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Dworzynski, P.

Publications and source records attributed to Dworzynski, P..

2 recordsLinked to original sources

Nationwide prediction of type 2 diabetes comorbidities

Identification of individuals at risk of developing disease comorbidities represents an important task in tackling the growing personal and societal burdens associated with chronic diseases. We employed machine learning techniques to investigate to what extent data from longitudinal, nationwide Danish health registers can be used to predict individuals at high risk of developing type 2 diabetes (T2D) comorbidities. Based on register data spanning hospitalizations, drug prescriptions and contacts with primary care contractors from >200,000 individuals newly diagnosed with T2D, we used logistic regression-, random forest- and gradient boosting models to predict five-year risk of heart failure (HF), myocardial infarction (MI), stroke (ST), cardiovascular disease (CVD) and chronic kidney disease (CKD). For HF, MI, CVD, and CKD, register-based models outperformed a reference model leveraging canonical individual characteristics by achieving area under the receiver operating characteristic curve improvements of 0.06, 0.03, 0.06, and 0.07, respectively. The top 1,000 patients predicted to be at highest risk exhibited observed incidence ratios exceeding 4.99, 3.52, 2.92 and 4.71 respectively. In summary, prediction of T2D comorbidities utilizing Danish registers led to consistent albeit modest performance improvements over reference models, suggesting that register data could be leveraged to systematically identify individuals at risk of developing disease comorbidities.

bioinformatics

Implementations of the chemical structural and compositional similarity metric in R and Python

MotivationTandem mass spectrometry (MS/MS) has the potential to substantially improve metabolomics by acquiring spectra of fragmented ions. These fragmentation spectra can be represented as a molecular network, by measuring cosine distances between them, thus identifying signals from the same or similar molecules. Metrics that enable comparison between pairs of samples based on their metabolite profiles are in great need. Taking inspiration from the successful phylogeny-aware beta-diversity measures used in microbiome research, integrating chemical similarity information about the features in addition to their abundances could lead to better insights when comparing metabolite profiles. Chemical Structural and Compositional Similarity (CSCS) is a recently published similarity metric comparing the full set of signals and their chemical similarity between two samples. Efficient, scalable and easily accessible implementations of this algorithm is currently lacking. Here, we present an easily accessible and scalable implementation of CSCS in both python and R, including a version not weighted by intensity information. ResultsWe provide a new implementation of the CSCS algorithm that is over 300 times faster than the published implementation in R, making the algorithm suitable for large-scale metabolomics applications. We also show that adding chemical information enriches existing methods. Furthermore, the R implementation includes functions for exporting molecular networks directly from the mass spectral molecular networking platform GNPS for ease of use for downstream applications. Contactbrejnrod@sund.ku.dk Availabilitygithub.com/askerdb/rCSCS, github.com/askerdb/pyCSCS

bioinformatics