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低剂量巴氯芬疗法可提高慢性脊髓损伤男性患者的血浆胰岛素样生长因子-1浓度,但无法以可预测且持续的方式使其升至正常范围。

Low-dose baclofen therapy raised plasma insulin-like growth factor-1 concentrations, but not into the normal range in a predictable and sustained manner in men with chronic spinal cord injury.

作者信息

Bauman William A, La Fountaine Michael F, Cirnigliaro Christopher M, Kirshblum Steven C, Spungen Ann M

机构信息

James J. Peters VA Medical Center, Bronx, NY, USA.

出版信息

J Spinal Cord Med. 2013 Sep;36(5):476-82. doi: 10.1179/2045772312Y.0000000061.

Abstract

OBJECTIVE

To evaluate, whether once-daily oral baclofen administration increases and/or sustains plasma insulin-like growth factor-1 (IGF-1) concentration in 11 men with chronic spinal cord injury (SCI) and IGF-1 deficiency (i.e. <250 ng/ml).

DESIGN

Prospective, open-label, dose titration study. Baclofen was administered at 20 mg/day for 8 weeks; then increased to 40 mg/day for another 8 weeks. Plasma IGF-1 and self-reported side effects were measured at baseline and every other week for the duration of the study.

RESULTS

The subjects were 43 ± 12 years old, had duration of injury of 20 ± 12 years; eight subjects had a complete motor injury, and eight had paraplegia. Nine of 11 subjects completed the 20 mg/day treatment and 5 subjects completed the 40 mg/day treatment. Plasma IGF-1 levels improved with each baclofen dose; however, only one subject increased from baseline and remained above the targeted physiological range of 250 ng/ml throughout treatment. A significant increase in IGF-1concentration was observed between baseline and week 2 (154 ± 63 vs. 217 ± 69 ng/ml; P < 0.05), weeks 8 and 10 (188 ± 95 vs. 228 ± 93 ng/ml; P < 0.05), and weeks 8 and 16 (188 ± 95 vs. 259 ± 92 ng/ml; P < 0.05). No serious side effects were observed at 20 mg/day; the 40 mg/day dose was less well tolerated.

CONCLUSION

Baclofen was not effective at sustaining plasma IGF-1 concentrations in the physiological range in men with chronic SCI.

摘要

目的

评估每日一次口服巴氯芬是否能提高和/或维持11名慢性脊髓损伤(SCI)且胰岛素样生长因子-1(IGF-1)缺乏(即<250 ng/ml)男性患者的血浆IGF-1浓度。

设计

前瞻性、开放标签、剂量滴定研究。巴氯芬以20毫克/天的剂量给药8周;然后增加到40毫克/天,再给药8周。在研究开始时及研究期间每隔一周测量血浆IGF-1和自我报告的副作用。

结果

受试者年龄为43±12岁,受伤时间为20±12年;8名受试者有完全性运动损伤,8名受试者患有截瘫。11名受试者中有9名完成了每日20毫克的治疗,5名受试者完成了每日40毫克的治疗。随着巴氯芬剂量的增加,血浆IGF-1水平有所改善;然而,只有一名受试者的IGF-1水平从基线上升,并在整个治疗过程中保持在250 ng/ml的目标生理范围之上。在基线与第2周(154±63 vs. 217±69 ng/ml;P<0.05)、第8周与第10周(188±95 vs.228±93 ng/ml;P<0.05)以及第8周与第16周(188±95 vs. 259±92 ng/ml;P<0.05)之间观察到IGF-1浓度显著增加。每日20毫克剂量时未观察到严重副作用;每日40毫克剂量的耐受性较差。

结论

巴氯芬在维持慢性SCI男性患者血浆IGF-1浓度在生理范围内无效。

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