Bauman William A, La Fountaine Michael F, Cirnigliaro Christopher M, Kirshblum Steven C, Spungen Ann M
James J. Peters VA Medical Center, Bronx, NY, USA.
J Spinal Cord Med. 2013 Sep;36(5):476-82. doi: 10.1179/2045772312Y.0000000061.
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).
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.
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.
Baclofen was not effective at sustaining plasma IGF-1 concentrations in the physiological range in men with chronic SCI.
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。
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。
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。
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。