Emily J Hill, Samuel Blaise Marcucci, Kelly DeLano, Jesus Abanto, Russell P Sawyer, Luca Marsili, Kevin R Duque, Qin Sun, Daniel Woo, Carl D Langefeld, Deborah A Hall, Dawn Skirpan, Nathaly Chinchihualpa Paredes, Cynthia Spikes, Deepa Agrawal Bajaj, Nathan Gregor, Shea Stivers, Abhimanyu Mahajan, Jessica G Woo, Alberto J Espay
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Other studies have found worsened PD symptoms and outcomes associated with lower individual SES. If environmental factors associated with lower SES influence PD biology in a way that worsens symptoms, those processes should also increase PD risk. We set out to determine whether community disadvantage, rather than individual SES, is associated with motor or cognitive symptom severity in PD and atypical parkinsonisms.</p><p><strong>Methods: </strong>Community disadvantage was defined using the Material Community Deprivation Index, a compound score of multiple poverty markers. In our Cincinnati Cohort Biomarkers Program, a cohort that includes PD and atypical parkinsonisms, we tested for associations between community disadvantage and motor symptom severity (Movement Disorders Society Unified PD Rating Scale part III; MDS-UPDRS III), motor disability (Hoehn and Yahr stage [HY]), and cognition (Montreal Cognitive Assessment [MoCA]). We considered age, sex, disease duration, levodopa equivalent daily dose, education years, and race as covariates in multiple regression analyses.</p><p><strong>Results: </strong>A total of 565 people with PD or atypical parkinsonisms were included (458 idiopathic PD and 107 atypical parkinsonisms). Their mean age was 69 years, and 65% were men. The mean disease duration was 7 years, and the mean MDS-UPDRS III score was 30. The majority (75%) were HY stage 2, and the mean cognitive screening score was nondemented (MoCA 25/30). Worse community disadvantage was significantly associated with worse MDS-UPDRS III score (β 1.58, <i>p</i> = 0.01; adjusted for age, sex, and disease duration) and HY stage (OR 1.27, <i>p</i> = 0.04, adjusted for age, sex, disease duration, and education years). Community disadvantage was not significantly associated with MoCA score (<i>p</i> = 0.45).</p><p><strong>Discussion: </strong>Community disadvantage was associated with worse motor symptom severity and motor disability in PD, suggesting that there are modifiable social and environmental factors that can affect parkinsonian symptom severity.</p>","PeriodicalId":19136,"journal":{"name":"Neurology. 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Previous literature suggests a potential disconnect between the effect of socioeconomic status (SES) on PD risk and severity. A recent study found that people with PD in the United States were more likely to come from well-resourced communities. Multiple possible explanations were proposed, including that lower SES could be protective against PD risk. Other studies have found worsened PD symptoms and outcomes associated with lower individual SES. If environmental factors associated with lower SES influence PD biology in a way that worsens symptoms, those processes should also increase PD risk. We set out to determine whether community disadvantage, rather than individual SES, is associated with motor or cognitive symptom severity in PD and atypical parkinsonisms.</p><p><strong>Methods: </strong>Community disadvantage was defined using the Material Community Deprivation Index, a compound score of multiple poverty markers. 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引用次数: 0
摘要
