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  1. Article ; Online: Node-degree aware edge sampling mitigates inflated classification performance in biomedical random walk-based graph representation learning.

    Cappelletti, Luca / Rekerle, Lauren / Fontana, Tommaso / Hansen, Peter / Casiraghi, Elena / Ravanmehr, Vida / Mungall, Christopher J / Yang, Jeremy J / Spranger, Leonard / Karlebach, Guy / Caufield, J Harry / Carmody, Leigh / Coleman, Ben / Oprea, Tudor I / Reese, Justin / Valentini, Giorgio / Robinson, Peter N

    Bioinformatics advances

    2024  Volume 4, Issue 1, Page(s) vbae036

    Abstract: Motivation: Graph representation learning is a family of related approaches that learn low-dimensional vector representations of nodes and other graph elements called embeddings. Embeddings approximate characteristics of the graph and can be used for a ... ...

    Abstract Motivation: Graph representation learning is a family of related approaches that learn low-dimensional vector representations of nodes and other graph elements called embeddings. Embeddings approximate characteristics of the graph and can be used for a variety of machine-learning tasks such as novel edge prediction. For many biomedical applications, partial knowledge exists about positive edges that represent relationships between pairs of entities, but little to no knowledge is available about negative edges that represent the explicit lack of a relationship between two nodes. For this reason, classification procedures are forced to assume that the vast majority of unlabeled edges are negative. Existing approaches to sampling negative edges for training and evaluating classifiers do so by uniformly sampling pairs of nodes.
    Results: We show here that this sampling strategy typically leads to sets of positive and negative examples with imbalanced node degree distributions. Using representative heterogeneous biomedical knowledge graph and random walk-based graph machine learning, we show that this strategy substantially impacts classification performance. If users of graph machine-learning models apply the models to prioritize examples that are drawn from approximately the same distribution as the positive examples are, then performance of models as estimated in the validation phase may be artificially inflated. We present a degree-aware node sampling approach that mitigates this effect and is simple to implement.
    Availability and implementation: Our code and data are publicly available at https://github.com/monarch-initiative/negativeExampleSelection.
    Language English
    Publishing date 2024-03-04
    Publishing country England
    Document type Journal Article
    ISSN 2635-0041
    ISSN (online) 2635-0041
    DOI 10.1093/bioadv/vbae036
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: GRAPE for fast and scalable graph processing and random-walk-based embedding.

    Cappelletti, Luca / Fontana, Tommaso / Casiraghi, Elena / Ravanmehr, Vida / Callahan, Tiffany J / Cano, Carlos / Joachimiak, Marcin P / Mungall, Christopher J / Robinson, Peter N / Reese, Justin / Valentini, Giorgio

    Nature computational science

    2023  Volume 3, Issue 6, Page(s) 552–568

    Abstract: Graph representation learning methods opened new avenues for addressing complex, real-world problems represented by graphs. However, many graphs used in these applications comprise millions of nodes and billions of edges and are beyond the capabilities ... ...

    Abstract Graph representation learning methods opened new avenues for addressing complex, real-world problems represented by graphs. However, many graphs used in these applications comprise millions of nodes and billions of edges and are beyond the capabilities of current methods and software implementations. We present GRAPE (Graph Representation Learning, Prediction and Evaluation), a software resource for graph processing and embedding that is able to scale with big graphs by using specialized and smart data structures, algorithms, and a fast parallel implementation of random-walk-based methods. Compared with state-of-the-art software resources, GRAPE shows an improvement of orders of magnitude in empirical space and time complexity, as well as competitive edge- and node-label prediction performance. GRAPE comprises approximately 1.7 million well-documented lines of Python and Rust code and provides 69 node-embedding methods, 25 inference models, a collection of efficient graph-processing utilities, and over 80,000 graphs from the literature and other sources. Standardized interfaces allow a seamless integration of third-party libraries, while ready-to-use and modular pipelines permit an easy-to-use evaluation of graph-representation-learning methods, therefore also positioning GRAPE as a software resource that performs a fair comparison between methods and libraries for graph processing and embedding.
    MeSH term(s) Vitis ; Algorithms ; Software ; Learning ; Libraries
    Language English
    Publishing date 2023-06-26
    Publishing country United States
    Document type Journal Article
    ISSN 2662-8457
    ISSN (online) 2662-8457
    DOI 10.1038/s43588-023-00465-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: An Original HPLC Method with Coulometric Detection to Monitor Hydroxyl Radical Generation via Fenton Chemistry.

