Evidence map›Paper›PMID 41877846›Full record

ArticleClinical ophthalmology (Auckland, N.Z.)2026

Genotype Association of VEGF Polymorphism rs2010963 with Strabismus in a Pakistani Cohort: A Case-Control Study.

Muhammad Ahmad Khalid, Noor-Ul-Ain Amin, Conain Nehal, Sana Nadeem, Kwang Min Woo, Muhammad Usman Jamil, Maleeha Azam

Abstract read
In one paragraph

Article in Clinical ophthalmology (Auckland, N.Z.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
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

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

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

7 authors.

Muhammad Ahmad KhalidDepartment of Science, Buckingham Browne and Nichols School, Cambridge, MA, USA.
Noor-Ul-Ain AminDepartment of Biosciences, COMSATS University Islamabad, Islamabad, Pakistan.
Conain NehalDepartment of Biosciences, COMSATS University Islamabad, Islamabad, Pakistan.
Sana NadeemDepartment of Ophthalmology, Foundation University Medical College, Foundation University Islamabad, Islamabad, Pakistan.ORCID 0000-0003-3994-8774
Kwang Min WooDepartment of Ophthalmology, New England Eye Center, Boston, MA, USA.
Muhammad Usman JamilDepartment of Ophthalmology, New England Eye Center, Boston, MA, USA.ORCID 0000-0001-9642-1886
Maleeha AzamDepartment of Biosciences, COMSATS University Islamabad, Islamabad, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: This study was conducted to investigate the associations between specific genetic variation in VEGF and the prevalence of strabismus, with particular focus on VEGF polymorphism rs2010963 and whether presence of GG phenotype increases the odds of strabismus compared to GC or CC allele in a Pakistani cohort. Patients and Methods: Blood samples from 43 strabismus patients and 170 non-diabetic healthy normal controls from a previously published study from our group were used for comparison. Genotyping of the selected single nucleotide polymorphism (SNP) was carried out using polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) for 43 samples of strabismus. Genotype and allele frequencies were then computed for all patients. Logistic regression was used to evaluate the association between the rs2010963 genotype and the risk of strabismus. A p-value of < 0.05 was considered statistically significant. Results: Of the 43 strabismus patients, 27 (66%) had exotropia, followed by esotropia in 14 patients (34%). Their genotype frequency included 24 (56%) patients with the GG genotype, 14 (33%) with the GC genotype, and 5 (12%) with the CC genotype. Among the 170 normal controls, 50 (29%) had the GG genotype, 60 (35%) had the GC genotype, and 60 (35%) had the CC genotype. Individuals with the GG phenotype had significantly higher odds of having strabismus compared to those with CC genotype (OR = 5.76, 95% CI [2.05-16.20], p = 0.0009). GG phenotype was also associated with higher odds to those with GC phenotype, but the result was not statistically significant (OR = 2.06 [0.96-4.39], p = 0.062). Conclusion: This study explored the association of VEGFA polymorphism rs2010963 and strabismus in a Pakistani cohort. The GG genotype was more frequent in strabismus cases than in controls (56% vs 29%), and a significant association was found between rs2010963 and strabismus which should be confirmed in larger, preferably age-matched cohorts.

Indexed as

genotypePakistaniSouth AsianstrabismusVEGF

Identifiers

PMID41877846
PMCPMC13007781

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.