背景与目的:社会经济因素与帕金森病(PD)的关系尚不清楚。先前的文献表明,社会经济地位(SES)对PD风险和严重程度的影响之间存在潜在的脱节。最近的一项研究发现,美国PD患者更有可能来自资源丰富的社区。提出了多种可能的解释,包括较低的社会经济地位可以预防帕金森病的风险。其他研究发现,PD症状和结果的恶化与个体社会地位较低有关。如果与低SES相关的环境因素以一种恶化症状的方式影响PD生物学,那么这些过程也应该增加PD的风险。我们开始确定社区劣势,而不是个体SES,是否与PD和非典型帕金森病的运动或认知症状严重程度有关。方法:采用多种贫困指标的复合评分——物质社区剥夺指数来定义社区劣势。在我们的辛辛那提队列生物标志物项目中,一个包括帕金森病和非典型帕金森病的队列,我们测试了社区劣势和运动症状严重程度之间的关系(运动障碍协会统一帕金森病评定量表第三部分;MDS-UPDRS III)、运动障碍(Hoehn和Yahr阶段[HY])和认知(蒙特利尔认知评估[MoCA])。在多元回归分析中,我们考虑了年龄、性别、病程、左旋多巴当量日剂量、受教育年限和种族作为协变量。结果:共纳入565例PD或非典型帕金森病患者(特发性PD 458例,非典型帕金森107例)。他们的平均年龄为69岁,65%是男性。平均病程为7年,MDS-UPDRS III平均评分为30分。大多数(75%)为HY 2期,平均认知筛查评分为无痴呆(MoCA 25/30)。社区劣势越严重,MDS-UPDRS评分越差(β 1.58, p = 0.01;经年龄、性别和病程调整后)和HY分期(OR 1.27, p = 0.04,经年龄、性别、病程和教育年限调整后)。社区劣势与MoCA评分无显著相关(p = 0.45)。讨论:社区劣势与PD患者运动症状严重程度和运动障碍相关,提示存在可改变的社会和环境因素影响帕金森症状严重程度。
Community Disadvantage Is Associated With More Severe Motor Symptoms in Parkinson Disease.
Background and objectives: The relationship between socioeconomic factors and Parkinson disease (PD) is unclear. Previous literature suggests a potential disconnect between the effect of socioeconomic status (SES) on PD risk and severity. A recent study found that people with PD in the United States were more likely to come from well-resourced communities. Multiple possible explanations were proposed, including that lower SES could be protective against PD risk. Other studies have found worsened PD symptoms and outcomes associated with lower individual SES. If environmental factors associated with lower SES influence PD biology in a way that worsens symptoms, those processes should also increase PD risk. We set out to determine whether community disadvantage, rather than individual SES, is associated with motor or cognitive symptom severity in PD and atypical parkinsonisms.
Methods: Community disadvantage was defined using the Material Community Deprivation Index, a compound score of multiple poverty markers. In our Cincinnati Cohort Biomarkers Program, a cohort that includes PD and atypical parkinsonisms, we tested for associations between community disadvantage and motor symptom severity (Movement Disorders Society Unified PD Rating Scale part III; MDS-UPDRS III), motor disability (Hoehn and Yahr stage [HY]), and cognition (Montreal Cognitive Assessment [MoCA]). We considered age, sex, disease duration, levodopa equivalent daily dose, education years, and race as covariates in multiple regression analyses.
Results: A total of 565 people with PD or atypical parkinsonisms were included (458 idiopathic PD and 107 atypical parkinsonisms). Their mean age was 69 years, and 65% were men. The mean disease duration was 7 years, and the mean MDS-UPDRS III score was 30. The majority (75%) were HY stage 2, and the mean cognitive screening score was nondemented (MoCA 25/30). Worse community disadvantage was significantly associated with worse MDS-UPDRS III score (β 1.58, p = 0.01; adjusted for age, sex, and disease duration) and HY stage (OR 1.27, p = 0.04, adjusted for age, sex, disease duration, and education years). Community disadvantage was not significantly associated with MoCA score (p = 0.45).
Discussion: Community disadvantage was associated with worse motor symptom severity and motor disability in PD, suggesting that there are modifiable social and environmental factors that can affect parkinsonian symptom severity.
期刊介绍:
Neurology® Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. The journal publishes original articles in all areas of neurogenetics including rare and common genetic variations, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease genes, and genetic variations with a putative link to diseases. Articles include studies reporting on genetic disease risk, pharmacogenomics, and results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology® Genetics, but studies using model systems for treatment trials, including well-powered studies reporting negative results, are welcome.