Vorwort

Die Beiträge des vorliegenden Bandes sind in einer doppelten Weise mit Manfred G. Schmidt verbunden. Sie wurden von Schülern oder von wissenschaftlichen Weggefährten verfasst und sie beziehen sich inhaltlich auf sein Werk. Die thematische Breite der Beiträge entspricht der Breite seines Werkes: Die Aufsätze analysieren Staatstätigkeiten –Wirtschafts-, Sozial- und Bildungspolitiken --, sie untersuchen Parteien, Institutionen, Demokratien und Autokratien, sie beantworten theoretisch-konzeptuelle oder empirische Fragen, sie nutzen die vergleichende Methode oder liefern einen Beitrag zum Verständnis des politischen Systems Deutschlands und sie sprengen engere Fachgrenzen, indem sie wissenschaftliche Kontexte und praktische Folgen von politikwissenschaftlicher Forschung und Lehre thematisieren. Zu all’ diesen Themen hat Manfred Schmidt wichtige Beiträge geliefert. Es war ein Vergnügen diese Festschrift zusammenzustellen. Die schwerste Entscheidung betraf die anzufragenden Kolleginnen und Kollegen. Einfach war die Identifikation von Kollegen am Heidelberger Institut, die besonders eng mit Manfred Schmidt zusammengearbeitet haben und von Schülern und von ihm geprägten Wissenschaftlern, die heute politikwissenschaftliche Professuren innehaben oder auf dem Weg dorthin sind. Bei der Auswahl von Autoren aus dem großen Kreis der Doktoranden spielten auch der Zufall und die Erreichbarkeit eine Rolle. Besonders schwierig war es, die Zahl der etablierten Forscher und Forscherinnen zu limitieren, die das Werk von Manfred G. Schmidt besonders schätzen und mit ihm in verschiedenen Funktionen wissenschaftlich verbunden waren. Mit guten Gründen hätte ich noch viele andere Kolleginnen und Kollegen anfragen können. Nur die Begrenzung des Seitenumfangs hat mich daran gehindert. Daraus wird auch schon deutlich, dass es keineswegs schwierig war, die Autoren zu gewinnen. Für viele war es eine Freude und Ehre an diesem Band mitzuwirken. Ich bedanke mich ganz herzlichen bei allen, die so engagiert zu diesem Projekt beigetragen haben. Frank Castles hat sich Zeit genommen, mit mir auf dem Krindenhof oberhalb des Thunersees die Konzeption des Bandes zu diskutieren; Dietmar Braun, Wolfgang Merkel und Ferdinand Müller-Rommel und viele andere Kollegen standen jederzeit mit Rat und Tat zur Verfügung. Ein besonderer Dank geht an die Mitarbeiterinnen und Mitarbeiter meiner Arbeitsgruppe – allen voran David Weisstanner und Monique Stoll – die in vielen Stunden mühevoller und konzentrierter Arbeit Korrekturen in die Manuskripte übertrugen, die Literaturlisten überprüften und anglichen sowie Tabellen und Graphiken standardisierten. Manfred Schmidts Heidelberger Sekretärin, Ingeborg Zimmermann, begleitete und unterstützte die Arbeiten aufmerksam und mit Feuereifer. Klaus Armingeon im Januar 2013.

β-Glucan Antigenemia Anticipates Diagnosis of Blood Culture–Negative Intraabdominal Candidiasis

