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The rs6265 Polymorphism of the BDNF Gene in the Population of Patients with Multiple Sclerosis in the Tomsk Region
Objectives . To study the effects of the rs6265 polymorphism of the brain-derived neurotrophic factor ( BDNF ) gene on the risk of developing multiple sclerosis (MS), its main clinical characteristics, and the nature of responses to pathogenetic therapy. Materials and methods . The study group consi...
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Published in: | Neuroscience and behavioral physiology 2023-11, Vol.53 (9), p.1497-1501 |
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container_title | Neuroscience and behavioral physiology |
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creator | Titova, M. A. Alifirova, V. M. Kamenskikh, E. M. Musina, N. F. Nikolaeva, T. N. Paderina, D. Z. Boiko, A. S. Ivanova, S. A. |
description | Objectives
. To study the effects of the rs6265 polymorphism of the brain-derived neurotrophic factor (
BDNF
) gene on the risk of developing multiple sclerosis (MS), its main clinical characteristics, and the nature of responses to pathogenetic therapy.
Materials and methods
. The study group consisted of 321 patients and the control group of 266 healthy people. DNA was extracted from venous blood using the standard phenol-chloroform method. Genotyping was carried out by real-time polymerase chain reaction (PCR) using competing TaqMan probes complementary to the polymorphic nucleotide sequence.
Results
. Carriage of the C allele and the CC genotype of the rs6265 polymorphism of the
BDNF
gene was found to be a factor determining a more favorable course of MS.
Conclusions
. Carriers of this genotype had a low rate of progression of MS, a lower frequency of exacerbations, and a less marked degree of disability, while disease duration was comparable; carriers also had a higher frequency of more optimal responses to therapy with first- and second-line MS disease-modifying drugs. |
doi_str_mv | 10.1007/s11055-023-01544-z |
format | article |
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. To study the effects of the rs6265 polymorphism of the brain-derived neurotrophic factor (
BDNF
) gene on the risk of developing multiple sclerosis (MS), its main clinical characteristics, and the nature of responses to pathogenetic therapy.
Materials and methods
. The study group consisted of 321 patients and the control group of 266 healthy people. DNA was extracted from venous blood using the standard phenol-chloroform method. Genotyping was carried out by real-time polymerase chain reaction (PCR) using competing TaqMan probes complementary to the polymorphic nucleotide sequence.
Results
. Carriage of the C allele and the CC genotype of the rs6265 polymorphism of the
BDNF
gene was found to be a factor determining a more favorable course of MS.
Conclusions
. Carriers of this genotype had a low rate of progression of MS, a lower frequency of exacerbations, and a less marked degree of disability, while disease duration was comparable; carriers also had a higher frequency of more optimal responses to therapy with first- and second-line MS disease-modifying drugs.</description><identifier>ISSN: 0097-0549</identifier><identifier>EISSN: 1573-899X</identifier><identifier>DOI: 10.1007/s11055-023-01544-z</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Behavioral Sciences ; Biomedical and Life Sciences ; Biomedicine ; Brain-derived neurotrophic factor ; Chloroform ; DNA probes ; Gene polymorphism ; Genotyping ; Methods of Investigation and Diagnostics ; Multiple sclerosis ; Neurobiology ; Neurosciences ; Nucleotide sequence ; Polymerase chain reaction ; Polymorphism</subject><ispartof>Neuroscience and behavioral physiology, 2023-11, Vol.53 (9), p.1497-1501</ispartof><rights>Springer Nature Switzerland AG 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c185z-9d77f1c03208e1446db6c652119294dfd6e4dd6a6ffcff5f3e08aa2124d698fb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Titova, M. A.</creatorcontrib><creatorcontrib>Alifirova, V. M.</creatorcontrib><creatorcontrib>Kamenskikh, E. M.</creatorcontrib><creatorcontrib>Musina, N. F.</creatorcontrib><creatorcontrib>Nikolaeva, T. N.</creatorcontrib><creatorcontrib>Paderina, D. Z.</creatorcontrib><creatorcontrib>Boiko, A. S.</creatorcontrib><creatorcontrib>Ivanova, S. A.</creatorcontrib><title>The rs6265 Polymorphism of the BDNF Gene in the Population of Patients with Multiple Sclerosis in the Tomsk Region</title><title>Neuroscience and behavioral physiology</title><addtitle>Neurosci Behav Physi</addtitle><description>Objectives
. To study the effects of the rs6265 polymorphism of the brain-derived neurotrophic factor (
BDNF
) gene on the risk of developing multiple sclerosis (MS), its main clinical characteristics, and the nature of responses to pathogenetic therapy.
Materials and methods
. The study group consisted of 321 patients and the control group of 266 healthy people. DNA was extracted from venous blood using the standard phenol-chloroform method. Genotyping was carried out by real-time polymerase chain reaction (PCR) using competing TaqMan probes complementary to the polymorphic nucleotide sequence.
Results
. Carriage of the C allele and the CC genotype of the rs6265 polymorphism of the
BDNF
gene was found to be a factor determining a more favorable course of MS.
