Holmberg Björn, Johansson Jan-Ove, Poewe Werner, Wenning Gregor, Quinn Niall P, Mathias Chris, Tolosa Eduardo, Cardozo Adriana, Dizdar Nil, Rascol Olivier, Slaoui Tarik
Movement Disorders Unit, Sahlgrenska University Hospital, Göteborg University, Göteborg, Sweden.
Mov Disord. 2007 Jun 15;22(8):1138-44. doi: 10.1002/mds.21501.
The objective of this study was to investigate tolerability and possible neurotrophic effects of growth hormone (GH) in treatment of multiple system atrophy (MSA). In this double-blind pilot study, MSA patients were randomized to recombinant human growth hormone (r-hGH, n = 22), 1 mg every second day (6 months) followed by alternating daily injections of 1 mg and 0.5 mg (6 months), or matched placebo (n = 21). Safety analysis demonstrated no obvious between-group differences. In both groups, there was progressive worsening of Unified Parkinson's Disease Rating Scale total score, which tended to be less in r-hGH-treated patients (12.9% at 6 months, 25.3% at 12 months) than in placebo (17.0% and 35.7%). Similarly, there was a trend to less worsening in Unified MSA Rating Scale total score with r-hGH (13.2% and 21.2%) than with placebo (21.1% and 36.5%). Cardiovascular reflex autonomic testing also tended to show less deterioration with r-hGH than with placebo at 12 months. However, 95% CI did not indicate treatment differences for any efficacy measures. In conclusion, r-hGH administration in MSA patients for up to 1 year appears safe and might influence disease symptoms, signs and, possibly, progression. The results support further studies utilizing higher doses in more patients.
本研究的目的是调查生长激素(GH)治疗多系统萎缩(MSA)的耐受性及可能的神经营养作用。在这项双盲试验性研究中,MSA患者被随机分为重组人生长激素(r-hGH,n = 22)组,每两天注射1 mg(6个月),随后交替每日注射1 mg和0.5 mg(6个月),或匹配的安慰剂组(n = 21)。安全性分析显示组间无明显差异。两组中,帕金森病统一评定量表总分均呈进行性恶化,r-hGH治疗的患者恶化程度(6个月时为12.9%,12个月时为25.3%)往往低于安慰剂组(分别为17.0%和35.7%)。同样,r-hGH组统一MSA评定量表总分恶化程度(分别为13.2%和21.2%)也有低于安慰剂组(分别为21.1%和36.5%)的趋势。心血管反射自主神经测试也显示,12个月时r-hGH组恶化程度低于安慰剂组。然而,95%置信区间并未显示任何疗效指标存在治疗差异。总之,MSA患者使用r-hGH治疗长达1年似乎是安全的,且可能会影响疾病症状、体征以及可能的疾病进展。结果支持在更多患者中使用更高剂量进行进一步研究。