Effect of levocarnitine combined with Yougui Capsule on oligospermia and asthenospermia in male patients
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摘要:目的 探讨左卡尼汀、右归胶囊联合治疗对男性少精、弱精患者的临床疗效及不良反应。方法 选取80例男性少精、弱精患者,随机分为研究组、对照组各40例,对照组单独采用左卡尼汀治疗,研究组同时联合右归胶囊治疗。治疗3个月后,比较2组总有效率、不良反应发生率、精液质量参数及性激素变化情况。结果 治疗后,研究组的总有效率87.5%、血浆睾酮(T)水平(812.3±130.2) ng/dL、卵泡刺激素(FSH)水平(9.1±3.5) IU/L, 分别显著优于对照组的65.0%、(778.4±113.2) ng/dL、(8.0±2.1) IU/L(P < 0.05); 研究组不良反应发生率为2.5%, 显著低于对照组的20.0%(P < 0.05); 研究组患者的精液质量参数显著优于对照组(P < 0.05)。结论 男性少精、弱精患者采用左卡尼汀、右归胶囊联合治疗,能有效提高性激素水平、精子质量,改善生育功能,不良反应少,疗效安全可靠。Abstract:Objective To analyze the clinical efficacy of levocarnitine combined with Yougui Capsule on oligospermia and asthenospermia in male patients and its adverse effects.Methods Eighty male patients with oligospermia admitted to our hospital were randomly divided into study group and control group, with 40 cases in each group. The control group was treated with levocarnitine alone, and study group was additionally given Yougui Capsule. The total effective rate, incidence of adverse reactions, semen quality parameters and changes of sex hormones were compared between the two groups after 3 months of treatment.Results The total effective rate, plasma testosterone (T) level, and follicle stimulating hormone (FSH) in the study group were 87.50%, (812.3±130.2) ng/dL, and (9.1±3.5) IU/L, respectively, which were superior to 65.0%, (778.4±113.2) ng/dL, (8.0±2.1) IU/L, in the control group(P < 0.05). The incidence rate of adverse reactions in the study group was significantly lower than that of the control group (2.50% vs. 20.00%, P < 0.05). The semen quality parameters of the study group were significantly better than the control group(P < 0.05).Conclusion The combination of levocarnitine and Yougui Capsule can effectively improve the sex hormone level and sperm quality, improve the reproductive function, which have fewer adverse reactions, and is safe and reliable.
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Keywords:
- oligospermia in male /
- levocarnitine /
- clinical efficacy /
- asthenospermia /
- Yougui Capsule /
- adverse reactions
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表 1 2组患者治疗总有效率比较[n(%)]
组别 n 治愈 显效 有效 总有效 对照组 40 12(30.0) 14(35.0) 14(35.0) 26(65.0) 研究组 40 23(57.5) 12(30.0) 5(12.5) 35(87.5)* 与对照组比较,*P < 0.05。 表 2 2组性激素水平比较(x±s)
组别 时点 T/(ng/dL) FSH/(IU/L) PRL/(ng/mL) P/(ng/mL) LH/(IU/L) 对照组(n=40) 治疗前 574.2±74.9 9.4±4.0 14.3±4.4 0.6±0.3 9.8±3.5 治疗后 778.4±113.2 8.0±2.1 13.7±3.6 0.5±0.4 10.6±2.5 研究组(n=40) 治疗前 572.3±75.3 9.3±3.9 14.5±4.3 0.5±0.3 9.6±3.6 治疗后 812.3±130.2* 9.1±3.5* 13.8±3.7 0.6±0.4 10.8±2.7 T: 血浆睾酮; FSH: 卵泡刺激素; PRL: 催乳素; P: 孕酮; LH: 黄体生成激素。与对照组比较, *P < 0.05。 表 3 2组患者不良反应发生情况比较[n(%)]
组别 n 口干 便秘 胃肠道不适 肝肾功能损伤 合计 对照组 40 3(7.5) 2(5.0) 3(7.5) 0 8(20.0) 研究组 40 1(2.5) 0 0 0 1(2.5)* 与对照组比较,*P < 0.05。 表 4 2组精液质量参数比较(x±s)
组别 时点 a级精子/% a级精子+b级精子/% 精子活动率/% 精子密度/(×106/mL) 对照组(n=40) 治疗前 11.0±5.6 30.6±5.5 32.9±6.3 13.6±3.0 治疗后 18.2±9.5 39.2±4.7 65.1±5.4 20.4±6.8 研究组(n=40) 治疗前 11.4±5.8 30.4±5.8 33.2±6.1 13.8±3.2 治疗后 24.2±6.8* 48.1±8.7* 72.5±4.6* 27.1±9.3* 与对照组比较, *P < 0.05。 -
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