    Catapano, Maria Carmen / Protti, Michele / Fontana, Tommaso / Mandrioli, Roberto / Mladěnka, Přemysl / Mercolini, Laura

    Molecules (Basel, Switzerland)

    2019  Volume 24, Issue 17

    Abstract: Hydroxyl radicals (•OH) can be generated via Fenton chemistry catalyzed by transition metals. An in vitro Fenton system was developed to test both the inhibition and stimulation of •OH formation, by monitoring salicylate aromatic hydroxylation ... ...

    Abstract Hydroxyl radicals (•OH) can be generated via Fenton chemistry catalyzed by transition metals. An in vitro Fenton system was developed to test both the inhibition and stimulation of •OH formation, by monitoring salicylate aromatic hydroxylation derivatives as markers of •OH production. The reaction was optimized with either iron or copper, and target analytes were determined by means of an original HPLC method coupled to coulometric detection. The method granted good sensitivity and precision, while method applicability was tested on antioxidant compounds with and without chelating properties in different substance to metal ratios. This analytical approach shows how Fenton's reaction can be monitored by HPLC coupled to coulometric detection, as a powerful tool for studying molecules' redox behavior.
    MeSH term(s) Chemistry Techniques, Synthetic ; Chromatography, High Pressure Liquid ; Hydrogen Peroxide/chemistry ; Hydroxyl Radical/analysis ; Hydroxyl Radical/chemical synthesis ; Iron/chemistry ; Limit of Detection ; Molecular Structure ; Reproducibility of Results
    Chemical Substances Fenton's reagent ; Hydroxyl Radical (3352-57-6) ; Hydrogen Peroxide (BBX060AN9V) ; Iron (E1UOL152H7)
    Language English
    Publishing date 2019-08-23
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 1413402-0
    ISSN 1420-3049 ; 1431-5165 ; 1420-3049
    ISSN (online) 1420-3049
    ISSN 1431-5165 ; 1420-3049
    DOI 10.3390/molecules24173066
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Book ; Online: Het-node2vec

    Valentini, Giorgio / Casiraghi, Elena / Cappelletti, Luca / Fontana, Tommaso / Reese, Justin / Robinson, Peter

    second order random walk sampling for heterogeneous multigraphs embedding

    2021  

    Abstract: The development of Graph Representation Learning methods for heterogeneous graphs is fundamental in several real-world applications, since in several contexts graphs are characterized by different types of nodes and edges. We introduce a an algorithmic ... ...

    Abstract The development of Graph Representation Learning methods for heterogeneous graphs is fundamental in several real-world applications, since in several contexts graphs are characterized by different types of nodes and edges. We introduce a an algorithmic framework (Het-node2vec) that extends the original node2vec node-neighborhood sampling method to heterogeneous multigraphs. The resulting random walk samples capture both the structural characteristics of the graph and the semantics of the different types of nodes and edges. The proposed algorithms can focus their attention on specific node or edge types, allowing accurate representations also for underrepresented types of nodes/edges that are of interest for the prediction problem under investigation. These rich and well-focused representations can boost unsupervised and supervised learning on heterogeneous graphs.

    Comment: 20 pages, 5 figures
    Keywords Computer Science - Machine Learning ; Computer Science - Social and Information Networks ; Physics - Physics and Society
    Subject code 004
    Publishing date 2021-01-05
    Publishing country us
    Document type Book ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  5. Article ; Online: An open source knowledge graph ecosystem for the life sciences.

