Evidence map›Paper›PMID 41628149›Full record

ArticlePloS one2026

Differences in drug intake levels (high versus low takers) do not necessarily imply distinct drug user types: Insights from a new cluster-based model.

Diego M Castaneda, Martin O Job

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Diego M CastanedaDepartment of Biomedical Sciences, Cooper Medical School of Rowan University, Camden, New Jersey, United States of America.
Martin O JobDepartment of Biomedical Sciences, Cooper Medical School of Rowan University, Camden, New Jersey, United States of America.ORCID https://orcid.org/0000-0003-0764-3992

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA current model categorizes drug takers into high versus low takers (HT and LT) based on their drug intake levels, with the assumption that these groups represent different phenotypes. When several drug doses are considered, the inverted u-shaped dose-response curves (IUDR) of HT are shifted upwards and rightward, relative to that of LT. However, these IUDR 'shifts' are not quantitative metrics and may be subjective. Also, differences in intake levels do not necessarily imply distinctions in other variables (such as demand elasticity) that are important for drug user phenotypology. With supporting evidence from a recent report, we hypothesized that, contrary to assumptions in the field, HT and LT do not necessarily represent distinct phenotypes.

methodsMale Sprague Dawley rats (n = 12) self-administered different doses of cocaine, and we obtained IUDR and demand curves per individual. We developed a new model to quantify the variables that defined the structure of the IUDR and we employed behavioral economic principles to obtain variables that defined the demand curve. We conducted principal component analysis/gaussian mixtures model clustering of variables from both IUDR and demand curves, to identify/compare the clusters that were revealed to HT/LT groups that were distinguished via median split.

resultsThe cluster-based model identified groups more distinct than LT versus HT. LT and HT were composed of mixtures of individuals from these distinct clusters. LT/HT were not very different when several other variables were considered.

conclusionsDifferences in drug intake levels (HT versus LT) do not necessarily imply distinct phenotypes.

Indexed as

CocaineAnimalsCluster AnalysisDose-Response Relationship, DrugMaleRatsRats, Sprague-DawleySelf AdministrationCocaine

Identifiers

PMID41628149
PMCPMC12863560

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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 OpenQuestion graph.