Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/7377
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dc.contributor.authorBalkarli, A.-
dc.contributor.authorSengül, C.-
dc.contributor.authorTepeli, E.-
dc.contributor.authorBalkarli, H.-
dc.contributor.authorCobankara, Veli-
dc.date.accessioned2019-08-16T12:29:26Z
dc.date.available2019-08-16T12:29:26Z
dc.date.issued2014-
dc.identifier.issn1471-2474-
dc.identifier.urihttps://hdl.handle.net/11499/7377-
dc.identifier.urihttps://doi.org/10.1186/1471-2474-15-191-
dc.description.abstractBackground: SNAP-25 protein is contributory to plasma membrane and synaptic vesicle fusions that are critical points in neurotransmission. SNAP-25 gene is associated with behavioral symptoms, personality and psychological disorders. In addition, SNAP-25 protein can be related to different neurotransmitter functions due to its association with vesicle membrane transition and fusion. This is important because neurologic, cognitive, and psychologic disorders in fibromyalgia syndrome (FMS) can be related to this function. This relationship may be enlightening for etiopathogenesis of FMS and treatment approaches. We aimed to study a SNAP-25 gene polymorphism, which is related to many psychiatric diseases, and FMS association in this prospective study. Methods. We included 71 patients who were diagnosed according to new criteria and 57 matched healthy women in this study. Both groups were evaluated regarding age, height, weight, BMI, education level, marital and occupational status. A new diagnosis of FMS was made from criteria scoring, SF-36, Beck depression scale, and VAS that were applied to the patient group. SNAP-25 gene polymorphism and disease activity score correlations were compared. Results: Mean age was 38±5,196 and 38.12±4.939 in patient and control groups, respectively (p=0.542). No significant difference was found between groups regarding age, height, weight, BMI, education level, marital or occupational status (p > 0.05). Ddel T/C genotype was significantly higher in the patient group (p = 0.009). MnlI gene polymorphism did not show a correlation with any score whereas a significant correlation was found between Ddel T/C genotype and Beck depression scale and VAS score (p ; 0.05). Conclusion: FMS etiopathogenesis is not clearly known. Numerous neurologic, cognitive and psychological disorders were found during studies looking at cause. Our study showed increased SNAP-25 Ddel T/C genotype in FMS patients compared to the control group, which is related to behavioral symptoms, personality and psychological disorders in FMS patients. © 2014Balkarli et al.; licensee BioMed Central Ltd.en_US
dc.language.isoenen_US
dc.publisherBioMed Central Ltd.en_US
dc.relation.ispartofBMC Musculoskeletal Disordersen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectFibromyalgiaen_US
dc.subjectSynaptosomal-associated protein 25 gene polymorphismen_US
dc.subjectsynaptosomal associated protein 25en_US
dc.subjectSNAP25 protein, humanen_US
dc.subjectadulten_US
dc.subjectageen_US
dc.subjectarticleen_US
dc.subjectBeck Depression Inventoryen_US
dc.subjectbehavior disorderen_US
dc.subjectbody heighten_US
dc.subjectbody massen_US
dc.subjectbody weighten_US
dc.subjectcase control studyen_US
dc.subjectcontrolled studyen_US
dc.subjectdisease activity scoreen_US
dc.subjecteducational statusen_US
dc.subjectemployment statusen_US
dc.subjectetiologyen_US
dc.subjectfemaleen_US
dc.subjectfibromyalgiaen_US
dc.subjectgenetic associationen_US
dc.subjectgenotypeen_US
dc.subjecthumanen_US
dc.subjectmajor clinical studyen_US
dc.subjectmarriageen_US
dc.subjectmental diseaseen_US
dc.subjectmiddle ageden_US
dc.subjectpersonality disorderen_US
dc.subjectprospective studyen_US
dc.subjectShort Form 36en_US
dc.subjectsingle nucleotide polymorphismen_US
dc.subjectvisual analog scaleen_US
dc.subjectageden_US
dc.subjectArticleen_US
dc.subjectdisease activityen_US
dc.subjectgenetic polymorphismen_US
dc.subjectcentral nervous system sensitizationen_US
dc.subjectdepressionen_US
dc.subjectgeneticsen_US
dc.subjectnerve conductionen_US
dc.subjectpain measurementen_US
dc.subjectphysiologyen_US
dc.subjectpsychologyen_US
dc.subjectsymptom assessmenten_US
dc.subjectsyndromeen_US
dc.subjectAdulten_US
dc.subjectCase-Control Studiesen_US
dc.subjectCentral Nervous System Sensitizationen_US
dc.subjectDepressive Disorderen_US
dc.subjectFemaleen_US
dc.subjectHumansen_US
dc.subjectNeural Conductionen_US
dc.subjectPain Measurementen_US
dc.subjectPolymorphism, Single Nucleotideen_US
dc.subjectSymptom Assessmenten_US
dc.subjectSynaptosomal-Associated Protein 25en_US
dc.subjectSyndromeen_US
dc.titleSynaptosomal-associated protein 25 (Snap-25) gene Polymorphism frequency in fibromyalgia syndrome and relationship with clinical symptomsen_US
dc.typeArticleen_US
dc.identifier.volume15en_US
dc.identifier.issue1en_US
dc.authorid0000-0003-1264-7971-
dc.identifier.doi10.1186/1471-2474-15-191-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid24885975en_US
dc.identifier.scopus2-s2.0-84903317027en_US
dc.identifier.wosWOS:000338143800002en_US
dc.identifier.scopusqualityQ1-
dc.ownerPamukkale University-
item.openairetypeArticle-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
item.grantfulltextopen-
item.cerifentitytypePublications-
crisitem.author.dept14.02. Internal Medicine-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
TR Dizin İndeksli Yayınlar Koleksiyonu / TR Dizin Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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