Evidence map›Paper›PMID 38409164›Full record

ArticleNature communications2024

Targeting HDAC6 to treat heart failure with preserved ejection fraction in mice.

Sara Ranjbarvaziri, Aliya Zeng, Iris Wu, Amara Greer-Short, Farshad Farshidfar, Ana Budan, Emma Xu, Reva Shenwai, Matthew Kozubov, Cindy Li and 9 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
16.5field-weighted citation impact, top 1% 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

41 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
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  8. Nuclear Proteome Map of Mouse Heart Chambers.Molecular & cellular proteomics : MCP · 2026
    Article
  9. Article
  10. Article
  11. Cardiac epigenome in heart development and disease.Nature reviews. Cardiology · 2026
    Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Normal cardiac lymphatics and their mimics.American journal of physiology. Heart and circulatory physiology · 2026
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 1 institution in 1 country.

Sara Ranjbarvaziri *Tenaya Therapeutics, South San Francisco, CA, USA.
Aliya Zeng *Tenaya Therapeutics, South San Francisco, CA, USA.
Iris WuTenaya Therapeutics, South San Francisco, CA, USA.ORCID 0000-0001-7515-4766
Amara Greer-ShortTenaya Therapeutics, South San Francisco, CA, USA.
Farshad FarshidfarTenaya Therapeutics, South San Francisco, CA, USA.
Ana BudanTenaya Therapeutics, South San Francisco, CA, USA.
Emma XuTenaya Therapeutics, South San Francisco, CA, USA.
Reva ShenwaiTenaya Therapeutics, South San Francisco, CA, USA.
Matthew KozubovTenaya Therapeutics, South San Francisco, CA, USA.
Cindy LiTenaya Therapeutics, South San Francisco, CA, USA.
Melissa Van PellTenaya Therapeutics, South San Francisco, CA, USA.
Francis GraftonTenaya Therapeutics, South San Francisco, CA, USA.
Charles E MacKayTenaya Therapeutics, South San Francisco, CA, USA.
Xiaomei SongTenaya Therapeutics, South San Francisco, CA, USA.
James R PriestTenaya Therapeutics, South San Francisco, CA, USA.
Gretchen ArgastTenaya Therapeutics, South San Francisco, CA, USA.
Mohammad A MandegarTenaya Therapeutics, South San Francisco, CA, USA.
Timothy HoeyTenaya Therapeutics, South San Francisco, CA, USA.
Jin YangTenaya Therapeutics, South San Francisco, CA, USA. flairjinyang@gmail.com.ORCID 0000-0001-8985-1319
Rapt Therapeutics (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heart failure with preserved ejection fraction (HFpEF) poses therapeutic challenges due to the limited treatment options. Building upon our previous research that demonstrates the efficacy of histone deacetylase 6 (HDAC6) inhibition in a genetic cardiomyopathy model, we investigate HDAC6's role in HFpEF due to their shared mechanisms of inflammation and metabolism. Here, we show that inhibiting HDAC6 with TYA-018 effectively reverses established heart failure and its associated symptoms in male HFpEF mouse models. Additionally, in male mice lacking Hdac6 gene, HFpEF progression is delayed and they are resistant to TYA-018's effects. The efficacy of TYA-018 is comparable to a sodium-glucose cotransporter 2 (SGLT2) inhibitor, and the combination shows enhanced effects. Mechanistically, TYA-018 restores gene expression related to hypertrophy, fibrosis, and mitochondrial energy production in HFpEF heart tissues. Furthermore, TYA-018 also inhibits activation of human cardiac fibroblasts and enhances mitochondrial respiratory capacity in cardiomyocytes. In this work, our findings show that HDAC6 impacts on heart pathophysiology and is a promising target for HFpEF treatment.

Indexed as

CardiomyopathiesHeart FailureAnimalsHistone Deacetylase 6HumansMaleMiceMyocytes, CardiacStroke VolumeHDAC6 protein, humanHdac6 protein, mouseHistone Deacetylase 6

Identifiers

PMID38409164
PMCPMC10897156
OpenAlexW4392157832

What Socratic 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 Socratic graph.