    Callahan, Tiffany J / Tripodi, Ignacio J / Stefanski, Adrianne L / Cappelletti, Luca / Taneja, Sanya B / Wyrwa, Jordan M / Casiraghi, Elena / Matentzoglu, Nicolas A / Reese, Justin / Silverstein, Jonathan C / Hoyt, Charles Tapley / Boyce, Richard D / Malec, Scott A / Unni, Deepak R / Joachimiak, Marcin P / Robinson, Peter N / Mungall, Christopher J / Cavalleri, Emanuele / Fontana, Tommaso /
    Valentini, Giorgio / Mesiti, Marco / Gillenwater, Lucas A / Santangelo, Brook / Vasilevsky, Nicole A / Hoehndorf, Robert / Bennett, Tellen D / Ryan, Patrick B / Hripcsak, George / Kahn, Michael G / Bada, Michael / Baumgartner, William A / Hunter, Lawrence E

    Scientific data

    2024  Volume 11, Issue 1, Page(s) 363

    Abstract: Translational research requires data at multiple scales of biological organization. Advancements in sequencing and multi-omics technologies have increased the availability of these data, but researchers face significant integration challenges. Knowledge ... ...

    Abstract Translational research requires data at multiple scales of biological organization. Advancements in sequencing and multi-omics technologies have increased the availability of these data, but researchers face significant integration challenges. Knowledge graphs (KGs) are used to model complex phenomena, and methods exist to construct them automatically. However, tackling complex biomedical integration problems requires flexibility in the way knowledge is modeled. Moreover, existing KG construction methods provide robust tooling at the cost of fixed or limited choices among knowledge representation models. PheKnowLator (Phenotype Knowledge Translator) is a semantic ecosystem for automating the FAIR (Findable, Accessible, Interoperable, and Reusable) construction of ontologically grounded KGs with fully customizable knowledge representation. The ecosystem includes KG construction resources (e.g., data preparation APIs), analysis tools (e.g., SPARQL endpoint resources and abstraction algorithms), and benchmarks (e.g., prebuilt KGs). We evaluated the ecosystem by systematically comparing it to existing open-source KG construction methods and by analyzing its computational performance when used to construct 12 different large-scale KGs. With flexible knowledge representation, PheKnowLator enables fully customizable KGs without compromising performance or usability.
    MeSH term(s) Algorithms ; Biological Science Disciplines ; Pattern Recognition, Automated ; Translational Research, Biomedical ; Knowledge Bases
    Language English
    Publishing date 2024-04-11
    Publishing country England
    Document type Journal Article
    ZDB-ID 2775191-0
    ISSN 2052-4463 ; 2052-4463
    ISSN (online) 2052-4463
    ISSN 2052-4463
    DOI 10.1038/s41597-024-03171-w
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: NSAID use and clinical outcomes in COVID-19 patients: a 38-center retrospective cohort study

    Reese, Justin T. / Coleman, Ben / Chan, Lauren / Blau, Hannah / Callahan, Tiffany J. / Cappelletti, Luca / Fontana, Tommaso / Bradwell, Katie R. / Harris, Nomi L. / Casiraghi, Elena / Valentini, Giorgio / Karlebach, Guy / Deer, Rachel / McMurry, Julie A. / Haendel, Melissa A. / Chute, Christopher G. / Pfaff, Emily / Moffitt, Richard / Spratt, Heidi /
    Singh, Jasvinder A. / Mungall, Christopher J. / Williams, Andrew E. / Robinson, Peter N.

    Virol J. 2022 Dec., v. 19, no. 1 p.84-84

    2022  

    Abstract: BACKGROUND: Non-steroidal anti-inflammatory drugs (NSAIDs) are commonly used to reduce pain, fever, and inflammation but have been associated with complications in community-acquired pneumonia. Observations shortly after the start of the COVID-19 ... ...

