Evidence map›Paper›PMID 31561001›Full record

ArticleThe Journal of steroid biochemistry and molecular biology2019

Simultaneous quantification of estrogens and glucocorticoids in human adipose tissue by liquid-chromatography-tandem mass spectrometry.

Sofia Laforest, Mélissa Pelletier, Nina Denver, Brigitte Poirier, Sébastien Nguyen, Brian R Walker, Francine Durocher, Natalie Z M Homer, Caroline Diorio, André Tchernof and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of steroid biochemistry and molecular biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 29 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

11 authors at 3 institutions in 2 countries.

Sofia LaforestCHU de Québec-Université Laval Research Center (Endocrinology and Nephrology Division), School of Nutrition, Faculty of Agriculture and Food Sciences, Université Laval, Québec, Canada; Quebec Heart Lung Institute, Québec, Canada.
Mélissa PelletierCHU de Québec-Université Laval Research Center (Endocrinology and Nephrology Division), School of Nutrition, Faculty of Agriculture and Food Sciences, Université Laval, Québec, Canada; Quebec Heart Lung Institute, Québec, Canada.
Nina DenverMass Spectrometry Core, Edinburgh Clinical Research Facility, Queen's Medical Research Institute, Edinburgh, United Kingdom; Institute of Cardiovascular and Medical Sciences, College of Medical, Veterinary and Life Sciences, University of Glasgow, University Avenue, Glasgow, United Kingdom; Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Cathedral Street, Glasgow, United Kingdom.
Brigitte PoirierCHU de Québec-Université Laval Research Center (Oncology Division), Université Laval Cancer Research Center and Department of Surgery, Faculty of Medicine, Université Laval, Québec, Canada; Centre des maladies du sein Deschênes-Fabia, Hôpital Saint-Sacrement, Québec, Canada.
Sébastien NguyenCHU de Québec-Université Laval Research Center (Oncology Division), Université Laval Cancer Research Center and Department of Surgery, Faculty of Medicine, Université Laval, Québec, Canada.
Brian R WalkerUniversity/BHF Centre for Cardiovascular Science, Queen's Medical Research Institute, University of Edinburgh, 47, Little France Crescent, Edinburgh, EH16 4TJ, UK; Newcastle University, Newcastle upon Tyne, NE1 7RU, UK.
Francine DurocherCHU de Québec-Université Laval Research Center (Endocrinology and Nephrology Division), Université Laval Cancer Research Center and Department of Molecular Medicine, Faculty of Medicine, Université Laval, Québec, Canada.
Natalie Z M HomerMass Spectrometry Core, Edinburgh Clinical Research Facility, Queen's Medical Research Institute, Edinburgh, United Kingdom; University/BHF Centre for Cardiovascular Science, Queen's Medical Research Institute, University of Edinburgh, 47, Little France Crescent, Edinburgh, EH16 4TJ, UK.
Caroline DiorioCentre des maladies du sein Deschênes-Fabia, Hôpital Saint-Sacrement, Québec, Canada; CHU de Québec-Université Laval Research Center (Oncology Division), Université Laval Cancer Research Center and Department of Social and Preventive Medicine, Faculty of Medicine, Université Laval, Québec, Canada.
André TchernofCHU de Québec-Université Laval Research Center (Endocrinology and Nephrology Division), School of Nutrition, Faculty of Agriculture and Food Sciences, Université Laval, Québec, Canada; Quebec Heart Lung Institute, Québec, Canada.
Ruth AndrewMass Spectrometry Core, Edinburgh Clinical Research Facility, Queen's Medical Research Institute, Edinburgh, United Kingdom; University/BHF Centre for Cardiovascular Science, Queen's Medical Research Institute, University of Edinburgh, 47, Little France Crescent, Edinburgh, EH16 4TJ, UK. Electronic address: ruth.andrew@ed.ac.uk.
Université Laval · CAThe Queen's Medical Research Institute · GBMontreal Heart Institute · CA

Funding

Biotechnology and Biological Sciences Research Council BB/N503691/1Medical Research Council MC_PC_12014
6 · The paper itself

Abstract

The presence of estrogens, androgens and glucocorticoids as well as their receptors and steroid converting enzymes in adipose tissue has been established. Their contribution to diseases such as obesity, diabetes and hormone-dependent cancers is an active area of research. Our objective was to develop a LC-MS/MS method to quantify bioactive estrogens and glucocorticoids simultaneously in human adipose tissue. Estrogens and glucocorticoids were extracted from adipose tissue samples using solid-phase extraction. Estrogens were derivatized using 1-(2,4-dinitro-5-fluorophenyl)-4-methylpiperazine (PPZ) and methyl iodide to generate a permanently charged molecule (MPPZ). Steroids were separated and quantified by LC-MS/MS. The limit of quantitation for the steroids was between 15 and 100 pg per sample. Accuracy and precision were acceptable (<20%). Using this method, estradiol, estrone, cortisone and cortisol were quantified in adipose tissue from women with and without breast cancer. This novel assay of estrogens and glucocorticoids by LC-MS/MS coupled with derivatization allowed simultaneous quantification of a panel of steroids in human adipose tissue across the endogenous range of concentrations encountered in health and disease.

Indexed as

Adipose TissueBreast NeoplasmsChromatography, LiquidCortisoneEstradiolEstrogensEstroneFemaleGlucocorticoidsHumansHydrocortisoneSpectrometry, Mass, Electrospray IonizationTandem Mass SpectrometryCortisoneEstradiolEstrogensEstroneGlucocorticoidsHydrocortisoneAdiposeCortisolCortisoneDerivatizationEstradiolEstrone

Identifiers

PMID31561001
PMCPMC7099401
OpenAlexW2974723071

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.