目的探讨脊柱微创通道镜系统辅助椎间孔腰椎椎体间融合术(TLIF)对腰椎退行性疾病患者脊髓功能及血清P物质(SP)、前列腺素E2(PGE2)水平的影响。方法选取51例腰椎退行性疾病患者,按照入院次序单双号法分为A组(n=25)及B组(n=26)。A组行脊...目的探讨脊柱微创通道镜系统辅助椎间孔腰椎椎体间融合术(TLIF)对腰椎退行性疾病患者脊髓功能及血清P物质(SP)、前列腺素E2(PGE2)水平的影响。方法选取51例腰椎退行性疾病患者,按照入院次序单双号法分为A组(n=25)及B组(n=26)。A组行脊柱微创通道镜系统辅助TLIF术治疗,B组行常规TLIF术治疗。比较两组手术指标,腰腿部疼痛与功能障碍状况,脊髓功能,血清P物质(SP)、前列腺素E2(PGE2)水平。结果A组术中失血量、术后引流量均少于B组,下床活动时间短于B组(P<0.05);术后4周两组腰腿部视觉模拟评分法(VAS)与Oswestry障碍指数(ODI)评分均较术前均明显改善(P<0.05);术后7 d两组各项脊髓功能指标较术前均明显改善,且A组改善幅度优于B组(P<0.05);术后3 d A组血清SP水平高于B组,而血清PGE2水平低于B组(P<0.05)。结论脊柱微创通道镜系统辅助TLIF术可显著改善腰椎退行性疾病患者脊髓功能以及疼痛介质水平。展开更多
背景失眠障碍是一种常见的精神疾病,给患者的生活和健康带来严重的负面影响。传统的认知行为疗法(CBT-I)是一种有效的非药物治疗方法,但其操作复杂、耗时长、依从性低等缺点限制了其在真实世界的应用。简版行为疗法(BBT-I)是一种基于CB...背景失眠障碍是一种常见的精神疾病,给患者的生活和健康带来严重的负面影响。传统的认知行为疗法(CBT-I)是一种有效的非药物治疗方法,但其操作复杂、耗时长、依从性低等缺点限制了其在真实世界的应用。简版行为疗法(BBT-I)是一种基于CBT-I的简化治疗方法,其疗效与CBT-I相当,更适合在真实世界中推广。然而,BBT-I是否适用于中国失眠障碍人群暂不明确,而通过线上方式进行BBT-I的研究更是缺乏。目的本研究旨在探讨通过微信小程序进行的在线BBT-I(eBBT-I)对中国失眠障碍患者失眠改善的疗效,以及其对患者睡眠信念和态度的影响。方法本研究采用前瞻性非随机对照研究的设计,将2023年2—11月来自暨南大学附属第一医院精神医学科睡眠门诊的失眠障碍患者设为干预组,将线上和线下招募的失眠障碍志愿者设为对照组,干预组接受为期2周的eBBT-I治疗,对照组接受精神卫生教育的伪干预。在干预前后分别测量患者的失眠严重程度指数量表(ISI)和简版睡眠信念与态度问卷(DBAS-16)得分,以评估干预效果。结果研究最终共纳入35例干预组患者和30例对照组患者。主要结局指标:组别与时间对ISI得分存在交互作用(P<0.05);组别与时间分别对ISI得分主效应显著(P<0.05)。干预前3d(基线)两组ISI得分比较,差异无统计学意义(P>0.05);干预后14d干预组ISI得分低于对照组(P<0.05);干预组干预后14 d ISI得分低于组内干预前(P<0.05)。次要结局指标:组别与时间对DBAS-16得分不存在交互作用(P>0.05);时间对DBAS-16得分主效应显著(P<0.05);组别对DBAS-16得分主效应不显著(P>0.05)。干预前3 d(基线)、干预后14 d两组DBAS-16得分比较,差异无统计学意义(P>0.05);干预组干预后14 d DBAS-16得分高于组内干预前(P<0.05)。结论eBBT-I有效地改善了失眠障碍患者的失眠症状和负面影响,但对睡眠信念与态度的改善效果仍有待提升。本研究支持了eBBT-I在中国失眠障碍患者失眠治疗中的可行性和有效性。展开更多
BACKGROUND MicroRNAs(miRNAs)regulate gene expression and play a critical role in cancer physiology.However,there is still a limited understanding of the function and regulatory mechanism of miRNAs in gastric cancer(GC...BACKGROUND MicroRNAs(miRNAs)regulate gene expression and play a critical role in cancer physiology.However,there is still a limited understanding of the function and regulatory mechanism of miRNAs in gastric cancer(GC).AIM To investigate the role and molecular mechanism of miRNA-145-5p(miR145-5p)in the progression of GC.METHODS Real-time polymerase chain reaction(RT-PCR)was used to detect miRNA expression in human GC tissues and cells.The ability of cancer cells to migrate and invade was assessed using wound-healing and transwell assays,respectively.Cell proliferation was measured using cell counting kit-8 and colony formation assays,and apoptosis was evaluated using flow cytometry.Expression of the epithelial-mesenchymal transition(EMT)-associated protein was determined by Western blot.Targets of