11 results on '"Saßmannshausen Z"'
Search Results
2. Auf dem Weg zur automatisierten Koloskopie-Berichterstellung: Eine künstliche Intelligenz zur Identifikation und Unterscheidung individueller Polypen
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Chiang, Y., additional, Sodmann, P., additional, Kafetzis, I., additional, Lux, T. J., additional, Saßmannshausen, Z., additional, Troya, J., additional, Brand, M., additional, Zoller, W. G., additional, Meining, A., additional, and Hann, A., additional
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- 2023
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3. Genetic findings in patients with different forms of pulmonary hypertension
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Eichstaedt, C., Sassmannshausen, Z., Gall, H., Seyfarth, H. J., Lerche, M., Halank, M., Xanthouli, P., Harutyunova, S., Egenlauf, B., Milger, K., Rosenkranz, S., Ewert, R., Lankeit, M., Lange, T., Hinderhofer, K., Gruenig, E., Eichstaedt, C., Sassmannshausen, Z., Gall, H., Seyfarth, H. J., Lerche, M., Halank, M., Xanthouli, P., Harutyunova, S., Egenlauf, B., Milger, K., Rosenkranz, S., Ewert, R., Lankeit, M., Lange, T., Hinderhofer, K., and Gruenig, E.
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- 2020
4. Genetic findings in patients with different forms of pulmonary hypertension
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Eichstaedt, C, additional, Saßmannshausen, Z, additional, Gall, H, additional, Seyfarth, HJ, additional, Lerche, M, additional, Halank, M, additional, Xanthouli, P, additional, Harutyunova, S, additional, Egenlauf, B, additional, Milger, K, additional, Rosenkranz, S, additional, Ewert, R, additional, Lankeit, M, additional, Lange, TJ, additional, Hinderhofer, K, additional, and Grünig, E, additional
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- 2020
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5. ProDOL: a general method to determine the degree of labeling for staining optimization and molecular counting.
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Tashev SA, Euchner J, Yserentant K, Hänselmann S, Hild F, Chmielewicz W, Hummert J, Schwörer F, Tsopoulidis N, Germer S, Saßmannshausen Z, Fackler OT, Klingmüller U, and Herten DP
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- Humans, CD4-Positive T-Lymphocytes metabolism, Adaptor Proteins, Signal Transducing metabolism, Lymphocyte Activation, HIV-1, Staining and Labeling methods, Microscopy, Fluorescence methods
- Abstract
Determining the label to target ratio, also known as the degree of labeling (DOL), is crucial for quantitative fluorescence microscopy and a high DOL with minimal unspecific labeling is beneficial for fluorescence microscopy in general. Yet robust, versatile and easy-to-use tools for measuring cell-specific labeling efficiencies are not available. Here we present a DOL determination technique named protein-tag DOL (ProDOL), which enables fast quantification and optimization of protein-tag labeling. With ProDOL various factors affecting labeling efficiency, including substrate type, incubation time and concentration, as well as sample fixation and cell type can be easily assessed. We applied ProDOL to investigate how human immunodeficiency virus-1 pathogenesis factor Nef modulates CD4 T cell activation measuring total and activated copy numbers of the adapter protein SLP-76 in signaling microclusters. ProDOL proved to be a versatile and robust tool for labeling calibration, enabling determination of labeling efficiencies, optimization of strategies and quantification of protein stoichiometry., (© 2024. The Author(s).)
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- 2024
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6. Assisted documentation as a new focus for artificial intelligence in endoscopy: the precedent of reliable withdrawal time and image reporting.
