Evidence map›Paper›PMID 40053300›Full record

Observational studyEpilepsia open2025

Bromodomain-containing protein 2 gene polymorphism among patients with photosensitive epilepsy in Indonesia.

Diah Kurnia Mirawati, Muhana Fawwazy Ilyas, Muhammad Hafizhan, Stefanus Erdana Putra, Suroto Suroto, Subandi Subandi, Rivan Danuaji, Pepi Budianto, Yetty Hambarsari, Baarid Luqman Hamidi and 6 more

Abstract readObservational Study
In one paragraph

Observational study in Epilepsia open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Observational
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

16 authors.

Diah Kurnia MirawatiDepartment of Neurology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia.ORCID https://orcid.org/0000-0002-0558-5680
Muhana Fawwazy IlyasDepartment of Neurology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia.ORCID https://orcid.org/0000-0002-0176-9773
Muhammad HafizhanDepartment of Neurology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia.ORCID https://orcid.org/0000-0002-6051-5300
Stefanus Erdana PutraDepartment of Neurology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia.ORCID https://orcid.org/0000-0003-2613-0711
Suroto SurotoDepartment of Neurology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia.ORCID https://orcid.org/0000-0001-8507-9077
Subandi SubandiDepartment of Neurology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia.ORCID https://orcid.org/0000-0003-4407-117X
Rivan DanuajiDepartment of Neurology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia.ORCID https://orcid.org/0000-0003-0370-572X
Pepi BudiantoDepartment of Neurology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia.ORCID https://orcid.org/0000-0002-6201-151X
Yetty HambarsariDepartment of Neurology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia.ORCID https://orcid.org/0000-0002-8549-9546
Baarid Luqman HamidiDepartment of Neurology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia.ORCID https://orcid.org/0000-0003-3253-6451
Hanindia Riani PrabaningtyasDepartment of Neurology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia.ORCID https://orcid.org/0000-0002-1130-5649
Ervina Arta Jayanti HutabaratDepartment of Neurology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia.ORCID https://orcid.org/0000-0003-1772-2897
Ira RistinawatiDepartment of Neurology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia.ORCID https://orcid.org/0000-0001-6319-6854
Teddy TejomuktiDepartment of Neurology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia.ORCID https://orcid.org/0000-0001-7375-7192
Raden Andi Ario TedjoDepartment of Neurology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia.ORCID https://orcid.org/0000-0002-7764-7748
Faris Khairuddin SyahDepartment of Neurology, Faculty of Medicine, Universitas Sebelas Maret, Surakarta, Indonesia.ORCID https://orcid.org/0000-0002-9011-9368

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesGenetic-associated epilepsy in the Indonesian population is rarely discussed, and no study was specifically studied about photosensitive epilepsy. The fundamental goal of this research endeavor was to evaluate whether the single nucleotide polymorphism (SNP) of the Bromodomain-Containing Protein 2 (BRD2) gene gives vulnerability to photosensitive epilepsy among Indonesian descent.

methodsThis observational case-control study includes patients of Indonesian descent with Javanese ancestry. Clinical and neurophysiological data, along with electroencephalographic (EEG) recordings, were used to diagnose epilepsy and photosensitive epilepsy. Blood samples were collected and analyzed for BRD2 gene SNPs (rs206781, rs188245, and rs15912) using polymerase chain reaction (PCR), electrophoresis, and the Sanger sequencing method.

resultsThis study included 27 participants, consisting of 17 patients in the epilepsy group (nine patients with photosensitive epilepsy and eight patients without photosensitive epilepsy) and 10 patients in the non-epilepsy group. Significant statistical differences were found in genotype (rs206781, p = 0.008 and rs188245, p = 0.004) and allele frequencies (rs206781, p < 0.001 and rs188245, p < 0.001) of the BRD2 gene in Indonesian descent with Javanese race patients diagnosed with photosensitive epilepsy and in those without this condition. SIGNIFICANCE: Our study corroborates the observation that genetic diversity within the BRD2 locus (rs206781 and rs188245) is associated with PE in Indonesian descendants of the Javanese race. To acquire a complete knowledge of the development of photosensitive epilepsy, further polymorphism studies at other SNP locations or genes are necessary. PLAIN LANGUAGE SUMMARY: This study investigated whether genetic differences in the BRD2 gene were linked to photosensitive epilepsy (a type of epilepsy triggered by visual stimuli like flashing lights) in individuals of Indonesian Javanese descent. We analyzed deoxyribonucleic acid (DNA) samples from patients with epilepsy, including those with photosensitive epilepsy, and found that certain variations in the BRD2 gene were significantly more common in people with photosensitive epilepsy. These findings imply that genetic factors, specifically variations in the BRD2 gene, could elevate the risk of individuals in this population experiencing photosensitive epilepsy.

Indexed as

Epilepsy, ReflexGenetic Predisposition to DiseasePolymorphism, Single NucleotideProtein Serine-Threonine KinasesAdolescentAdultBromodomain Containing ProteinsCase-Control StudiesChildElectroencephalographyFemaleGene FrequencyGenotypeHumansIndonesiaMaleBRD2 protein, humanBromodomain Containing ProteinsProtein Serine-Threonine KinasesTranscription FactorsBRD2Indonesianphotosensitive epilepsypolymorphismreflex epilepsy

Identifiers

PMID40053300
PMCPMC12014917

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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.