miR-145-5p were predicated using bioinformatics analysis and verified using a dual-luciferase reporter system.Serpin family E member 1(SERPINE1)expression in GC tissues and cells was evaluated using RT-PCR and immunohistochemical staining.The correlation between SERPINE1 expression and overall patient survival was determined using Kaplan-Meier plot analysis.The association between SERPINE1 and GC progression was also tested.A rescue experiment of SERPINE1 overexpression was conducted to verify the relationship between this protein and miR-145-5p.The mechanism by which miR-145-5p influences GC progression was further explored by assessing tumor formation in nude mice.RESULTS GC tissues and cells had reduced miR-145-5p expression and SERPINE1 was identified as a direct target of this miRNA.Overexpression of miR-145-5p was associated with decreased GC cell proliferation,invasion,migration,and EMT,and these effects were reversed by forcing SERPINE1 expression.Kaplan-Meier plot analysis revealed that patients with higher SERPINE1 expression had a shorter survival rate than those with lower SERPINE1 expression.Nude mouse tumorigenesis experiments confirmed that miR-145-5p targets SERPINE1 to regulate extracellular signal-regulated kinase-1/2(ERK1/2).CONCLUSION This study found that miR-145-5p inhibits tumor progression and is expressed in lower amounts in patients with GC.MiR-145-5p was found to affect GC cell proliferation,migration,and invasion by negatively regulating SERPINE1 levels and controlling the ERK1/2 pathway.展开更多
文摘目的探讨脊柱微创通道镜系统辅助椎间孔腰椎椎体间融合术(TLIF)对腰椎退行性疾病患者脊髓功能及血清P物质(SP)、前列腺素E2(PGE2)水平的影响。方法选取51例腰椎退行性疾病患者,按照入院次序单双号法分为A组(n=25)及B组(n=26)。A组行脊柱微创通道镜系统辅助TLIF术治疗,B组行常规TLIF术治疗。比较两组手术指标,腰腿部疼痛与功能障碍状况,脊髓功能,血清P物质(SP)、前列腺素E2(PGE2)水平。结果A组术中失血量、术后引流量均少于B组,下床活动时间短于B组(P<0.05);术后4周两组腰腿部视觉模拟评分法(VAS)与Oswestry障碍指数(ODI)评分均较术前均明显改善(P<0.05);术后7 d两组各项脊髓功能指标较术前均明显改善,且A组改善幅度优于B组(P<0.05);术后3 d A组血清SP水平高于B组,而血清PGE2水平低于B组(P<0.05)。结论脊柱微创通道镜系统辅助TLIF术可显著改善腰椎退行性疾病患者脊髓功能以及疼痛介质水平。
文摘背景失眠障碍是一种常见的精神疾病,给患者的生活和健康带来严重的负面影响。传统的认知行为疗法(CBT-I)是一种有效的非药物治疗方法,但其操作复杂、耗时长、依从性低等缺点限制了其在真实世界的应用。简版行为疗法(BBT-I)是一种基于CBT-I的简化治疗方法,其疗效与CBT-I相当,更适合在真实世界中推广。然而,BBT-I是否适用于中国失眠障碍人群暂不明确,而通过线上方式进行BBT-I的研究更是缺乏。目的本研究旨在探讨通过微信小程序进行的在线BBT-I(eBBT-I)对中国失眠障碍患者失眠改善的疗效,以及其对患者睡眠信念和态度的影响。方法本研究采用前瞻性非随机对照研究的设计,将2023年2—11月来自暨南大学附属第一医院精神医学科睡眠门诊的失眠障碍患者设为干预组,将线上和线下招募的失眠障碍志愿者设为对照组,干预组接受为期2周的eBBT-I治疗,对照组接受精神卫生教育的伪干预。在干预前后分别测量患者的失眠严重程度指数量表(ISI)和简版睡眠信念与态度问卷(DBAS-16)得分,以评估干预效果。结果研究最终共纳入35例干预组患者和30例对照组患者。主要结局指标:组别与时间对ISI得分存在交互作用(P<0.05);组别与时间分别对ISI得分主效应显著(P<0.05)。干预前3d(基线)两组ISI得分比较,差异无统计学意义(P>0.05);干预后14d干预组ISI得分低于对照组(P<0.05);干预组干预后14 d ISI得分低于组内干预前(P<0.05)。次要结局指标:组别与时间对DBAS-16得分不存在交互作用(P>0.05);时间对DBAS-16得分主效应显著(P<0.05);组别对DBAS-16得分主效应不显著(P>0.05)。干预前3 d(基线)、干预后14 d两组DBAS-16得分比较,差异无统计学意义(P>0.05);干预组干预后14 d DBAS-16得分高于组内干预前(P<0.05)。结论eBBT-I有效地改善了失眠障碍患者的失眠症状和负面影响,但对睡眠信念与态度的改善效果仍有待提升。本研究支持了eBBT-I在中国失眠障碍患者失眠治疗中的可行性和有效性。
