Please use this identifier to cite or link to this item: 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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