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Lux TJ, Saßmannshausen Z, Kafetzis I, Sodmann P, Herold K, Sudarevic B, Schmitz R, Zoller WG, Meining A, and Hann A
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- Humans, Colonoscopy, Algorithms, Documentation, Artificial Intelligence, Endoscopy, Gastrointestinal
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BACKGROUND : Reliable documentation is essential for maintaining quality standards in endoscopy; however, in clinical practice, report quality varies. We developed an artificial intelligence (AI)-based prototype for the measurement of withdrawal and intervention times, and automatic photodocumentation. METHOD: A multiclass deep learning algorithm distinguishing different endoscopic image content was trained with 10 557 images (1300 examinations, nine centers, four processors). Consecutively, the algorithm was used to calculate withdrawal time (AI prediction) and extract relevant images. Validation was performed on 100 colonoscopy videos (five centers). The reported and AI-predicted withdrawal times were compared with video-based measurement; photodocumentation was compared for documented polypectomies. RESULTS: Video-based measurement in 100 colonoscopies revealed a median absolute difference of 2.0 minutes between the measured and reported withdrawal times, compared with 0.4 minutes for AI predictions. The original photodocumentation represented the cecum in 88 examinations compared with 98/100 examinations for the AI-generated documentation. For 39/104 polypectomies, the examiners' photographs included the instrument, compared with 68 for the AI images. Lastly, we demonstrated real-time capability (10 colonoscopies). CONCLUSION : Our AI system calculates withdrawal time, provides an image report, and is real-time ready. After further validation, the system may improve standardized reporting, while decreasing the workload created by routine documentation., Competing Interests: The authors declare that they have no conflict of interest., (The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/).)
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- 2023
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7. Artificial intelligence-based polyp size measurement in gastrointestinal endoscopy using the auxiliary waterjet as a reference.
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Sudarevic B, Sodmann P, Kafetzis I, Troya J, Lux TJ, Saßmannshausen Z, Herlod K, Schmidt SA, Brand M, Schöttker K, Zoller WG, Meining A, and Hann A
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- Humans, Artificial Intelligence, Colonoscopy methods, Surgical Instruments, Colonic Polyps diagnostic imaging, Colonic Polyps pathology, Colonography, Computed Tomographic methods, Colorectal Neoplasms diagnostic imaging, Colorectal Neoplasms pathology
- Abstract
Background: Measurement of colorectal polyp size during endoscopy is mainly performed visually. In this work, we propose a novel polyp size measurement system (Poseidon) based on artificial intelligence (AI) using the auxiliary waterjet as a measurement reference., Methods: Visual estimation, biopsy forceps-based estimation, and Poseidon were compared using a computed tomography colonography-based silicone model with 28 polyps of defined sizes. Four experienced gastroenterologists estimated polyp sizes visually and with biopsy forceps. Furthermore, the gastroenterologists recorded images of each polyp with the waterjet in proximity for the application of Poseidon. Additionally, Poseidon's measurements of 29 colorectal polyps during routine clinical practice were compared with visual estimates., Results: In the silicone model, visual estimation had the largest median percentage error of 25.1 % (95 %CI 19.1 %-30.4 %), followed by biopsy forceps-based estimation: median 20.0 % (95 %CI 14.4 %-25.6 %). Poseidon gave a significantly lower median percentage error of 7.4 % (95 %CI 5.0 %-9.4 %) compared with other methods. During routine colonoscopies, Poseidon presented a significantly lower median percentage error (7.7 %, 95 %CI 6.1 %-9.3 %) than visual estimation (22.1 %, 95 %CI 15.1 %-26.9 %)., Conclusion: In this work, we present a novel AI-based method for measuring colorectal polyp size with significantly higher accuracy than other common sizing methods., Competing Interests: The authors declare that they have no conflict of interest., (The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).)
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- 2023
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8. Characterization of a novel Plasmodium falciparum merozoite surface antigen and potential vaccine target.
