Loeb Mark B, Molloy D William, Smieja Marek, Standish Tim, Goldsmith Charles H, Mahony Jim, Smith Stephanie, Borrie Michael, Decoteau Earl, Davidson Warren, McDougall Allan, Gnarpe Judy, O'DONNell Martin, Chernesky Max
Department of Pathology and Molecular Medicine, Biostatistics Hamilton Regional Laboratory Medicine Program, Hamilton, Ontario, Canada.
J Am Geriatr Soc. 2004 Mar;52(3):381-7. doi: 10.1111/j.1532-5415.2004.52109.x.
To assess whether doxycycline and rifampin have a therapeutic role in patients with Alzheimer's disease (AD).
Randomized, triple-blind, controlled trial.
Three tertiary care and two community geriatric clinics in Canada.
One hundred one patients with probable AD and mild to moderate dementia.
Oral daily doses of doxycycline 200 mg and rifampin 300 mg for 3 months.
The primary outcome was a change in Standardized Alzheimer's Disease Assessment Scale cognitive subscale (SADAScog) at 6 months. Secondary outcomes were changes in the SADAScog at 12 months and tests of dysfunctional behavior, depression, and functional status.
There was significantly less decline in the SADAScog score at 6 months in the antibiotic group than in the placebo group, (-2.75 points, 95% confidence interval (CI)=-5.28 to -0.22, P=.034). At 12 months, the difference between groups in the SADAScog was -4.31 points (95% CI=-9.17-0.56, P=.079). The antibiotic group showed significantly less dysfunctional behavior at 3 months. There was no significant difference in adverse events between groups (P=.34). There were no differences in Chlamydia pneumoniae detection using polymerase chain reaction or antibodies (immunoglobulin (Ig)G or IgA) between groups.
Therapy with doxycycline and rifampin may have a therapeutic role in patients with mild to moderate AD. The mechanism is unlikely to be due to their effect on C. pneumoniae. More research is needed to investigate these agents.
评估强力霉素和利福平对阿尔茨海默病(AD)患者是否具有治疗作用。
随机、三盲、对照试验。
加拿大的三家三级医疗中心和两家社区老年诊所。
101例可能患有AD且有轻度至中度痴呆的患者。
每日口服200毫克强力霉素和300毫克利福平,持续3个月。
主要结局是6个月时标准化阿尔茨海默病评估量表认知子量表(SADAScog)的变化。次要结局是12个月时SADAScog的变化以及功能失调行为、抑郁和功能状态测试。
抗生素组6个月时SADAScog评分的下降显著低于安慰剂组(-2.75分,95%置信区间(CI)=-5.28至-0.22,P = 0.034)。12个月时,两组间SADAScog的差异为-4.31分(95% CI = -9.17 - 0.56,P = 0.079)。抗生素组在3个月时功能失调行为显著较少。两组间不良事件无显著差异(P = 0.34)。两组间使用聚合酶链反应或抗体(免疫球蛋白(Ig)G或IgA)检测肺炎衣原体无差异。
强力霉素和利福平治疗可能对轻度至中度AD患者具有治疗作用。其机制不太可能是由于它们对肺炎衣原体的作用。需要更多研究来调查这些药物。