Carrier Status for p.Gly61Glu and p.Arg368His CYP1B1 Mutations Causing Primary Congenital Glaucoma in Iran

Abstract Purpose: To estimate carrier frequencies of CYP1B1 mutations p.Gly61Glu and p.Arg368His, respectively, in Talesh and the east of Guilan province in Iran with a maximum error of 2%. Previously, it was shown that these CYP1B1 mutations may be relatively prevalent in these regions. Methods: Po...

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Autores principales: Ali Heshmati, Peyman Taghizadeh, Hamid Ahmadieh, Mehdi Yaseri, Fatemeh Suri, Mahsa Alizadeh, Marjan Dadashzadeh, Hajar Khatami, Monireh Moradkhah Navi, Parisa Zamanparvar, Hassan Behboudi, Elahe Elahi
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Publicado: Knowledge E 2021
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spelling oai:doaj.org-article:b4b18880fe45485489ffda447c4f575e2021-11-09T08:05:35ZCarrier Status for p.Gly61Glu and p.Arg368His CYP1B1 Mutations Causing Primary Congenital Glaucoma in Iran2008-20102008-322X10.18502/jovr.v16i4.9747https://doaj.org/article/b4b18880fe45485489ffda447c4f575e2021-10-01T00:00:00Zhttps://doi.org/10.18502/jovr.v16i4.9747https://doaj.org/toc/2008-2010https://doaj.org/toc/2008-322XAbstract Purpose: To estimate carrier frequencies of CYP1B1 mutations p.Gly61Glu and p.Arg368His, respectively, in Talesh and the east of Guilan province in Iran with a maximum error of 2%. Previously, it was shown that these CYP1B1 mutations may be relatively prevalent in these regions. Methods: Population-based screenings were performed. DNA was extracted from saliva samples of 1036 individuals from Talesh and 3029 individuals from the east of Guilan. P.Gly61Glu and p.Arg368His screenings were performed, respectively, by RFLP and ARMS-based PCR protocols. For confirmation, the DNA of individuals with mutations was sequenced using the Sanger protocol. Results: Nine individuals from Talesh (0.86%; 95%CI: 0.45–1.64%) carried the p.Gly61Glu mutation, and 73 from the east of Guilan (2.41%; 95%CI: 1.91–3.04%) carried p.Arg368His. There was no significant difference in frequencies between urban and rural regions of the various cities, nor among four cities within the east of Guilan. Conclusion: The frequencies of p.Gly61Glu carriers in Talesh and of p.Arg368His carriers in the east of Guilan were within the 95% confidence interval of a previous study based on screenings of fewer individuals. The reliability of the recent estimates is higher, as the confidence interval for p.Gly61Glu decreased from 6.5% to 1.19% and the interval for p.Arg368His decreased from 4% to 1.13%. Based on the new findings, the maximum expected frequency of p.Gly61Glu carriers in Talesh is 1.64%, and of p.Arg368His carriers in the east of Guilan is 3%. The need for performing premarital screenings in the respective cities can be evaluated.Ali HeshmatiPeyman TaghizadehHamid AhmadiehMehdi YaseriFatemeh SuriMahsa AlizadehMarjan DadashzadehHajar KhatamiMonireh Moradkhah NaviParisa ZamanparvarHassan BehboudiElahe ElahiKnowledge Earticlecyp1b1guilaniranp.arg368hisp.gly61gluprimary congenital glaucomaOphthalmologyRE1-994ENJournal of Ophthalmic & Vision Research, Vol 16, Iss 4, Pp 574-581 (2021)
institution DOAJ
collection DOAJ
language EN
topic cyp1b1
guilan
iran
p.arg368his
p.gly61glu
primary congenital glaucoma
Ophthalmology
RE1-994
spellingShingle cyp1b1
guilan
iran
p.arg368his
p.gly61glu
primary congenital glaucoma
Ophthalmology
RE1-994
Ali Heshmati
Peyman Taghizadeh
Hamid Ahmadieh
Mehdi Yaseri
Fatemeh Suri
Mahsa Alizadeh
Marjan Dadashzadeh
Hajar Khatami
Monireh Moradkhah Navi
Parisa Zamanparvar
Hassan Behboudi
Elahe Elahi
Carrier Status for p.Gly61Glu and p.Arg368His CYP1B1 Mutations Causing Primary Congenital Glaucoma in Iran
description Abstract Purpose: To estimate carrier frequencies of CYP1B1 mutations p.Gly61Glu and p.Arg368His, respectively, in Talesh and the east of Guilan province in Iran with a maximum error of 2%. Previously, it was shown that these CYP1B1 mutations may be relatively prevalent in these regions. Methods: Population-based screenings were performed. DNA was extracted from saliva samples of 1036 individuals from Talesh and 3029 individuals from the east of Guilan. P.Gly61Glu and p.Arg368His screenings were performed, respectively, by RFLP and ARMS-based PCR protocols. For confirmation, the DNA of individuals with mutations was sequenced using the Sanger protocol. Results: Nine individuals from Talesh (0.86%; 95%CI: 0.45–1.64%) carried the p.Gly61Glu mutation, and 73 from the east of Guilan (2.41%; 95%CI: 1.91–3.04%) carried p.Arg368His. There was no significant difference in frequencies between urban and rural regions of the various cities, nor among four cities within the east of Guilan. Conclusion: The frequencies of p.Gly61Glu carriers in Talesh and of p.Arg368His carriers in the east of Guilan were within the 95% confidence interval of a previous study based on screenings of fewer individuals. The reliability of the recent estimates is higher, as the confidence interval for p.Gly61Glu decreased from 6.5% to 1.19% and the interval for p.Arg368His decreased from 4% to 1.13%. Based on the new findings, the maximum expected frequency of p.Gly61Glu carriers in Talesh is 1.64%, and of p.Arg368His carriers in the east of Guilan is 3%. The need for performing premarital screenings in the respective cities can be evaluated.
format article
author Ali Heshmati
Peyman Taghizadeh
Hamid Ahmadieh
Mehdi Yaseri
Fatemeh Suri
Mahsa Alizadeh
Marjan Dadashzadeh
Hajar Khatami
Monireh Moradkhah Navi
Parisa Zamanparvar
Hassan Behboudi
Elahe Elahi
author_facet Ali Heshmati
Peyman Taghizadeh
Hamid Ahmadieh
Mehdi Yaseri
Fatemeh Suri
Mahsa Alizadeh
Marjan Dadashzadeh
Hajar Khatami
Monireh Moradkhah Navi
Parisa Zamanparvar
Hassan Behboudi
Elahe Elahi
author_sort Ali Heshmati
title Carrier Status for p.Gly61Glu and p.Arg368His CYP1B1 Mutations Causing Primary Congenital Glaucoma in Iran
title_short Carrier Status for p.Gly61Glu and p.Arg368His CYP1B1 Mutations Causing Primary Congenital Glaucoma in Iran
title_full Carrier Status for p.Gly61Glu and p.Arg368His CYP1B1 Mutations Causing Primary Congenital Glaucoma in Iran
title_fullStr Carrier Status for p.Gly61Glu and p.Arg368His CYP1B1 Mutations Causing Primary Congenital Glaucoma in Iran
title_full_unstemmed Carrier Status for p.Gly61Glu and p.Arg368His CYP1B1 Mutations Causing Primary Congenital Glaucoma in Iran
title_sort carrier status for p.gly61glu and p.arg368his cyp1b1 mutations causing primary congenital glaucoma in iran
publisher Knowledge E
publishDate 2021
url https://doaj.org/article/b4b18880fe45485489ffda447c4f575e
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