Rationale: Life-threatening intraabdominal candidiasis (IAC) occurs in 30 to 40% of high-risk surgical intensive care unit (ICU) patients. Although early IAC diagnosis is crucial, blood cultures are negative, and the role of Candida score/colonization indexes is not established. Objectives: The aim of this prospective Fungal Infection Network of Switzerland (FUNGINOS) cohort study was to assess accuracy of 1,3-β-d-glucan (BG) antigenemia for diagnosis of IAC. Methods: Four hundred thirty-four consecutive adults with abdominal surgery or acute pancreatitis and ICU stay 72 hours or longer were screened: 89 (20.5%) at high risk for IAC were studied (68 recurrent gastrointestinal tract perforation, 21 acute necrotizing pancreatitis). Diagnostic accuracy of serum BG (Fungitell), Candida score, and colonization indexes was compared. Measurements and Main Results: Fifty-eight of 89 (65%) patients were colonized by Candida; 29 of 89 (33%) presented IAC (27 of 29 with negative blood cultures). Nine hundred twenty-one sera were analyzed (9/patient): median BG was 253 pg/ml (46–9,557) in IAC versus 99 pg/ml (8–440) in colonization (P < 0.01). Sensitivity and specificity of two consecutive BG measurements greater than or equal to 80 pg/ml were 65 and 78%, respectively. In recurrent gastrointestinal tract perforation it was 75 and 77% versus 90 and 38% (Candida score ≥ 3), 79 and 34% (colonization index ≥ 0.5), and 54 and 63% (corrected colonization index ≥ 0.4), respectively. BG positivity anticipated IAC diagnosis (5 d) and antifungal therapy (6 d). Severe sepsis/septic shock and death occurred in 10 of 11 (91%) and 4 of 11 (36%) patients with BG 400 pg/ml or more versus 5 of 18 (28%, P = 0.002) and 1 of 18 (6%, P = 0.05) with BG measurement less than 400 pg/ml. β-Glucan decreased in IAC responding to therapy and increased in nonresponse. Conclusions: BG antigenemia is superior to Candida score and colonization indexes and anticipates diagnosis of blood culture–negative IAC. This proof-of-concept observation in strictly selected high-risk surgical ICU patients deserves investigation of BG-driven preemptive therapy.

Tagungsbericht «Gesundheitsrecht am Puls der Zeit»: Symposium der UFL zum Thema Herausforderung Alter am 23. November 2012 in Triesen FL

Bereits zum dritten Mal führte die Private Universität im Fürstentum Liechtenstein UFL im November 2012 ihr jährliches Symposium zum Gesundheitsrecht durch. Dieses Mal beschäftigten sich die Referate mit dem Thema Alter und Altern, und zwar nicht nur aus rechtlicher Perspektive, sondern mit Blick über die Disziplinengrenzen hinaus.

Verkehrsmedizin im Kindes- und Jugendalter

Mit dem Begriff «Verkehrsmedizin» verbinden die meisten Ärzte die ausschliessliche Beurteilung der Fahrfähigkeit und Fahreignung (Tabelle 1) von Motorfahrzeuglenkern. Die Verkehrsmedizin gilt damit als «Erwachsenengebiet» – Kinder fahren ja nicht Auto! Kinder und Jugendliche können und dürfen in der Schweiz jedoch – abhängig vom Alter – in verschiedener Weise aktiv am Strassenverkehr und an der privaten Binnenschifffahrt teilnehmen. Kinder und Jugendliche müssen analog zu den Erwachsenen gewisse medizinische Mindestanforderungen erfüllen, um sicher am Strassenverkehr und – als nachrangiges Problem – an der privaten Binnenschifffahrt teilnehmen zu können. Nachfolgend soll auf die gesetzlich erlaubten Möglichkeiten der aktiven Verkehrsteilnahme von Kindern und Jugendlichen (bis zum vollendeten 16. Lebensjahr) und auf die für eine sichere Verkehrsteilnahme notwendigen medizinischen Voraussetzungen eingegangen werden. Ergänzend werden die juristische Problematik der Fahrfähigkeits-/Fahreignungsaufklärung sowie die Bedeutung verkehrsmedizinischer Überlegungen für die Berufswahl angesprochen.

