major HPB surgery frequently present with relevant preoperative nutritional and cellular impairments that are not adequately identified by BMI and serum albumin. Incorporation of BIA into routine preoperative assessment may improve risk stratification and support targeted nutritional optimization in this high-risk surgical population.
- 30 August 2026
- Published by MDPI AG in Diagnostics
- Vol. 16 (17) , 2792
Open AccessPreoperative Bioelectrical Impedance Analysis Identifies Altered Body Composition, Which Is Associated with Severe Postoperative Complications in Major Hepatopancreaticobiliary Surgery
Background: Altered body composition is common in patients undergoing major hepatopancreaticobiliary (HPB) surgery and may be associated with increased postoperative morbidity. Conventional markers such as body mass index (BMI) and serum albumin have limited sensitivity for detecting early nutritional changes. Bioelectrical impedance analysis (BIA) provides an objective assessment of body composition, and phase angle (PA) may serve as a proxy for cellular status. Methods: This single-center retrospective observational cohort study included 73 patients undergoing major HPB surgery. Preoperative BIA-derived variables included resistance (R), reactance (Xc), PA, fat-free mass index (FFMI), fat mass index (FMI), and the Body Composition Chart (BCC). Nutritional Risk Screening 2002 (NRS 2002), serum albumin, and prealbumin were assessed preoperatively. BIA-derived data were compared with published healthy reference data. Postoperative complications were graded according to the Clavien–Dindo classification. Results: Patients demonstrated significant alterations in BIA-derived variables compared with healthy controls. Xc and PA were significantly reduced across all analyzable/matched sex and BMI strata (all p < 0.05). The median PA in the surgical cohort was 4.3° and significantly lower than reference values for both female and male patients (p < 0.001). FFMI and FMI distributions indicated a high prevalence of adverse body composition phenotypes, including low fat-free mass and increased adiposity. In multivariable Firth penalized logistic regression, a BCC classification outside the green reference zone (odds ratio (OR) 3.32, 95% confidence interval (CI) 1.04–12.87, p = 0.043) and higher Eastern Cooperative Oncology Group (ECOG) performance status (OR 2.07, 95% CI 1.08–4.24, p = 0.028) were independently associated with severe postoperative complications. Conclusions: Patients undergoing major HPB surgery frequently present with relevant preoperative nutritional and cellular impairments that are not adequately identified by BMI and serum albumin. Incorporation of BIA into routine preoperative assessment may improve risk stratification and support targeted nutritional optimization in this high-risk surgical population.
- Open Access
- 5 June 2026
- Published by Elsevier in Neuropeptides
- Vol. 118, 102635
Expression of the Galanin system in the human pancreas, pancreatitis, and pancreatic cancer: Association with nodal involvement and perineural invasion
- 5 June 2026
- Published by Elsevier in Neuropeptides
- Vol. 118, 102635
Open AccessExpression of the Galanin system in the human pancreas, pancreatitis, and pancreatic cancer: Association with nodal involvement and perineural invasion
- Open Access
Galanin System in the Human Bile Duct and Perihilar Cholangiocarcinoma
Background: Perihilar cholangiocarcinoma (pCCA) is characterised by poor outcomes. Early diagnosis is essential for patient survival. The peptide galanin (GAL) and its receptors GAL1–3 are expressed in various tumours. Detailed characterisation of the GAL system in pCCA is lacking. Our study sought to characterise GAL and GAL1–3 receptor (GAL1–3–R) expression in the healthy human bile duct, in cholestasis and pCCA. Methods: Immunohistochemical staining was performed in healthy controls (n = 5) and in the peritumoural tissues (with and without cholestasis) (n = 20) and tumour tissues of pCCA patients (n = 33) using validated antibodies. The score values of GAL and GAL1–3–R expression were calculated and statistically evaluated. Results: GAL and GAL1–R were expressed in various bile duct cell types. GAL2–R was only slightly but still expressed in almost all the examined tissues, and GAL3–R specifically in cholangiocytes and capillaries. In a small pCCA patient cohort (n = 18), high GAL expression correlated with good survival, whereas high GAL3–R correlated with poor survival. Conclusions: Our in-depth characterisation of the GAL system in the healthy human biliary duct and pCCA in a small patient cohort revealed that GAL and GAL3–R expression in tumour cells of pCCA patients could potentially represent suitable biomarkers for survival.