Conclusions
. Carriers of this genotype had a low rate of progression of MS, a lower frequency of exacerbations, and a less marked degree of disability, while disease duration was comparable; carriers also had a higher frequency of more optimal responses to therapy with first- and second-line MS disease-modifying drugs.</description><subject>Behavioral Sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Brain-derived neurotrophic factor</subject><subject>Chloroform</subject><subject>DNA probes</subject><subject>Gene polymorphism</subject><subject>Genotyping</subject><subject>Methods of Investigation and Diagnostics</subject><subject>Multiple sclerosis</subject><subject>Neurobiology</subject><subject>Neurosciences</subject><subject>Nucleotide sequence</subject><subject>Polymerase chain reaction</subject><subject>Polymorphism</subject><issn>0097-0549</issn><issn>1573-899X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kMFOwzAQRC0EEqXwA5wscTbYju3ERyi0IBWooEjcrDSx25QkDnYi1H49bgPixmlXu_NmVwPAOcGXBOP4yhOCOUeYRggTzhjaHoAB4XGEEinfD8EAYxkjzJk8Bifer3GA4gQPgJuvNHReUMHhzJabyrpmVfgKWgPbsLq5fRrDia41LOr9YGabrkzbwtY7ySx0um49_CraFXzsyrZoSg1fs1I76wv_S81t5T_gi14G7hQcmbT0-uynDsHb-G4-ukfT58nD6HqKMpLwLZJ5HBuS4YjiRBPGRL4QmeCUEEkly00uNMtzkQpjMmO4iTRO0pQSynIhE7OIhuCi922c_ey0b9Xadq4OJxWVJOKx5FwGFe1VWXjYO21U44oqdRtFsNplq_psVchW7bNV2wBFPeSDuF5q92f9D_UNR5h9Ag</recordid><startdate>20231101</startdate><enddate>20231101</enddate><creator>Titova, M. 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A. ; Alifirova, V. M. ; Kamenskikh, E. M. ; Musina, N. F. ; Nikolaeva, T. N. ; Paderina, D. Z. ; Boiko, A. S. ; Ivanova, S. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c185z-9d77f1c03208e1446db6c652119294dfd6e4dd6a6ffcff5f3e08aa2124d698fb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Behavioral Sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Brain-derived neurotrophic factor</topic><topic>Chloroform</topic><topic>DNA probes</topic><topic>Gene polymorphism</topic><topic>Genotyping</topic><topic>Methods of Investigation and Diagnostics</topic><topic>Multiple sclerosis</topic><topic>Neurobiology</topic><topic>Neurosciences</topic><topic>Nucleotide sequence</topic><topic>Polymerase chain reaction</topic><topic>Polymorphism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Titova, M. A.</creatorcontrib><creatorcontrib>Alifirova, V. M.</creatorcontrib><creatorcontrib>Kamenskikh, E. M.</creatorcontrib><creatorcontrib>Musina, N. F.</creatorcontrib><creatorcontrib>Nikolaeva, T. N.</creatorcontrib><creatorcontrib>Paderina, D. Z.</creatorcontrib><creatorcontrib>Boiko, A. S.</creatorcontrib><creatorcontrib>Ivanova, S. A.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Physical Education Index</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><jtitle>Neuroscience and behavioral physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Titova, M. A.</au><au>Alifirova, V. M.</au><au>Kamenskikh, E. M.</au><au>Musina, N. F.</au><au>Nikolaeva, T. N.</au><au>Paderina, D. Z.</au><au>Boiko, A. S.</au><au>Ivanova, S. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The rs6265 Polymorphism of the BDNF Gene in the Population of Patients with Multiple Sclerosis in the Tomsk Region</atitle><jtitle>Neuroscience and behavioral physiology</jtitle><stitle>Neurosci Behav Physi</stitle><date>2023-11-01</date><risdate>2023</risdate><volume>53</volume><issue>9</issue><spage>1497</spage><epage>1501</epage><pages>1497-1501</pages><issn>0097-0549</issn><eissn>1573-899X</eissn><abstract>Objectives
. To study the effects of the rs6265 polymorphism of the brain-derived neurotrophic factor (
BDNF
) gene on the risk of developing multiple sclerosis (MS), its main clinical characteristics, and the nature of responses to pathogenetic therapy.
Materials and methods
. The study group consisted of 321 patients and the control group of 266 healthy people. DNA was extracted from venous blood using the standard phenol-chloroform method. Genotyping was carried out by real-time polymerase chain reaction (PCR) using competing TaqMan probes complementary to the polymorphic nucleotide sequence.
Results
. Carriage of the C allele and the CC genotype of the rs6265 polymorphism of the
BDNF
gene was found to be a factor determining a more favorable course of MS.
Conclusions
. Carriers of this genotype had a low rate of progression of MS, a lower frequency of exacerbations, and a less marked degree of disability, while disease duration was comparable; carriers also had a higher frequency of more optimal responses to therapy with first- and second-line MS disease-modifying drugs.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><doi>10.1007/s11055-023-01544-z</doi><tpages>5</tpages></addata></record> |
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subjects | Behavioral Sciences Biomedical and Life Sciences Biomedicine Brain-derived neurotrophic factor Chloroform DNA probes Gene polymorphism Genotyping Methods of Investigation and Diagnostics Multiple sclerosis Neurobiology Neurosciences Nucleotide sequence Polymerase chain reaction Polymorphism |
title | The rs6265 Polymorphism of the BDNF Gene in the Population of Patients with Multiple Sclerosis in the Tomsk Region |
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