Evidence map›Paper›PMID 24065618›Full record

ArticleJournal of cardiovascular translational research2013

Evaluation of docosahexaenoic acid in a dog model of hypertension induced left ventricular hypertrophy.

William C Stanley, James W Cox, Girma Asemu, Kelly A O'Connell, Erinne R Dabkowski, Wenhong Xu, Eduardo Hertel Ribeiro, Kadambari C Shekar, Stephen W Hoag, Sharad Rastogi and 3 more

Abstract read
In one paragraph

Article in Journal of cardiovascular translational research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.2field-weighted citation impact, top 41% 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

5 citing papers in PubMed, 9 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

13 authors at 6 institutions in 3 countries.

William C StanleyDiscipline of Physiology, University of Sydney, Anderson Stuart Building (F13), Sydney, NSW, 2006, Australia. wstanley@usyd.edu.au.
James W CoxDivision of Cardiology, Department of Medicine, University of Maryland, Baltimore, MD, USA.
Girma AsemuDivision of Cardiology, Department of Medicine, University of Maryland, Baltimore, MD, USA.
Kelly A O'ConnellDivision of Cardiology, Department of Medicine, University of Maryland, Baltimore, MD, USA.
Erinne R DabkowskiDivision of Cardiology, Department of Medicine, University of Maryland, Baltimore, MD, USA.
Wenhong XuDivision of Cardiology, Department of Medicine, University of Maryland, Baltimore, MD, USA.
Eduardo Hertel RibeiroDivision of Cardiology, Department of Medicine, University of Maryland, Baltimore, MD, USA.
Kadambari C ShekarDivision of Cardiology, Department of Medicine, University of Maryland, Baltimore, MD, USA.
Stephen W HoagDepartment of Pharmaceutical Sciences, School of Pharmacy, University of Maryland, Baltimore, MD, USA.
Sharad RastogiDepartment of Medicine, Division of Cardiovascular Medicine, Henry Ford Health System, Detroit, MI, USA.
Hani N SabbahDepartment of Medicine, Division of Cardiovascular Medicine, Henry Ford Health System, Detroit, MI, USA.
Caroline DaneaultDepartment of Nutrition and Montreal Heart Institute, Université de Montréal, Montreal, QC, Canada.
Christine des RosiersDepartment of Nutrition and Montreal Heart Institute, Université de Montréal, Montreal, QC, Canada.
University of Maryland, Baltimore · USUniversity of Maryland, College Park · USHenry Ford Health System · USMontreal Heart Institute · CAUniversité de Montréal · CAUniversity of Sydney · AU

Funding

Substrate Selection and Oxidative Stress in Heart FailureP01HL074237 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI STANLEY, WILLIAM C · 2003 to 2013
$19.9M
Interdisciplinary Training Program Muscle BiologyT32AR007592 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI Aikaterini Kontrogianni-Konstantopoulos · 1996 to 2026
$11.7M
Docosahexaenoic Acid, Mitochondrial Dysfunction and Cardiac Reperfusion InjuryR21HL110731 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI STANLEY, WILLIAM C · 2011 to 2012
$422k
NHLBI NIH HHS HL074237NHLBI NIH HHS HL110731NHLBI NIH HHS P01 HL074237NHLBI NIH HHS R21 HL110731NIAMS NIH HHS T32 AR007592
6 · The paper itself

Abstract

Marine n-3 polyunsaturated fatty acids alter cardiac phospholipids and prevent cardiac pathology in rodents subjected to pressure overload. This approach has not been evaluated in humans or large animals with hypertension-induced pathological hypertrophy. We evaluated docosahexaenoic acid (DHA) in old female dogs with hypertension caused by 16 weeks of aldosterone infusion. Aldosterone-induced hypertension resulted in concentric left ventricular (LV) hypertrophy and impaired diastolic function in placebo-treated dogs. DHA supplementation increased DHA and depleted arachidonic acid in cardiac phospholipids, but did not improve LV parameters compared to placebo. Surprisingly, DHA significantly increased serum aldosterone concentration and blood pressure compared to placebo. Cardiac mitochondrial yield was decreased in placebo-treated hypertensive dogs compared to normal animals, which was prevented by DHA. Extensive analysis of mitochondrial function found no differences between DHA and placebo groups. In conclusion, DHA did not favorably impact mitochondrial or LV function in aldosterone hypertensive dogs.

Indexed as

AldosteroneAnimalsArachidonic AcidBlood PressureDisease Models, AnimalDocosahexaenoic AcidsDogsFemaleFibrosisHypertensionHypertrophy, Left VentricularMitochondria, HeartMyocardiumPhospholipidsTime FactorsVentricular Function, LeftAldosteroneArachidonic AcidDocosahexaenoic AcidsPhospholipids

Identifiers

PMID24065618
PMCPMC4793776
OpenAlexW2032102473

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.