Evidence map›Paper›PMID 26858998›Full record

ArticleThe Analyst2016

Quantification of cortisol in human eccrine sweat by liquid chromatography - tandem mass spectrometry.

Min Jia, Wade M Chew, Yelena Feinstein, Perry Skeath, Esther M Sternberg

Open access · hybridAbstract read
In one paragraph

Article in The Analyst, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.0field-weighted citation impact, top 16% 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

37 citing papers in PubMed, 106 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Min JiaArizona Center for Integrative Medicine, College of Medicine, the University of Arizona, Tucson, AZ 85724, USA. mjia@email.arizona.edu esternberg@email.arizona.edu.
Wade M ChewArizona Cancer Center, The University of Arizona, Tucson, AZ 85724, USA.
Yelena FeinsteinCenter for Toxicology, College of Pharmacy, The University of Arizona, Tucson, AZ 85724, USA.
Perry SkeathArizona Center for Integrative Medicine, College of Medicine, the University of Arizona, Tucson, AZ 85724, USA. mjia@email.arizona.edu esternberg@email.arizona.edu.
Esther M SternbergArizona Center for Integrative Medicine, College of Medicine, the University of Arizona, Tucson, AZ 85724, USA. mjia@email.arizona.edu esternberg@email.arizona.edu.
University of Arizona · US

Funding

VITAMIN AP30CA023074 · NCI · UNIVERSITY OF ARIZONA · PI Dan Theodorescu · 1985 to 2026
$110.2M
SOUTHWEST ENVIRONMENTAL HEALTH SCIENCES CENTERP30ES006694 · NIEHS · UNIVERSITY OF ARIZONA · PI DEAN BILLHEIMER · 1994 to 2026
$36.7M
AB 4000 QTRAP MASS SPECTROMETER: PLANT SCIENCESS10RR022384 · NCRR · UNIVERSITY OF ARIZONA · PI TSAPRAILIS, GEORGE · 2006 to 2006
$357k
NCI NIH HHS CA023074NCI NIH HHS P30 CA023074NCRR NIH HHS 1S10RR022384-01NCRR NIH HHS S10 RR022384NIEHS NIH HHS ES06694NIEHS NIH HHS P30 ES006694
6 · The paper itself

Abstract

Cortisol has long been recognized as the "stress biomarker" in evaluating stress related disorders. Plasma, urine or saliva are the current source for cortisol analysis. The sampling of these biofluids is either invasive or has reliability problems that could lead to inaccurate results. Sweat has drawn increasing attention as a promising source for non-invasive stress analysis. A sensitive HPLC-MS/MS method was developed for the quantitation of cortisol ((11β)-11,17,21-trihydroxypregn-4-ene-3,20-dione) in human eccrine sweat. At least one unknown isomer that has previously not been reported and could potentially interfere with quantification was separated from cortisol with mixed mode RP HPLC. Detection of cortisol was carried out using atmospheric pressure chemical ionization (APCI) and selected reaction monitoring (SRM) in positive ion mode, using cortisol-9,11,12,12-D4 as internal standard. LOD and LOQ were estimated to be 0.04 ng ml(-1) and 0.1 ng ml(-1), respectively. Linear range of 0.10-25.00 ng ml(-1) was obtained. Intraday precision (2.5%-9.7%) and accuracy (0.5%-2.1%), interday precision (12.3%-18.7%) and accuracy (7.1%-15.1%) were achieved. This method has been successfully applied to the cortisol analysis of human eccrine sweat samples. This is the first demonstration that HPLC-MS/MS can be used for the sensitive and highly specific determination of cortisol in human eccrine sweat in the presence of at least one isomer that has similar hydrophobicity as cortisol. This study demonstrated that human eccrine sweat could be used as a promising source for non-invasive assessment of stress biomarkers such as cortisol and other steroid hormones.

Indexed as

Analytic Sample Preparation MethodsChromatography, High Pressure LiquidClinical Chemistry TestsExocrine GlandsHumansHydrocortisoneReproducibility of ResultsSweatTandem Mass SpectrometryTime FactorsHydrocortisone

Identifiers

PMID26858998
PMCPMC5376102
OpenAlexW2260554414

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.