ArticlePloS one2026
Evaluating machine learning algorithms at predicting developmental trajectories using sequential dataset truncation of voluntary alcohol consumption in adolescent mice.
Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundAdolescent alcohol consumption is a known risk factor for developing alcohol use disorder (AUD) in adulthood, but individual susceptibility varies widely, contributed to by differences in factors that are not well-understood. Identifying patterns of developmental trajectories in voluntary alcohol consumption behavior during adolescence could provide insight into biological underpinnings of AUD risk. Machine learning (ML) offers powerful pattern recognition capabilities that may help forecast future behavioral trajectories based on early-stage data.
objectiveThis study aimed to evaluate the performance of twelve supervised ML algorithms in predicting developmental trajectories of voluntary alcohol consumption behavior in adolescent mice using sequentially truncated datasets.
methodsSimulated balanced datasets of alcohol consumption in adolescent mice were generated based on previously published biological data. We applied a sequential dataset truncation strategy to train and evaluate ML models on progressively longer spans of behavioral data. Prediction accuracy for trajectory pattern classification was assessed for each truncation point, and goodness-of-fit was modeled using four curve-fitting equations, including locally estimated scatterplot smoothing (LOESS), which provided best fit and was selected for downstream comparative analysis.
resultsLOESS-fitted accuracy progression curves enabled quantitative comparison across models. Six ML algorithms-Random Forest, Logistic Regression, Multilayer Perceptron, Linear Discriminant Analysis, K-Nearest Neighbors, and Support Vector Machine-achieved outstanding results, with 98% or better prediction accuracy by experiment end and 90% or better accuracy at midpoint. Four additional algorithms-Stochastic Gradient Descent, Decision Tree, Gradient Boosting Classifier, and Multinomial Naive Bayes-achieved acceptable accuracy values (77-95% at midpoint, and 91-96% at experiment end). In contrast, two models (Quadratic Discriminant Analysis and Gaussian Process Classifier) performed poorly and displayed declining accuracy trends with more data.
conclusionsThis study demonstrates that certain supervised ML algorithms can accurately predict behavioral outcomes from early-stage data. This approach holds promise for guiding molecular and cellular analyses at time points prior to behavioral phenotype's fully manifesting, making it possible to identify potential biological drivers that initiate the onset of harmful behavior of alcohol consumption during adolescence development.
Indexed as
Identifiers
What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.