Evidence map›Paper›PMID 33511378›Full record

ArticleArchives of autoimmune diseases2020

Utilization of electronic health records for the assessment of adiponectin receptor autoantibodies during the progression of cardio-metabolic comorbidities.

Michael J Pugia, Meeta Pradhan, Rong Qi, Doreen L Eastes, Anna Vorsilak, Bradley J Mills, Zane Baird, Aruna Wijeratne, Scott M McAhren, Amber Mosley and 2 more

Open access · greenAbstract read
In one paragraph

Article in Archives of autoimmune diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 44% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

12 authors at 4 institutions in 1 country.

Michael J PugiaBioanalytical Research Core, Indiana Biosciences Research Institute, Indianapolis IN, USA.
Meeta PradhanApplied Data Sciences Center, Indiana Biosciences Research Institute, Indianapolis IN, USA.
Rong QiApplied Data Sciences Center, Indiana Biosciences Research Institute, Indianapolis IN, USA.
Doreen L EastesBioanalytical Research Core, Indiana Biosciences Research Institute, Indianapolis IN, USA.
Anna VorsilakBioanalytical Research Core, Indiana Biosciences Research Institute, Indianapolis IN, USA.
Bradley J MillsApplied Data Sciences Center, Indiana Biosciences Research Institute, Indianapolis IN, USA.
Zane BairdBioanalytical Research Core, Indiana Biosciences Research Institute, Indianapolis IN, USA.
Aruna WijeratneIndiana University School of Medicine, Indianapolis IN, USA.
Scott M McAhrenEli Lilly and Company, Lilly Corporate Center, Indianapolis IN, USA.
Amber MosleyIndiana University School of Medicine, Indianapolis IN, USA.
Anantha ShekharIndiana University School of Medicine, Indianapolis IN, USA.
Daniel H RobertsonApplied Data Sciences Center, Indiana Biosciences Research Institute, Indianapolis IN, USA.
Indiana Biosciences Research Institute · USIndiana University – Purdue University Indianapolis · USEli Lilly (United States) · USIndiana University School of Medicine

Funding

Indiana Clinical and Translational Science Institute (UL1)UL1TR000006 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI SHEKHAR, ANANTHA · 2012 to 2013
$5.6M
NCATS NIH HHS UL1 TR000006
6 · The paper itself

Abstract

backgroundDiabetes is a complex, multi-symptomatic disease whose complications drives increases in healthcare costs as the diabetes prevalence grows rapidly world-wide. Real-world electronic health records (EHRs) coupled with patient biospecimens, biological understanding, and technologies can characterize emerging diagnostic autoimmune markers resulting from proteomic discoveries.

methodsCirculating autoantibodies for C-terminal fragments of adiponectin receptor 1 (IgG-CTF) were measured by immunoassay to establish the reference range using midpoint samples from 1862 participants in a 20-year observational study of type 2 diabetes and cardiovascular arterial disease (CVAD) conducted by the Fairbanks Institute. The White Blood Cell elastase activity in these patients was assessed using immunoassays for Bikunin and Uristatin. Participants were assigned to four cohorts (healthy, T2D, CV, CV+T2D) based on analysis of their EHRs and the diagnostic biomarkers values and patient status were assessed ten-years post-sample.

resultsThe IgG-CTF reference range was determined to be 75-821 ng/mL and IgG-CTF out-of-range values did not predict cohort or comorbidity as determined from the EHRs at 10 years after sample collection nor did IgG-CTF demonstrate a significant risk for comorbidity or death. Many patients at sample collection time had other conditions (hypertension, hyperlipidemia, or other risk factors) of which only hypertension, Uristatin and Bikunin values correlated with increased risk of developing additional comorbidities (odds ratio 2.58-13.11, P<0.05).

conclusionsThis study confirms that retrospective analysis of biorepositories coupled with EHRs can establish reference ranges for novel autoimmune diagnostic markers and provide insights into prediction of specific health outcomes and correlations to other markers.

Identifiers

PMID33511378
PMCPMC7839988
OpenAlexW3122559941

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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.