Evidence map›Paper›PMID 31080742›Full record

ArticleJournal of clinical & translational endocrinology2019

Metabolic dysfunction in Emirati subjects in Abu Dhabi: Relationship to levels of soluble RAGEs.

Abdishakur Abdulle, Claire K Inman, Abdelkarim Saleh, Mohamed Noshi, Divya Galani, Laila Abdelwareth, Habiba Alsafar, Abubaker Elfatih, Hefsa Al Shamsi, Raghib Ali and 5 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical & translational endocrinology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 42% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Observational
  4. Review
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

15 authors at 4 institutions in 2 countries.

Abdishakur AbdullePublic Health Research Center, New York University Abu Dhabi, United Arab Emirates.
Claire K InmanPublic Health Research Center, New York University Abu Dhabi, United Arab Emirates.
Abdelkarim SalehDepartment of Medicine, Sheikh Khalifa Medical City, United Arab Emirates.
Mohamed NoshiDepartment of Medicine, Sheikh Khalifa Medical City, United Arab Emirates.
Divya GalaniPublic Health Research Center, New York University Abu Dhabi, United Arab Emirates.
Laila AbdelwarethDepartment of Pathology, Cleveland Clinic Abu Dhabi, United Arab Emirates.
Habiba AlsafarCenter for Biotechnology, Khalifa University of Science & Technology, Abu Dhabi, United Arab Emirates.
Abubaker ElfatihDepartment of Medicine, Sheikh Khalifa Medical City, United Arab Emirates.
Hefsa Al ShamsiDepartment of Medicine, Sheikh Khalifa Medical City, United Arab Emirates.
Raghib AliPublic Health Research Center, New York University Abu Dhabi, United Arab Emirates.
Huilin LiDepartment of Population Health, New York University School of Medicine, NY, USA.
Ravichandran RamasamyDepartment of Medicine, New York University School of Medicine, NY, USA.
Ann Marie SchmidtDepartment of Medicine, New York University School of Medicine, NY, USA.
Mahmoud M BenbarkaDepartment of Medicine, Sheikh Khalifa Medical City, United Arab Emirates.
Mohamed H HassanDepartment of Medicine, Sheikh Khalifa Medical City, United Arab Emirates.
Shaikh Khalifa Medical City · AENew York University Abu Dhabi · AENew York University · USKhalifa University of Science and Technology · AE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe United Arab Emirates is experiencing increasing rates of type 2 diabetes (T2D) and its complications. As soluble levels of the receptor for advanced glycation end products, (sRAGE), and endogenous secretory RAGE (esRAGE), the latter an alternatively spliced form of

methodsIn a case-control study, we recruited Emirati subjects with T2D and controls from the Sheikh Khalifa Medical City in Abu Dhabi. Anthropomorphic characteristics, levels of plasma sRAGE and esRAGE, and routine chemistry variables were measured.

resultsTwo hundred and sixteen T2D subjects and 215 control subjects (mean age, 57.4 ± 12.1 CONCLUSION/DISCUSSION: Levels of sRAGE, but not esRAGE, were associated with T2D status in Abu Dhabi, but not after correction for eGFR. Elevated levels of plasma insulin in both control and T2D subjects suggests the presence of metabolic dysfunction, even in subjects without diabetes.

Indexed as

ADAM10, a disintegrin and metalloproteinase domain-containing protein 10AGEs, advanced glycation endproductsARIC, Atherosclerosis Risk in CommunitiesBMI, body mass indexCARDS, Collaborative Atorvastatin Diabetes StudyCV, coefficient of variationDBP, diastolic blood pressureeGFR, estimated glomerular filtration rateELISA, enzyme-linked immunosorbent assayesRAGE (endogenous secretory RAGE)esRAGE, endogenous secretory RAGEESRD, end stage renal diseaseFBG, fasting blood glucoseHbA1c, glycosylated hemoglobinHDL, high density lipoproteinhsCRP, high sensitivity C-reactive proteinInsulin resistanceKidney functionLADA, latent autoimmune diabetes of the adultLDL, low density lipoproteinMMP, matrix metalloproteinaseRAGE, receptor for advanced glycation endproductsReceptor for advanced glycation endproducts (RAGE)SBP, systolic blood pressureSKMC, Sheikh Khalifa Medical CitySoluble RAGE (sRAGE)sRAGE, soluble RAGET2D, type 2 diabetesTG, triglyceridesType 2 diabetesUAEHFS, United Arab Emirates Healthy Futures StudyUAE, United Arab EmiratesW/H ratio, Waist/Hip circumference ratio

Identifiers

PMID31080742
PMCPMC6503160
OpenAlexW2940483374

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.