Evidence map›Paper›PMID 28752301›Full record

ArticleJournal of endocrinological investigation2018

Gender differences in the association of ELMO1 genetic variants with type 2 diabetes in Tunisian Arabs.

A Turki, S Mzoughi, N Mtitaoui, M Khairallah, H Marmouch, S Hammami, T Mahjoub, W Y Almawi

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Article in Journal of endocrinological investigation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 22% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

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  4. Comparative Morphological, Metabolic and Transcriptome Analyses inFrontiers in cell and developmental biology · 2022
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  6. Interaction betweenDiabetology & metabolic syndrome · 2019
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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 3 institutions in 1 country.

A TurkiResearch Laboratory of Human Genome and Multifactorial Diseases, Faculty of Pharmacy of Monastir, University of Monastir, Monastir, Tunisia.
S MzoughiResearch Laboratory of Human Genome and Multifactorial Diseases, Faculty of Pharmacy of Monastir, University of Monastir, Monastir, Tunisia.
N MtitaouiResearch Laboratory of Human Genome and Multifactorial Diseases, Faculty of Pharmacy of Monastir, University of Monastir, Monastir, Tunisia.
M KhairallahDepartment of Ophthalmology, Fattouma Bourguiba University Hospital, Monastir, Tunisia.
H MarmouchDepartment of Endocrinology and Internal Medicine, Fattouma Bourguiba University Hospital, Monastir, Tunisia.
S HammamiDepartment of Endocrinology and Internal Medicine, Fattouma Bourguiba University Hospital, Monastir, Tunisia.
T MahjoubResearch Laboratory of Human Genome and Multifactorial Diseases, Faculty of Pharmacy of Monastir, University of Monastir, Monastir, Tunisia.
W Y AlmawiFaculty of Sciences, El Manar University, Tunis, Tunisia. wassim.almawi@outlook.com.
University of Monastir · TNHospital Fatuma Bourguiba Monastir · TNTunis El Manar University · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePolymorphisms of the engulfment and cell motility 1 (ELMO1) gene were recently associated with type 2 diabetes (T2DM) and its complications. We investigated the association of rs10255208, rs7782979, and rs2041801 ELMO1 gene variants with T2DM in Tunisian Arabs.

methodsSubjects comprised 900 T2DM patients and 600 normoglycemic controls. ELMO1 genotyping was done by PCR-RFLP; the contribution of ELMO1 variants to T2DM was analyzed by Haploview and regression analysis.

resultsMinor allele frequencies of rs7782979 and rs10255208 ELMO1 variants were significantly higher among unselected T2DM cases than controls, and significant differences in the distribution of rs7782979 genotypes were seen between T2DM cases and control subjects, which was seen in male but not female subjects. Three-locus ELMO1 haplotype analysis identified haplotype GAA to be positively associated, and haplotypes GCA, AAA, and GCG to be negatively associated with T2DM. The distribution of these haplotypes was gender-dependent for some (GCA, GCG, AAG), and gender-independent for others (GAA, AAA). This translated into altered risk of T2DM in male or female subjects, which persisted after adjusting for BMI, systolic and diastolic blood pressure, and serum lipid profile.

conclusionThese results confirm role for ELMO1 as T2DM susceptibility locus, which appears to be gender-dependent.

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideAdaptor Proteins, Signal TransducingArabsBiomarkersCase-Control StudiesDiabetes Mellitus, Type 2FemaleFollow-Up StudiesGene FrequencyGenotypeHaplotypesHumansMaleMiddle AgedPrognosisAdaptor Proteins, Signal TransducingBiomarkersELMO1 protein, humanAlleleELMO1HaplotypeTunisiaType 2 diabetes

Identifiers

PMID28752301
OpenAlexW2740173520

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Registered trials

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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.