Open AccessGalanin System in the Human Bile Duct and Perihilar Cholangiocarcinoma
Background: Perihilar cholangiocarcinoma (pCCA) is characterised by poor outcomes. Early diagnosis is essential for patient survival. The peptide galanin (GAL) and its receptors GAL1–3 are expressed in various tumours. Detailed characterisation of the GAL system in pCCA is lacking. Our study sought to characterise GAL and GAL1–3 receptor (GAL1–3–R) expression in the healthy human bile duct, in cholestasis and pCCA. Methods: Immunohistochemical staining was performed in healthy controls (n = 5) and in the peritumoural tissues (with and without cholestasis) (n = 20) and tumour tissues of pCCA patients (n = 33) using validated antibodies. The score values of GAL and GAL1–3–R expression were calculated and statistically evaluated. Results: GAL and GAL1–R were expressed in various bile duct cell types. GAL2–R was only slightly but still expressed in almost all the examined tissues, and GAL3–R specifically in cholangiocytes and capillaries. In a small pCCA patient cohort (n = 18), high GAL expression correlated with good survival, whereas high GAL3–R correlated with poor survival. Conclusions: Our in-depth characterisation of the GAL system in the healthy human biliary duct and pCCA in a small patient cohort revealed that GAL and GAL3–R expression in tumour cells of pCCA patients could potentially represent suitable biomarkers for survival.
- Open Access
Expression of the microRNA-200 Family, microRNA-205, and Markers of Epithelial–Mesenchymal Transition as Predictors for Endoscopic Submucosal Dissection over Esophagectomy in Esophageal Adenocarcinoma: A Single-Center Experience
Endoscopic submucosal dissection (ESD) is an effective treatment of early esophageal adenocarcinomas (EACs). The decision of ESD over esophagectomy is based on clinical evaluation of tumor depth and invasion. On a molecular level, tumor invasion is strongly associated with epithelial-to-mesenchymal transition (EMT). Here, we investigated whether localized ESD-resected and surgically resected EAC samples displayed different expression profiles of EMT protein and microRNA markers and whether these different expression profiles were able to retrospectively discriminate localized and surgically resected samples. By doing this, we aimed to evaluate whether preoperative measurement of EMT marker expression might support the decision regarding ESD over surgery. The results showed that ESD-resected samples displayed an epithelial expression profile, i.e., high expression of epithelial protein markers, whereas surgically resected samples displayed high expression of mesenchymal markers. In addition, the anti-EMT microRNA-205 was significantly more expressed in ESD-resected samples, whereas we found no significant differences in the expression levels of microRNA-200 family members. Furthermore, in our retrospective approach, we have demonstrated that measurement of selected EMT markers and microRNA-205 has significant discrimination power to distinguish ESD-resected and surgically resected samples. We suggest that the assessment of EMT status of EAC samples on a molecular level may support clinical evaluation regarding the applicability of ESD.
Open AccessExpression of the microRNA-200 Family, microRNA-205, and Markers of Epithelial–Mesenchymal Transition as Predictors for Endoscopic Submucosal Dissection over Esophagectomy in Esophageal Adenocarcinoma: A Single-Center Experience
Endoscopic submucosal dissection (ESD) is an effective treatment of early esophageal adenocarcinomas (EACs). The decision of ESD over esophagectomy is based on clinical evaluation of tumor depth and invasion. On a molecular level, tumor invasion is strongly associated with epithelial-to-mesenchymal transition (EMT). Here, we investigated whether localized ESD-resected and surgically resected EAC samples displayed different expression profiles of EMT protein and microRNA markers and whether these different expression profiles were able to retrospectively discriminate localized and surgically resected samples. By doing this, we aimed to evaluate whether preoperative measurement of EMT marker expression might support the decision regarding ESD over surgery. The results showed that ESD-resected samples displayed an epithelial expression profile, i.e., high expression of epithelial protein markers, whereas surgically resected samples displayed high expression of mesenchymal markers. In addition, the anti-EMT microRNA-205 was significantly more expressed in ESD-resected samples, whereas we found no significant differences in the expression levels of microRNA-200 family members. Furthermore, in our retrospective approach, we have demonstrated that measurement of selected EMT markers and microRNA-205 has significant discrimination power to distinguish ESD-resected and surgically resected samples. We suggest that the assessment of EMT status of EAC samples on a molecular level may support clinical evaluation regarding the applicability of ESD.