Space-based space surveillance and tracking demonstrator: mission and system design

This paper presents the capabilities of a Space-Based Space Surveillance (SBSS) demonstration mission for Space Surveillance and Tracking (SST) based on a micro-satellite platform. The results have been produced in the frame of ESA’s "Assessment Study for Space Based Space Surveillance Demonstration Mission" performed by the Airbus Defence and Space consortium. The assessment of SBSS in an SST system architecture has shown that both an operational SBSS and also already a well- designed space-based demonstrator can provide substantial performance in terms of surveillance and tracking of beyond-LEO objects. Especially the early deployment of a demonstrator, possible by using standard equipment, could boost initial operating capability and create a self-maintained object catalogue. Furthermore, unique statistical information about small-size LEO debris (mm size) can be collected in-situ. Unlike classical technology demonstration missions, the primary goal is the demonstration and optimisation of the functional elements in a complex end-to-end chain (mission planning, observation strategies, data acquisition, processing, etc.) until the final products can be offered to the users and with low technological effort and risk. The SBSS system concept takes the ESA SST System Requirements into account and aims at fulfilling SST core requirements in a stand-alone manner. Additionally, requirements for detection and characterisation of small-sizedLEO debris are considered. The paper presents details of the system concept, candidate micro-satellite platforms, the instrument design and the operational modes. Note that the detailed results of performance simulations for space debris coverage and cataloguing accuracy are presented in a separate paper “Capability of a Space-based Space Surveillance System to Detect and Track Objects in GEO, MEO and LEO Orbits” by J. Silha (AIUB) et al., IAC-14, A6, 1.1x25640.

Reevaluation of the MASTER-2009 MLI and H-10 Debris Modeling

The current paper is an excerpt from the doctoral thesis ”Multi-Layer Insulation as Contribution to Orbital Debris”written at the Institute of Aerospace Systems of the Technische Universit ̈at of Braunschweig. The Multi-Layer In-sulation (MLI) population included in ESA’s MASTER-2009 (M eteoroid and Space-Debris Terrestrial Environment Reference) software is based on models for two mechanisms: One model simulates the release of MLI debris during fragmentation events while another estimates the continuo us release of larger MLI pieces due to aging related deterioration of the material. The aim of the thesis was to revise the MLI models from the base up followed by a re-validation of the simulated MLI debris population. The validation is based on comparison to measurement data of the GEO and GTO debris environment obtained by the Astronomical Institute of the University of Bern (AIUB) using ESA’s Space Debris Telescope (ESASDT), the 1-m Zeiss telescope located at the Optical Ground Station (OGS) at the Teide Observatory at Tenerife, Spain. The re-validation led to the conclusion that MLI may cover a much smaller portion of the observed objects than previously published. Further investigation of the resulting discrepancy revealed that the contribution of altogether nine known Ariane H-10 upper stage explosion events which occurred between 1984 and 2002 has very likely been underestimated in past simulations.

Eosinophilia in Dermatologic Disorders

Eosinophil infiltration can be observed in skin disorders, such as allergic/immunologic, autoimmune, infectious, and neoplastic diseases. Clinical presentations are variable and include eczematous, papular, urticarial, bullous, nodular, and fibrotic lesions; pruritus is a common symptom in all. In this review, we present representative eosinophilic skin diseases according to their clinical pattern, together with histologic findings and diagnostic procedures. We also discuss the potential roles of eosinophils in the pathogenesis of dermatologic disorder. Current pathogenesis-based diagnostic and therapeutic approaches are outlined.

Metabolism, oxidative stress and territorial behaviour in a female colour polymorphic cichlid fish

Intrasexual selection on body coloration is thought to play an important role in the evolution of colour polymorphism, but its physiological underpinnings have received limited attention. In the colour polymorphic cichlid Neochromis omnicaeruleus, three fully sympatric female colour morphs— a plain morph (P) and two conspicuously coloured blotched morphs, black-and-white blotched (WB) and orange blotched (OB)—differ in agonistic behaviour. We compared routine metabolic rate (when females were housed in social isolation), short-term energetic costs of interacting with a same-colour rival housed in an adjacent transparent chamber and oxidative stress between the three female colour morphs. WB females had a lower routine metabolic rate compared with the other colour morphs. WB females also had a lower active metabolic rate during inter-female interactions than OB females, while OB females used more oxygen per unit aggressive act than the other two colour morphs. However, there were no consistent differences in oxidative stress between the three morphs. Concerted divergence in colour, behaviour and metabolism might contribute to the evolution of these polymorphisms in sympatry.

