Neurophysiology and genetics of burning mouth syndrome

dc.contributor.authorKolkka M.
dc.contributor.authorForssell H.
dc.contributor.authorVirtanen A.
dc.contributor.authorPuhakka A.
dc.contributor.authorPesonen U.
dc.contributor.authorJääskeläinen S.K.
dc.contributor.organizationfi=biolääketieteen laitos|en=Institute of Biomedicine|
dc.contributor.organizationfi=hammaslääketieteen laitos|en=Institute of Dentistry|
dc.contributor.organizationfi=kliininen neurofysiologia|en=Clinical Neurophysiology|
dc.contributor.organizationfi=lääketieteellinen tiedekunta|en=Faculty of Medicine|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.13290506867
dc.contributor.organization-code1.2.246.10.2458963.20.64787032594
dc.contributor.organization-code1.2.246.10.2458963.20.77952289591
dc.contributor.organization-code1.2.246.10.2458963.20.82306181437
dc.converis.publication-id39901870
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/39901870
dc.date.accessioned2022-10-28T13:50:13Z
dc.date.available2022-10-28T13:50:13Z
dc.description.abstract<p>Background and aims: Neuropathic mechanisms are involved in burning mouth syndrome (BMS), and variation of the dopamine D2 receptor (DRD2) gene contributes to experimental pain perception. We investigated whether neurophysiologic findings differ in BMS patients compared to healthy controls, and whether 957C>T polymorphism of the DRD2 gene influences thermal sensitivity or pain experience in BMS.<br /><br />Methods: Forty‐five BMS patients (43 women), mean age 62.5 years, and 32 healthy controls (30 women), mean age 64.8 years, participated. Patients estimated pain intensity, interference, suffering and sleep with Numeric Rating Scale. Blink reflex tests of the supraorbital (SON), mental (MN) and lingual (LN) nerves, and thermal quantitative sensory testing were done. The results were analysed with ANOVA. DRD2 gene 957C>T polymorphism was determined in 31 patients, and its effects on neurophysiologic and clinical variables were analysed.<br /><br />Results: Cool (p = 0.0090) and warm detection thresholds (p = 0.0229) of the tongue were higher in BMS patients than controls. The stimulation threshold for SON BR was higher in patients than in controls (p = 0.0056). The latencies of R2 component were longer in BMS patients than in controls (p = 0.0005) at the SON distribution. Habituation of SON BR did not differ between the groups. The heat pain thresholds were highest (p = 0.0312) in homozygous patients with 957TT, who also reported most interference (p = 0.0352) and greatest suffering (p = 0.0341). Genotype 957CC associated with sleep disturbances (p = 0.0254).<br /><br />Conclusions: Burning mouth syndrome patients showed thermal hypoesthesia within LN distribution compatible with small fibre neuropathy. The DRD2 957C>T genotype influences perception and experience of BMS pain.</p><p><br />Significance: The results confirm earlier findings of neuropathic pain in BMS. The DRD2 957 C>T genotype influences perception and experience of clinical pain in BMS.<br /></p>
dc.format.pagerange1153
dc.format.pagerange1161
dc.identifier.jour-issn1090-3801
dc.identifier.olddbid184641
dc.identifier.oldhandle10024/167735
dc.identifier.urihttps://www.utupub.fi/handle/11111/38944
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/full/10.1002/ejp.1382
dc.identifier.urnURN:NBN:fi-fe2021042823800
dc.language.isoen
dc.okm.affiliatedauthorKolkka, Marina
dc.okm.affiliatedauthorForssell, Heli
dc.okm.affiliatedauthorPesonen, Ullamari
dc.okm.affiliatedauthorJääskeläinen, Satu
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline1184 Genetics, developmental biology, physiologyen_GB
dc.okm.discipline3112 Neurosciencesen_GB
dc.okm.discipline313 Dentistryen_GB
dc.okm.discipline1184 Genetiikka, kehitysbiologia, fysiologiafi_FI
dc.okm.discipline3112 Neurotieteetfi_FI
dc.okm.discipline313 Hammaslääketieteetfi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherBlackwell Publishing Ltd
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.doi10.1002/ejp.1382
dc.relation.ispartofjournalEuropean Journal of Pain
dc.relation.issue6
dc.relation.volume23
dc.source.identifierhttps://www.utupub.fi/handle/10024/167735
dc.titleNeurophysiology and genetics of burning mouth syndrome
dc.year.issued2019

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