Evidence map›Paper›PMID 33911618›Full record

ArticleAnnals of dermatology2019

Polydeoxyribonucleotides Improve Diabetic Wound Healing in Mouse Animal Model for Experimental Validation.

Tae-Rin Kwon, Sung Won Han, Jong Hwan Kim, Byung Chul Lee, Jae Min Kim, Ji Yeon Hong, Beom Joon Kim

Open access · hybridAbstract read
In one paragraph

Article in Annals of dermatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 17% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 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

7 authors at 1 institution in 1 country.

Tae-Rin KwonDepartment of Dermatology, Chung-Ang University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-9892-7714
Sung Won HanDepartment of Dermatology, Chung-Ang University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-0040-3542
Jong Hwan KimDepartment of Medicine, Graduate School, Chung-Ang University, Seoul, Korea.ORCID https://orcid.org/0000-0001-6201-9602
Byung Chul LeeDepartment of Dermatology, Chung-Ang University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-6858-4853
Jae Min KimDepartment of Dermatology, Chung-Ang University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-7333-3883
Ji Yeon HongDepartment of Dermatology, Chung-Ang University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-5632-8449
Beom Joon KimDepartment of Dermatology, Chung-Ang University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-2320-7621
Chung-Ang University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWound healing mechanisms is believed to have effects similar to wound healing disorders in diabetic patients, including abnormal inflammatory cells, angiogenesis disorders, and reduced collagen synthesis. Therefore, reestablishment of structural and promoted angiogenesis could be beneficial to promote wound healing process.

objectiveTherefore, we investigated whether the polydeoxyribonucleotide (PDRN) that was self-production in Korea, could be useful as an intradermal injection for promoting wound healing. Also, we validate for wound healing effect of PDRN using healing-impaired (db/db) mice.

methodsIn this study, we confirmed the effects of PDRN by creating wound models in

resultsTime course observations revealed that mice treated with PDRN showed accelerated wound closure and epidermal and dermal regeneration, enhanced angiogenesis. The wound area and depth decreased at 3, 6, 9, and 12 days after skin injury. Histological evaluation showed an increase of vascular endothelial growth factor, CD31, and collagen fibers in the PDRN group compared with the control group, indicating that PDRN was effective in the treatment of delayed wound healing caused by diabetes.

conclusionThis study suggests that our PDRN has a wound healing effect in transgenic animal models with cells and diabetes through angiogenesis.

Indexed as

CD31Diabetes mouse modelPolyribonucleotideVascular endothelial growth factor AWound healing

Identifiers

PMID33911618
PMCPMC7992745
OpenAlexW2956669871

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.