Evidence map›Paper›PMID 31554182›Full record

ArticleCells2019

Potential Roles of Adiponectin Isoforms in Human Obesity with Delayed Wound Healing.

Jiyoon Ryu, Colleen A Loza, Huan Xu, Min Zhou, Jason T Hadley, Jielei Wu, Huayu You, Huaiqing Wang, Jihong Yang, Juli Bai and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. 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

13 authors at 2 institutions in 1 country.

Jiyoon RyuDepartment of Cell Systems & Anatomy, University of Texas Health Science Center, San Antonio, TX 78229-3900, USA. Ryuj@uthscsa.edu.ORCID 0000-0001-7365-0555
Colleen A LozaDepartment of Cell Systems & Anatomy, University of Texas Health Science Center, San Antonio, TX 78229-3900, USA.
Huan XuDepartment of Cell Systems & Anatomy, University of Texas Health Science Center, San Antonio, TX 78229-3900, USA.
Min ZhouDepartment of Cell Systems & Anatomy, University of Texas Health Science Center, San Antonio, TX 78229-3900, USA.
Jason T HadleyDepartment of Cell Systems & Anatomy, University of Texas Health Science Center, San Antonio, TX 78229-3900, USA.
Jielei WuDepartment of Cell Systems & Anatomy, University of Texas Health Science Center, San Antonio, TX 78229-3900, USA.
Huayu YouDepartment of Cell Systems & Anatomy, University of Texas Health Science Center, San Antonio, TX 78229-3900, USA.
Huaiqing WangDepartment of Cell Systems & Anatomy, University of Texas Health Science Center, San Antonio, TX 78229-3900, USA.
Jihong YangDepartment of Cell Systems & Anatomy, University of Texas Health Science Center, San Antonio, TX 78229-3900, USA.
Juli BaiDepartment of Pharmacology, University of Texas Health Science Center, San Antonio, TX 78229-3900, USA.
Feng LiuDepartment of Pharmacology, University of Texas Health Science Center, San Antonio, TX 78229-3900, USA.
Christie BialowasDivision of Plastic Surgery, Department of Surgery, Albany Medical Center, 50 New Scotland Ave, 1st Floor, Albany, NY 12208-3403, USA.
Lily Q DongDepartment of Cell Systems & Anatomy, University of Texas Health Science Center, San Antonio, TX 78229-3900, USA. DongQ@uthscsa.edu.
The University of Texas Health Science Center at San Antonio · USAlbany Medical Center Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adiponectin is an adipokine with anti-insulin resistance and anti-inflammatory functions. It exists in serum predominantly in three multimeric complexes: the trimer, hexamer, and high-molecular-weight forms. Although recent studies indicate that adiponectin promotes wound healing in rodents, its role in the wound healing process in humans is unknown. This study investigated the expression levels of adiponectin in adipose tissue and serum of women who experienced either normal or delayed wound healing after abdominal plastic surgery. We found that obese women with delayed healing had slightly lower total adiponectin levels in their adipose tissue compared with women with normal healing rates. Among the different isoforms of adiponectin, levels of the trimer forms were significantly reduced in adipose tissue, but not the serum, of obese women with delayed healing compared to women who healed normally. This study provides clinical evidence for a potential role of low-molecular-weight oligomers of adiponectin in the wound healing process as well as implications for an autocrine and/or paracrine mechanism of adiponectin action in adipose tissues.

Indexed as

AdiponectinAdipose TissueAdultAgedAutocrine CommunicationCase-Control StudiesFemaleHumansMiddle AgedObesityParacrine CommunicationProtein IsoformsTime FactorsWound HealingYoung AdultAdiponectinADIPOQ protein, humanProtein Isoformsadiponectinhumanmultimerswomanwound healing

Identifiers

PMID31554182
PMCPMC6830100
OpenAlexW2975512783

What OpenQuestion 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 OpenQuestion graph.