Alvarez X A, Franco A, Fernández-Novoa L, Cacabelos R
EuroEspes Research Center, Santa Marta de Babío, A Coruña, Spain.
Mol Chem Neuropathol. 1996 Oct-Dec;29(2-3):237-52. doi: 10.1007/BF02815005.
In this study, we have evaluated the levels of blood histamine, serum interleukin-1 beta (IL-1 beta), and plasma tumor necrosis factor-alpha (TNF-alpha) in 20 patients with mild to moderate Alzheimer disease (AD; 13 early onset and 7 late-onset AD subjects) and in 20 age-matched control subjects (C). AD patients showed higher concentrations of histamine (AD = 452.9 +/- 237.9 pmol/mL; C = 275.3 +/- 151.5 pmol/mL; p < 0.05) and IL-1 beta (AD = 211.2 +/- 31.1 pg/mL; C = 183.4 +/- 24.4 pg/mL; p < 0.01), and lower values of TNF-alpha (AD = 3.59 +/- 2.02 pg/mL; C = 9.47 +/- 2.64 pg/mL; p < 0.001) than elderly controls. Increased levels of histamine and decreased levels of TNF-alpha were observed in both early onset AD (EOAD) and late-onset AD (LOAD) patients, but only EOAD subjects had elevated serum IL-1 beta values compared with age-matched controls. Age negatively correlated with histamine (r = -0.57; p < 0.05) and positively with IL-1 beta levels (r = 0.48; p < 0.05) in healthy subjects, but not in AD, whereas a positive correlation between TNF-alpha scores and age was only found in AD patients (r = 0.46; p < 0.05). Furthermore, histamine and TNF-alpha values correlated negatively in AD (r = -0.50, p < 0.05). In addition, cognitive impairment increased in patients with lower TNF-alpha and higher histamine and IL-1 beta levels, as indicated by the correlations between mental performance scores and histamine (r = -0.37, ns), IL-1 beta (r = -0.33, ns) and TNF-alpha levels (r = 0.42, p < 0.05). Finally, histamine concentrations decreased as depression scores increased in AD (r = -0.63, p < 0.01). These data suggest a dysfunction in cytokine and histamine regulation in AD, probably indicating changes associated with inflammatory processes.
在本研究中,我们评估了20例轻度至中度阿尔茨海默病(AD;13例早发型和7例晚发型AD患者)及20例年龄匹配的对照者(C)的血液组胺、血清白细胞介素-1β(IL-1β)和血浆肿瘤坏死因子-α(TNF-α)水平。AD患者的组胺浓度(AD = 452.9±237.9 pmol/mL;C = 275.3±151.5 pmol/mL;p < 0.05)和IL-1β浓度(AD = 211.2±31.1 pg/mL;C = 183.4±24.4 pg/mL;p < 0.01)高于老年对照者,而TNF-α值(AD = 3.59±2.02 pg/mL;C = 9.47±2.64 pg/mL;p < 0.001)低于老年对照者。早发型AD(EOAD)和晚发型AD(LOAD)患者均观察到组胺水平升高和TNF-α水平降低,但只有EOAD患者与年龄匹配的对照者相比血清IL-1β值升高。在健康受试者中,年龄与组胺呈负相关(r = -0.57;p < 0.05),与IL-1β水平呈正相关(r = 0.48;p < 0.05),但在AD患者中并非如此,而仅在AD患者中发现TNF-α评分与年龄呈正相关(r = 0.46;p < 0.05)。此外,AD患者中组胺和TNF-α值呈负相关(r = -0.50,p < 0.05)。另外,如心理表现评分与组胺(r = -0.37,无统计学意义)、IL-1β(r = -0.33,无统计学意义)和TNF-α水平(r = 0.42,p < 0.05)之间的相关性所示,TNF-α水平较低、组胺和IL-1β水平较高患者的认知障碍加重。最后,AD患者中抑郁评分增加时组胺浓度降低(r = -0.63,p < 0.01)。这些数据表明AD患者细胞因子和组胺调节功能存在障碍,可能提示与炎症过程相关的变化。