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Niaré K, Chege T, Rosenkranz M, Mwai K, Saßmannshausen Z, Odera D, Nyamako L, Tuju J, Alfred T, Waitumbi JN, Ogutu B, Sirima SB, Awandare G, Kouriba B, Rayner JC, and Osier FHA
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- Animals, Humans, Plasmodium falciparum, Merozoites, Antigens, Protozoan genetics, Protozoan Proteins, Antigens, Surface, Prospective Studies, Immunoglobulin G, Burkina Faso, Malaria, Falciparum, Parasites, Malaria Vaccines
- Abstract
Introduction: Detailed analyses of genetic diversity, antigenic variability, protein localization and immunological responses are vital for the prioritization of novel malaria vaccine candidates. Comprehensive approaches to determine the most appropriate antigen variants needed to provide broad protection are challenging and consequently rarely undertaken., Methods: Here, we characterized PF3D7_1136200, which we named Asparagine-Rich Merozoite Antigen (ARMA) based on the analysis of its sequence, localization and immunogenicity. We analyzed IgG and IgM responses against the common variants of ARMA in independent prospective cohort studies in Burkina Faso (N = 228), Kenya (N = 252) and Mali (N = 195) using a custom microarray, Div-KILCHIP., Results: We found a marked population structure between parasites from Africa and Asia. African isolates shared 34 common haplotypes, including a dominant pair although the overall selection pressure was directional (Tajima's D = -2.57; Fu and Li's F = -9.69; P < 0.02). ARMA was localized to the merozoite surface, IgG antibodies induced Fc-mediated degranulation of natural killer cells and strongly inhibited parasite growth in vitro. We found profound serological diversity, but IgG and IgM responses were highly correlated and a hierarchical clustering analysis identified only three major serogroups. Protective IgG and IgM antibodies appeared to target both cross-reactive and distinct epitopes across variants. However, combinations of IgG and IgM antibodies against selected variants were associated with complete protection against clinical episodes of malaria., Discussion: Our systematic strategy exploits genomic data to deduce the handful of antigen variants with the strongest potential to induce broad protection and may be broadly applicable to other complex pathogens for which effective vaccines remain elusive., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest, (Copyright © 2023 Niaré, Chege, Rosenkranz, Mwai, Saßmannshausen, Odera, Nyamako, Tuju, Alfred, Waitumbi, Ogutu, Sirima, Awandare, Kouriba, Rayner and Osier.)
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- 2023
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9. Pilot study of a new freely available computer-aided polyp detection system in clinical practice.
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Lux TJ, Banck M, Saßmannshausen Z, Troya J, Krenzer A, Fitting D, Sudarevic B, Zoller WG, Puppe F, Meining A, and Hann A
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- Colonoscopy methods, Computers, Humans, Pilot Projects, Prospective Studies, Randomized Controlled Trials as Topic, Adenoma diagnosis, Colonic Polyps diagnosis, Colorectal Neoplasms diagnosis
- Abstract
Purpose: Computer-aided polyp detection (CADe) systems for colonoscopy are already presented to increase adenoma detection rate (ADR) in randomized clinical trials. Those commercially available closed systems often do not allow for data collection and algorithm optimization, for example regarding the usage of different endoscopy processors. Here, we present the first clinical experiences of a, for research purposes publicly available, CADe system., Methods: We developed an end-to-end data acquisition and polyp detection system named EndoMind. Examiners of four centers utilizing four different endoscopy processors used EndoMind during their clinical routine. Detected polyps, ADR, time to first detection of a polyp (TFD), and system usability were evaluated (NCT05006092)., Results: During 41 colonoscopies, EndoMind detected 29 of 29 adenomas in 66 of 66 polyps resulting in an ADR of 41.5%. Median TFD was 130 ms (95%-CI, 80-200 ms) while maintaining a median false positive rate of 2.2% (95%-CI, 1.7-2.8%). The four participating centers rated the system using the System Usability Scale with a median of 96.3 (95%-CI, 70-100)., Conclusion: EndoMind's ability to acquire data, detect polyps in real-time, and high usability score indicate substantial practical value for research and clinical practice. Still, clinical benefit, measured by ADR, has to be determined in a prospective randomized controlled trial., (© 2022. The Author(s).)
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- 2022
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10. Development and evaluation of a deep learning model to improve the usability of polyp detection systems during interventions.
