Evidence map›Paper›PMID 27226402›Full record

ArticleNMR in biomedicine2016

Functional and anatomical characterization of brown adipose tissue in heart failure with blood oxygen level dependent magnetic resonance.

Marcello Panagia, Yin-Ching Iris Chen, Howard H Chen, Laura Ernande, Chan Chen, Wei Chao, Kenneth Kwong, Marielle Scherrer-Crosbie, David E Sosnovik

Open access · greenAbstract read
In one paragraph

Article in NMR in biomedicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Molecular Imaging of Brown Adipose Tissue Mass.International journal of molecular sciences · 2021
    Review
  8. Review
  9. Article
  10. Review
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

9 authors at 3 institutions in 2 countries.

Marcello PanagiaCardiology Section, Boston Medical Center, Boston, MA, USA.
Yin-Ching Iris ChenMartinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Boston, MA, USA.
Howard H ChenMartinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Boston, MA, USA.
Laura ErnandeCardiology Division, Massachusetts General Hospital, Boston, MA, USA.
Chan ChenDepartment of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Wei ChaoDepartment of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Kenneth KwongMartinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Boston, MA, USA.
Marielle Scherrer-CrosbieCardiology Division, Massachusetts General Hospital, Boston, MA, USA.
David E SosnovikCardiology Division, Massachusetts General Hospital, Boston, MA, USA.
Massachusetts General Hospital · USBoston Medical Center · USHarvard University · US

Funding

ULTRAHIGH FIELD TECHNOLOGY FOR FUNCTIONAL IMAGINGP41RR014075 · NCRR · MASSACHUSETTS GENERAL HOSPITAL · PI WALD, LAWRENCE L · 1999 to 2011
$16.4M
Cardiac MRI-Tractography In Vivo: Integrated Imaging of Structure and FunctionR01HL112831 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI SOSNOVIK, DAVID E · 2013 to 2016
$3.0M
Molecular and Microstructural Imaging of Cardiomyocyte Apoptosis and AutophagyR01HL093038 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI SOSNOVIK, DAVID E · 2008 to 2012
$2.2M
Role of TLR-cfB Signaling in SepsisR01GM097259 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE · PI CHAO, WEI · 2012 to 2015
$1.9M
Role of Toll-like Receptor 4 (TLR4) in Ischemic Myocardial InjuryR01GM080906 · NIGMS · MASSACHUSETTS GENERAL HOSPITAL · PI CHAO, WEI · 2007 to 2011
$1.6M
Multiplexed Imaging of Energy Metabolism in Murine Models of Heart FailureK08HL123744 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI PANAGIA, MARCELLO · 2014 to 2018
$767k
Multiplexed Molecular Imaging of Cell Death PathwaysR00HL121152 · NHLBI · TUFTS MEDICAL CENTER · PI CHEN, HOWARD H. · 2017 to 2019
$747k
Detection of Brown Adipose Tissue Using Contrast UltrasoundR21DK092909 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI SCHERRER-CROSBIE, MARIELLE · 2011 to 2012
$450k
Multiplexed Molecular Imaging of Cell Death PathwaysK99HL121152 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI CHEN, HOWARD H. · 2014 to 2015
$298k
NCRR NIH HHS P41 RR014075NHLBI NIH HHS K08 HL123744NHLBI NIH HHS K99 HL121152NHLBI NIH HHS R00 HL121152NHLBI NIH HHS R01 HL093038NHLBI NIH HHS R01 HL112831NIDDK NIH HHS R21 DK092909NIGMS NIH HHS R01 GM080906NIGMS NIH HHS R01 GM097259
6 · The paper itself

Abstract

Recent studies have suggested that brown adipose tissue (BAT) plays an important role in obesity, insulin resistance and heart failure. The characterization of BAT in vivo, however, has been challenging. No technique to comprehensively image BAT anatomy and function has been described. Moreover, the impact on BAT of the neuroendocrine activation seen in heart failure has only recently begun to be evaluated in vivo. The aim of this study was to use MRI to characterize the impact of heart failure on the morphology and function of BAT. Mice subjected to permanent ligation of the left coronary artery were imaged with MRI 6 weeks later. T2 weighted MRI of BAT volume and blood oxygen level dependent MRI of BAT function were performed. T2 * maps of BAT were obtained at multiple time points before and after administration of the β3 adrenergic agonist CL 316 243 (CL). Blood flow to BAT was studied after CL injection using the flow alternating inversion recovery (FAIR) approach. Excised BAT tissue was analyzed for lipid droplet content and for uncoupling protein 1 (UCP1) mRNA expression. BAT volume was significantly lower in heart failure (51 ± 1 mm(3) versus 65 ± 3 mm(3) ; p < 0.05), and characterized by a reduction in lipid globules and a fourfold increase in UCP1 mRNA (p < 0.05). CL injection increased BAT T2 * in healthy animals but not in mice with heart failure (24 ± 4% versus 6 ± 2%; p < 0.01), consistent with an increase in flow in control BAT. This was confirmed by a significant difference in the FAIR response in BAT in control and heart failure mice. Heart failure results in the chronic activation of BAT, decreased BAT lipid stores and decreased BAT volume, and it is associated with a marked decrease in ability to respond to acute physiological stimuli. This may have important implications for substrate utilization and overall metabolic homeostasis in heart failure. Copyright © 2016 John Wiley & Sons, Ltd.

Indexed as

Adipose Tissue, BrownAnimalsCardiac Imaging TechniquesFemaleHeart FailureLipid DropletsMagnetic Resonance ImagingMaleMiceMice, Inbred C57BLOximetryOxygenOxygenBOLDbrown adipose tissueheart failureMRI

Identifiers

PMID27226402
PMCPMC4912044
OpenAlexW2395667525

What OpenQuestion holds

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Registered trials

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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.