TY - JOUR
T1 - Using machine learning for real-time BAC estimation from a new-generation transdermal biosensor in the laboratory
AU - Fairbairn, Catharine E.
AU - Kang, Dahyeon
AU - Bosch, Nigel
N1 - This research was supported by NIH National Institute on Alcohol Abuse and Alcoholism grant R01AA025969 to Catharine Fairbairn. Our thanks to Brynne Velia and the students of the Alcohol Research Laboratory for their help in the conduct of this research. BACtrack Skyn devices used in this research were issued free of charge from the company BACtrack. At the time this research was conducted, no price was associated with the BACtrack Skyn, and, to our knowledge, all researchers who requested Skyn were provided with a complementary device.
PY - 2020/11/1
Y1 - 2020/11/1
N2 - Background: Transdermal biosensors offer a noninvasive, low-cost technology for the assessment of alcohol consumption with broad potential applications in addiction science. Older-generation transdermal devices feature bulky designs and sparse sampling intervals, limiting potential applications for transdermal technology. Recently a new-generation of transdermal device has become available, featuring smartphone connectivity, compact designs, and rapid sampling. Here we present initial laboratory research examining the validity of a new-generation transdermal sensor prototype. Methods: Participants were young drinkers administered alcohol (target BAC = .08 %) or no-alcohol in the laboratory. Participants wore transdermal sensors while providing repeated breathalyzer (BrAC) readings. We assessed the association between BrAC (measured BrAC for a specific time point) and eBrAC (BrAC estimated based only on transdermal readings collected in the immediately preceding time interval). Extra-Trees machine learning algorithms, incorporating transdermal time series features as predictors, were used to create eBrAC. Results: Failure rates for the new-generation prototype sensor were high (16 %–34 %). Among participants with useable new-generation sensor data, models demonstrated strong capabilities for separating drinking from non-drinking episodes, and significant (moderate) ability to differentiate BrAC levels within intoxicated participants. Differences between eBrAC and BrAC were 60 % higher for models based on data from old-generation vs new-generation devices. Model comparisons indicated that both time series analysis and machine learning contributed significantly to final model accuracy. Conclusions: Results provide favorable preliminary evidence for the accuracy of real-time BAC estimates from a new-generation sensor. Future research featuring variable alcohol doses and real-world contexts will be required to further validate these devices.
AB - Background: Transdermal biosensors offer a noninvasive, low-cost technology for the assessment of alcohol consumption with broad potential applications in addiction science. Older-generation transdermal devices feature bulky designs and sparse sampling intervals, limiting potential applications for transdermal technology. Recently a new-generation of transdermal device has become available, featuring smartphone connectivity, compact designs, and rapid sampling. Here we present initial laboratory research examining the validity of a new-generation transdermal sensor prototype. Methods: Participants were young drinkers administered alcohol (target BAC = .08 %) or no-alcohol in the laboratory. Participants wore transdermal sensors while providing repeated breathalyzer (BrAC) readings. We assessed the association between BrAC (measured BrAC for a specific time point) and eBrAC (BrAC estimated based only on transdermal readings collected in the immediately preceding time interval). Extra-Trees machine learning algorithms, incorporating transdermal time series features as predictors, were used to create eBrAC. Results: Failure rates for the new-generation prototype sensor were high (16 %–34 %). Among participants with useable new-generation sensor data, models demonstrated strong capabilities for separating drinking from non-drinking episodes, and significant (moderate) ability to differentiate BrAC levels within intoxicated participants. Differences between eBrAC and BrAC were 60 % higher for models based on data from old-generation vs new-generation devices. Model comparisons indicated that both time series analysis and machine learning contributed significantly to final model accuracy. Conclusions: Results provide favorable preliminary evidence for the accuracy of real-time BAC estimates from a new-generation sensor. Future research featuring variable alcohol doses and real-world contexts will be required to further validate these devices.
KW - Alcohol
KW - Biosensor
KW - Blood alcohol concentration
KW - Machine learning
KW - Real-time
KW - Transdermal
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U2 - 10.1016/j.drugalcdep.2020.108205
DO - 10.1016/j.drugalcdep.2020.108205
M3 - Article
C2 - 32853998
AN - SCOPUS:85089750081
SN - 0376-8716
VL - 216
JO - Drug and Alcohol Dependence
JF - Drug and Alcohol Dependence
M1 - 108205
ER -