Servello A, Andreozzi P, Bechini F, De Angelis R, Pontecorvo M L, Vulcano A, Cerra E, Vigliotta M T, Artini M, Selan L, Ettorre E
Dipartimento di Sanità Pubblica e Malattie Infettiva La Sapienza Università di Roma, Roma, Italia -
Minerva Med. 2014 Apr;105(2):167-74.
Vascular dementia (VaD) is defined as a loss of cognitive function resulting from ischemic, hypoperfusive, or hemorrhagic brain lesions due to cerebrovascular disease or cardiovascular pathology. The main types of VaD are: Small Vessel Disease Dementia (sVAD), Large vessel disease dementia, hypoperfusive-ischemic dementia and hemorragic dementia. The sVAD is divided into two main categories: subcortical ischemic vascular dementia (SIVD) and cortical dementia. Currently, no drugs are approved for the treatment of VaD. This study aimed to determine whether rivastigmine, a second generation cholinesterase inhibitor with selectivity for the CNS, with capacity to inhibit both acetylcholinesterase (AChE) and butyryl-cholinesterase (BuChE), slows the rate of cognitive decline associated with VaD.
Study subjects were 27 male and 43 female outpatients aged 80.03±6.53 years, with Mini-Mental State Examination (MMSE) score ranging batween 22 and 12, affected by VaD. They were included in the study if they were undergoing pharmacological treatment with acetylsalicylic acid 100 mg for at least six months. Patients were divided into two groups: one group was treated with ASA 100 mg and rivastigmine patch 9.5 mg (Rivastigmine group), the other just with ASA 100 mg (ASA group). All patients were followed for 6 months, with a first evaluation (T0) and a second examination after six mounths of treatment (T1).
Statistically data proved as the Rivastigmine group showed constant values at MMSE, compared with patients of the ASA group who experienced decline of their cognitive performances. The same result was found in CDR, ADL, GDS and NPI scales. It is remarkable to underline as Rivastigmine-treated patients had a mean improvement in GDS scales, in comparison with patients of the ASA group who showed a worsening of mood.
Rivastigmine-therapy improves cognitive performance in elderly with SIVD.
血管性痴呆(VaD)被定义为由于脑血管疾病或心血管病变导致的缺血性、灌注不足性或出血性脑损伤所引起的认知功能丧失。VaD的主要类型包括:小血管疾病性痴呆(sVAD)、大血管疾病性痴呆、灌注不足-缺血性痴呆和出血性痴呆。sVAD主要分为两类:皮质下缺血性血管性痴呆(SIVD)和皮质性痴呆。目前,尚无获批用于治疗VaD的药物。本研究旨在确定卡巴拉汀(一种对中枢神经系统具有选择性的第二代胆碱酯酶抑制剂,能够抑制乙酰胆碱酯酶(AChE)和丁酰胆碱酯酶(BuChE))是否能减缓与VaD相关的认知衰退速度。
研究对象为27名男性和43名女性门诊患者,年龄80.03±6.53岁,受VaD影响,简易精神状态检查表(MMSE)评分在22至12之间。如果他们正在接受100毫克乙酰水杨酸的药物治疗至少六个月,则被纳入研究。患者分为两组:一组接受100毫克ASA和9.5毫克卡巴拉汀贴片治疗(卡巴拉汀组),另一组仅接受100毫克ASA治疗(ASA组)。所有患者随访6个月,进行首次评估(T0)以及治疗6个月后的第二次检查(T1)。
统计学数据表明,与认知能力下降的ASA组患者相比,卡巴拉汀组患者的MMSE值保持稳定。在CDR、ADL、GDS和NPI量表中也发现了相同的结果。值得注意的是,与情绪恶化的ASA组患者相比,接受卡巴拉汀治疗的患者在GDS量表上平均有所改善。
卡巴拉汀治疗可改善老年SIVD患者的认知表现。