中国医药导报
中國醫藥導報
중국의약도보
CHINA MEDICAL HERALD
2014年
29期
64-67,71
,共5页
张玉琦%陈炯华%李桂林%张峰%陈彩霞%夏鸣华%张长松%赵幸福
張玉琦%陳炯華%李桂林%張峰%陳綵霞%夏鳴華%張長鬆%趙倖福
장옥기%진형화%리계림%장봉%진채하%하명화%장장송%조행복
老年%抑郁症%米氮平%脑源性神经营养因子
老年%抑鬱癥%米氮平%腦源性神經營養因子
노년%억욱증%미담평%뇌원성신경영양인자
Elderly%Major depression%Mirtazapine%BDNF
目的:探讨米氮平治疗老年抑郁症的临床效果和安全性及其对血清脑源性神经营养因子(BDNF)的影响。方法2011年12月~2013年10月就诊于南京医科大学附属精神卫生中心,符合《中国精神疾病分类方案与诊断标准》第3版(CCMD-3)抑郁症诊断标准的老年抑郁症患者62例,进行为期8周的开放性米氮平治疗,以汉密尔顿抑郁量表(HAMD)和临床疗效总评量表(CGI)为评估临床疗效的工具。在入组时和8周的开放性治疗结束时检测BDNF。结果完成研究的老年抑郁症患者58例,所用米氮平的平均剂量为(31.3±7.8)mg/d。米氮平治疗8周后HAMD总分、病情严重程度、疗效总评和疗效指数与治疗前相比明显下降,差异有高度统计学意义(P<0.01);治疗后体重稍有增加,但差异无统计学意义(P>0.05);BDNF较治疗前明显升高,差异有高度统计学意义(P<0.01)。副作用主要为过度镇静、入睡时下肢不适、头晕、腹泻。结论米氮平治疗老年抑郁症安全、有效,能提高BDNF水平。
目的:探討米氮平治療老年抑鬱癥的臨床效果和安全性及其對血清腦源性神經營養因子(BDNF)的影響。方法2011年12月~2013年10月就診于南京醫科大學附屬精神衛生中心,符閤《中國精神疾病分類方案與診斷標準》第3版(CCMD-3)抑鬱癥診斷標準的老年抑鬱癥患者62例,進行為期8週的開放性米氮平治療,以漢密爾頓抑鬱量錶(HAMD)和臨床療效總評量錶(CGI)為評估臨床療效的工具。在入組時和8週的開放性治療結束時檢測BDNF。結果完成研究的老年抑鬱癥患者58例,所用米氮平的平均劑量為(31.3±7.8)mg/d。米氮平治療8週後HAMD總分、病情嚴重程度、療效總評和療效指數與治療前相比明顯下降,差異有高度統計學意義(P<0.01);治療後體重稍有增加,但差異無統計學意義(P>0.05);BDNF較治療前明顯升高,差異有高度統計學意義(P<0.01)。副作用主要為過度鎮靜、入睡時下肢不適、頭暈、腹瀉。結論米氮平治療老年抑鬱癥安全、有效,能提高BDNF水平。
목적:탐토미담평치료노년억욱증적림상효과화안전성급기대혈청뇌원성신경영양인자(BDNF)적영향。방법2011년12월~2013년10월취진우남경의과대학부속정신위생중심,부합《중국정신질병분류방안여진단표준》제3판(CCMD-3)억욱증진단표준적노년억욱증환자62례,진행위기8주적개방성미담평치료,이한밀이돈억욱량표(HAMD)화림상료효총평량표(CGI)위평고림상료효적공구。재입조시화8주적개방성치료결속시검측BDNF。결과완성연구적노년억욱증환자58례,소용미담평적평균제량위(31.3±7.8)mg/d。미담평치료8주후HAMD총분、병정엄중정도、료효총평화료효지수여치료전상비명현하강,차이유고도통계학의의(P<0.01);치료후체중초유증가,단차이무통계학의의(P>0.05);BDNF교치료전명현승고,차이유고도통계학의의(P<0.01)。부작용주요위과도진정、입수시하지불괄、두훈、복사。결론미담평치료노년억욱증안전、유효,능제고BDNF수평。
Objective To investigate the clinical efficacy and safety of Mirtazapine in treatment of elderly depression and impact on serum brain-derived neurotrophic factor (BDNF). Methods From December 2011 to October 2013 for treatment at Wuxi Mental Health Center Affiliated to Nanjing Medical University, 62 elders who met diagnostic criteria for major depression in Chinese Classification of Mental Disorders (CCMD-3) were treated with Mirtazapine for 8 weeks, Hamilton depression scale (HAMD) and clinical global impression (CGI) were used to assess clinical efficacy of Mirtazapine. Serum BDNF at enrolled and after 8 weeks of open treatment was detected. Results Fifty eight patients completed the study, the mean dose of Mirtazapine was (31.3±7.8) mg/d. After 8 weeks of Mirtazapine treatment, HAMD total score, severity of illness, global improvement and efficacy index were decreased significantly compared with before treatment (P< 0.01). The body weight slight increased after treatment, but the difference was not statistical-ly significant (P>0.05). BDNF was statistically significant higher than pre-treatment (P<0.01). The main side effects were excessive sedation, lower extremity discomfort when falling asleep, dizziness, and diarrhea. Conclusion Mirtazap-ine in treatment of elderly depression is safe and effective, and it can increase BDNF levels.