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The BDNF Val66Met polymorphism is associated with the functional connectivity dynamics of pain modulatory systems in primary dysmenorrhea
Primary dysmenorrhea (PDM), menstrual pain without an organic cause, is a prevailing problem in women of reproductive age. We previously reported alterations of structure and functional connectivity (FC) in the periaqueductal gray (PAG) of PDM subjects. Given that the brain derived neurotrophic fact...
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Published in: | Scientific reports 2016-03, Vol.6 (1), p.23639-23639, Article 23639 |
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description | Primary dysmenorrhea (PDM), menstrual pain without an organic cause, is a prevailing problem in women of reproductive age. We previously reported alterations of structure and functional connectivity (FC) in the periaqueductal gray (PAG) of PDM subjects. Given that the brain derived neurotrophic factor (BDNF) acts as a pain modulator within the PAG and the
BDNF
Val66Met polymorphism contributes towards susceptibility to PDM, the present study of imaging genetics set out to investigate the influence of, firstly, the
BDNF
Val66Met single nucleotide polymorphism and, secondly, the genotype-pain interplays on the descending pain modulatory systems in the context of PAG-seeded FC patterning. Fifty-six subjects with PDM and 60 controls participated in the current study of resting-state functional magnetic resonance imaging (fMRI) during the menstruation and peri-ovulatory phases; in parallel, blood samples were taken for genotyping. Our findings indicate that the
BDNF
Val66Met polymorphism is associated with the diverse functional expressions of the descending pain modulatory systems. Furthermore, PAG FC patterns in pain-free controls are altered in women with PDM in a genotype-specific manner. Such resilient brain dynamics may underpin the individual differences and shed light on the vulnerability for chronic pain disorders of PDM subjects. |
doi_str_mv | 10.1038/srep23639 |
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BDNF
Val66Met polymorphism contributes towards susceptibility to PDM, the present study of imaging genetics set out to investigate the influence of, firstly, the
BDNF
Val66Met single nucleotide polymorphism and, secondly, the genotype-pain interplays on the descending pain modulatory systems in the context of PAG-seeded FC patterning. Fifty-six subjects with PDM and 60 controls participated in the current study of resting-state functional magnetic resonance imaging (fMRI) during the menstruation and peri-ovulatory phases; in parallel, blood samples were taken for genotyping. Our findings indicate that the
BDNF
Val66Met polymorphism is associated with the diverse functional expressions of the descending pain modulatory systems. Furthermore, PAG FC patterns in pain-free controls are altered in women with PDM in a genotype-specific manner. Such resilient brain dynamics may underpin the individual differences and shed light on the vulnerability for chronic pain disorders of PDM subjects.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/srep23639</identifier><identifier>PMID: 27010666</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>45/77 ; 59/57 ; 631/378/1689/2610 ; 631/378/2583 ; 692/1807/410/2610 ; 692/420/2489/144 ; Adult ; Brain Mapping ; Brain-derived neurotrophic factor ; Brain-Derived Neurotrophic Factor - genetics ; Chronic pain ; Dysmenorrhea - physiopathology ; Female ; Functional magnetic resonance imaging ; Gene polymorphism ; Genotyping ; Humanities and Social Sciences ; Humans ; Menstruation ; Methionine - genetics ; multidisciplinary ; Neural networks ; Neuroimaging ; Pain ; Pain - physiopathology ; Periaqueductal gray area ; Polymorphism, Single Nucleotide ; Science ; Science (multidisciplinary) ; Single-nucleotide polymorphism ; Valine - genetics ; Young Adult</subject><ispartof>Scientific reports, 2016-03, Vol.6 (1), p.23639-23639, Article 23639</ispartof><rights>The Author(s) 2016</rights><rights>Copyright Nature Publishing Group Mar 2016</rights><rights>Copyright © 2016, Macmillan Publishers Limited 2016 Macmillan Publishers Limited</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-a4a0699daf4932ff338a6caeb9605fbcfd5ca407f205433fd221888d141586fc3</citedby><cites>FETCH-LOGICAL-c438t-a4a0699daf4932ff338a6caeb9605fbcfd5ca407f205433fd221888d141586fc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1898684128/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1898684128?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,25734,27905,27906,36993,36994,44571,53772,53774,74875</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27010666$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wei, Shyh-Yuh</creatorcontrib><creatorcontrib>Chao, Hsiang-Tai</creatorcontrib><creatorcontrib>Tu, Cheng-Hao</creatorcontrib><creatorcontrib>Lin, Ming-Wei</creatorcontrib><creatorcontrib>Li, Wei-Chi</creatorcontrib><creatorcontrib>Low, Intan</creatorcontrib><creatorcontrib>Shen, Horng-Der</creatorcontrib><creatorcontrib>Chen, Li-Fen</creatorcontrib><creatorcontrib>Hsieh, Jen-Chuen</creatorcontrib><title>The BDNF Val66Met polymorphism is associated with the functional connectivity dynamics of pain modulatory systems in primary dysmenorrhea</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Primary dysmenorrhea (PDM), menstrual pain without an organic cause, is a prevailing problem in women of reproductive age. We previously reported alterations of structure and functional connectivity (FC) in the periaqueductal gray (PAG) of PDM subjects. Given that the brain derived neurotrophic factor (BDNF) acts as a pain modulator within the PAG and the
BDNF
Val66Met polymorphism contributes towards susceptibility to PDM, the present study of imaging genetics set out to investigate the influence of, firstly, the
BDNF
