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度洛西汀治疗中国广泛性焦虑障碍患者的临床疗效和安全性:一项前后研究。

Clinical efficacy and safety of low-dose doxepin in Chinese patients with generalized anxiety disorder: A before-after study.

机构信息

Department of Neurology, Jinshan Hospital, Fudan University, Shanghai, China.

Department of Geriatric Cognitive Disorders, Shanghai Jinshan Zhongren Geriatric Nursing Hospital, Shanghai, China.

出版信息

Medicine (Baltimore). 2022 Oct 21;101(42):e31201. doi: 10.1097/MD.0000000000031201.

Abstract

Clinical and animal studies have reported that low-dose doxepin may have positive effects on generalized anxiety disorder (GAD); however, its effectiveness and clinical safety are less well understood. This study is a before-after study and aims to investigate the effectiveness and side effects of low-dose doxepin by evaluating Hamilton Anxiety Scale (HAMA) scores, hormones, blood glucose, serum lipids, body weight, and body mass index (BMI) in patients with GAD. Forty-nine patients (20 males and 29 females) with GAD were randomly assigned to receive low-dose doxepin (6.25 mg-12.5 mg per day) for 12 weeks between February 2015 and March 2016. HAMA scores, fasting blood glucose (FBG) body weight, BMI, and some serum biochemical indexes, such as adrenocorticotropic hormone (ACTH), free triiodothyronine (FT3), total cholesterol (TC), triglyceride (TG), and low-density lipoprotein cholesterol (LDLC), and FBG, were assessed during pretreatment and post-treatment. Mean scores of HAMA decreased from 19.50 ± 1.22 to 8.50 ± 3.61 after low-dose doxepin treatment (P < .01). The serum levels of ACTH (4.33 ± 2.14 vs 6.12 ± 3.02 pmol/L), FT3 (4.78 ± 0.51 vs 5.15 ± 0.52 pg/mL), TC (4.55 ± 1.01 vs 5.93 ± 1.66 mmol/L), TG (1.69 ± 1.51 vs 3.39 ± 2.86 mmol/L), and LDLC (2.43 ± 0.88 vs 3.76 ± 1.25 mmol/L), and FBG (5.06 ± 0.43 vs 5.78 ± 0.81 mmol/L) were higher than that pretreatment with a significant difference (P < .01). Bodyweight (62.00 ± 7.45 vs 64.00 ± 6.44 kg, P = .23) and BMI (23.70 ± 2.35 vs 24.48 ± 2.11 kg/m2, P = .14) had no difference after treatment. These results suggest that low-dose doxepin has beneficial clinical efficacy and safety. Low-dose doxepin can ameliorate anxiety in GAD patients and has some effects on neuroendocrine systems and the metabolic activity of serum glucose and lipid.

摘要

临床和动物研究报告称,低剂量多塞平可能对广泛性焦虑症(GAD)有积极影响;然而,其疗效和临床安全性了解较少。本研究为前后研究,旨在通过评估汉密尔顿焦虑量表(HAMA)评分、激素、空腹血糖、血清脂质、体重和体重指数(BMI),探讨低剂量多塞平治疗 GAD 患者的有效性和副作用。49 例 GAD 患者(男 20 例,女 29 例)于 2015 年 2 月至 2016 年 3 月期间随机分为低剂量多塞平组(每日 6.25-12.5mg),疗程 12 周。在治疗前和治疗后评估 HAMA 评分、空腹血糖(FBG)、体重、BMI 和一些血清生化指标,如促肾上腺皮质激素(ACTH)、游离三碘甲状腺原氨酸(FT3)、总胆固醇(TC)、甘油三酯(TG)、低密度脂蛋白胆固醇(LDLC)和 FBG。低剂量多塞平治疗后 HAMA 平均评分从 19.50±1.22 降至 8.50±3.61(P<.01)。ACTH(4.33±2.14 与 6.12±3.02 pmol/L)、FT3(4.78±0.51 与 5.15±0.52 pg/mL)、TC(4.55±1.01 与 5.93±1.66 mmol/L)、TG(1.69±1.51 与 3.39±2.86 mmol/L)、LDLC(2.43±0.88 与 3.76±1.25 mmol/L)和 FBG(5.06±0.43 与 5.78±0.81 mmol/L)血清水平高于治疗前,差异有统计学意义(P<.01)。治疗后体重(62.00±7.45 与 64.00±6.44kg,P=.23)和 BMI(23.70±2.35 与 24.48±2.11kg/m2,P=.14)无差异。这些结果表明,低剂量多塞平具有良好的临床疗效和安全性。低剂量多塞平可改善 GAD 患者的焦虑症状,对神经内分泌系统和血清葡萄糖及脂质代谢活性有一定影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07d1/9592331/b0c07fb354b6/medi-101-e31201-g001.jpg

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