Evidence map›Paper›PMID 36602653›Full record

ArticleReproductive sciences (Thousand Oaks, Calif.)2023

Differential Association of FTO Gene variants and Haplotypes with the Susceptibility to Polycystic Ovary Syndrome According To Obesity in Women with PCOS.

Wassim Y Almawi, Rita Nemr, Tomiris Atazhanova, Zainab H Malalla, Sameh Sarray, Fekria E Mustafa, Naeema A Mahmood

Abstract read
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In one paragraph

Article in Reproductive sciences (Thousand Oaks, Calif.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.5field-weighted citation impact, top 12% 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, 9 citations in OpenAlex.

  1. FTO-mediated NR1D1 mScientific reports · 2026
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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

7 authors at 5 institutions in 4 countries.

Wassim Y AlmawiSchool of Medicine, Nazarbayev University, Astana, Kazakhstan. wassim.almawi@outlook.com.ORCID 0000-0003-1633-9757
Rita NemrSchool of Medicine, Lebanese American University, Beirut, Lebanon.
Tomiris AtazhanovaSchool of Medicine, Nazarbayev University, Astana, Kazakhstan.
Zainab H MalallaDepartment of Medical Biochemistry, Arabian Gulf University, Manama, Bahrain.
Sameh SarrayDepartment of Medical Biochemistry, Arabian Gulf University, Manama, Bahrain.
Fekria E MustafaDepartment of Obstetrics and Gynecology, Salmaniya Medical Complex, Manama, Bahrain.
Naeema A MahmoodDepartment of Obstetrics and Gynecology, Salmaniya Medical Complex, Manama, Bahrain.
Arabian Gulf University · BHSalmaniya Medical Complex · BHBrock University · CALebanese American University · LBNazarbayev University · KZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We explored the relation between FTO single gene variants (rs1861868, rs9939973, rs1421085, rs1121980, rs17817449, rs8050136, rs9939609, rs9930506, and rs8044769) and polycystic ovary syndrome (PCOS), in particular, according to the obesity status. This retrospective population-based case-control study involved women with PCOS (583) and 713 eumenorrheic control women; genotyping was done by real-time PCR. Significantly higher minor allele frequency (MAF) of rs9939973, rs17817449, rs9939609, and rs9930506 and lower MAF of rs1121980 were seen in PCOS cases. Lower risk of PCOS was associated with rs1121980 and rs8050136 heterozygous and minor allele-homozygous genotypes, while an elevated risk of PCOS was seen with minor allele-homozygous rs9939973, rs17817449, and r9939609 heterozygous and genotypes and minor allele-homozygous rs9930506 and rs8044769 genotype. While none of the tested FTO SNPs variants was associated with PCOS in normal body weight/lean subjects, rs9939973, rs9939609, and rs9930506 were negatively associated with PCOS in overweight subjects. In comparison, rs1861868 was negatively, while rs8044769 was positively associated with PCOS in obese subjects. Haplotype analysis identified haplotypes GACCTCTAT, AACCTCTAT, AACCTATAT and AGTTGCAGC, and GACCTCTAC to be positively associated with PCOS, while haplotypes GGTTGAAGC, GACCTATAT, GGTTGCAGC, and GATCTATAT were negatively associated with PCOS. Apart from GGTTGAAGC, these haplotypes remained associated with altered risk of PCOS after adjusting for covariates. In addition to rs17817449, rs9939609, rs9930506, and rs1121980, this study is the first to demonstrate association of rs9939973 and rs8044769 with altered risk of PCOS and the first to confirm the BMI dependency on the association of FTO variants with PCOS. This underscores the role of FTO gene variants as predisposing factors of PCOS.

Indexed as

Polycystic Ovary SyndromeAlpha-Ketoglutarate-Dependent Dioxygenase FTOBody Mass IndexCase-Control StudiesFemaleGene FrequencyGenetic Predisposition to DiseaseGenotypeHaplotypesHumansObesityPolymorphism, Single NucleotideRetrospective StudiesAlpha-Ketoglutarate-Dependent Dioxygenase FTOFTO protein, humanAllelesGenotypesHaplotypesInsulin resistancePolycystic ovary syndrome

Identifiers

PMID36602653
OpenAlexW4313546149

What OpenQuestion holds

Textmetadata
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.