Evidence mapPaperPMID 40757266Full record

ArticleInternational journal of women's health2025

Molecular Variants in

Mohammed Alfaifi, Adel Abo Mansour, Bijesh Yadav, Imran Ali Khan

Abstract read
In one paragraph

Article in International journal of women's health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
field-weighted citation impact
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

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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.

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

4 authors.

Mohammed AlfaifiDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Khalid University, Abha, Saudi Arabia.
Adel Abo MansourDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Khalid University, Abha, Saudi Arabia.
Bijesh YadavDepartment of Population Health, Division of Biostatistics, King Abdullah International Medical Research Center, Ministry of National Guard-Health Affairs, Riyadh, Saudi Arabia.
Imran Ali KhanMedical Genomics Research Department, King Abdullah International Medical Research Center, King Saud bin Abdulaziz University for Health Sciences, Ministry of National Guard Health Affairs, Riyadh, 11481, Saudi Arabia.ORCID 0000-0002-9746-5300

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Gestational Diabetes Mellitus (GDM) is defined as impaired glucose intolerance resulting in hyperglycemia. SIRT1 deficiency and single nucleotide polymorphisms (SNPs) were also related to diabetes. No documented studies were carried out between GDM and Objective: This study was designed to explore the molecular association carried out between GDM women and Methods/Design: Serum samples were used for studying biochemical parameters, genotyping and Sanger sequencings for rs4746720 and rs10823112 SNPs. Statistical analysis was carried out between GDM and non-GDM women for anthropometric, biochemical and molecular data. Results: A total of 120 GDM and 120 non-GDM women were recruited based on inclusion and exclusion criteria. Different forms of glucose values have confirmed the statistical association levels between GDM and non-GDM women (p < 0.05). Penalized logistic regression analysis showed the positive association with FBG, OGTT-2hr and HDLc levels (p < 0.05) in GDM women. The rs4746720 SNP was associated with GDM (p = 0.01). ANOVA analysis has confirmed the strong association with FBG (p = 0.002), PPBG (p = 0.0001) and HDLc (p = 0.0003) levels in rs4746720 SNP; while in rs10823112 SNP, both PPBG (p = 0.0001) and HDLc (p = 0.01) were associated. Linkage disequilibrium and GMDR analysis showed significant associations (p < 0.05). Conclusion: This study confirms rs4746720 SNP and glucose levels played a role in this study.

Indexed as

GDMnon-GDM womenrs10823112rs4746720SIRT1SNPs

Identifiers

PMID40757266
PMCPMC12316047

What Socratic holds

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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 Socratic graph.