Association of lectin pathway proteins with intra-abdominal Candida infection in high-risk surgical intensive-care unit patients. A prospective cohort study within the fungal infection network of Switzerland

OBJECTIVES Human studies on the role of mannose-binding lectin (MBL) in patients with invasive candidiasis have yielded conflicting results. We investigated the influence of MBL and other lectin pathway proteins on Candida colonization and intra-abdominal candidiasis (IAC) in a cohort of high-risk patients. METHODS Prospective observational cohort study of 89 high-risk intensive-care unit (ICU) patients. Levels of lectin pathway proteins at study entry and six MBL2 single-nucleotide polymorphisms were analyzed by sandwich-type immunoassays and genotyping, respectively, and correlated with development of heavy Candida colonization (corrected colonization index (CCI) ≥0.4) and occurrence of IAC during a 4-week period. RESULTS Within 4 weeks after inclusion a CCI ≥0.4 and IAC was observed in 47% and 38% of patients respectively. Neither serum levels of MBL, ficolin-1, -2, -3, MASP-2 or collectin liver 1 nor MBL2 genotypes were associated with a CCI ≥0.4. Similarly, none of the analyzed proteins was found to be associated with IAC with the exception of lower MBL levels (HR 0.74, p = 0.02) at study entry. However, there was no association of MBL deficiency (<0.5 μg/ml), MBL2 haplo- or genotypes with IAC. CONCLUSION Lectin pathway protein levels and MBL2 genotype investigated in this study were not associated with heavy Candida colonization or IAC in a cohort of high-risk ICU patients.

Exploration of genetic susceptibility to pancreatic cancer: A GWAS approach

Pancreatic cancer is the 4th most common cause for cancer death in the United States, accompanied by less than 5% five-year survival rate based on current treatments, particularly because it is usually detected at a late stage. Identifying a high-risk population to launch an effective preventive strategy and intervention to control this highly lethal disease is desperately needed. The genetic etiology of pancreatic cancer has not been well profiled. We hypothesized that unidentified genetic variants by previous genome-wide association study (GWAS) for pancreatic cancer, due to stringent statistical threshold or missing interaction analysis, may be unveiled using alternative approaches. To achieve this aim, we explored genetic susceptibility to pancreatic cancer in terms of marginal associations of pathway and genes, as well as their interactions with risk factors. We conducted pathway- and gene-based analysis using GWAS data from 3141 pancreatic cancer patients and 3367 controls with European ancestry. Using the gene set ridge regression in association studies (GRASS) method, we analyzed 197 pathways from the Kyoto Encyclopedia of Genes and Genomes (KEGG) database. Using the logistic kernel machine (LKM) test, we analyzed 17906 genes defined by University of California Santa Cruz (UCSC) database. Using the likelihood ratio test (LRT) in a logistic regression model, we analyzed 177 pathways and 17906 genes for interactions with risk factors in 2028 pancreatic cancer patients and 2109 controls with European ancestry. After adjusting for multiple comparisons, six pathways were marginally associated with risk of pancreatic cancer ( P < 0.00025): Fc epsilon RI signaling, maturity onset diabetes of the young, neuroactive ligand-receptor interaction, long-term depression (Ps < 0.0002), and the olfactory transduction and vascular smooth muscle contraction pathways (P = 0.0002; Nine genes were marginally associated with pancreatic cancer risk (P < 2.62 × 10−5), including five reported genes (ABO, HNF1A, CLPTM1L, SHH and MYC), as well as four novel genes (OR13C4, OR 13C3, KCNA6 and HNF4 G); three pathways significantly interacted with risk factors on modifying the risk of pancreatic cancer (P < 2.82 × 10−4): chemokine signaling pathway with obesity ( P < 1.43 × 10−4), calcium signaling pathway (P < 2.27 × 10−4) and MAPK signaling pathway with diabetes (P < 2.77 × 10−4). However, none of the 17906 genes tested for interactions survived the multiple comparisons corrections. In summary, our current GWAS study unveiled unidentified genetic susceptibility to pancreatic cancer using alternative methods. These novel findings provide new perspectives on genetic susceptibility to and molecular mechanisms of pancreatic cancer, once confirmed, will shed promising light on the prevention and treatment of this disease. ^