低频重复经颅磁刺激联合艾司西酞普兰治疗青少年抑郁伴睡眠障碍的临床效果
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Clinical efficacy of low frequency repetitive transcranial magnetic stimulation combined with escitalopram for sleep disorders in adolescents with depressive
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    摘要:

    目的 研究低频重复经颅磁刺激(LF-rTMS)(1 Hz)联合艾司西酞普兰治疗青少年抑郁伴 睡眠障碍的临床效果。方法 选取 2023 年 1 月— 2024 年 1 月在喀什地区第一人民医院综合心理科就 诊的 82 例青少年抑郁伴睡眠障碍患者为研究对象,根据治疗方法不同分为对照组(40 例,予以艾司西 酞普兰治疗)与研究组(42 例,予以 LF-rTMS 联合艾司西酞普兰治疗)。比较两组临床疗效、汉密尔顿焦 虑量表(HAMA)评分、17 项汉密尔顿抑郁量表(HAMD-17)评分、匹兹堡睡眠质量指数(PSQI)评分、睡眠 质量、多导睡眠图指标、生活质量、血清指标及不良反应发生率。结果 研究组治疗有效率高于对照组 [90.48%(38/42)比 72.50%(29/40)],差异有统计学意义(χ2 =4.430,P< 0.05);研究组 HAMA、HAMD 及 PSQI评分治疗前后差值均高于对照组[(7.16±1.28)分比(6.38±1.05)分、(12.86±1.60)分比(8.64±2.35)分、 (6.63±1.05)分 比(4.97±0.43)分],差 异 均 有 统 计 学 意 义(t=3.009、9.546、9.283,均P< 0.01);研 究 组睡眠总时间(TST)、睡眠潜伏期(SL)、觉醒次数(NW)、觉醒时间(AT)治疗前后差值均高于对照组 [(3.01±0.76)h 比(1.12±0.69)h、(27.34±7.75)min 比(23.06±1.24) min、(1.68±0.38)次比(1.02±0.15)次、 (67.53±4.71)min比(62.57±4.12)min],差异均有统计学意义(t=11.772、3.450、10.248、5.065,均P< 0.001); 研究组生活质量生理、社会、情感、躯体评分治疗前后差值均高于对照组[(13.40±3.55)分比(9.01±1.68)分、 (20.38±1.01)分 比(12.76±0.73)分、(10.93±1.89)分 比(7.12±0.79)分、(7.45±2.13)分 比(4.12±1.76)分],差 异均有统计学意义(t=7.099、38.990、11.834、7.697,均P<0.001);研究组γ-氨基丁酸(GABA)、5-羟色胺 (5-HT)、脑源性神经营养因子(BDNF)水平治疗前后差值均高于对照组[(2.84±0.27) ng/ml比(2.31±0.25) ng/ml、 (56.44±9.83) ng/ml比(36.02±8.35) ng/ml、(6.51±0.24) ng/ml比(5.63±0.32) ng/ml],差异均有统计学意义(t=9.211、 10.114、14.132,均P<0.001);两组不良反应发生率比较,差异无统计学意义(P>0.05)。结论 LF-rTMS 联合艾司西酞普兰治疗青少年抑郁伴睡眠障碍患者,能改善其抑郁症状及睡眠质量,提高其生活质量, 改善血清相关指标,具有较好的临床应用价值。

    Abstract:

    Objective To explore the clinical efficacy of low frequency repetitive transcranial magnetic stimulation (LF-rTMS) (1 Hz) combined with escitalopram for sleep disorders in adolescents with depressive. Methods A total of 82 sleep disorders in adolescents with depressive disorder who attended the Department of Comprehensive Psychology of the Kashgar First People's Hospital from January 2023 to January 2024 were retrospectively selected for the study. The study subjects were divided into control group (40 cases, escitalopram) and study group (42 cases, LF-rTMS in combination with escitalopram) according to the treatment method. Clinical efficacy, Hamilton Anxiety Scale (HAMA) scores, Hamilton Depression Scale-17 (HAMD-17) scores, Pittsburgh Sleep Quality Index (PSQI) scores, quality of sleep, polysomnographic indices, quality of life, serum indices, and the incidence of adverse reactions were compared between the two groups. Results The treatment efficiency of study group was higher than that of control group [90.48% (38/42) vs. 72.50% (29/40)], and the difference was statistically significant (χ2 =4.430, P < 0.05). The pre- and post-treatment differences of HAMA, HAMD and PSQI scores in study group were significantly higher than those in control group [(7.16±1.28) vs. (6.38±1.05), (12.86±1.60) vs. (8.64±2.35), (6.63±1.05) vs. (4.97±0.43) scores], and the differences were all statistically significant (t=3.009, 9.546, 9.283; all P < 0.01). The pre-and post-treatment differences in total sleep time (TST), sleep latency (SL), number of awakenings (NW), and awakening time (AT) in study group were higher than those in control group [(3.01±0.76) h vs. (1.12±0.69) h, (27.34±7.75) min vs. (23.06±1.24) min, (1.68±0.38) times vs. (1.02±0.15) times, (67.53±4.71) min vs. (62.57±4.12) min], and the differences were statistically significant (t=11.772, 3.450,10.248, 5.065; all P < 0.001). The pre- and post-treatment differences in the physical, social, emotional, and somatic scores of quality of life in study group were higher than those in control group [(13.40±3.55) vs. (9.01±1.68), (20.38±1.01) vs. (12.76±0.73), (10.93±1.89) vs. (7.12±0.79), (7.45±2.13) vs. (4.12±1.76) scores], and the differences were statistically significant (t=7.099, 38.990, 11.834, 7.697; all P < 0.001). The pre- and post-treatment differences in gamma-aminobutyric acid (GABA),5-hydroxytryptamine (5-HT), and brain-derived neurotrophic factor (BDNF) in study group was higher than that in control group [(2.84±0.27) ng/ml vs. (2.31±0.25) ng/ml, (56.44±9.83) ng/ml vs. (36.02±8.35) ng/ml, (6.51±0.24) ng/ml vs. (5.63±0.32) ng/ml], and the differences were statistically significant (t=9.211, 10.114,14.132; all P < 0.001). The difference in the incidence of adverse reactions between the two groups was not statistically significant (P > 0.05). Conclusions Combined treatment with LF-rTMS and Escitalopram for depressive adolescents with sleep disorders can improve their depressive symptoms and sleep quality, enhance the patients' quality of life, and improve relevant serum indexes, which has good clinical application value.

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木太里甫江·木合台尔,穆耶赛尔·阿布都克尤木,麦尔巴·阿布都克尤木.低频重复经颅磁刺激联合艾司西酞普兰治疗青少年抑郁伴睡眠障碍的临床效果[J].神经疾病与精神卫生,2025,25(4):270-275
DOI :10.3969/j. issn.1009-6574.2025.04.007.

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  • 在线发布日期: 2025-04-25