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Dive into the research topics where Sieglinde Zelzer is active.

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Featured researches published by Sieglinde Zelzer.


Obesity | 2013

Uric acid best predicts metabolically unhealthy obesity with increased cardiovascular risk in youth and adults.

Harald Mangge; Sieglinde Zelzer; Peter Puerstner; Wolfgang J. Schnedl; Gloria Reeves; Teodor T. Postolache; Daniel Weghuber

The obesity prevalence is growing worldwide and largely responsible for cardiovascular disease, the most common cause of death in the western world. The rationale of this study was to distinguish metabolically healthy from unhealthy overweight/obese young and adult patients as compared to healthy normal weight age matched controls by an extensive anthropometric, laboratory, and sonographic vascular assessment.


Obesity | 2014

Obesity-related dysregulation of the tryptophan-kynurenine metabolism: role of age and parameters of the metabolic syndrome.

Harald Mangge; Kelli L. Summers; Andreas Meinitzer; Sieglinde Zelzer; Gunter Almer; Ruth Prassl; Wolfgang J. Schnedl; Eva Z. Reininghaus; Katharina Paulmichl; Daniel Weghuber; Dietmar Fuchs

Obesity‐related immune mediated systemic inflammation was associated with the development of the metabolic syndrome by induction of the tryptophan (TRP)–kynurenine (KYN) pathway. The study aimed to assess whether this holds true across the lifespan from juvenility to adulthood.


Antimicrobial Agents and Chemotherapy | 2005

Isocratic High-Performance Liquid Chromatographic Method with Ultraviolet Detection for Simultaneous Determination of Levels of Voriconazole and Itraconazole and Its Hydroxy Metabolite in Human Serum

GholamAli Khoschsorur; Franz Fruehwirth; Sieglinde Zelzer

ABSTRACT A simple, specific method is presented for simultaneous determination of voriconazole and itraconazole and its metabolite, hydroxyitraconazole, in human serum using one-step liquid-liquid extraction and high-performance liquid chromatography. Linearity tests ranged from 0.1 to 8.0 μg/ml; the minimum detectable concentration was 0.03 μg/ml.


Free Radical Research | 2010

An inter-laboratory validation of methods of lipid peroxidation measurement in UVA-treated human plasma samples

Nicolle Breusing; Tilman Grune; Luka Andrisic; Mustafa Atalay; Grzegorz Bartosz; Fiorella Biasi; Suzana Borović; Laura Bravo; Isidre Casals; Rosario Casillas; Anca Dinischiotu; Joanna Drzewinska; Heidemarie Faber; Norsyahida Mohd Fauzi; Agnieszka Gajewska; Juan Gambini; Daniela Gradinaru; Tarja Kokkola; Antonín Lojek; Wojciech Łuczaj; Denisa Margina; Cinzia Mascia; Raquel Mateos; Andreas Meinitzer; Maria Teresa Mitjavila; Lidija Mrakovcic; Maria Cristina Munteanu; Martina Podborská; Giuseppe Poli; Paulina Sicińska

Abstract Lipid peroxidation products like malondialdehyde, 4-hydroxynonenal and F2-isoprostanes are widely used as markers of oxidative stress in vitro and in vivo. This study reports the results of a multi-laboratory validation study by COST Action B35 to assess inter-laboratory and intra-laboratory variation in the measurement of lipid peroxidation. Human plasma samples were exposed to UVA irradiation at different doses (0, 15 J, 20 J), encoded and shipped to 15 laboratories, where analyses of malondialdehyde, 4-hydroxynonenal and isoprostanes were conducted. The results demonstrate a low within-day-variation and a good correlation of results observed on two different days. However, high coefficients of variation were observed between the laboratories. Malondialdehyde determined by HPLC was found to be the most sensitive and reproducible lipid peroxidation product in plasma upon UVA treatment. It is concluded that measurement of malondialdehyde by HPLC has good analytical validity for inter-laboratory studies on lipid peroxidation in human EDTA-plasma samples, although it is acknowledged that this may not translate to biological validity.


Translational Research | 2012

Link between leptin and interleukin-6 levels in the initial phase of obesity related inflammation

Ingeborg Stelzer; Sieglinde Zelzer; Reinhard B. Raggam; Florian Prüller; Martie Truschnig-Wilders; Andreas Meinitzer; Wolfgang J. Schnedl; Renate Horejsi; Reinhard Möller; Daniel Weghuber; Gloria Reeves; Teodor T. Postolache; Harald Mangge

The mechanisms underlying the pathogenesis of obesity-related atherosclerosis remain to be clarified. To investigate the preclinical phase, interleukin-6 (IL-6) plasma levels were analyzed together with clinical, anthropometric, inflammatory, and metabolic variables in a well-defined cohort of 677 young and middle-aged overweight/obese and normal-weight subjects. In the juvenile and adult overweight/obese study group, IL-6 levels were increased significantly compared with normal-weight, age-matched controls (P < 0.001). In both juveniles and adults, higher levels of IL-6 were observed in obese compared with overweight participants. Subjects with metabolic syndrome (MS) had significantly higher IL-6 levels than those without MS. In juveniles, leptin, and in adults, the waist-to-height ratio, turned out to be the best predictor of IL-6 plasma levels in a multiple stepwise regression model. Taken together, in every age group, interleukin-6 is associated positively with the grade of overweight. Interestingly, leptin, which is the best known adipokine, is associated predictively with interleukin-6 plasma levels only in juveniles, which may indicate an important role of this molecule in the initiation of obesity-related inflammation.


