Evidence map›Paper›PMID 34805366›Full record

ReviewAnnals of translational medicine2021

Mitochondrial bioenergetics and D-ribose in HFpEF: a brief narrative review.

Kathryn J Krueger, Faith K Rahman, Qiuhua Shen, James Vacek, John B Hiebert, Janet D Pierce

Open access · diamondAbstract readReview
In one paragraph

Review in Annals of translational medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 12 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

6 authors at 2 institutions in 1 country.

Kathryn J KruegerSchool of Nursing, University of Kansas Medical Center, Kansas City, KS, USA.
Faith K RahmanSchool of Nursing, University of Kansas Medical Center, Kansas City, KS, USA.
Qiuhua ShenSchool of Nursing, University of Kansas Medical Center, Kansas City, KS, USA.
James VacekThe University of Kansas Health System, Kansas City, KS, USA.
John B HiebertSchool of Nursing, University of Kansas Medical Center, Kansas City, KS, USA.
Janet D PierceSchool of Nursing, University of Kansas Medical Center, Kansas City, KS, USA.
University of Kansas Medical Center · USUniversity of Kansas · US

Funding

Reducing symptom burden in patients with heart failure with preserved ejection fraction using ubiquinol and/or D-riboseR01AG054486 · NIA · UNIVERSITY OF KANSAS MEDICAL CENTER · PI PIERCE, JANET DOREEN · 2017 to 2019
$1.7M
NIA NIH HHS R01 AG054486
6 · The paper itself

Abstract

objectiveIn this review article, we briefly describe the status of treatment options for HFpEF and the role of mitochondrial dysfunction in the pathogenesis of HFpEF as an alternative therapeutic target. We also examine the mechanisms of D-ribose in cellular energy production and discuss the potential disadvantages and benefits of supplemental use of D-ribose in patients with HFpEF.

backgroundHeart failure is a major cardiovascular disease that impacts over 6 million Americans and is one of the leading causes for morbidity and mortality. Patients with heart failure often experience shortness of breath and fatigue along with impaired physical capacity, all leading to poor quality of life. As a subtype of heart failure, heart failure with preserved ejection fraction (HFpEF) is characterized with impaired diastolic function. Currently, there are no effective treatments specifically for HFpEF, thus clinicians and researchers are searching for therapies to improve cardiac function. Emerging evidence indicate that mitochondrial dysfunction and impaired cardiac bioenergetics are among the underlying mechanisms for HFpEF. There is increased interest in investigating the use of supplements such as D-ribose to enhance mitochondrial function and improve production of adenosine triphosphate (ATP).

methodsFor this narrative review, more than 100 relevant scientific articles were considered from various databases (e.g., PubMed, Web of Science, CINAHL, and Google Scholar) using the keywords "Heart Failure", "HFpEF", "D-ribose", "ATP", "Mitochondria", Bioenergetics", and "Cellular Respiration".

conclusionsIt is essential to find potential targeted therapeutic treatments for HFpEF. Since there is evidence that the HFpEF is related to impaired myocardial bioenergetics, enhancing mitochondrial function could augment cardiac function. Using a supplement such as D-ribose could improve mitochondrial function by increasing ATP and enhancing cardiac performance for patients with HFpEF. There is a recently completed clinical trial with HFpEF patients that indicates D-ribose increases ATP production and improves cardiac ejection fraction.

Indexed as

adenosine triphosphateD-riboseHeart failure with preserved ejection fraction (HFpEF)mitochondria

Identifiers

PMID34805366
PMCPMC8573443
OpenAlexW3198927193

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.