首页|抗抑郁药联合肠道菌群调节剂治疗抑郁症疗效分析

抗抑郁药联合肠道菌群调节剂治疗抑郁症疗效分析

Efficacy of antidepressants combined with intestinal flora regulators in the treatment of depression

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目的 分析抗抑郁药物联合肠道菌群调节剂用于抑郁症患者的临床疗效.方法 回顾性分析丽水市第二人民医院2019年1月至2021年12月收治的抑郁症患者92例的临床资料,采用病例对照研究根据治疗方式不同,将其分为对照组(n=46)、观察组(n=46).对照组应用草酸艾司西酞普兰片治疗,观察组应用草酸艾司西酞普兰片联合双歧三联活菌治疗,两组疗程2个月.比较两组抑郁、焦虑程度、睡眠质量、生活质量、炎症因子水平及不良反应发生情况.结果 治疗2个月后,观察组汉密尔顿抑郁量表评分、汉密尔顿焦虑量表评分分别为(16.49±2.96)分、(7.58±1.66)分,均低于对照组的(18.51±3.13)分、(9.31±2.01)分(t=3.18、4.50,P=0.002、P<0.001).治疗4周、8周,观察组匹兹堡睡眠质量问卷评分分别为(10.39±2.30)分、(8.11±1.82)分,均明显低于对照组的(14.25±2.66)分、(10.49±2.07)分(t=7.40、5.86,均P<0.001).治疗2个月后,观察组简明健康状况调查问卷总分为(73.50±9.16)分,高于对照组的(65.23±7.29)分(t=4.79,P<0.001);观察组白细胞介素6和肿瘤坏死因子 α 水平分别为(9.33±2.72)ng/L、(16.71±4.46)ng/L,均低于对照组的(13.59±4.05)ng/L、(23.20±5.03)ng/L(t=5.92、6.55,均P<0.001).两组不良反应发生率差异无统计学意义(P<0.05).结论 抗抑郁药物联合肠道菌群调节剂可显著减轻抑郁症患者焦虑、抑郁及失眠程度,改善生活质量,降低炎症因子水平,且不良反应少,安全性高.
Objective To analyze the clinical efficacy of antidepressants combined with intestinal flora regulators in patients with depression.Methods The clinical data of 92 patients with depression admitted to the Second People's Hospital of Lishui from January 2019 to December 2021 were retrospectively analyzed.In the case-control study,the patients were divided into a control group(n=46)and an observation group(n=46)according to different treatment methods.The control group received treatment with escitalopram oxalate tablets,while the observation group received treatment with escitalopram oxalate tablets and bifidobacterium triple viable preparation.Both groups were treated for 2 months.The degrees of depression and anxiety,sleep quality,quality of life,levels of inflammatory factors,and the incidence of adverse reactions were compared between the two groups.Results After 2 months of treatment,the scores of Hamilton Depression Scale and Hamilton Anxiety Scale in the observation group were(16.49±2.96)points and(7.58±1.66)points,respectively,which were significantly lower than those in the control group[(18.51±3.13)points and(9.31±2.01)points,t=3.18,4.50,P=0.002,P<0.001).After 4 and 8 weeks of treatment,the scores of Pittsburgh Sleep Quality Index in the observation group were(10.39±2.30)points and(8.11±1.82)points,respectively,which were significantly lower than those in the control group[(14.25±2.66)points,(10.49±2.07)points,t=7.40,5.86,both P<0.001].After 2 months of treatment,the total score of the Short Form-36 Health Survey in the observation group was(73.50±9.16)points,which was significantly higher than that in the control group[(65.23±7.29)points,t=4.79,P<0.001].The levels of interleukin-6 and tumor necrosis factor-α in the observation group were(9.33±2.72)ng/L and(16.71±4.46)ng/L,respectively,which were significantly lower than those in the control group[(13.59±4.05)ng/L,(23.20±5.03)ng/L,t=5.92,6.55,both P<0.001].There was no significant difference in the incidence of adverse reactions between the two groups(P>0.05).Conclusion The combined use of antidepressants and intestinal flora regulators can obviously reduce the severity of anxiety,depression,and insomnia in patients with depression,improve their quality of life,and lower the levels of inflammatory factors,with minimal adverse reactions and high safe.

Depressive disorderAntidepressive agentsDepressionAnxietySleepQuality of lifeInterleukin-6Tumor necrosis factor-alpha

康艳宝、赵龙友

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丽水市第二人民医院五病区,丽水 323000

抑郁症 抗抑郁药 抑郁 焦虑 睡眠 生活质量 白细胞介素6 肿瘤坏死因子α

浙江省基础公益研究计划

LGF20H090016

2024

中国基层医药
中华医学会,安徽医科大学

中国基层医药

影响因子:1.003
ISSN:1008-6706
年,卷(期):2024.31(8)
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