Val66Met single nucleotide polymorphism and, secondly, the genotype-pain interplays on the descending pain modulatory systems in the context of PAG-seeded FC patterning. Fifty-six subjects with PDM and 60 controls participated in the current study of resting-state functional magnetic resonance imaging (fMRI) during the menstruation and peri-ovulatory phases; in parallel, blood samples were taken for genotyping. Our findings indicate that the
BDNF
Val66Met polymorphism is associated with the diverse functional expressions of the descending pain modulatory systems. Furthermore, PAG FC patterns in pain-free controls are altered in women with PDM in a genotype-specific manner. Such resilient brain dynamics may underpin the individual differences and shed light on the vulnerability for chronic pain disorders of PDM subjects.</description><subject>45/77</subject><subject>59/57</subject><subject>631/378/1689/2610</subject><subject>631/378/2583</subject><subject>692/1807/410/2610</subject><subject>692/420/2489/144</subject><subject>Adult</subject><subject>Brain Mapping</subject><subject>Brain-derived neurotrophic factor</subject><subject>Brain-Derived Neurotrophic Factor - genetics</subject><subject>Chronic pain</subject><subject>Dysmenorrhea - physiopathology</subject><subject>Female</subject><subject>Functional magnetic resonance imaging</subject><subject>Gene polymorphism</subject><subject>Genotyping</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Menstruation</subject><subject>Methionine - genetics</subject><subject>multidisciplinary</subject><subject>Neural networks</subject><subject>Neuroimaging</subject><subject>Pain</subject><subject>Pain - 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genetics</topic><topic>Chronic pain</topic><topic>Dysmenorrhea - physiopathology</topic><topic>Female</topic><topic>Functional magnetic resonance imaging</topic><topic>Gene polymorphism</topic><topic>Genotyping</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>Menstruation</topic><topic>Methionine - genetics</topic><topic>multidisciplinary</topic><topic>Neural networks</topic><topic>Neuroimaging</topic><topic>Pain</topic><topic>Pain - physiopathology</topic><topic>Periaqueductal gray area</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Single-nucleotide polymorphism</topic><topic>Valine - genetics</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wei, Shyh-Yuh</creatorcontrib><creatorcontrib>Chao, Hsiang-Tai</creatorcontrib><creatorcontrib>Tu, Cheng-Hao</creatorcontrib><creatorcontrib>Lin, Ming-Wei</creatorcontrib><creatorcontrib>Li, Wei-Chi</creatorcontrib><creatorcontrib>Low, Intan</creatorcontrib><creatorcontrib>Shen, Horng-Der</creatorcontrib><creatorcontrib>Chen, Li-Fen</creatorcontrib><creatorcontrib>Hsieh, Jen-Chuen</creatorcontrib><collection>SpringerOpen</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Proquest Health & Medical Complete</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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 One Sustainability</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Science Journals</collection><collection>Biological Science Database</collection><collection>Publicly Available Content (ProQuest)</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 Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wei, Shyh-Yuh</au><au>Chao, Hsiang-Tai</au><au>Tu, Cheng-Hao</au><au>Lin, Ming-Wei</au><au>Li, Wei-Chi</au><au>Low, Intan</au><au>Shen, Horng-Der</au><au>Chen, Li-Fen</au><au>Hsieh, Jen-Chuen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The BDNF Val66Met polymorphism is associated with the functional connectivity dynamics of pain modulatory systems in primary dysmenorrhea</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2016-03-24</date><risdate>2016</risdate><volume>6</volume><issue>1</issue><spage>23639</spage><epage>23639</epage><pages>23639-23639</pages><artnum>23639</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Primary dysmenorrhea (PDM), menstrual pain without an organic cause, is a prevailing problem in women of reproductive age. We previously reported alterations of structure and functional connectivity (FC) in the periaqueductal gray (PAG) of PDM subjects. Given that the brain derived neurotrophic factor (BDNF) acts as a pain modulator within the PAG and the
BDNF
Val66Met polymorphism contributes towards susceptibility to PDM, the present study of imaging genetics set out to investigate the influence of, firstly, the
BDNF
Val66Met single nucleotide polymorphism and, secondly, the genotype-pain interplays on the descending pain modulatory systems in the context of PAG-seeded FC patterning. Fifty-six subjects with PDM and 60 controls participated in the current study of resting-state functional magnetic resonance imaging (fMRI) during the menstruation and peri-ovulatory phases; in parallel, blood samples were taken for genotyping. Our findings indicate that the
BDNF
Val66Met polymorphism is associated with the diverse functional expressions of the descending pain modulatory systems. Furthermore, PAG FC patterns in pain-free controls are altered in women with PDM in a genotype-specific manner. Such resilient brain dynamics may underpin the individual differences and shed light on the vulnerability for chronic pain disorders of PDM subjects.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>27010666</pmid><doi>10.1038/srep23639</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 45/77 59/57 631/378/1689/2610 631/378/2583 692/1807/410/2610 692/420/2489/144 Adult Brain Mapping Brain-derived neurotrophic factor Brain-Derived Neurotrophic Factor - genetics Chronic pain Dysmenorrhea - physiopathology Female Functional magnetic resonance imaging Gene polymorphism Genotyping Humanities and Social Sciences Humans Menstruation Methionine - genetics multidisciplinary Neural networks Neuroimaging Pain Pain - physiopathology Periaqueductal gray area Polymorphism, Single Nucleotide Science Science (multidisciplinary) Single-nucleotide polymorphism Valine - genetics Young Adult |
title | The BDNF Val66Met polymorphism is associated with the functional connectivity dynamics of pain modulatory systems in primary dysmenorrhea |
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