Evidence map›Paper›PMID 30225964›Full record

ArticleDiabetes, obesity & metabolism2019

Empagliflozin reduces myocardial ketone utilization while preserving glucose utilization in diabetic hypertensive heart disease: A hyperpolarized

Desiree Abdurrachim, Xing Qi Teo, Chern Chiuh Woo, Wei Xin Chan, Janise Lalic, Carolyn S P Lam, Philip Teck Hock Lee

Abstract read
In one paragraph

Article in Diabetes, obesity & metabolism, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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, 1 synthesis or guideline pooled it.

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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

7 authors.

Desiree AbdurrachimSingapore Bioimaging Consortium, Agency for Science, Technology and Research, Singapore.
Xing Qi TeoSingapore Bioimaging Consortium, Agency for Science, Technology and Research, Singapore.
Chern Chiuh WooSingapore Bioimaging Consortium, Agency for Science, Technology and Research, Singapore.
Wei Xin ChanSingapore Bioimaging Consortium, Agency for Science, Technology and Research, Singapore.
Janise LalicSingapore Bioimaging Consortium, Agency for Science, Technology and Research, Singapore.
Carolyn S P LamSingapore Bioimaging Consortium, Agency for Science, Technology and Research, Singapore.
Philip Teck Hock LeeSingapore Bioimaging Consortium, Agency for Science, Technology and Research, Singapore.ORCID 0000-0002-4885-5994

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo investigate the effects of the sodium-glucose co-transporter-2 inhibitor empagliflozin on myocardial ketone body utilization in diabetic, obese rats with spontaneously hypertensive heart failure (SHHF), after 6 months of treatment. MATERIALS AND

methodsMyocardial ketone body utilization was measured in vivo real time using a novel ketone probe (hyperpolarized [3-

resultsAt baseline, myocardial ketone and glucose utilization were both higher in SHHF compared with control rats. Six months of empagliflozin treatment in SHHF rats was associated with less obesity, lower blood pressure, reduced blood glucose and insulin levels, and increased fasting blood β-hydroxybutyrate levels, as expected. Contrary to the hypothesis, myocardial ketone body utilization was lower in empagliflozin-treated SHHF rats, while glucose utilization and cardiac function were unaltered and hepatic congestion was reduced, compared with vehicle-treated SHHF rats.

conclusionsIn diabetic hypertensive heart disease, empagliflozin reduces afterload without altering myocardial function and glucose utilization in the face of falling blood glucose levels, but does not enhance myocardial ketone utilization despite increased circulating levels.

Indexed as

Carbon-13 Magnetic Resonance SpectroscopyDiabetes Mellitus, ExperimentalAnimalsBenzhydryl CompoundsBlood PressureDiabetic AngiopathiesGlucoseGlucosidesHeartKetonesMaleMyocardiumObesityRatsRats, Inbred SHRRats, Sprague-DawleyBenzhydryl CompoundsempagliflozinGlucoseGlucosidesKetonesanimal pharmacologycardiovascular diseasediabetes complicationsempagliflozinexperimental pharmacologyglucose metabolism

Identifiers

PMID30225964
PMCPMC6587455

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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.