Evidence map›Paper›PMID 26491214›Full record

ArticleDisease markers2015

Association of Angiotensin Converting Enzyme Insertion-Deletion Polymorphism with Hypertension in Emiratis with Type 2 Diabetes Mellitus and Its Interaction with Obesity Status.

Habiba Alsafar, Ahmed Hassoun, Shaikha Almazrouei, Wala Kamal, Mustafa Almaini, Unini Odama, Naushad Rais

Open access · hybridAbstract read
In one paragraph

Article in Disease markers, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The Predisposition for Type 2 Diabetes Mellitus and Metabolic Syndrome.Balkan journal of medical genetics : BJMG · 2023
    Article
  5. The Association ofInternational journal of molecular sciences · 2022
    Article
  6. Article
  7. Role of angiotensin II in aging.Frontiers in aging neuroscience · 2022
    Review
  8. Article
  9. Article
  10. Article
  11. Association betweenInternational journal of molecular and cellular medicine · 2017
    Article
  12. Review
  13. Article
  14. Article
  15. 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

7 authors at 5 institutions in 3 countries.

Habiba AlsafarDepartment of Biomedical Engineering, Khalifa University of Science, Technology & Research, P.O. Box 127788, Abu Dhabi, UAE.
Ahmed HassounDubai Diabetes Centre, Dubai Health Authority, Dubai, UAE.
Shaikha AlmazroueiDepartment of Biomedical Engineering, Khalifa University of Science, Technology & Research, P.O. Box 127788, Abu Dhabi, UAE.
Wala KamalSchool of Life Sciences, Manipal University, P.O. Box 345050, Dubai, UAE.
Mustafa AlmainiImmunology Clinics, Mafraq Hospital, Abu Dhabi, UAE.
Unini OdamaLandmark Nephrology and Hypertension Clinic, Talladega, AL, USA.
Naushad RaisSchool of Life Sciences, Manipal University, P.O. Box 345050, Dubai, UAE.
Khalifa University of Science and Technology · AEManipal Academy of Higher Education · INDubai Health Authority · AEHypertension Institute · USMafraq Hospital · AE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The association of Angiotensin Converting Enzyme (ACE) insertion-deletion (I/D) polymorphism with Type 2 Diabetes Mellitus (T2DM) and hypertension has been extensively studied throughout various ethnic populations but largely with inconsistent findings. We investigated these associations in Emirati population and their interaction with obesity status. Saliva samples were collected from a total of 564 Emiratis (277 T2DM and 297 healthy). DNA was extracted and the samples were genotyped for ACE I/D polymorphism by a PCR based method followed by gel electrophoresis. Upon evaluation of the ACE I/D polymorphism amongst all T2DM, hypertensive patients, and respective controls regardless of obesity status, ACE DD genotype was not found to be associated with either T2DM [odds ratio (OR) = 1.34, p = 0.086] or hypertension [odd ratio (OR) = 1.02, p = 0.93]. When the genetic variants amongst the nonobese and obese population were analyzed separately, the risk genotype ACE DD conferred significantly increased risk of hypertension in nonobese population [odds ratio (OR) = 1.80, p = 0.02] but was found to be protective against the hypertension in the obese group ((OR) = 0.54, p = 0.01). However, there was no effect of obesity status on the association of ACE genotypes with T2DM. The risk of hypertension associated with ACE DD is modulated by obesity status and hence future genetic association studies should take obesity into account for the interpretation of data. We also confirmed that ACE I/D polymorphism is not associated with T2DM risk in Emirati population.

Indexed as

INDEL MutationPolymorphism, GeneticAdultAgedCase-Control StudiesDiabetes Mellitus, Type 2FemaleHumansHypertensionMaleMiddle AgedObesityPeptidyl-Dipeptidase AACE protein, humanPeptidyl-Dipeptidase A

Identifiers

PMID26491214
PMCPMC4603605
OpenAlexW1872554778

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.