Institute of Applied Health Sciences, University of Aberdeen, Polwarth Building, Foresterhill, Aberdeen, AB25 2ZD, UK.
University of Aberdeen Medical School, Foresterhill, Aberdeen, AB25 2ZD, UK.
J Neurol. 2022 Aug;269(8):4288-4298. doi: 10.1007/s00415-022-11058-2. Epub 2022 Mar 21.
There are few long-term data on the incidence, baseline predictors, and outcomes of dementia in Parkinson's disease (PD) from prospective community-based incident cohorts.
The PINE study prospectively identified all incident PD patients in Aberdeen along with age-sex-matched, community-based controls who consented to standardized annual life-long follow-up. Each year, a clinical expert reviewed the diagnosis of PD and the presence of dementia according to DSM-IV-based criteria. Age-sex stratified incidence rates for dementia in PD and controls were calculated and compared with hazard ratios (HR) adjusted for age, sex, education, and socioeconomic status. Cox proportional-hazard modelling was used to assess baseline predictors for PD dementia and the influence of dementia on survival and institutionalization.
201 patients (mean age 72.6yrs) and 260 controls (mean age 75.4yrs) were followed for median 9.5 years. The incidence of dementia was 7.4 (PD) versus 2.1 (controls) per 100 person-years (adjusted HR 6.0, 95%CI 4.1-8.7), with a sixfold increase from under 60 to over 80 years in PD but no sex difference. Independent baseline predictors of PD dementia were older age at diagnosis, self-reported cognitive symptoms, dream enactment, lower MMSE scores, worse motor UPDRS scores, and the ApoE genotype. PD dementia increased the rates of subsequent death and institutionalization (32.0 and 26.9 per 100 person-years, respectively).
The incidence of dementia in PD is high, increases markedly with age, is increased in those with baseline subjective cognitive symptoms as well as other established risk factors, and is associated with high rates of death and institutionalization.
来自前瞻性社区发病队列的研究中,关于帕金森病(PD)患者痴呆的发病率、基线预测因子和结局的长期数据较少。
PINE 研究前瞻性地确定了阿伯丁所有新发 PD 患者,以及年龄性别匹配的、同意进行标准化年度终生随访的社区对照者。每年,临床专家根据 DSM-IV 标准审查 PD 和痴呆的诊断。计算 PD 和对照组中痴呆的年龄性别分层发病率,并与年龄、性别、教育程度和社会经济地位调整后的危险比(HR)进行比较。使用 Cox 比例风险模型评估 PD 痴呆的基线预测因子以及痴呆对生存和住院的影响。
201 名患者(平均年龄 72.6 岁)和 260 名对照者(平均年龄 75.4 岁)中位随访 9.5 年。痴呆的发病率为 PD 患者 7.4(每 100 人年)与对照组 2.1(每 100 人年)(调整 HR 6.0,95%CI 4.1-8.7),PD 患者从 60 岁以下到 80 岁以上增加了 6 倍,但无性别差异。PD 痴呆的独立基线预测因子包括诊断时年龄较大、自我报告的认知症状、梦境行为、较低的 MMSE 评分、较差的运动 UPDRS 评分和 ApoE 基因型。PD 痴呆增加了随后死亡和住院的发生率(分别为 32.0 和 26.9 每 100 人年)。
PD 患者痴呆的发病率较高,随年龄显著增加,与基线主观认知症状以及其他已确立的危险因素增加有关,且与高死亡率和住院率相关。