Evidence map›Paper›PMID 39664781›Full record

ArticleLaryngoscope investigative otolaryngology2024

Higher expression of mir-31-5p is associated with reduced risk of head and neck keloid recurrence following surgical resection.

Albert M Levin, Oghenefejiro Okifo, Katherine Buhl, Takahiro Ouchi, Bianca Parker, Jessica Tan, Indrani Datta, Xiangguo Dai, Yalei Chen, Nallasivam Palanisamy and 11 more

Abstract read
In one paragraph

Article in Laryngoscope investigative otolaryngology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

21 authors.

Albert M LevinDepartment of Public Health Science Henry Ford Health Detroit Michigan USA.
Oghenefejiro OkifoDepartment of Otolaryngology Henry Ford Hospital Detroit Michigan USA.ORCID https://orcid.org/0000-0001-7794-944X
Katherine BuhlDepartment of Otolaryngology Henry Ford Hospital Detroit Michigan USA.
Takahiro OuchiDepartment of Otolaryngology Henry Ford Hospital Detroit Michigan USA.
Bianca ParkerDepartment of Otolaryngology Henry Ford Hospital Detroit Michigan USA.
Jessica TanDepartment of Otolaryngology Henry Ford Hospital Detroit Michigan USA.
Indrani DattaDepartment of Pathology Henry Ford Hospital Detroit Michigan USA.
Xiangguo DaiDepartment of Otolaryngology Henry Ford Hospital Detroit Michigan USA.
Yalei ChenDepartment of Public Health Science Henry Ford Health Detroit Michigan USA.
Nallasivam PalanisamyDepartment of Urology Henry Ford Hospital Detroit Michigan USA.
Jesse VeenstraDepartment of Dermatology Henry Ford Hospital Detroit Michigan USA.
Shannon CarskadonDepartment of Urology Henry Ford Hospital Detroit Michigan USA.
Jia LiDepartment of Public Health Science Henry Ford Health Detroit Michigan USA.
David OzogDepartment of Dermatology Henry Ford Hospital Detroit Michigan USA.
Christian E KellerDepartment of Pathology Henry Ford Hospital Detroit Michigan USA.ORCID https://orcid.org/0000-0002-0801-340X
Dhananjay ChitaleDepartment of Pathology Henry Ford Hospital Detroit Michigan USA.
Kevin R BobbittDepartment of Public Health Science Henry Ford Health Detroit Michigan USA.
Howard C CrawfordHenry Ford Cancer Institute Detroit Michigan USA.
Nina SteeleHenry Ford Cancer Institute Detroit Michigan USA.
Qing-Sheng MiDepartment of Dermatology Henry Ford Hospital Detroit Michigan USA.
Lamont R JonesDepartment of Otolaryngology Henry Ford Hospital Detroit Michigan USA.ORCID https://orcid.org/0000-0001-9638-232X

Funding

Characterization of Keloid Specific Exosomes and Determination of Exosomal Critical Signaling Pathways in the Keloid MicroenvironmentK08GM128156 · NIGMS · HENRY FORD HEALTH SYSTEM · PI JONES, LAMONT · 2018 to 2022
$894k
NIGMS NIH HHS K08 GM128156
6 · The paper itself

Abstract

Objective: In this study, we aimed to evaluate mir-31-5p as a prognostic biomarker of keloid disease (KD) recurrence using a retrospective, treatment naïve, surgical cohort of head and neck KD cases from Henry Ford Health. Methods: Using a tissue microarray, mir-31-5p expression was measured with miRNAscope, and mir-31-5p cell positivity was determined with QuPath. Logistic regression was used to test the association between mir-31-5p positive cells and KD recurrence at 1 year. In an independent dataset, associations between mir-31-5p and messenger RNA (mRNA) expression were assessed. Ingenuity Pathway Analysis identified target genes and pathways impacted by mir-31-5p. Results: Of the 58 KD patients, 42 (72%) received adjuvant triamcinolone injections, and 8 recurred (14%). mir-31-5p was expressed in 48 (83%) specimens. Increasing mir-31-5p expression was associated with decreased risk of recurrence ( Conclusion: Taken together, our data supports the association between mir-31-5p expression and KD recurrence. Its potential as a prognostic biomarker should be further investigated. Level of Evidence: Level 2.

Indexed as

biomarkerfibroproliferativein situ hybridizationkeloidmicroarraymicroRNA

Identifiers

PMID39664781
PMCPMC11632843

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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.