Abstract:Introduction:Migraine is a complex, recurrent headache disorder that is one of the most common complaints in neurology practice. The role of various genes in its pathogenesis is being studied. We did this study to see whether an association exists between ACE gene I/D polymorphism and migraine in our region.Materials and Methods:The study included 100 patients diagnosed with migraine and 121 healthy controls. The study subject were age and gender matched. The analysis was based on Polymerase Chain Reaction (PC… Show more
“…Concerning the ACE -I/D polymorphism, the present meta-analysis showed a significant association between the variant of interest and the risk of migraine and both clinical subtypes such as MA and MWA. This present study supports the independent study by Jasrotia and group and Joshi and group 13 , 17 in contrast non-significant association was observed by Wani and group 24 . Interestingly all studies 13 , 17 , 24 were from north India, thus disparity between such might be due to different sample sizes i.e., control and case subjects.…”
Section: Discussionsupporting
confidence: 91%
“…This present study supports the independent study by Jasrotia and group and Joshi and group 13 , 17 in contrast non-significant association was observed by Wani and group 24 . Interestingly all studies 13 , 17 , 24 were from north India, thus disparity between such might be due to different sample sizes i.e., control and case subjects. Evidence from the meta-analysis published in 2016 powered with 7334 patients and 22,990 control showed no relationship between the ACE I/D polymorphism and any migraine but upon subgrouping based on the criteria of ethnicity, they observed a protective effect against migraine with aura and without aura at least in the Turkish population 41 .…”
Section: Discussionsupporting
confidence: 91%
“…2 ) (Paint—Microsoft Apps). Only nine genes have been studied more than two times in the Indian population and thus were found eligible for the meta-analysis and these include six studies which have explored MTHFR gene 13 , 16 – 18 , 22 , 23 , three studies for ACE (I/D polymorphism) 13 , 17 , 24 , LRP1- rs11172113 19 , 26 , 28 , PRDM16- rs2651899 19 , 26 , TRPM8- rs10166942 and rs10504861 21 , 26 , ESR1 PvuII and XbaI 15 , 29 , 37 , DAO- rs10156191, rs2052129 20 , 35 and TNF-α G308A 25 , 30 . Figure 1 Selection of literature according to PRISMA (Preferred Reporting Items for Systematics Reviews and Meta-Analysis) guidelines.…”
Section: Resultsmentioning
confidence: 99%
“…There are 3 studies 13 , 17 , 24 (Supplementary Table 3 S1) that observed the frequency and association of polymorphism in the population of the Indian population. After pooling such independent studies, we found that the overall frequency of risk and wild allele was 0.410 (n = 289/704) and 0.589 (n = 415/704) in the patient group respectively.…”
Section: Resultsmentioning
confidence: 99%
“… S. No Gene Protein Chr Function SNPs Diagnosis Case/controls State Region ReL Comment Ref 1 ACE Angiotensin I converting enzyme 17q23.3 It catalyzes the conversion of angiotensin I into a physiologically active peptide angiotensin II. Angiotensin II is a potent vasopressor and aldosterone-stimulating peptide that controls blood pressure and fluid-electrolyte balance I/D IHS 100/121 Kashmir NI X We were not able to find a statistically significant association between ACE gene I/D polymorphism with migraine Wani et al 24 ACE I/D IHS 102/150 Jammu NI ✓ ACE I/D polymorphism analysis revealed that D allele and DD genotype is considerably associated with the risk for migraine in population of North India (Jammu region) Jasrotia et al 17 ACE I/D IHS 150/150 Lucknow, UP NI ✓ ACE DD genotype showed significant association in migraine patients Joshi et al 13 2 ANKK1 Ankyrin repeat and kinase domain containing 1 11q23.2 A TaqIA polymorphism (rs1800497) is located 9.5 kb downstream from DRD2 gene. It causes an amino acid change (Glu713Lys) in the C-terminal ankyrin repeat domain of ANKK1 (ankyrin repeats ...…”
Migraine is a complex disorder with multigenic inheritance and is characterized by the cardinal symptom of unilateral headache. Many genes are responsible for increasing the susceptibility of disease within different populations. Therefore, our primary aim in this review was to catalog the many genes that have been studied in India and after collecting the necessary information, we calculated a more precise risk relationship between an identified variation and migraine. The gene and its associated risk variant were discovered in the Indian population using a PRISMA-based systematic literature review guideline from online databases such as PubMed & Google Scholar. We constructed pooled odds ratios with 95% confidence intervals using multiple genetic models. Also, we looked for heterogeneity using Cochran's Q Test and the I2 statistic. Publication bias was analyzed using Begg's and Egger's tests. A p-value less than 0.05 was judged to be statistically significant for all tests. After a critical analysis, a total of 24 studies explored about 21 genes with 31 variants out of which only nine genes have been studied more than two times in the Indian population and thus were found eligible for the meta-analysis. It has been found, that the ACE-DD variant (allele model: OR: 1.37 [1.11–1.69], I2 = 0%/ fixed model), ESR1-PvuII (allele model: OR: 1.47 [1.24–1.74], I2 = 0%/ fixed model) significantly increases the risk of migraine in Indian population. Also, a protective role of the LRP1-rs11172113variant was observed for both migraine and its clinical subtype i.e., MA (allelic model: OR of 0.65 [0.50–0.83] I2 = 44% and allele: OR: 0.54 [0.37–0.78], I2 = 52%) respectively. Overall, the results of this meta-analysis indicated that the ACE-DD variant and the ESR1-PvuII were associated with an increased risk of migraine in the Indian community, while the LRP1-rs11172113 variant was associated with protection from migraine in this population.
