6 research outputs found
Crowdsourcing digital health measures to predict Parkinson's disease severity: the Parkinson's Disease Digital Biomarker DREAM Challenge
Consumer wearables and sensors are a rich source of data about patients' daily disease and symptom burden, particularly in the case of movement disorders like Parkinson's disease (PD). However, interpreting these complex data into so-called digital biomarkers requires complicated analytical approaches, and validating these biomarkers requires sufficient data and unbiased evaluation methods. Here we describe the use of crowdsourcing to specifically evaluate and benchmark features derived from accelerometer and gyroscope data in two different datasets to predict the presence of PD and severity of three PD symptoms: tremor, dyskinesia, and bradykinesia. Forty teams from around the world submitted features, and achieved drastically improved predictive performance for PD status (best AUROCâ=â0.87), as well as tremor- (best AUPRâ=â0.75), dyskinesia- (best AUPRâ=â0.48) and bradykinesia-severity (best AUPRâ=â0.95)
Spatial variation of fixed charge density in knee joint cartilage from sodium MRI â Implication on knee joint mechanics under static loading
The effects of fixed charge density (FCD) and cartilage swelling have not been demonstrated on cartilage mechanics on knee joint level before. In this study, we present how the spatial and local variations of FCD affects the mechanical response of the knee joint cartilage during standing (half of the body weight, 13 minutes) using finite element (FE) modeling. The FCD distribution of tibial cartilage of an asymptomatic subject was determined using sodium (23Na) MRI at 7T and implemented into a 3-D FE-model of the knee joint (Subject-specific model, FCD: 0.18±0.08 mEq/ml). Tissue deformation in the Subject-specific model was validated against experimental, in vivo loading of the joint conducted with a MR-compatible compression device. For comparison, models with homogeneous FCD distribution (homogeneous model) and FCD distribution obtained from literature (literature model) were created. Immediately after application of the load (dynamic response), the variations in FCD had minor effects on cartilage stresses and strains. After 13 minutes of standing, the spatial and local variations in FCD had most influence on axial strains. In the superficial tibial cartilage in the Subject-specific model, axial strains were increased up to +13% due to smaller FCD (mean â11%), as compared to the homogeneous model. Compared to the literature model, those were decreased up to â18% due to greater FCD (mean +7%). The findings demonstrate that the spatial and local FCD variations in cartilage modulates strains in knee joint cartilage. Thereby, the results highlight the mechanical importance of site-specific content of proteoglycans in cartilage
Colour and decay resistance and its relationships in Eperua grandiflora
Eperua grandiflora, which is widely distributed in the French Guiana forest region, shows high variability in decay resistance. Further information concerning this wood
quality parameter is necessary, but standard testing methods are complex and
time-consuming. We assessed the use of colorimetry to determine durability
in heartwood samples from a range of trees. Eperua grandiflora colour parameters were measured using a CIELAB system, revealing that the tree effect was greater than the radial position and height effects. The wood samples were exposed to Coriolus versicolor and Antrodia sp. according to two European standards (En 350-1 and XP CEN TS 15083-1). Eperua grandiflora is more susceptible to brown rot. These two standards did not give the same durability classes. The high variation in natural durability was due to the tree effect. These two properties were found to be correlated and the assessment also
distinguished the extreme durability classes but they are not sufficient to
classify the class of durability of this species.Ătude de la variabilitĂ© de la couleur, de la durabilitĂ©
naturelle et recherche de corrĂ©lations chez Eperua grandiflora. Eperua grandiflora, essence largement rĂ©pandue dans les forĂȘts de Guyane soufre d'un
défaut majeur : une grande variabilité de sa durabilité
naturelle Ă l'Ă©gard des champignons lignivores. Dans un premier
temps, nous avons étudié la variabilité de la mesure de la
couleur selon le systÚme CIElab afin de vérifier si la
colorimĂ©trie peut ĂȘtre utilisĂ©e comme un indicateur de la
durabilitĂ© naturelle. Nous avons Ă©tudiĂ© la rĂ©sistance de cette essence Ă
l'échelle inter, et intra-arbres à l'égard de Coriolus versicolor et Antrodia sp., conformément aux normes européennes en vigueur : EN 350-1 et XP TS
15083-1. Les rĂ©sultats ont rĂ©vĂ©lĂ© qu'Eperua grandiflora est plus sensible au champignon de pourriture brune. De mĂȘme, l'utilisation des normes a montrĂ© que l'on n'obtenait pas
les mĂȘmes classes de durabilitĂ©. La variabilitĂ© de la
durabilité et de la couleur est plus importante à l'échelle
inter-arbres qu'à l'échelle intra-arbre. Enfin, ces deux propriétés sont corrélées mais nous ne
pouvons envisager d'utiliser la colorimétrie comme indicateur de la
durabilité naturelle, car elle ne permet de différencier que les
classes extrĂȘmes
Crowdsourcing digital health measures to predict Parkinsonâs disease severity: The Parkinsonâs Disease Digital Biomarker DREAM Challenge.
Consumer wearables and sensors are a rich source of data about patientsâ daily disease and symptom burden, particularly in the case of movement disorders like Parkinsonâs disease (PD). However, interpreting these complex data into so-called digital biomarkers requires complicated analytical approaches, and validating these biomarkers requires sufficient data and unbiased evaluation methods. Here we describe the use of crowdsourcing to specifically evaluate and benchmark features derived from accelerometer and gyroscope data in two different datasets to predict the presence of PD and severity of three PD symptoms: tremor, dyskinesia, and bradykinesia. Forty teams from around the world submitted features, and achieved drastically improved predictive performance for PD status (best AUROC = 0.87), as well as tremor- (best AUPR = 0.75), dyskinesia- (best AUPR = 0.48) and bradykinesia-severity (best AUPR = 0.95)