文摘BACKGROUND MicroRNAs(miRNAs)regulate gene expression and play a critical role in cancer physiology.However,there is still a limited understanding of the function and regulatory mechanism of miRNAs in gastric cancer(GC).AIM To investigate the role and molecular mechanism of miRNA-145-5p(miR145-5p)in the progression of GC.METHODS Real-time polymerase chain reaction(RT-PCR)was used to detect miRNA expression in human GC tissues and cells.The ability of cancer cells to migrate and invade was assessed using wound-healing and transwell assays,respectively.Cell proliferation was measured using cell counting kit-8 and colony formation assays,and apoptosis was evaluated using flow cytometry.Expression of the epithelial-mesenchymal transition(EMT)-associated protein was determined by Western blot.Targets of miR-145-5p were predicated using bioinformatics analysis and verified using a dual-luciferase reporter system.Serpin family E member 1(SERPINE1)expression in GC tissues and cells was evaluated using RT-PCR and immunohistochemical staining.The correlation between SERPINE1 expression and overall patient survival was determined using Kaplan-Meier plot analysis.The association between SERPINE1 and GC progression was also tested.A rescue experiment of SERPINE1 overexpression was conducted to verify the relationship between this protein and miR-145-5p.The mechanism by which miR-145-5p influences GC progression was further explored by assessing tumor formation in nude mice.RESULTS GC tissues and cells had reduced miR-145-5p expression and SERPINE1 was identified as a direct target of this miRNA.Overexpression of miR-145-5p was associated with decreased GC cell proliferation,invasion,migration,and EMT,and these effects were reversed by forcing SERPINE1 expression.Kaplan-Meier plot analysis revealed that patients with higher SERPINE1 expression had a shorter survival rate than those with lower SERPINE1 expression.Nude mouse tumorigenesis experiments confirmed that miR-145-5p targets SERPINE1 to regulate extracellular signal-regulated kinase-1/2(ERK1/2).CONCLUSION This study found that miR-145-5p inhibits tumor progression and is expressed in lower amounts in patients with GC.MiR-145-5p was found to affect GC cell proliferation,migration,and invasion by negatively regulating SERPINE1 levels and controlling the ERK1/2 pathway.
