Evidence map›Paper›PMID 30102726›Full record

ArticlePloS one2018

Association of weight gain and fifteen adipokines with declining beta-cell function in Mexican Americans.

Anny H Xiang, Mary Helen Black, Yu-Hsiang Shu, Jun Wu, Adrienne MacKay, Corinna Koebnick, Richard M Watanabe, Thomas A Buchanan

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 19% 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, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Observational
  4. Article
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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

8 authors at 2 institutions in 1 country.

Anny H XiangDepartment of Research & Evaluation, Kaiser Permanente Southern California, Pasadena, CA, United States of America.ORCID 0000-0003-2786-1268
Mary Helen BlackDepartment of Research & Evaluation, Kaiser Permanente Southern California, Pasadena, CA, United States of America.
Yu-Hsiang ShuDepartment of Research & Evaluation, Kaiser Permanente Southern California, Pasadena, CA, United States of America.
Jun WuDepartment of Research & Evaluation, Kaiser Permanente Southern California, Pasadena, CA, United States of America.
Adrienne MacKayDepartment of Preventive Medicine, Keck School of Medicine of USC, Los Angeles, CA, United States of America.
Corinna KoebnickDepartment of Research & Evaluation, Kaiser Permanente Southern California, Pasadena, CA, United States of America.
Richard M WatanabeDepartment of Preventive Medicine, Keck School of Medicine of USC, Los Angeles, CA, United States of America.
Thomas A BuchananDiabetes and Obesity Research Institute, University of Southern California, Los Angeles, CA, United States of America.
Kaiser Permanente · USUniversity of Southern California · US

Funding

The Role of Adipokines in Glucose Regulation and Metabolic DeclineR01DK100302 · NIDDK · KAISER FOUNDATION RESEARCH INSTITUTE · PI XIANG, ANNY H · 2014 to 2016
$1.1M
NIDDK NIH HHS R01 DK100302
6 · The paper itself

Abstract

Obesity and adipokines are associated with development of type 2 diabetes. However, limited longitudinal studies have examined their roles on declining β-cell function over time. This report assessed three adiposity measures (BMI, percent body fat, trunk fat), insulin resistance, and fifteen adipokines in relationship to longitudinal change in β-cell function measured by disposition index (DI) from frequently-sampled-intravenous-glucose-tolerance testing. The results showed that three factors were significantly and independently associated with rate of change in DI over time: rate of change in BMI (negative), rate of change in IL-6 (negative), and baseline adiponectin (positive). The association was the strongest for changing BMI and was largely explained by changing insulin resistance; the association with changing IL-6 was also largely explained by changing insulin resistance. Baseline adiponectin remained positively associated after adjustment for changing insulin resistance, suggesting an independent effect of adiponectin to preserve or improve β-cell function. These findings provide evidence and potential mechanisms for the role of obesity in promoting β-cell dysfunction, highlighting the potential importance of mitigating obesity and its metabolic effects in preventing and treating type 2 diabetes.

Indexed as

Insulin ResistanceWeight GainAdipokinesAdultFemaleGlucose Tolerance TestHumansInsulin-Secreting CellsLongitudinal StudiesMaleMexican AmericansObesityAdipokines

Identifiers

PMID30102726
PMCPMC6089433
OpenAlexW2886925822

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.