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Dive into the research topics where Andreas Rembert Koczulla is active.

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Featured researches published by Andreas Rembert Koczulla.


European Respiratory Journal | 2013

Detection of obstructive sleep apnoea by an electronic nose

Timm Greulich; Akira Hattesohl; Antje Grabisch; Janine Koepke; Severin Schmid; Sarah Noeske; Christoph Nell; Marion Wencker; Rudolf A. Jörres; Claus Vogelmeier; Ulrich Köhler; Andreas Rembert Koczulla

Diagnosis of obstructive sleep apnoea syndrome (OSAS) is technically demanding, cost-intensive and time-consuming. The measurement of volatile organic compounds by an electronic nose is an innovative method that determines distinct molecular patterns of exhaled breath in different patient groups. We addressed the following questions: What is the diagnostic accuracy of an electronic nose in the detection of OSAS and the ability to detect effects of standard therapy in patients with OSAS? Are these results related to changes in distinct markers of airway inflammation and extracellular remodelling? We included 40 OSAS patients and 20 healthy controls. Exhaled breath of all participants was analysed using the Cyranose 320 electronic nose. Pharyngeal washings were performed to sample the upper airway compartment. For statistical analysis linear discriminant analysis was employed. We identified a linear discriminant function separating OSAS from control (p<0.0001). The corresponding area under the receiver-operating curve was 0.85 (95% CI 0.75–0.96; sensitivity 0.93 and specificity 0.7). In pharyngeal washing fluids of OSAS patients, we observed higher levels of &agr;1-antitrypsin and markers of extracellular remodelling compared to controls. The electronic nose can distinguish between OSAS patients and controls with high accuracy.


BMC Pulmonary Medicine | 2014

Benefits of whole body vibration training in patients hospitalised for COPD exacerbations - a randomized clinical trial

Timm Greulich; Christoph Nell; Janine Koepke; J Fechtel; M Franke; Bernd Schmeck; Daniel Haid; Sandra Apelt; Silke Filipovic; Klaus Kenn; Sabina Janciauskiene; Claus Vogelmeier; Andreas Rembert Koczulla

BackgroundPatients with stable COPD show improvements in exercise capacity and muscular function after the application of whole body vibration. We aimed to evaluate whether this modality added to conventional physiotherapy in exacerbated hospitalised COPD patients would be safe and would improve exercise capacity and quality of life.Methods49 hospitalised exacerbated COPD patients were randomized (1:1) to undergo physiotherapy alone or physiotherapy with the addition of whole body vibration. The primary endpoint was the between-group difference of the 6-minute walking test (day of discharge – day of admission). Secondary assessments included chair rising test, quality of life, and serum marker analysis.ResultsWhole body vibration did not cause procedure-related adverse events. Compared to physiotherapy alone, it led to significantly stronger improvements in 6-minute walking test (95.55 ± 76.29 m vs. 6.13 ± 81.65 m; p = 0.007) and St. Georges Respiratory Questionnaire (-6.43 ± 14.25 vs. 5.59 ± 19.15, p = 0.049). Whole body vibration increased the expression of the transcription factor peroxisome proliferator receptor gamma coactivator-1-α and serum levels of irisin, while it decreased serum interleukin-8.ConclusionWhole body vibration during hospitalised exacerbations did not cause procedure-related adverse events and induced clinically significant benefits regarding exercise capacity and health-related quality of life that were associated with increased serum levels of irisin, a marker of muscle activity.Trial registrationGerman Clinical Trials Register DRKS00005979. Registered 17 March 2014.


Respirology | 2011

Discrimination between COPD patients with and without alpha 1-antitrypsin deficiency using an electronic nose

Akira Hattesohl; Rudolf A. Jörres; Holger Dressel; Severin Schmid; Claus Vogelmeier; Timm Greulich; Sarah Noeske; Robert Bals; Andreas Rembert Koczulla

Background and objective:  To compare the volatile organic compound patterns of patients with COPD with and without alpha 1‐antitrypsin (AAT) deficiency using electronic nose technology.


