Evidence map›Paper›PMID 36471785›Full record

ArticleNature aging2022

Landscape of somatic mutations in aging human heart muscle cells.

Abstract readComment
In one paragraph

Article in Nature aging, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. SomaticExperimental and therapeutic medicine · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

0 authors.

Funding

Single cell, whole genome analysis of the aging human cardiomyocyte Diversity SupplementR01HL152063 · NHLBI · BOSTON CHILDREN'S HOSPITAL · PI CHOUDHURY, SANGITA · 2021 to 2025
$4.3M
NHLBI NIH HHS R01 HL152063
6 · The paper itself

Abstract

Using single-cell whole-genome sequencing, we identified and characterized the landscape of somatic single-nucleotide variants (sSNVs) in single cardiomyocytes from individuals across the human lifespan. Aged cardiomyocytes were found to have a higher burden of sSNVs and show mutational signatures that suggest failed repair of oxidative DNA damage.

Indexed as

AgingMyocytes, CardiacAgedDNA DamageHumansMutationOxidative Stress

Identifiers

PMID36471785
PMCPMC9719721

What OpenQuestion holds

Textmetadata
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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.