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A Method to Study the C924T Polymorphism of the Thromboxane A2 Receptor Gene
Published on: April 1, 2019
Association of MTHFR gene polymorphisms with migraine in North Indian population
Sukhvinder Kaur1, Arif Ali2, Anil Kumar Pandey3
1Department of Biosciences, UGC-PDF, Gene Expression Lab, Jamia Millia Islamia, New Delhi, India. singhrp12@rediffmail.com.
Abstract:
Polymorphisms in MTHFR gene are mostly associated with increased levels of homocysteine in the absence of dietary folate and are a risk factor for complex neurovascular diseases like migraine. The aim of present case-control study was to determine the association between MTHFR gene polymorphisms (C667T; rs 1801133, A1298C; rs 1801131) with migraine susceptibility. In total, 100 patients with migraine (23with MA and 77 with MO) and age-sex matched 100 healthy controls were included in this study from OPD of ESIC Medical College & Hospital, Faridabad. Genotyping was done by PCR-RFLP method. Genotypic and allelic frequencies were compared by SPSS 24 version. Genotypic results indicated a non-significant increase in frequencies of CT and TT in C667T SNP in migraine patients with control (52 and 10% vs. 42 and 7%: p > 0.05), but CC genotype in A1298C was found to be a risk factor in migraine patients than controls (30 vs. 17% respectively: p < 0.05). On comparing migraine subclasses, migraine with aura (MA) and without aura (MO) with control groups, the present study suggests that in MTHFR polymorphisms, the prevalence of 677CT genotype and T allele in C667T SNP influences susceptibility to MA (p < 0.05) but not to MO. Meanwhile, CC genotype in A1298C SNP could be a risk factor for migraine patients without aura (p < 0.05).
Insights
Methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms are linked to migraine susceptibility. The A1298C CC genotype is a risk factor for migraine, while C677T influences migraine with aura.
Area of Science:
- Genetics
- Neurology
- Molecular Biology
Background:
- Polymorphisms in the methylenetetrahydrofolate reductase (MTHFR) gene are associated with elevated homocysteine levels, particularly with insufficient dietary folate.
- These MTHFR gene variations are implicated as risk factors for complex neurovascular disorders, including migraine.
Purpose of the Study:
- To investigate the association between MTHFR gene polymorphisms (C677T and A1298C) and the susceptibility to migraine.
- To differentiate the impact of these polymorphisms on migraine with aura (MA) and migraine without aura (MO).
Main Methods:
- A case-control study involving 100 migraine patients and 100 age- and sex-matched healthy controls.
- Genotyping of MTHFR gene polymorphisms (C677T; rs 1801133, A1298C; rs 1801131) was performed using the Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-RFLP) technique.
- Genotypic and allelic frequencies were analyzed using SPSS version 24.
Main Results:
- The CC genotype of the A1298C single nucleotide polymorphism (SNP) was significantly more frequent in migraine patients compared to controls (30% vs. 17%, p < 0.05).
- The 677CT genotype and T allele of the C677T SNP were associated with an increased susceptibility to migraine with aura (MA) (p < 0.05).
- No significant association was found between C677T polymorphisms and migraine without aura (MO), nor between A1298C polymorphisms and MA.
Conclusions:
- The A1298C CC genotype may serve as a risk factor for overall migraine susceptibility.
- Specific MTHFR polymorphisms, particularly the C677T variant, appear to influence susceptibility to migraine with aura.
- Further research is warranted to elucidate the precise mechanisms linking MTHFR gene variations to different migraine subtypes.
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