    Abstract BACKGROUND: Non-steroidal anti-inflammatory drugs (NSAIDs) are commonly used to reduce pain, fever, and inflammation but have been associated with complications in community-acquired pneumonia. Observations shortly after the start of the COVID-19 pandemic in 2020 suggested that ibuprofen was associated with an increased risk of adverse events in COVID-19 patients, but subsequent observational studies failed to demonstrate increased risk and in one case showed reduced risk associated with NSAID use. METHODS: A 38-center retrospective cohort study was performed that leveraged the harmonized, high-granularity electronic health record data of the National COVID Cohort Collaborative. A propensity-matched cohort of 19,746 COVID-19 inpatients was constructed by matching cases (treated with NSAIDs at the time of admission) and 19,746 controls (not treated) from 857,061 patients with COVID-19 available for analysis. The primary outcome of interest was COVID-19 severity in hospitalized patients, which was classified as: moderate, severe, or mortality/hospice. Secondary outcomes were acute kidney injury (AKI), extracorporeal membrane oxygenation (ECMO), invasive ventilation, and all-cause mortality at any time following COVID-19 diagnosis. RESULTS: Logistic regression showed that NSAID use was not associated with increased COVID-19 severity (OR: 0.57 95% CI: 0.53–0.61). Analysis of secondary outcomes using logistic regression showed that NSAID use was not associated with increased risk of all-cause mortality (OR 0.51 95% CI: 0.47–0.56), invasive ventilation (OR: 0.59 95% CI: 0.55–0.64), AKI (OR: 0.67 95% CI: 0.63–0.72), or ECMO (OR: 0.51 95% CI: 0.36–0.7). In contrast, the odds ratios indicate reduced risk of these outcomes, but our quantitative bias analysis showed E-values of between 1.9 and 3.3 for these associations, indicating that comparatively weak or moderate confounder associations could explain away the observed associations. CONCLUSIONS: Study interpretation is limited by the observational design. Recording of NSAID use may have been incomplete. Our study demonstrates that NSAID use is not associated with increased COVID-19 severity, all-cause mortality, invasive ventilation, AKI, or ECMO in COVID-19 inpatients. A conservative interpretation in light of the quantitative bias analysis is that there is no evidence that NSAID use is associated with risk of increased severity or the other measured outcomes. Our results confirm and extend analogous findings in previous observational studies using a large cohort of patients drawn from 38 centers in a nationally representative multicenter database.
    Keywords COVID-19 infection ; acute kidney injury ; cohort studies ; databases ; fever ; ibuprofen ; inflammation ; mortality ; pain ; pneumonia ; regression analysis ; risk ; risk reduction ; telemedicine
    Language English
    Dates of publication 2022-12
    Size p. 84.
    Publishing place BioMed Central
    Document type Article ; Online
    ZDB-ID 2160640-7
    ISSN 1743-422X
    ISSN 1743-422X
    DOI 10.1186/s12985-022-01813-2
    Database NAL-Catalogue (AGRICOLA)

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  7. Article: Explainable Machine Learning for Early Assessment of COVID-19 Risk Prediction in Emergency Departments.

    Casiraghi, Elena / Malchiodi, Dario / Trucco, Gabriella / Frasca, Marco / Cappelletti, Luca / Fontana, Tommaso / Esposito, Alessandro Andrea / Avola, Emanuele / Jachetti, Alessandro / Reese, Justin / Rizzi, Alessandro / Robinson, Peter N / Valentini, Giorgio

    IEEE access : practical innovations, open solutions

    2020  Volume 8, Page(s) 196299–196325

    Abstract: Between January and October of 2020, the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus has infected more than 34 million persons in a worldwide pandemic leading to over one million deaths worldwide (data from the Johns Hopkins ... ...

    Abstract Between January and October of 2020, the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus has infected more than 34 million persons in a worldwide pandemic leading to over one million deaths worldwide (data from the Johns Hopkins University). Since the virus begun to spread, emergency departments were busy with COVID-19 patients for whom a quick decision regarding in- or outpatient care was required. The virus can cause characteristic abnormalities in chest radiographs (CXR), but, due to the low sensitivity of CXR, additional variables and criteria are needed to accurately predict risk. Here, we describe a computerized system primarily aimed at extracting the most relevant radiological, clinical, and laboratory variables for improving patient risk prediction, and secondarily at presenting an explainable machine learning system, which may provide simple decision criteria to be used by clinicians as a support for assessing patient risk. To achieve robust and reliable variable selection, Boruta and Random Forest (RF) are combined in a 10-fold cross-validation scheme to produce a variable importance estimate not biased by the presence of surrogates. The most important variables are then selected to train a RF classifier, whose rules may be extracted, simplified, and pruned to finally build an associative tree, particularly appealing for its simplicity. Results show that the radiological score automatically computed through a neural network is highly correlated with the score computed by radiologists, and that laboratory variables, together with the number of comorbidities, aid risk prediction. The prediction performance of our approach was compared to that that of generalized linear models and shown to be effective and robust. The proposed machine learning-based computational system can be easily deployed and used in emergency departments for rapid and accurate risk prediction in COVID-19 patients.
    Language English
    Publishing date 2020-10-26
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2687964-5
    ISSN 2169-3536
    ISSN 2169-3536
    DOI 10.1109/ACCESS.2020.3034032
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: KG-COVID-19: a framework to produce customized knowledge graphs for COVID-19 response.