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Brand M, Troya J, Krenzer A, Saßmannshausen Z, Zoller WG, Meining A, Lux TJ, and Hann A
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- Artificial Intelligence, Colonoscopy methods, Humans, Sensitivity and Specificity, Colonic Polyps diagnosis, Colonic Polyps pathology, Colonic Polyps surgery, Deep Learning
- Abstract
Background: The efficiency of artificial intelligence as computer-aided detection (CADe) systems for colorectal polyps has been demonstrated in several randomized trials. However, CADe systems generate many distracting detections, especially during interventions such as polypectomies. Those distracting CADe detections are often induced by the introduction of snares or biopsy forceps as the systems have not been trained for such situations. In addition, there are a significant number of non-false but not relevant detections, since the polyp has already been previously detected. All these detections have the potential to disturb the examiner's work., Objectives: Development and evaluation of a convolutional neuronal network that recognizes instruments in the endoscopic image, suppresses distracting CADe detections, and reliably detects endoscopic interventions., Methods: A total of 580 different examination videos from 9 different centers using 4 different processor types were screened for instruments and represented the training dataset (519,856 images in total, 144,217 contained a visible instrument). The test dataset included 10 full-colonoscopy videos that were analyzed for the recognition of visible instruments and detections by a commercially available CADe system (GI Genius, Medtronic)., Results: The test dataset contained 153,623 images, 8.84% of those presented visible instruments (12 interventions, 19 instruments used). The convolutional neuronal network reached an overall accuracy in the detection of visible instruments of 98.59%. Sensitivity and specificity were 98.55% and 98.92%, respectively. A mean of 462.8 frames containing distracting CADe detections per colonoscopy were avoided using the convolutional neuronal network. This accounted for 95.6% of all distracting CADe detections., Conclusions: Detection of endoscopic instruments in colonoscopy using artificial intelligence technology is reliable and achieves high sensitivity and specificity. Accordingly, the new convolutional neuronal network could be used to reduce distracting CADe detections during endoscopic procedures. Thus, our study demonstrates the great potential of artificial intelligence technology beyond mucosal assessment., (© 2022 The Authors. United European Gastroenterology Journal published by Wiley Periodicals LLC on behalf of United European Gastroenterology.)
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- 2022
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11. Gene panel diagnostics reveals new pathogenic variants in pulmonary arterial hypertension.
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Eichstaedt CA, Saßmannshausen Z, Shaukat M, Cao D, Xanthouli P, Gall H, Sommer N, Ghofrani HA, Seyfarth HJ, Lerche M, Halank M, Kleymann J, Benjamin N, Harutyunova S, Egenlauf B, Milger K, Rosenkranz S, Ewert R, Klose H, Hoeper MM, Olsson KM, Lankeit M, Lange TJ, Hinderhofer K, and Grünig E
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- Activin Receptors, Type II genetics, Adenosine Triphosphatases genetics, Familial Primary Pulmonary Hypertension diagnosis, Familial Primary Pulmonary Hypertension epidemiology, Familial Primary Pulmonary Hypertension genetics, Genetic Predisposition to Disease genetics, Humans, Membrane Transport Proteins genetics, Mutation genetics, Protein Serine-Threonine Kinases, Hypertension, Pulmonary diagnosis, Hypertension, Pulmonary genetics, Hypertension, Pulmonary pathology, Pulmonary Arterial Hypertension diagnosis, Pulmonary Arterial Hypertension genetics
- Abstract
Background: A genetic predisposition can lead to the rare disease pulmonary arterial hypertension (PAH). Most mutations have been identified in the gene BMPR2 in heritable PAH. However, as of today 15 further PAH genes have been described. The exact prevalence across these genes particularly in other PAH forms remains uncertain. We present the distribution of mutations across PAH genes identified at the largest German referral centre for genetic diagnostics in PAH over a course of > 3 years., Methods: Our PAH-specific gene diagnostics panel was used to sequence 325 consecutive PAH patients from March 2017 to October 2020. For the first year the panel contained thirteen PAH genes: ACVRL1, BMPR1B, BMPR2, CAV1, EIF2AK4, ENG, GDF2, KCNA5, KCNK3, KLF2, SMAD4, SMAD9 and TBX4. These were extended by the three genes ATP13A3, AQP1 and SOX17 from March 2018 onwards following the genes' discovery., Results: A total of 79 mutations were identified in 74 patients (23%). Of the variants 51 (65%) were located in the gene BMPR2 while the other 28 variants were found in ten further PAH genes. We identified disease-causing variants in the genes AQP1, KCNK3 and SOX17 in families with at least two PAH patients. Mutations were not only detected in patients with heritable and idiopathic but also with associated PAH., Conclusions: Genetic defects were identified in 23% of the patients in a total of 11 PAH genes. This illustrates the benefit of the specific gene panel containing all known PAH genes., (© 2022. The Author(s).)
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- 2022
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