American Journal of Respiratory Cell and Molecular Biology | 2013

Role of IL-18 in Second-Hand Smoke–Induced Emphysema

Adelheid Kratzer; Jonas Salys; Claudia A. Nold-Petry; Carlyne D. Cool; Martin R. Zamora; Russ Bowler; Andreas Rembert Koczulla; Sabina Janciauskiene; Michael G. Edwards; Charles A. Dinarello; Laimute Taraseviciene-Stewart

Chronic second-hand smoke (SHS) exposure comprises the main risk factor for nonsmokers to develop chronic obstructive pulmonary disease (COPD). However, the mechanisms behind the chronic inflammation and lung destruction remain incompletely understood. In this study, we show that chronic exposure of Sprague-Dawley rats to SHS results in a significant increase of proinflammatory cytokine IL-18 and chemokine (C-C motif) ligand 5 in the bronchoalveolar lavage fluid (BALF) and a significant decrease of vascular endothelial growth factor (VEGF) in the lung tissue. SHS exposure resulted in progressive alveolar airspace enlargement, cell death, pulmonary vessel loss, vessel muscularization, collagen deposition, and right ventricular hypertrophy. Alveolar macrophages displayed a foamy phenotype and a decreased expression of the natural inhibitor of IL-18, namely, IL-18 binding protein (IL-18BP). Moreover, IL-18 down-regulated the expression of VEGF receptor-1 and VEGFR receptor-2, and induced apoptosis in pulmonary microvascular endothelial cells in vitro. We also observed a trend toward increased concentrations of IL-18 in the BALF of patients with COPD. Our findings suggest that IL-18-mediated endothelial cell death may contribute to vascular destruction and disappearance in SHS-induced COPD. Moreover, IL-18 and IL-18BP are potential new targets for therapeutics.


PLOS ONE | 2011

Comparison of two devices and two breathing patterns for exhaled breath condensate sampling.

Eva-Maria Hüttmann; Timm Greulich; Akira Hattesohl; Severin Schmid; Sarah Noeske; Christian Herr; Gerrit John; Rudolf A. Jörres; Bernd Müller; Claus Vogelmeier; Andreas Rembert Koczulla

Introduction Analysis of exhaled breath condensate (EBC) is a noninvasive method to access the epithelial lining fluid of the lungs. Due to standardization problems the method has not entered clinical practice. The aim of the study was to assess the comparability for two commercially available devices in healthy controls. In addition, we assessed different breathing patterns in healthy controls with protein markers to analyze the source of the EBC. Methods EBC was collected from ten subjects using the RTube and ECoScreen Turbo in a randomized crossover design, twice with every device - once in tidal breathing and once in hyperventilation. EBC conductivity, pH, surfactant protein A, Clara cell secretory protein and total protein were assessed. Bland-Altman plots were constructed to display the influence of different devices or breathing patterns and the intra-class correlation coefficient (ICC) was calculated. The volatile organic compound profile was measured using the electronic nose Cyranose 320. For the analysis of these data, the linear discriminant analysis, the Mahalanobis distances and the cross-validation values (CVV) were calculated. Results Neither the device nor the breathing pattern significantly altered EBC pH or conductivity. ICCs ranged from 0.61 to 0.92 demonstrating moderate to very good agreement. Protein measurements were greatly influenced by breathing pattern, the device used, and the way in which the results were reported. The electronic nose could distinguish between different breathing patterns and devices, resulting in Mahalanobis distances greater than 2 and CVVs ranging from 64% to 87%. Conclusion EBC pH and (to a lesser extent) EBC conductivity are stable parameters that are not influenced by either the device or the breathing patterns. Protein measurements remain uncertain due to problems of standardization. We conclude that the influence of the breathing maneuver translates into the necessity to keep the volume of ventilated air constant in further studies.