    Reese, Justin / Unni, Deepak / Callahan, Tiffany J / Cappelletti, Luca / Ravanmehr, Vida / Carbon, Seth / Fontana, Tommaso / Blau, Hannah / Matentzoglu, Nicolas / Harris, Nomi L / Munoz-Torres, Monica C / Robinson, Peter N / Joachimiak, Marcin P / Mungall, Christopher J

    bioRxiv : the preprint server for biology

    2020  

    Abstract: Integrated, up-to-date data about SARS-CoV-2 and coronavirus disease 2019 (COVID-19) is crucial for the ongoing response to the COVID-19 pandemic by the biomedical research community. While rich biological knowledge exists for SARS-CoV-2 and related ... ...

    Abstract Integrated, up-to-date data about SARS-CoV-2 and coronavirus disease 2019 (COVID-19) is crucial for the ongoing response to the COVID-19 pandemic by the biomedical research community. While rich biological knowledge exists for SARS-CoV-2 and related viruses (SARS-CoV, MERS-CoV), integrating this knowledge is difficult and time consuming, since much of it is in siloed databases or in textual format. Furthermore, the data required by the research community varies drastically for different tasks - the optimal data for a machine learning task, for example, is much different from the data used to populate a browsable user interface for clinicians. To address these challenges, we created KG-COVID-19, a flexible framework that ingests and integrates biomedical data to produce knowledge graphs (KGs) for COVID-19 response. This KG framework can also be applied to other problems in which siloed biomedical data must be quickly integrated for different research applications, including future pandemics.
    Bigger picture: An effective response to the COVID-19 pandemic relies on integration of many different types of data available about SARS-CoV-2 and related viruses. KG-COVID-19 is a framework for producing knowledge graphs that can be customized for downstream applications including machine learning tasks, hypothesis-based querying, and browsable user interface to enable researchers to explore COVID-19 data and discover relationships.
    Keywords covid19
    Language English
    Publishing date 2020-08-18
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2020.08.17.254839
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Supervised learning with word embeddings derived from PubMed captures latent knowledge about protein kinases and cancer.

    Ravanmehr, Vida / Blau, Hannah / Cappelletti, Luca / Fontana, Tommaso / Carmody, Leigh / Coleman, Ben / George, Joshy / Reese, Justin / Joachimiak, Marcin / Bocci, Giovanni / Hansen, Peter / Bult, Carol / Rueter, Jens / Casiraghi, Elena / Valentini, Giorgio / Mungall, Christopher / Oprea, Tudor I / Robinson, Peter N

    NAR genomics and bioinformatics

    2021  Volume 3, Issue 4, Page(s) lqab113

    Abstract: Inhibiting protein kinases (PKs) that cause cancers has been an important topic in cancer therapy for years. So far, almost 8% of >530 PKs have been targeted by FDA-approved medications, and around 150 protein kinase inhibitors (PKIs) have been tested in ...

    Abstract Inhibiting protein kinases (PKs) that cause cancers has been an important topic in cancer therapy for years. So far, almost 8% of >530 PKs have been targeted by FDA-approved medications, and around 150 protein kinase inhibitors (PKIs) have been tested in clinical trials. We present an approach based on natural language processing and machine learning to investigate the relations between PKs and cancers, predicting PKs whose inhibition would be efficacious to treat a certain cancer. Our approach represents PKs and cancers as semantically meaningful 100-dimensional vectors based on word and concept neighborhoods in PubMed abstracts. We use information about phase I-IV trials in ClinicalTrials.gov to construct a training set for random forest classification. Our results with historical data show that associations between PKs and specific cancers can be predicted years in advance with good accuracy. Our tool can be used to predict the relevance of inhibiting PKs for specific cancers and to support the design of well-focused clinical trials to discover novel PKIs for cancer therapy.
    Language English
    Publishing date 2021-12-08
    Publishing country England
    Document type Journal Article
    ISSN 2631-9268
    ISSN (online) 2631-9268
    DOI 10.1093/nargab/lqab113
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: NSAID use and clinical outcomes in COVID-19 patients: a 38-center retrospective cohort study.

