Analysis of the mutations in exon 10 of MEFV gene in patients with premature coronary heart disease in west Azerbaijan province of Iran
Introduction: Premature coronary heart disease (PCHD) affects public health and leads to death. PCHD has several genetic and environmental risk factors. The aim of this study was to analysis of the mutations in exon 10 of MEFV gene in patients with PCHD in West Azerbaijan province of Iran. Methods:...
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| Format: | Article |
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Tabriz University of Medical Sciences
2018-03-01
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| Series: | Journal of Cardiovascular and Thoracic Research |
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| Online Access: | https://jcvtr.tbzmed.ac.ir/PDF/jcvtr-10-20.pdf |
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| author | Morteza Bagheri Kamal Khadem-Vatani Mir Hossein Seyed Mohammad Zad Isa Abdi Rad Behzad Rahimi Alireza Rostamzadeh Mojtaba Godarzi Shabnam Ashena |
| author_facet | Morteza Bagheri Kamal Khadem-Vatani Mir Hossein Seyed Mohammad Zad Isa Abdi Rad Behzad Rahimi Alireza Rostamzadeh Mojtaba Godarzi Shabnam Ashena |
| author_sort | Morteza Bagheri |
| collection | DOAJ |
| description | Introduction: Premature coronary heart disease (PCHD) affects public health and leads to death. PCHD has several genetic and environmental risk factors. The aim of this study was to analysis of the mutations in exon 10 of MEFV gene in patients with PCHD in West Azerbaijan province of Iran. Methods: Totally 41 PCHD patients who were admitted to the cardiology unit of Sayedoshohada hospital (Urmia, Iran) enrolled in the study. Selection of the patients was done based on the strict criteria, that is, who had a minimum of one angiographically documented coronary artery with the stenosis of 50%. Mutations in exon 10 of MEFV gene were found by direct sequencing. Results: V726A, M680I, K695R, and A744S mutations with 2.44%, 1.22%, 1.22%, and 1.22%, allelic frequency were found, respectively. Five patients (12.2%) with PCHD carried at least one mutated MEFV allele. Heterozygote V726A was the most frequent mutation among tested cases (4.88%), followed by heterozygote M680I, heterozygote K695R, and heterozygote A744S. Conclusion: The results of the present study imply that the frequency of the MEFV gene exon 10 is significantly high in PCHD patients. This is the first report in its own kind in clinically diagnosed PCHD patients of Iranian Azeri Turkish population. |
| first_indexed | 2024-12-21T14:52:47Z |
| format | Article |
| id | doaj.art-6e7d79609867430584be0360d55a5f22 |
| institution | Directory Open Access Journal |
| issn | 2008-5117 2008-6830 |
| language | English |
| last_indexed | 2024-12-21T14:52:47Z |
| publishDate | 2018-03-01 |
| publisher | Tabriz University of Medical Sciences |
| record_format | Article |
| series | Journal of Cardiovascular and Thoracic Research |
| spelling | doaj.art-6e7d79609867430584be0360d55a5f222022-12-21T18:59:50ZengTabriz University of Medical SciencesJournal of Cardiovascular and Thoracic Research2008-51172008-68302018-03-01101202310.15171/jcvtr.2018.03JCVTR_19384_20170515133901Analysis of the mutations in exon 10 of MEFV gene in patients with premature coronary heart disease in west Azerbaijan province of IranMorteza Bagheri0Kamal Khadem-Vatani1Mir Hossein Seyed Mohammad Zad2Isa Abdi Rad3Behzad Rahimi4Alireza Rostamzadeh5Mojtaba Godarzi6Shabnam Ashena7Cellular and Molecular Research Center, Urmia University of Medical Sciences, Urmia, IranSeyyed-al Shohada University Hospital, Urmia University of Medical Sciences, Urmia, IranSeyyed-al Shohada University Hospital, Urmia University of Medical Sciences, Urmia, IranCellular and Molecular Research Center, Urmia University of Medical Sciences, Urmia, IranSeyyed-al Shohada University Hospital, Urmia University of Medical Sciences, Urmia, IranSeyyed-al Shohada University Hospital, Urmia University of Medical Sciences, Urmia, IranSeyyed-al Shohada University Hospital, Urmia University of Medical Sciences, Urmia, IranSeyyed-al Shohada University Hospital, Urmia University of Medical Sciences, Urmia, IranIntroduction: Premature coronary heart disease (PCHD) affects public health and leads to death. PCHD has several genetic and environmental risk factors. The aim of this study was to analysis of the mutations in exon 10 of MEFV gene in patients with PCHD in West Azerbaijan province of Iran. Methods: Totally 41 PCHD patients who were admitted to the cardiology unit of Sayedoshohada hospital (Urmia, Iran) enrolled in the study. Selection of the patients was done based on the strict criteria, that is, who had a minimum of one angiographically documented coronary artery with the stenosis of 50%. Mutations in exon 10 of MEFV gene were found by direct sequencing. Results: V726A, M680I, K695R, and A744S mutations with 2.44%, 1.22%, 1.22%, and 1.22%, allelic frequency were found, respectively. Five patients (12.2%) with PCHD carried at least one mutated MEFV allele. Heterozygote V726A was the most frequent mutation among tested cases (4.88%), followed by heterozygote M680I, heterozygote K695R, and heterozygote A744S. Conclusion: The results of the present study imply that the frequency of the MEFV gene exon 10 is significantly high in PCHD patients. This is the first report in its own kind in clinically diagnosed PCHD patients of Iranian Azeri Turkish population.https://jcvtr.tbzmed.ac.ir/PDF/jcvtr-10-20.pdfmefvpchdmutations |
| spellingShingle | Morteza Bagheri Kamal Khadem-Vatani Mir Hossein Seyed Mohammad Zad Isa Abdi Rad Behzad Rahimi Alireza Rostamzadeh Mojtaba Godarzi Shabnam Ashena Analysis of the mutations in exon 10 of MEFV gene in patients with premature coronary heart disease in west Azerbaijan province of Iran Journal of Cardiovascular and Thoracic Research mefv pchd mutations |
| title | Analysis of the mutations in exon 10 of MEFV gene in patients with premature coronary heart disease in west Azerbaijan province of Iran |
| title_full | Analysis of the mutations in exon 10 of MEFV gene in patients with premature coronary heart disease in west Azerbaijan province of Iran |
| title_fullStr | Analysis of the mutations in exon 10 of MEFV gene in patients with premature coronary heart disease in west Azerbaijan province of Iran |
| title_full_unstemmed | Analysis of the mutations in exon 10 of MEFV gene in patients with premature coronary heart disease in west Azerbaijan province of Iran |
| title_short | Analysis of the mutations in exon 10 of MEFV gene in patients with premature coronary heart disease in west Azerbaijan province of Iran |
| title_sort | analysis of the mutations in exon 10 of mefv gene in patients with premature coronary heart disease in west azerbaijan province of iran |
| topic | mefv pchd mutations |
| url | https://jcvtr.tbzmed.ac.ir/PDF/jcvtr-10-20.pdf |
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