PLOS ONE | 2017

Influence of lung CT changes in chronic obstructive pulmonary disease (COPD) on the human lung microbiome

Marion Engel; David Endesfelder; Brigitte Schloter-Hai; Susanne Kublik; Michael S. Granitsiotis; Piera Boschetto; Mariarita Stendardo; Imre Barta; Balazs Dome; Jean-François Deleuze; Anne Boland; Joachim Müller-Quernheim; Antje Prasse; Tobias Welte; Jens M. Hohlfeld; Deepak Subramanian; David Parr; Ivo Gut; Timm Greulich; Andreas Rembert Koczulla; Adam Nowinski; Dorota Gorecka; Dave Singh; Sumit Gupta; Christopher E. Brightling; Harald Hoffmann; Marion Frankenberger; Thomas Höfer; Dorothe Burggraf; Marion S. Heiss-Neumann

Background Changes in microbial community composition in the lung of patients suffering from moderate to severe COPD have been well documented. However, knowledge about specific microbiome structures in the human lung associated with CT defined abnormalities is limited. Methods Bacterial community composition derived from brush samples from lungs of 16 patients suffering from different CT defined subtypes of COPD and 9 healthy subjects was analyzed using a cultivation independent barcoding approach applying 454-pyrosequencing of 16S rRNA gene fragment amplicons. Results We could show that bacterial community composition in patients with changes in CT (either airway or emphysema type changes, designated as severe subtypes) was different from community composition in lungs of patients without visible changes in CT as well as from healthy subjects (designated as mild COPD subtype and control group) (PC1, Padj = 0.002). Higher abundance of Prevotella in samples from patients with mild COPD subtype and from controls and of Streptococcus in the severe subtype cases mainly contributed to the separation of bacterial communities of subjects. No significant effects of treatment with inhaled glucocorticoids on bacterial community composition were detected within COPD cases with and without abnormalities in CT in PCoA. Co-occurrence analysis suggests the presence of networks of co-occurring bacteria. Four communities of positively correlated bacteria were revealed. The microbial communities can clearly be distinguished by their associations with the CT defined disease phenotype. Conclusion Our findings indicate that CT detectable structural changes in the lung of COPD patients, which we termed severe subtypes, are associated with alterations in bacterial communities, which may induce further changes in the interaction between microbes and host cells. This might result in a changed interplay with the host immune system.


Respirology | 2010

Ambient temperature impacts on pH of exhaled breath condensate

Andreas Rembert Koczulla; Sarah Noeske; Christian Herr; Frank Dette; Olaf Pinkenburg; Severin Schmid; Rudolf A. Jörres; Claus Vogelmeier; Robert Bals

Background and objective:  Analysis of exhaled breath condensate (EBC) pH is a non‐invasive method to study airway inflammation. Low pH is correlated with inflammatory diseases like asthma and COPD. The aim of this study was to assess the influence of measurement temperature on pH values of EBC.


European Respiratory Journal | 2017

The prevalence of diagnosed α1-antitrypsin deficiency and its comorbidities: results from a large population-based database.

Timm Greulich; Christoph Nell; David Hohmann; Marco Grebe; Sabina Janciauskiene; Andreas Rembert Koczulla; Claus Vogelmeier

α1-Antitrypsin deficiency (AATD) is a genetically determined disorder that is associated with different clinical manifestations. We aimed to assess the prevalence of diagnosed AATD and its comorbidities using a large healthcare database. In this retrospective longitudinal observational study, we analysed data from 4 million insurants. Using International Classification of Diseases revision 10 (ICD-10) codes, we assessed the prevalence, comorbidities and healthcare utilisation of AATD patients (E88.0 repeatedly coded) relative to non-AATD patients with chronic obstructive pulmonary disease (COPD), emphysema or asthma. In our study population, we identified 673 AATD patients (590 aged ≥30 years), corresponding to a prevalence of 23.73 per 100 000 in all age groups and 29.36 per 100 000 in those ≥30 years. Based on the number of AATD cases detected in the sample size (673 out of 2 836 585), we extrapolated that there were 19 162 AATD cases in Germany during the years studied. AATD patients had a higher prevalence of arterial hypertension, chronic kidney disease and diabetes relative to non-AATD asthma or emphysema patients. When compared to non-AATD COPD patients, AATD patients had significantly more consultations and more frequent and longer hospitalisations. Our data strengthen the assumption that AATD is associated with a variety of other diseases. Healthcare utilisation appears to be higher among AATD patients as compared to patients with non-AATD-related obstructive lung diseases. AATD patients have higher healthcare utilisation relative to non-AATD COPD, emphysema and asthma patients http://ow.ly/pHHh303m025


