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https://hdl.handle.net/11499/7377
Title: | Synaptosomal-associated protein 25 (Snap-25) gene Polymorphism frequency in fibromyalgia syndrome and relationship with clinical symptoms | Authors: | Balkarli, A. Sengül, C. Tepeli, E. Balkarli, H. Cobankara, Veli |
Keywords: | Fibromyalgia Synaptosomal-associated protein 25 gene polymorphism synaptosomal associated protein 25 SNAP25 protein, human adult age article Beck Depression Inventory behavior disorder body height body mass body weight case control study controlled study disease activity score educational status employment status etiology female fibromyalgia genetic association genotype human major clinical study marriage mental disease middle aged personality disorder prospective study Short Form 36 single nucleotide polymorphism visual analog scale aged Article disease activity genetic polymorphism central nervous system sensitization depression genetics nerve conduction pain measurement physiology psychology symptom assessment syndrome Adult Case-Control Studies Central Nervous System Sensitization Depressive Disorder Female Humans Neural Conduction Pain Measurement Polymorphism, Single Nucleotide Symptom Assessment Synaptosomal-Associated Protein 25 Syndrome |
Publisher: | BioMed Central Ltd. | Abstract: | Background: 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. | URI: | https://hdl.handle.net/11499/7377 https://doi.org/10.1186/1471-2474-15-191 |
ISSN: | 1471-2474 |
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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