Evidence map›Paper›PMID 31568687›Full record

ArticleMolecular genetics & genomic medicine2019

Genetics of diabetic kidney disease: A follow-up study in the Arab population of the United Arab Emirates.

Wael M Osman, Herbert F Jelinek, Guan K Tay, Mohamed H Hassan, Wael Almahmeed, Ahsan H Khandoker, Kinda Khalaf, Habiba S Alsafar

Open access · goldAbstract read
In one paragraph

Article in Molecular genetics & genomic medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. 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

8 authors at 4 institutions in 2 countries.

Wael M OsmanCenter for Biotechnology, Khalifa University, Abu Dhabi, United Arab Emirates.ORCID 0000-0002-1921-8021
Herbert F JelinekSchool of Community Health, Charles Sturt University, Albury, Australia.ORCID 0000-0002-1573-3659
Guan K TayCenter for Biotechnology, Khalifa University, Abu Dhabi, United Arab Emirates.ORCID 0000-0001-6639-3298
Mohamed H HassanNephrology Division, Medical Institute, Sheikh Khalifa Medical City, Abu Dhabi, United Arab Emirates.ORCID 0000-0002-2110-0946
Wael AlmahmeedInstitute of Cardiac Science, Sheikh Khalifa Medical City, Abu Dhabi, United Arab Emirates.ORCID 0000-0003-0312-9910
Ahsan H KhandokerDepartment of Biomedical Engineering, Khalifa University, Abu Dhabi, United Arab Emirates.ORCID 0000-0002-0636-1646
Kinda KhalafDepartment of Biomedical Engineering, Khalifa University, Abu Dhabi, United Arab Emirates.ORCID 0000-0002-3878-2621
Habiba S AlsafarCenter for Biotechnology, Khalifa University, Abu Dhabi, United Arab Emirates.ORCID 0000-0001-7141-1438
Khalifa University of Science and Technology · AEShaikh Khalifa Medical City · AECharles Sturt University · AUEdith Cowan University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTwo genome-wide association studies in European and Japanese populations reported on new loci for diabetic kidney disease (DKD), including FTO. In this study, we have replicated these investigations on a cohort of 410 Type 2 diabetes mellitus (T2DM) patients of Arab origin from the United Arab Emirates (UAE). METHODS AND

resultsThe cohort included 145 diabetic patients diagnosed with DKD and 265 diabetics free of the disease. In general, we were able to confirm the association between the FTO locus and DKD, as reported in the Japanese population. Specifically, there were significant associations with two single nucleotide polymorphisms (SNPs), namely rs1421086 (p = .013, OR = 1.52 depending on allele G, 95% CI: 1.09-2.11) and rs17817449 (p = .0088, OR = 1.55 depending on allele C, 95% CI: 1.12-2.14) of the FTO locus. Both SNPs were in linkage disequilibrium with rs56094641, also as reported in the Japanese population. While the alleles of both SNPs, which increase the risk of DKD, were associated with higher Body Mass Index (BMI), their associations with DKD were independent of the BMI effects.

conclusionsThis study confirms that FTO is a multiethnic locus for DKD which is independent from any influence of BMI and/or obesity.

Indexed as

Polymorphism, Single NucleotideAgedAlpha-Ketoglutarate-Dependent Dioxygenase FTOArabsBody Mass IndexCase-Control StudiesCross-Sectional StudiesDiabetic NephropathiesFemaleGenetic Association StudiesHumansLinkage DisequilibriumMaleMiddle AgedUnited Arab EmiratesAlpha-Ketoglutarate-Dependent Dioxygenase FTOFTO protein, humandiabetic kidney diseaseFTOgeneticsType 2 diabetesUnited Arab Emirates

Identifiers

PMID31568687
PMCPMC6900378
OpenAlexW2978415392

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.