Aarsland D, Andersen K, Larsen J P, Lolk A, Nielsen H, Kragh-Sørensen P
Section of Geriatric Psychiatry, Rogaland Psychiatric Hospital, Stavanger, Norway.
Neurology. 2001 Mar 27;56(6):730-6. doi: 10.1212/wnl.56.6.730.
To calculate the incidence of and determine possible risk factors for dementia in PD.
Dementia has important clinical consequences for patients with PD and their caregivers, but the incidence is unknown.
A population-based cohort of nondemented patients with PD (n = 171) from the county of Rogaland, Norway, was assessed at baseline and 4.2 years later with a comprehensive evaluation of motor, cognitive, and neuropsychiatric symptoms. The diagnosis of dementia was made according to the Diagnostic and Statistical Manual of Mental Disorders, 3rd edition, revised (DSM-III-R) criteria, based on interview of the patient and a caregiver, cognitive rating scales, and neuropsychologic tests. A representative sample of 3,062 nondemented elderly subjects without PD served as control group.
Forty-three patients with PD were demented at follow-up evaluation, equivalent to an incidence rate of 95.3 per 1,000 person-years (95% CI, 68.2 to 122.0). The risk for the development of dementia in patients with PD relative to the control subjects after adjusting for age, sex, and education was 5.9 (95% CI, 3.9 to 9.1). Predictive factors at baseline for dementia in PD in addition to age were Hoehn & Yahr score >2 (OR, 3.4; 95% CI, 1.3 to 8.6) and Mini-Mental State Examination score < 29 (OR, 3.3; 95% CI, 1.3 to 8.2).
Patients with PD have an almost sixfold increased risk for becoming demented compared with subjects without PD.
计算帕金森病(PD)患者中痴呆症的发病率,并确定可能的风险因素。
痴呆症对PD患者及其照料者具有重要的临床影响,但其发病率尚不清楚。
对挪威罗加兰郡171例非痴呆PD患者进行基于人群的队列研究,在基线时和4.2年后对运动、认知和神经精神症状进行全面评估。根据《精神障碍诊断与统计手册》第3版修订版(DSM-III-R)标准,通过对患者及其照料者的访谈、认知评定量表和神经心理学测试来诊断痴呆症。选取3062例无PD的非痴呆老年受试者作为对照组。
在随访评估中,43例PD患者出现痴呆,发病率为每1000人年95.3例(95%可信区间,68.2至122.0)。在调整年龄、性别和教育程度后,PD患者发生痴呆的风险相对于对照组为5.9(95%可信区间,3.9至9.1)。除年龄外,PD患者痴呆的基线预测因素包括Hoehn&Yahr评分>2(比值比,3.4;95%可信区间,1.3至8.6)和简易精神状态检查表评分<29(比值比,3.3;95%可信区间,1.3至8.2)。
与非PD患者相比,PD患者患痴呆症的风险增加了近6倍。