Peskind Elaine R, Tsuang Debby W, Bonner Lauren T, Pascualy Marcella, Riekse Robert G, Snowden Mark B, Thomas Ronald, Raskind Murray A
Department of Veterans Affairs Northwest Network VISN 20 Mental Illness Research, Education and Clinical Center, Seattle, WA, USA.
Alzheimer Dis Assoc Disord. 2005 Jan-Mar;19(1):23-8. doi: 10.1097/01.wad.0000155067.16313.5e.
Enhanced behavioral responsiveness to central nervous system (CNS) norepinephrine (NE) in Alzheimer disease (AD) may contribute to the pathophysiology of disruptive behaviors such as aggression, uncooperativeness with necessary care, irritability, and pressured pacing. We evaluated the efficacy of the beta-adrenergic antagonist propranolol for treatment-resistant disruptive behaviors and overall behavioral status in nursing home residents with probable or possible AD.
Thirty-one subjects (age 85 +/- 8 [SD]) with probable or possible AD and persistent disruptive behaviors that interfered with necessary care were randomized to propranolol (n = 17) or placebo (n = 14) in a double-blind study. Stable doses of previously prescribed psychotropics were maintained at pre-study dose during the study. Following a propranolol or placebo dose titration period of up to 9 days (per a dosing algorithm), subjects were maintained on maximum achieved dose for 6 weeks. Primary outcome measures were the Neuropsychiatric Inventory (NPI) and the Clinical Global Impression of Change (CGIC).
Propranolol augmentation (mean achieved dose 106 +/- 38 mg/d) was significantly more effective than placebo for improving overall behavioral status on the total NPI score and CGIC. Improvement in individual NPI items within propranolol subjects was significant only for "agitation/aggression" and "anxiety," and reached borderline statistical significance favoring propranolol over placebo only for "agitation/aggression." Pressured pacing and irritability did not appear responsive to propranolol. In propranolol subjects rated "moderately improved" or "markedly improved" on the CGIC at the end of the double-blind study phase, improvement of overall behavioral status had diminished substantially after 6 months of open-label propranolol treatment.
Short-term propranolol augmentation treatment appeared modestly effective and well tolerated for overall behavioral status in nursing home residents with probable or possible AD complicated by disruptive behaviors. Propranolol may be helpful specifically for aggression and uncooperativeness (the behaviors assessed by the NPI "agitation/aggressiveness" item). However, the usefulness of propranolol in this very old and frail population was limited by the high frequency of relative contraindications to beta-adrenergic antagonist treatment and diminution of initial behavioral improvements over time.
阿尔茨海默病(AD)患者对中枢神经系统(CNS)去甲肾上腺素(NE)的行为反应增强,可能导致攻击、不配合必要护理、易怒和强迫性踱步等破坏性行为的病理生理过程。我们评估了β-肾上腺素能拮抗剂普萘洛尔对患有可能或疑似AD的养老院居民中难治性破坏性行为及整体行为状态的疗效。
在一项双盲研究中,将31名年龄为85±8(标准差)岁、患有可能或疑似AD且存在干扰必要护理的持续性破坏性行为的受试者随机分为普萘洛尔组(n = 17)或安慰剂组(n = 14)。在研究期间,将之前开具的精神药物稳定剂量维持在研究前的剂量。在长达9天的普萘洛尔或安慰剂剂量滴定期(根据给药算法)后,受试者维持在最大达到剂量6周。主要结局指标为神经精神科问卷(NPI)和临床总体印象变化量表(CGIC)。
在改善总体行为状态的NPI总分和CGIC方面,普萘洛尔增量治疗(平均达到剂量106±38mg/d)比安慰剂显著更有效。普萘洛尔组受试者个体NPI项目中仅“激越/攻击”和“焦虑”有显著改善,且仅“激越/攻击”在普萘洛尔优于安慰剂方面达到临界统计学显著性。强迫性踱步和易怒对普萘洛尔似乎无反应。在双盲研究阶段结束时,CGIC评定为“中度改善”或“显著改善”的普萘洛尔组受试者,在开放标签普萘洛尔治疗6个月后,总体行为状态的改善已大幅减弱。
短期普萘洛尔增量治疗对于患有可能或疑似AD并伴有破坏性行为的养老院居民的总体行为状态似乎有一定疗效且耐受性良好。普萘洛尔可能特别有助于治疗攻击和不配合行为(由NPI“激越/攻击性”项目评估的行为)。然而,在这个非常年老体弱的人群中,普萘洛尔的效用受到β-肾上腺素能拮抗剂治疗相对禁忌证的高发生率以及随着时间推移初始行为改善减弱的限制。