选择性5 -羟色胺再摄取抑制剂和5 -羟色胺去甲肾上腺素再摄取抑制剂:对原发性纤维肌痛患者小梁骨评分和骨密度的影响

H. Hamoud, Mohamed M. Ghait, Muhammad M Harb Yasser A Elmotaleb Elsayed
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摘要

背景:纤维肌痛是一种慢性肌肉骨骼疼痛疾病,其特征是多压痛点广泛性疼痛,睡眠障碍和疲劳,随后影响生活质量。我们研究的目的是确定原发性纤维肌痛患者服用SSRIs和SNRIs与BMD和TBS之间的相关性。方法和发现:对150名埃及参与者进行了横断面研究。将患者分为2个主要组:治疗组包括100例原发性骨髓纤维化患者(50例SSRI, 50例SNRI),对照组包括50例年龄匹配的受试者(25例健康个体,25例原发性骨髓纤维化但接受非SSRI和SNRI药物治疗)。与健康对照组相比,SSRI和SNRI治疗组的BMD和TBS显著降低。在老年人群中,SSRI组腰椎(L1-L4) BMD和TBS明显下降。同样,对照的原发性纤维肌痛患者也表现出低骨密度。结论:我们的研究表明,原发性骨髓纤维化患者,特别是老年人,使用SSRIs或SNRIs治疗具有低BMD和低TBS。此外,未接受SSRI或SNRI治疗的原发性纤维肌痛患者的骨密度也较低。因此,原发性骨髓纤维化可被认为是低骨密度的一个促成因素。
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Selective serotonin reuptake inhibitors and serotonin norepinephrine reuptake inhibitors: Impact on trabecular bone score and bone mineral density in primary fibromyalgia
Background: Fibromyalgia is a chronic musculoskeletal pain disorder characterized by widespread pain at multiple tender points, sleep disturbance and fatigue, which subsequently affect quality of life.The aim of our study is to determine the correlation between consumption of SSRIs and SNRIs in patients with primary fibromyalgia, and BMD and TBS. Methods and Findings: A cross-sectional study carried out on 150 Egyptian participants. Patients were divided into 2 main groups: treatment group including 100 patients (50 on SSRI, and 50 on SNRI) diagnosed with primary myelofibrosis, and control group including 50 age-matched subjects (25 healthy individual, and 25 with primary myelofibrosis but receiving medications other than SSRI and SNRI).BMD and TBS were significantly low in SSRI and SNRI treatment groups compared to healthy control. In older population, lumbar spine (L1-L4) BMD and TBS decreased significantly in SSRI group. Also, control patients with primary fibromyalgia showed low BMD. Conclusion: Our study showed that patients with primary myelofibrosis, especially old population, whose treatment involved SSRIs or SNRIs had low BMD and low TBS. Additionally, patients with primary fibromyalgia who neither received SSRI nor SNRI also experienced low BMD. Thus, primary myelofibrosis could be considered as a contributing factor for low BMD.
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