Bipolar Disorders | 2014

Tryptophan breakdown is increased in euthymic overweight individuals with bipolar disorder: a preliminary report.

Eva Z. Reininghaus; Roger S. McIntyre; Bernd Reininghaus; Simon Geisler; Susanne A. Bengesser; N. Lackner; Karen Hecht; Armin Birner; Fabian Kattnig; Renate Unterweger; Hans-Peter Kapfhammer; Sieglinde Zelzer; Dietmar Fuchs; Harald Mangge

Individuals with bipolar disorder (BD) are disproportionately affected by symptoms of being overweight and metabolic syndrome when compared to the general population. The pertinence of this observation is underscored by observations that excess weight is associated with a more complex illness presentation, course, and outcome in BD. We present the first preliminary report of our BIPFAT study, which explored shared hypothesized pathophysiological pathways between being overweight and having BD.


Clinica Chimica Acta | 2011

High density lipoprotein cholesterol level is a robust predictor of lipid peroxidation irrespective of gender, age, obesity, and inflammatory or metabolic biomarkers

Sieglinde Zelzer; Nina Fuchs; Gunter Almer; Reinhard B. Raggam; Florian Prüller; Martie Truschnig-Wilders; Wolfgang J. Schnedl; Renate Horejsi; Reinhard Möller; Daniel Weghuber; Rottraut Ille; Harald Mangge

BACKGROUND Obesity related dyslipidemia, chronic inflammation and oxidative stress were associated with atherosclerotic sequels. We analysed oxidized low-density lipoprotein (oxLDL) plasma levels of 797 participants of the STyrian Juvenile OBesity (STYJOBS) / Early DEteCTion of Atherosclerosis (EDECTA) Study cohort aged from 5 to 50 years. The rationale of STYJOBS/EDECTA is to investigate the preclinical phase of obesity by a well defined cohort of young and middle aged overweight/obese and normal weight subjects. METHODS AND RESULTS Plasma oxLDL was analysed by ELISA (Mercodia, Sweden). In the overweight/obese (OW/OB) study group, oxLDL levels were significantly increased compared to normal weighted controls (p<0.001). Probands with metabolic syndrome (MS) had significantly higher oxLDL levels than probands without MS; between overweight and obese participants, and between females and males, no significant difference was seen. In a multiple stepwise regression analysis including all study subjects, age, gender, anthropometric data, presence of metabolic syndrome, systolic, diastolic blood pressure, carotis communis intima media thickness, lipids, adipokines, metabolic, and inflammatory biomarkers, decreased high-density lipoprotein (HDL-cholesterol) and increased total cholesterol were the best predictors for increased oxLDL levels. CONCLUSION Decreased HDL-cholesterol is an important determinant of lipid peroxidation irrespective of obesity, age, gender, SAT distribution, and inflammatory/metabolic biomarkers.


Critical Care Medicine | 2013

Mild hypothermia attenuates circulatory and pulmonary dysfunction during experimental endotoxemia.

Michael Schwarzl; Sebastian Seiler; Markus Wallner; Dirk von Lewinski; Stefan Huber; Heinrich Maechler; Paul Steendijk; Sieglinde Zelzer; Martie Truschnig-Wilders; Barbara Obermayer-Pietsch; Andreas Lueger; Burkert Pieske; Heiner Post

Objective:We tested whether mild hypothermia impacts on circulatory and respiratory dysfunction during experimental endotoxemia. Design:Randomized controlled prospective experimental study. Setting:Large animal facility, Medical University of Graz, Austria. Subjects:Thirteen anesthetized and mechanically ventilated pigs. Interventions:Lipopolysaccharide was administered for 4 hours. With the beginning of lipopolysaccharide infusion, animals were assigned to either normothermia (38°C, n = 7) or mild hypothermia (33°C, n = 6, intravascular cooling) and followed for 8 hours in total. Measurements and Main Results:At the end of the protocol, cardiac output was lower in mild hypothermia than in normothermia (4.5 ± 0.4 L/min vs 6.6 ± 0.4 L/min, p < 0.05), but systemic vascular resistance (885 ± 77 dyn·s/cm5 vs 531 ± 29 dyn·s/cm5, p < 0.05) and (77% ± 6% vs 54% ± 3%, p < 0.05) were higher. Indices of left ventricular contractility in vivo were not different between groups. The high-frequency band in spectral analysis of heart rate variability indicated a better preserved vagal autonomic modulation of sinuatrial node activity in mild hypothermia versus normothermia (87 ± 5 vs 47 ± 5, normalized units, p < 0.05). Plasma norepinephrine levels were elevated compared with baseline in normothermia (2.13 ± 0.27 log pg/mL vs 0.27 ± 0.17 log pg/mL, p < 0.05) but not in mild hypothermia (1.02 ± 0.31 vs 0.55 ± 0.26, p = not significant). At 38°C in vitro, left ventricular muscle strips isolated from the mild hypothermia group had a higher force response to isoproterenol. SaO2 (100% ± 0% vs 92% ± 3%, p < 0.05) and the oxygenation index (PO2/FIO2, 386 ± 52 mm Hg vs 132 ± 32 mm Hg, p < 0.05) were substantially higher in mild hypothermia versus normothermia. Plasma cytokine levels were not consistently different between groups (interleukin 10) or higher (tumor necrosis factor-&agr; and interleukin 6 and 8) during mild hypothermia versus normothermia. Conclusion:The induction of mild hypothermia attenuates cardiac and respiratory dysfunction and counteracts sympathetic activation during experimental endotoxemia. This was not associated with lower plasma cytokine levels, indicating a reduction of cytokine responsiveness by mild hypothermia.


