少数民族神经退行性疾病的症状患病率

Tarun D. Singh, K. Josephs
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引用次数: 2

摘要

背景:在美国,预计1990年至2040年间,少数民族中每年神经退行性疾病的数量将增加524%,并且没有研究观察不同种族和少数民族阿尔茨海默氏痴呆(AD)、帕金森病(PD)和运动神经元病(MND)患者的症状/体征的发病率和流行程度。方法:回顾性分析2000年1月1日至2015年12月31日期间在罗切斯特梅奥诊所(Mayo Clinic, Rochester, MN)诊断为AD、PD或MND的所有少数亚组患者。我们将研究人群分为7组:黑人、亚洲人、南亚人、中东人、西班牙裔/拉丁裔、美洲印第安人/阿拉斯加原住民和夏威夷原住民/太平洋岛民。结果:在我们机构15年的时间框架内,共8927例被诊断为神经退行性疾病的患者中,472例为少数群体[PD=220 (46.6%);AD=90 (19.1%), MND=162(34.3%)]。最常见的种族/民族是黑人或非裔美国人135人(28.6%),亚洲人101人(21.4%),南亚人69人(14.6%),中东人60人(12.7%),西班牙裔/拉丁裔59人(12.5%)和美洲印第安人/阿拉斯加原住民/夏威夷原住民/太平洋岛民48人(10.2%)。PD组在微书写症、嗅觉缺失、左旋多巴引起的运动障碍、跌倒和肌张力障碍的频率上存在差异,AD组在执行功能障碍和视觉空间变化上存在差异,MND组在肌肉萎缩、肢体束动、无法行走、舌束动、窒息发作和吞咽困难上存在差异。结论:神经退行性疾病影响所有少数民族和民族,包括一些以前未报道的,不同少数民族/民族出现体征和症状的频率显著不同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Symptom Prevalence of Neurodegenerative Diseases among Minorities
Background: The annual number of neurodegenerative diseases among minorities is projected to increase by 524% between 1990 and 2040 in the US and there have been no studies looking at the incidence and prevalence of signs/symptoms among different racial and ethnic minority patients with Alzheimer's dementia (AD), Parkinson's disease (PD) and Motor neuron disease (MND).Methods: Retrospective review of all minority subgroups who presented to Mayo Clinic, Rochester (MN), with a diagnosis of AD, PD or MND between January 1st, 2000 and December 31st, 2015. We divided our study population into seven groups: Black, Asian, South Asian, Middle Eastern, Hispanic/Latino, American Indian/Alaskan Native and Native Hawaiian/Pacific Islander.Results: From a total of 8927 patients diagnosed with a neurodegenerative disease at our institution over the 15 year time frame, 472 were minority [PD=220 (46.6%); AD=90 (19.1%) and MND=162 (34.3%)]. The most common races/ethnicity were Black or African American in 135 (28.6%), Asian in 101 (21.4%), South Asian in 69 (14.6%), Middle eastern in 60 (12.7%), Hispanic/Latino in 59 (12.5%) and American Indian/Alaskan Native/Native Hawaiian/ Pacific Islander in 48 (10.2%). For PD, there were differences in the frequency of micrographia, anosmia, levodopa induced dyskinesia, falls and dystonia, while for AD there were differences in executive dysfunction and visual spatial changes and for MND difference were present for muscle atrophy, limb fasciculation, inability to ambulate, tongue fasciculation, choking episodes and dysphagia.Conclusion: Neurodegenerative diseases afflict all minority races and ethnicities, including some not previously reported and the frequency of presenting signs and symptoms significantly vary across different minority/ethnic groups.
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