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1.
PNAS Nexus ; 2(2): pgac315, 2023 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-36798622

RESUMO

Neurodevelopmental disorders are on the rise worldwide, with diagnoses that detect derailment from typical milestones by 3 to 4.5 years of age. By then, the circuitry in the brain has already reached some level of maturation that inevitably takes neurodevelopment through a different course. There is a critical need then to develop analytical methods that detect problems much earlier and identify targets for treatment. We integrate data from multiple sources, including neonatal auditory brainstem responses (ABR), clinical criteria detecting autism years later in those neonates, and similar ABR information for young infants and children who also received a diagnosis of autism spectrum disorders, to produce the earliest known digital screening biomarker to flag neurodevelopmental derailment in neonates. This work also defines concrete targets for treatment and offers a new statistical approach to aid in guiding a personalized course of maturation in line with the highly nonlinear, accelerated neurodevelopmental rates of change in early infancy.

2.
J Vis Exp ; (149)2019 07 24.
Artigo em Inglês | MEDLINE | ID: mdl-31403620

RESUMO

As Parkinson's disease (PD) is a heterogeneous disorder, personalized medicine is truly required to optimize care. In their current form, standard scores from paper and pencil symptom- measures traditionally used to track disease progression are too coarse (discrete) to capture the granularity of the clinical phenomena under consideration, in the face of tremendous symptom diversity. For this reason, sensors, wearables, and mobile devices are increasingly incorporated into PD research and routine care. These digital measures, while more precise, yield data that are less standardized and interpretable than traditional measures, and consequently, the two types of data remain largely siloed. Both of these issues present barriers to the broad clinical application of the field's most precise assessment tools. This protocol addresses both problems. Using traditional tasks to measure cognition and motor control, we test the participant, while co-registering biophysical signals unobtrusively using wearables. We then integrate the scores from traditional paper-and-pencil methods with the digital data that we continuously register. We offer a new standardized data type and unifying statistical platform that enables the dynamic tracking of change in the person's stochastic signatures under different conditions that probe different functional levels of neuromotor control, ranging from voluntary to autonomic. The protocol and standardized statistical framework offer dynamic digital biomarkers of physical and cognitive function in PD that correspond to validated clinical scales, while significantly improving their precision.


Assuntos
Cognição , Monitorização Fisiológica/instrumentação , Atividade Motora , Doença de Parkinson/diagnóstico , Doença de Parkinson/fisiopatologia , Idoso , Progressão da Doença , Feminino , Humanos , Estudos Longitudinais , Masculino , Dispositivos Eletrônicos Vestíveis , Adulto Jovem
3.
Artigo em Inglês | MEDLINE | ID: mdl-29556179

RESUMO

The variability inherently present in biophysical data is partly contributed by disparate sampling resolutions across instrumentations. This poses a potential problem for statistical inference using pooled data in open access repositories. Such repositories combine data collected from multiple research sites using variable sampling resolutions. One example is the Autism Brain Imaging Data Exchange repository containing thousands of imaging and demographic records from participants in the spectrum of autism and age-matched neurotypical controls. Further, statistical analyses of groups from different diagnoses and demographics may be challenging, owing to the disparate number of participants across different clinical subgroups. In this paper, we examine the noise signatures of head motion data extracted from resting state fMRI data harnessed under different sampling resolutions. We characterize the quality of the noise in the variability of the raw linear and angular speeds for different clinical phenotypes in relation to age-matched controls. Further, we use bootstrapping methods to ensure compatible group sizes for statistical comparison and report the ranges of physical involuntary head excursions of these groups. We conclude that different sampling rates do affect the quality of noise in the variability of head motion data and, consequently, the type of random process appropriate to characterize the time series data. Further, given a qualitative range of noise, from pink to brown noise, it is possible to characterize different clinical subtypes and distinguish them in relation to ranges of neurotypical controls. These results may be of relevance to the pre-processing stages of the pipeline of analyses of resting state fMRI data, whereby head motion enters the criteria to clean imaging data from motion artifacts.

4.
Sensors (Basel) ; 18(4)2018 Mar 29.
Artigo em Inglês | MEDLINE | ID: mdl-29596342

RESUMO

Wearable biosensors, such as those embedded in smart phones, can provide data to assess neuro-motor control in mobile settings, at homes, schools, workplaces and clinics. However, because most machine learning algorithms currently used to analyze such data require several steps that depend on human heuristics, the analyses become computationally expensive and rather subjective. Further, there is no standardized scale or set of tasks amenable to take advantage of such technology in ways that permit broad dissemination and reproducibility of results. Indeed, there is a critical need for fully objective automated analytical methods that easily handle the deluge of data these sensors output, while providing standardized scales amenable to apply across large sections of the population, to help promote personalized-mobile medicine. Here we use an open-access data set from Kaggle.com to illustrate the use of a new statistical platform and standardized data types applied to smart phone accelerometer and gyroscope data from 30 participants, performing six different activities. We report full distinction without confusion of the activities from the Kaggle set using a single parameter (linear acceleration or angular speed). We further extend the use of our platform to characterize data from commercially available smart shoes, using gait patterns within a set of experiments that probe nervous systems functioning and levels of motor control.

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