Stem Cells and Development | 2012

Exercise Increases the Frequency of Circulating Hematopoietic Progenitor Cells, But Reduces Hematopoietic Colony-Forming Capacity

Julia Kroepfl; Karin Pekovits; Ingeborg Stelzer; Robert Fuchs; Sieglinde Zelzer; Peter Hofmann; Peter Sedlmayr; Gottfried Dohr; Wolfgang Domej; Wolfram Mueller

Circulating hematopoietic progenitor cells (CPCs) may be triggered by physical exercise and/or normobaric hypoxia from the bone marrow. The aim of the study was to investigate the influence of physical exercise and normobaric hypoxia on CPC number and functionality in the peripheral blood as well as the involvement of oxidative stress parameters as possibly active agents. Ten healthy male subjects (25.3±4.4 years) underwent a standardized cycle incremental exercise test protocol (40 W+20 W/min) under either normoxic (FiO2 ∼0.21) or hypoxic conditions (FiO2<0.15, equals 3,500 m, 3 h xposure) within a time span of at least 1 week. Blood was drawn from the cubital vein before and 10, 30, 60, and 120 min after exercise. The number of CPCs in the peripheral blood was analyzed by flow cytometry (CD34/CD45-positive cells). The functionality of cells present was addressed by secondary colony-forming unit-granulocyte macrophage (CFU-GM) assays. To determine a possible correlation between the mobilization of CPCs and reactive oxygen species, parameters for oxidative stress such as malondialdehyde (MDA) and myeloperoxidase (MPO) were obtained. Data showed a significant increase of CPC release under normoxic as well as hypoxic conditions after 10 min of recovery (P<0.01). Most interestingly, although CD34+/CD45dim cells increased in number, the proliferative capacity of CPCs decreased significantly 10 min after cessation of exercise (P<0.05). A positive correlation between CPCs and MDA/MPO levels turned out to be significant for both normoxic and hypoxic conditions (P<0.05/P<0.01). Hypoxia did not provoke an additional effect. Although the CPC frequency increased, the functionality of CPCs decreased significantly after exercise, possibly due to the influence of increased oxidative stress levels.


Journal of Heart and Lung Transplantation | 2010

Myeloperoxidase and carbonyl proteins: Promising markers for non-invasive monitoring of graft rejection after heart transplantation

Sonja Koestenbauer; Philipp Stiegler; Vanessa Stadlbauer; Ursula Mayrhauser; Bettina Leber; Martin Schweiger; Andrae Wasler; Günther Prenner; Michael Sereinigg; Sieglinde Zelzer; Tatjana Stojakovic; Michael Scarpatetti; Antonia Griesbacher; Joachim Greilberger; Karlheinz Tscheliessnigg

BACKGROUND After heart transplantation (HTx), endomyocardial biopsy (EMB) is currently the standard method to diagnose acute graft rejection. A non-invasive marker of rejection would be desirable as an alternative or to permit more selective use of the costly and invasive EMB. METHODS In this retrospective study, outcomes of routinely taken EMBs were used to select 28 patients after HTx EMB Grade 0R (8 patients), 1R (9 patients) or 2R (11 patients). For these patients, myeloperoxidase (MPO) and carbonyl proteins (CP) in serum were measured using enzyme-linked immunoassay (ELISA). RESULTS MPO and CP levels in post-HTx patients with Grade 2R rejection were significantly (MPO: p < 0.01; CP: p < 0.001) elevated at the time of rejection compared with levels 1 month earlier. MPO and CP levels predicted Grade 2R rejection and the best cut-off point was 237.5 μg/l for MPO and 222.5 pmol/mg for CP, respectively. Clinically most important was the marked increase (doubling of basic values within 1 month) of MPO and CP levels in cases of Grade 2R rejection in post-HTx patients. CONCLUSIONS MPO and CP seem to be appropriate parameters to monitor rejection events non-invasively and to minimize the application of EMBs after HTx.

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Harald Mangge

Medical University of Graz

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Andreas Meinitzer

Medical University of Graz

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Armin Birner

Medical University of Graz

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Dietmar Fuchs

Innsbruck Medical University

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Florian Prüller

Medical University of Graz

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