    Reese, Justin T / Coleman, Ben / Chan, Lauren / Blau, Hannah / Callahan, Tiffany J / Cappelletti, Luca / Fontana, Tommaso / Bradwell, Katie R / Harris, Nomi L / Casiraghi, Elena / Valentini, Giorgio / Karlebach, Guy / Deer, Rachel / McMurry, Julie A / Haendel, Melissa A / Chute, Christopher G / Pfaff, Emily / Moffitt, Richard / Spratt, Heidi /
    Singh, Jasvinder A / Mungall, Christopher J / Williams, Andrew E / Robinson, Peter N

    Virology journal

    2022  Volume 19, Issue 1, Page(s) 84

    Abstract: Background: Non-steroidal anti-inflammatory drugs (NSAIDs) are commonly used to reduce pain, fever, and inflammation but have been associated with complications in community-acquired pneumonia. Observations shortly after the start of the COVID-19 ... ...

    Abstract Background: Non-steroidal anti-inflammatory drugs (NSAIDs) are commonly used to reduce pain, fever, and inflammation but have been associated with complications in community-acquired pneumonia. Observations shortly after the start of the COVID-19 pandemic in 2020 suggested that ibuprofen was associated with an increased risk of adverse events in COVID-19 patients, but subsequent observational studies failed to demonstrate increased risk and in one case showed reduced risk associated with NSAID use.
    Methods: A 38-center retrospective cohort study was performed that leveraged the harmonized, high-granularity electronic health record data of the National COVID Cohort Collaborative. A propensity-matched cohort of 19,746 COVID-19 inpatients was constructed by matching cases (treated with NSAIDs at the time of admission) and 19,746 controls (not treated) from 857,061 patients with COVID-19 available for analysis. The primary outcome of interest was COVID-19 severity in hospitalized patients, which was classified as: moderate, severe, or mortality/hospice. Secondary outcomes were acute kidney injury (AKI), extracorporeal membrane oxygenation (ECMO), invasive ventilation, and all-cause mortality at any time following COVID-19 diagnosis.
    Results: Logistic regression showed that NSAID use was not associated with increased COVID-19 severity (OR: 0.57 95% CI: 0.53-0.61). Analysis of secondary outcomes using logistic regression showed that NSAID use was not associated with increased risk of all-cause mortality (OR 0.51 95% CI: 0.47-0.56), invasive ventilation (OR: 0.59 95% CI: 0.55-0.64), AKI (OR: 0.67 95% CI: 0.63-0.72), or ECMO (OR: 0.51 95% CI: 0.36-0.7). In contrast, the odds ratios indicate reduced risk of these outcomes, but our quantitative bias analysis showed E-values of between 1.9 and 3.3 for these associations, indicating that comparatively weak or moderate confounder associations could explain away the observed associations.
    Conclusions: Study interpretation is limited by the observational design. Recording of NSAID use may have been incomplete. Our study demonstrates that NSAID use is not associated with increased COVID-19 severity, all-cause mortality, invasive ventilation, AKI, or ECMO in COVID-19 inpatients. A conservative interpretation in light of the quantitative bias analysis is that there is no evidence that NSAID use is associated with risk of increased severity or the other measured outcomes. Our results confirm and extend analogous findings in previous observational studies using a large cohort of patients drawn from 38 centers in a nationally representative multicenter database.
    MeSH term(s) Acute Kidney Injury ; Anti-Inflammatory Agents, Non-Steroidal/adverse effects ; COVID-19 ; COVID-19 Testing ; Cohort Studies ; Humans ; Pandemics ; Retrospective Studies
    Chemical Substances Anti-Inflammatory Agents, Non-Steroidal
    Language English
    Publishing date 2022-05-15
    Publishing country England
    Document type Journal Article ; Multicenter Study ; Research Support, U.S. Gov't, Non-P.H.S. ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2160640-7
    ISSN 1743-422X ; 1743-422X
    ISSN (online) 1743-422X
    ISSN 1743-422X
    DOI 10.1186/s12985-022-01813-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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