Drug Discovery Today | 2017

New concepts in asthma: clinical phenotypes and pathophysiological mechanisms

Andreas Rembert Koczulla; Claus Vogelmeier; Holger Garn; Harald Renz

Asthma is among the most common chronic inflammatory diseases worldwide. Recent evidence indicates that the pathogenesis shows a high degree of heterogeneity. Patient subsets have been identified that exhibit different cellular and molecular patterns of dysregulation. A prominent example is eosinophilic Th2-driven asthma. These unique and molecular patterns are termed endotypes. Characterization of endotypes has broad implications for therapeutic interventions. Although ∼80% of asthmatic patients respond well to standard anti-inflammatory therapies, the remaining subset particularly consisting of severe patients requires a more specialized endotype-specific approach. This interrelationship between clinical phenotypes, molecular endotypes and endotype-specific therapies is the focus of this review.


European Respiratory Journal | 2016

Emphysema- and airway-dominant COPD phenotypes defined by standardised quantitative computed tomography

Deepak Subramanian; Sumit Gupta; Dorothe Burggraf; Suzan J. vom Silberberg; Irene Heimbeck; Marion S. Heiss-Neumann; Karl Haeussinger; Chris Newby; Beverley Hargadon; Vimal Raj; Dave Singh; Umme Kolsum; Thomas P.J. Hofer; Khaled Al-shair; Niklas Luetzen; Antje Prasse; Joachim Müller-Quernheim; Giorgio Benea; S Leprotti; Piera Boschetto; Dorota Gorecka; Adam Nowinski; Karina Oniszh; Wolfgang zu Castell; Michael Hagen; Imre Barta; Balazs Dome; János Strausz; Timm Greulich; Claus Vogelmeier

EvA (Emphysema versus Airway disease) is a multicentre project to study mechanisms and identify biomarkers of emphysema and airway disease in chronic obstructive pulmonary disease (COPD). The objective of this study was to delineate objectively imaging-based emphysema-dominant and airway disease-dominant phenotypes using quantitative computed tomography (QCT) indices, standardised with a novel phantom-based approach. 441 subjects with COPD (Global Initiative for Chronic Obstructive Lung Disease (GOLD) stages 1–3) were assessed in terms of clinical and physiological measurements, laboratory testing and standardised QCT indices of emphysema and airway wall geometry. QCT indices were influenced by scanner non-conformity, but standardisation significantly reduced variability (p<0.001) and led to more robust phenotypes. Four imaging-derived phenotypes were identified, reflecting “emphysema-dominant”, “airway disease-dominant”, “mixed” disease and “mild” disease. The emphysema-dominant group had significantly higher lung volumes, lower gas transfer coefficient, lower oxygen (PO2) and carbon dioxide (PCO2) tensions, higher haemoglobin and higher blood leukocyte numbers than the airway disease-dominant group. The utility of QCT for phenotyping in the setting of an international multicentre study is improved by standardisation. QCT indices of emphysema and airway disease can delineate within a population of patients with COPD, phenotypic groups that have typical clinical features known to be associated with emphysema-dominant and airway-dominant disease. Standardisation of quantitative CT improves delineation of emphysema and airway phenotypes in a multicentre study http://ow.ly/10zjhV

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Robert Bals

University of Pennsylvania

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