Evidence map›Paper›PMID 27100333›Full record

Trial reportClinical toxicology (Philadelphia, Pa.)2016

Pharmacokinetic analysis and comparison of caffeine administered rapidly or slowly in coffee chilled or hot versus chilled energy drink in healthy young adults.

John R White, Jeannie M Padowski, Yili Zhong, Gang Chen, Shaman Luo, Philip Lazarus, Matthew E Layton, Sterling McPherson

Open access · hybridAbstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Clinical toxicology (Philadelphia, Pa.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
11.0field-weighted citation impact, top 1% of its field
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 113 citations in OpenAlex.

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  12. Leveraging the developmental neurotoxicityFrontiers in toxicology · 2026
    Article
  13. Systematic evaluation and comparison of theCurrent research in food science · 2026
    Article
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  20. Neuropathic pain: Mechanisms and therapeutic strategies.Frontiers in cell and developmental biology · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

John R Whitea Department of Pharmacotherapy , College of Pharmacy, WA State University , Spokane , WA , USA ;
Jeannie M Padowskib College of Medicine, WA State University , Spokane , WA , USA ;
Yili Zhongc Department of Pharmaceutical Sciences , College of Pharmacy, WA State University , Spokane , WA , USA ;
Gang Chenc Department of Pharmaceutical Sciences , College of Pharmacy, WA State University , Spokane , WA , USA ;
Shaman Luoc Department of Pharmaceutical Sciences , College of Pharmacy, WA State University , Spokane , WA , USA ;
Philip Lazarusc Department of Pharmaceutical Sciences , College of Pharmacy, WA State University , Spokane , WA , USA ;
Matthew E Laytonb College of Medicine, WA State University , Spokane , WA , USA ;
Sterling McPhersond Program of Excellence in Addictions Research (PEAR) , College of Nursing, WA State University , Spokane , WA , USA ;
Washington State University Spokane · USProvidence Health & Services · US

Funding

The UGT2A and 3A metabolizing enzymes and tobacco-related cancer riskR01ES025460 · NIEHS · WASHINGTON STATE UNIVERSITY · PI LAZARUS, PHILIP · 2015 to 2019
$2.8M
NIEHS NIH HHS R01 ES025460
6 · The paper itself

Abstract

contextThere is a paucity of data describing the impact of type of beverage (coffee versus energy drink), different rates of consumption and different temperature of beverages on the pharmacokinetic disposition of caffeine. Additionally, there is concern that inordinately high levels of caffeine may result from the rapid consumption of cold energy drinks.

objectiveThe objective of this study was to compare the pharmacokinetics of caffeine under various drink temperature, rate of consumption and vehicle (coffee versus energy drink) conditions. MATERIALS: Five caffeine (dose = 160 mg) conditions were evaluated in an open-label, group-randomized, crossover fashion. After the administration of each caffeine dose, 10 serial plasma samples were harvested. Caffeine concentration was measured via liquid chromatography-mass spectrometry (LC-MS), and those concentrations were assessed by non-compartmental pharmacokinetic analysis. The calculated mean pharmacokinetic parameters were analyzed statistically by one-way repeated measures analysis of variance (RM ANOVA). If differences were found, each group was compared to the other by all pair-wise multiple comparison.

resultsTwenty-four healthy subjects ranging in age from 18 to 30 completed the study. The mean caffeine concentration time profiles were similar with overlapping SDs at all measured time points. The ANOVA revealed significant differences in mean Cmax and Vd ss/F, but no pair-wise comparisons reached statistical significance. No other differences in pharmacokinetic parameters were found. DISCUSSION: The results of this study are consistent with previous caffeine pharmacokinetic studies and suggest that while rate of consumption, temperature of beverage and vehicle (coffee versus energy drink) may be associated with slightly different pharmacokinetic parameters, the overall impact of these variables is small.

conclusionThis study suggests that caffeine absorption and exposure from coffee and energy drink is similar irrespective of beverage temperature or rate of consumption.

Indexed as

CoffeeEnergy DrinksAdolescentAdultCaffeineCross-Over StudiesFemaleHumansMaleTemperatureYoung AdultCaffeineCoffeeCaffeinecoffeeenergy drinkspharmacokineticsrapid administration

Identifiers

PMID27100333
PMCPMC4898153
OpenAlexW2336330597

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.