“…Concerning the ACE -I/D polymorphism, the present meta-analysis showed a significant association between the variant of interest and the risk of migraine and both clinical subtypes such as MA and MWA. This present study supports the independent study by Jasrotia and group and Joshi and group 13 , 17 in contrast non-significant association was observed by Wani and group 24 . Interestingly all studies 13 , 17 , 24 were from north India, thus disparity between such might be due to different sample sizes i.e., control and case subjects.…”
Section: Discussionsupporting
confidence: 91%
“…This present study supports the independent study by Jasrotia and group and Joshi and group 13 , 17 in contrast non-significant association was observed by Wani and group 24 . Interestingly all studies 13 , 17 , 24 were from north India, thus disparity between such might be due to different sample sizes i.e., control and case subjects. Evidence from the meta-analysis published in 2016 powered with 7334 patients and 22,990 control showed no relationship between the ACE I/D polymorphism and any migraine but upon subgrouping based on the criteria of ethnicity, they observed a protective effect against migraine with aura and without aura at least in the Turkish population 41 .…”
Section: Discussionsupporting
confidence: 91%
“…2 ) (Paint—Microsoft Apps). Only nine genes have been studied more than two times in the Indian population and thus were found eligible for the meta-analysis and these include six studies which have explored MTHFR gene 13 , 16 – 18 , 22 , 23 , three studies for ACE (I/D polymorphism) 13 , 17 , 24 , LRP1- rs11172113 19 , 26 , 28 , PRDM16- rs2651899 19 , 26 , TRPM8- rs10166942 and rs10504861 21 , 26 , ESR1 PvuII and XbaI 15 , 29 , 37 , DAO- rs10156191, rs2052129 20 , 35 and TNF-α G308A 25 , 30 . Figure 1 Selection of literature according to PRISMA (Preferred Reporting Items for Systematics Reviews and Meta-Analysis) guidelines.…”
Section: Resultsmentioning
confidence: 99%
“…There are 3 studies 13 , 17 , 24 (Supplementary Table 3 S1) that observed the frequency and association of polymorphism in the population of the Indian population. After pooling such independent studies, we found that the overall frequency of risk and wild allele was 0.410 (n = 289/704) and 0.589 (n = 415/704) in the patient group respectively.…”
Section: Resultsmentioning
confidence: 99%
“… S. No Gene Protein Chr Function SNPs Diagnosis Case/controls State Region ReL Comment Ref 1 ACE Angiotensin I converting enzyme 17q23.3 It catalyzes the conversion of angiotensin I into a physiologically active peptide angiotensin II. Angiotensin II is a potent vasopressor and aldosterone-stimulating peptide that controls blood pressure and fluid-electrolyte balance I/D IHS 100/121 Kashmir NI X We were not able to find a statistically significant association between ACE gene I/D polymorphism with migraine Wani et al 24 ACE I/D IHS 102/150 Jammu NI ✓ ACE I/D polymorphism analysis revealed that D allele and DD genotype is considerably associated with the risk for migraine in population of North India (Jammu region) Jasrotia et al 17 ACE I/D IHS 150/150 Lucknow, UP NI ✓ ACE DD genotype showed significant association in migraine patients Joshi et al 13 2 ANKK1 Ankyrin repeat and kinase domain containing 1 11q23.2 A TaqIA polymorphism (rs1800497) is located 9.5 kb downstream from DRD2 gene. It causes an amino acid change (Glu713Lys) in the C-terminal ankyrin repeat domain of ANKK1 (ankyrin repeats ...…”
Migraine is a complex disorder with multigenic inheritance and is characterized by the cardinal symptom of unilateral headache. Many genes are responsible for increasing the susceptibility of disease within different populations. Therefore, our primary aim in this review was to catalog the many genes that have been studied in India and after collecting the necessary information, we calculated a more precise risk relationship between an identified variation and migraine. The gene and its associated risk variant were discovered in the Indian population using a PRISMA-based systematic literature review guideline from online databases such as PubMed & Google Scholar. We constructed pooled odds ratios with 95% confidence intervals using multiple genetic models. Also, we looked for heterogeneity using Cochran's Q Test and the I2 statistic. Publication bias was analyzed using Begg's and Egger's tests. A p-value less than 0.05 was judged to be statistically significant for all tests. After a critical analysis, a total of 24 studies explored about 21 genes with 31 variants out of which only nine genes have been studied more than two times in the Indian population and thus were found eligible for the meta-analysis. It has been found, that the ACE-DD variant (allele model: OR: 1.37 [1.11–1.69], I2 = 0%/ fixed model), ESR1-PvuII (allele model: OR: 1.47 [1.24–1.74], I2 = 0%/ fixed model) significantly increases the risk of migraine in Indian population. Also, a protective role of the LRP1-rs11172113variant was observed for both migraine and its clinical subtype i.e., MA (allelic model: OR of 0.65 [0.50–0.83] I2 = 44% and allele: OR: 0.54 [0.37–0.78], I2 = 52%) respectively. Overall, the results of this meta-analysis indicated that the ACE-DD variant and the ESR1-PvuII were associated with an increased risk of migraine in the Indian community, while the LRP1-rs11172113 variant was associated with protection from migraine in this population.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.