Evidence map›Paper›PMID 36979801›Full record

ArticleBiomedicines2023

Dysregulation of Serum MicroRNA after Intracerebral Hemorrhage in Aged Mice.

Dominic Robles, De-Huang Guo, Noah Watson, Diana Asante, Sangeetha Sukumari-Ramesh

Open access · goldFull text read
In one paragraph

Article in Biomedicines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. MiRNA Dysregulation in Brain Injury: AnCurrent neuropharmacology · 2025
    Article
  4. Article
  5. Article
  6. Review
  7. Article
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

5 authors at 1 institution in 1 country.

Dominic RoblesDepartment of Pharmacology and Toxicology, Medical College of Georgia, Augusta University, 1120 15th Street, CB3618, 30912 Augusta, Georgia.ORCID 0000-0001-5608-6075
De-Huang GuoDepartment of Pharmacology and Toxicology, Medical College of Georgia, Augusta University, 1120 15th Street, CB3618, 30912 Augusta, Georgia.
Noah WatsonDepartment of Pharmacology and Toxicology, Medical College of Georgia, Augusta University, 1120 15th Street, CB3618, 30912 Augusta, Georgia.
Diana AsanteDepartment of Pharmacology and Toxicology, Medical College of Georgia, Augusta University, 1120 15th Street, CB3618, 30912 Augusta, Georgia.
Sangeetha Sukumari-RameshDepartment of Pharmacology and Toxicology, Medical College of Georgia, Augusta University, 1120 15th Street, CB3618, 30912 Augusta, Georgia.
Augusta University · US

Funding

The Translocator Protein (TSPO) and Intracerebral HemorrhageR01NS107853 · NINDS · AUGUSTA UNIVERSITY · PI SUKUMARI-RAMESH, SANGEETHA · 2018 to 2021
$1.3M
Quantitative proteomic analysis of the aging brain after intracerebral hemorrhageR03AG077460 · NIA · AUGUSTA UNIVERSITY · PI SUKUMARI-RAMESH, SANGEETHA · 2022 to 2023
$154k
NIA NIH HHS R03 AG077460NIH HHS R01NS107853, R03AG077460NINDS NIH HHS R01 NS107853
6 · The paper itself

Abstract

Stroke is one of the most common diseases that leads to brain injury and mortality in patients, and intracerebral hemorrhage (ICH) is the most devastating subtype of stroke. Though the prevalence of ICH increases with aging, the effect of aging on the pathophysiology of ICH remains largely understudied. Moreover, there is no effective treatment for ICH. Recent studies have demonstrated the potential of circulating microRNAs as non-invasive diagnostic and prognostic biomarkers in various pathological conditions. While many studies have identified microRNAs that play roles in the pathophysiology of brain injury, few demonstrated their functions and roles after ICH. Given this significant knowledge gap, the present study aims to identify microRNAs that could serve as potential biomarkers of ICH in the elderly. To this end, sham or ICH was induced in aged C57BL/6 mice (18-24 months), and 24 h post-ICH, serum microRNAs were isolated, and expressions were analyzed. We identified 28 significantly dysregulated microRNAs between ICH and sham groups, suggesting their potential to serve as blood biomarkers of acute ICH. Among those microRNAs, based on the current literature, miR-124-3p, miR-137-5p, miR-138-5p, miR-219a-2-3p, miR-135a-5p, miR-541-5p, and miR-770-3p may serve as the most promising blood biomarker candidates of ICH, warranting further investigation.

Indexed as

agingintracerebral hemorrhagemicroRNA

Identifiers

PMID36979801
PMCPMC10044892
OpenAlexW4323663592

What Socratic holds

Textfull text, public
LicenceCC BY
measurements read31
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.