Barbara Sperner-Unterweger

Dr. Barbara Sperner-Unterweger

orcid

Research Focus & Metrics

Academic Career Length

40Years (1987-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 June 1996 in Quality of Life Research
Verified
Journal Article
Closed access
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ABA. E. Bonomi
A. E. Bonomi
DCD. F. Cella
D. F. Cella
EHE. A. Hahn
E. A. Hahn
KBK. Bjordal
K. Bjordal
BSBarbara Sperner-Unterweger
Barbara Sperner-Unterweger
RZR. Zittoun
R. Zittoun

1 September 2008 in Current Drug Metabolism
Verified
Journal Article
Closed access
PDF file
GNG. Neurauter
G. Neurauter
KSK. Schrocksnadel
K. Schrocksnadel
SSS. Scholl-Burgi
S. Scholl-Burgi
BSBarbara Sperner-Unterweger
Barbara Sperner-Unterweger
CSC. Schubert
C. Schubert
DFD. Fuchs
D. Fuchs
Neurospychiatric symptoms like mood changes and depression are common in patients with chronic inflammatory disorders such as infections, autoimmune diseases or cancer. The pathogenesis of these symptoms is still unclear. Pro-inflammatory stimuli interfere not only with the neural circuits and neurotransmitters of the serotonergic, but also with those of the adrenergic system. The proinflammatory cytokine interferon-γ stimulates the biosynthesis of 5,6,7,8-tetrahydrobiopterin (BH4), which is cofactor for several aromatic amino acid monooxygenases and thus is strongly involved in the biosynthesis of the neurotransmitter serotonin and the catecholamines dopamine, epinephrine (adrenaline) and norepinephrine (noradrenaline). In macrophages, interferon-γ also triggers the high output of reactive oxygen species, which can destroy the oxidation-labile BH4. Recent data suggest that oxidative loss of BH4 in chronic inflammatory conditions can reduce the biosynthesis of catecholamines, which may relate to disturbed adrenergic neurotransmitter pathways in patients.

1 October 2002 in Brain, Behavior, and Immunity
Verified
Journal Article
Closed access
BWBernhard Widner
Bernhard Widner
ALAndreas Laich
Andreas Laich
BSBarbara Sperner-Unterweger
Barbara Sperner-Unterweger
MLMaximilian Ledochowski
Maximilian Ledochowski
DFDietmar Fuchs
Dietmar Fuchs

28 July 2010 in The Oncologist
Verified
Journal Article
Open access
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AZAugust Zabernigg
August Zabernigg
EGEva-Maria Gamper
Eva-Maria Gamper
JGJohannes M. Giesinger
Johannes M. Giesinger
Gerhard RuedlGerhard Ruedl
Gerhard Ruedl
GKGeorg Kemmler
Georg Kemmler
BHBernhard Holzner
Bernhard Holzner
Learning Objectives: After completing this course, the reader will be able to: Evaluate the effect of various chemotherapy regimens on taste alterations.Investigate the effect of chemotherapy-induced taste alterations on patients and use available dietary approaches such as taste enhancement and substitution of proteins and nutrients of avoided food to improve quality of life. CME This article is available for continuing medical education credit at CME.TheOncologist.com. Background.: Taste alterations (TAs) are a frequent but under-recognized treatment side effect in cancer patients undergoing chemotherapy (CT). CT regimens with different toxicity profiles may vary in their impact on TAs, but research on this topic is lacking. This study assesses the prevalence of TAs and their relation to sociodemographic and clinical variables, especially CT regimens. Furthermore, the association between TAs and quality of life (QOL) is investigated. Patients and Methods.: TAs and QOL data were collected longitudinally in 197 cancer patients (lung cancer, 54.3%; pancreatic cancer, 19.3%; colorectal cancer, 26.4%; age, 65.2 ±10.4 years; male, 57.4%) who were receiving CT at the Department of Internal Medicine at Kufstein County Hospital, giving rise to a total of 1,024 assessment times. Patients completed the European Organization for Research and Treatment of Cancer (EORTC) QLQ-C30 questionnaire and two additional questions taken from the EORTC item bank concerning TAs. Statistical analyses were performed using mixed-effect models. Results.: The study showed that the prevalence of TAs in chemotherapy patients is alarmingly high (69.9%). There were clear differences in TA scores among treatment groups: patients receiving irinotecan reported significantly more TAs than patients in other treatment groups; patients receiving a combination of gemcitabine and a platinum agent reported the lowest TAs. Additionally, significant associations between TAs and several QOL dimensions were found, especially with appetite loss and fatigue. Conclusion.: The high prevalence of TAs and their impact on QOL in CT patients underscore the urgent need for increased attention to this side effect, both in research and in clinical practice.

1 March 2001 in Psychosomatics
Verified
Journal Article
Closed access
BHBernhard Holzner
Bernhard Holzner
GKGeorg Kemmler
Georg Kemmler
MKMartin Kopp
Martin Kopp
RMRoland Moschen
Roland Moschen
HSHansjo Rd Schweigkofler
Hansjo Rd Schweigkofler
BSBarbara Sperner-Unterweger
Barbara Sperner-Unterweger

1 September 1999 in Journal of Clinical Oncology
Verified
Journal Article
Closed access
GKGeorg Kemmler
Georg Kemmler
BHBernhard Holzner
Bernhard Holzner
MKMartin Kopp
Martin Kopp
MDMartina Dünser
Martina Dünser
RMRaimund Margreiter
Raimund Margreiter
BSBarbara Sperner-Unterweger
Barbara Sperner-Unterweger
PURPOSE: To compare two quality-of-life (QOL) questionnaires for cancer patients, the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-C30 (EORTC QLQ-C30) and the Functional Assessment of Cancer Therapy-General (Fact-G), on the basis of empirical data. PATIENTS AND METHODS: Two hundred forty-four patients with a diagnosis of breast cancer or Hodgkin's disease completed both the EORTC QLQ-C30 and the FACT-G (German language version) during the same session. Questionnaire data were analyzed on a subscale basis using correlation analysis, canonical correlation, and multiple linear regression. RESULTS: Correlations between corresponding subscales of the FACT-G and the EORTC QLQ-C30 ranged from r = .14 for the social domain (very poor agreement) to r = .66 for the physical domain (good agreement), with r values for the other domains lying between these extremes. Canonical correlation analysis for the two sets of subscales revealed that overall agreement between the two instruments was only moderate (first canonical correlation coefficient r = .85, but overall redundancy less than 40%). Of the five FACT-G subscales, only one, physical well-being, was well represented by the EORTC QLQ-C30 subscales (multiple linear regression, R2 = .67). Only three of eight EORTC QLQ-C30 subscales (physical functioning, global QOL, general symptoms) were represented fairly well by FACT-G subscales (R2 = .43 to .60). The lowest R2 values (< .15; ie, virtually no representation by the other instrument) were found for the FACT-G social well-being and relation with doctors and EORTC QLQ-C30 cognitive functioning subscales. CONCLUSION: For the sample investigated, the EORTC QLQ-C30 and the FACT-G were found to measure markedly different aspects of QOL, despite considerable overlap. Replicability provided, this implies that neither of the two QOL instruments can be replaced by the other and that a direct comparison of results obtained with the two instruments is not possible.