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J Public Health (Oxf). 2020 Nov 23;42(4):839-847. doi: 10.1093/pubmed/fdz167.
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Words hurt: Political rhetoric, emotions/affect, and psychological well-being among Mexican-origin youth.言语伤人:政治言论、情绪/情感与墨西哥裔青年的心理健康。
Soc Sci Med. 2019 May;228:240-251. doi: 10.1016/j.socscimed.2019.03.008. Epub 2019 Mar 11.
3
Social Relations and Health: Comparing "Invisible" Arab Americans to Blacks and Whites.社会关系与健康:将“隐形”的阿拉伯裔美国人与黑人和白人进行比较。
Soc Ment Health. 2018 Mar;8(1):84-92. doi: 10.1177/2156869317718234. Epub 2017 Jul 14.
4
Dementia Prevalence in Older Adults: Variation by Race/Ethnicity and Immigrant Status.老年人痴呆症的患病率:按种族/民族和移民身份的差异。
Am J Geriatr Psychiatry. 2019 Mar;27(3):241-250. doi: 10.1016/j.jagp.2018.11.003. Epub 2018 Nov 28.
5
Arab American Cognitive Aging: Opportunities for Advancing Research on Alzheimer's Disease Disparities.阿拉伯裔美国人的认知衰老:推进阿尔茨海默病差异研究的机遇。
Innov Aging. 2018 Feb 21;1(3):igx034. doi: 10.1093/geroni/igx034. eCollection 2017 Nov.
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Controversies and evidence for cardiovascular disease in the diverse Hispanic population.西班牙裔不同人群中心血管疾病的争议和证据。
J Vasc Surg. 2018 Mar;67(3):960-969. doi: 10.1016/j.jvs.2017.06.111. Epub 2017 Sep 23.
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Alzheimer's Disease in the Latino Community: Intersection of Genetics and Social Determinants of Health.拉丁裔社区的阿尔茨海默病:遗传学与健康社会决定因素的交集。
J Alzheimers Dis. 2017;58(4):979-992. doi: 10.3233/JAD-161261.
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Systematic review of dementia prevalence and incidence in United States race/ethnic populations.美国不同种族/族裔人群痴呆症患病率和发病率的系统评价
Alzheimers Dement. 2017 Jan;13(1):72-83. doi: 10.1016/j.jalz.2016.06.2360. Epub 2016 Sep 4.
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2016 Alzheimer's disease facts and figures.2016 年阿尔茨海默病事实和数据。
Alzheimers Dement. 2016 Apr;12(4):459-509. doi: 10.1016/j.jalz.2016.03.001.
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A Health Profile of Arab Americans in Michigan: A Novel Approach to Using a Hospital Administrative Database.密歇根州阿拉伯裔美国人的健康概况:利用医院行政数据库的新方法。
J Immigr Minor Health. 2016 Dec;18(6):1449-1454. doi: 10.1007/s10903-015-0296-8.

与中东/阿拉伯裔美国人和拉丁裔移民社区合作,增加参与阿尔茨海默病研究。

Partnering with Middle Eastern/Arab American and Latino Immigrant Communities to Increase Participation in Alzheimer's Disease Research.

机构信息

Department of Sociology, Anthropology, Criminology, Eastern Michigan University, Ypsilanti, MI.

Department of Translational Neuroscience, Michigan State University, Grand Rapids, MI.

出版信息

Ethn Dis. 2020 Nov 19;30(Suppl 2):765-774. doi: 10.18865/ed.30.S2.765. eCollection 2020.

DOI:10.18865/ed.30.S2.765
PMID:33250623
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7683026/
Abstract

PURPOSE

Recruitment and retention of US ethnic groups traditionally underrepresented in research continues to pose challenges. The Michigan Center for Contextual Factors in Alzheimer's Disease (MCCFAD) engages with two underserved immigrant communities in Michigan - Middle Eastern/Arab Americans in metro-Detroit and Latinos in the Grand Rapids area - to recruit and retain two Participant Resource Pools (PRP).

PROCEDURES

We adapt an existing community-based participatory research (CBPR) approach to recruit Middle Eastern/Arab American and Latino adults of all ages for Alzheimer's disease and related dementia (ADRD) research. Using American Community Survey (2014-2018) data, we compare socio-demographic characteristics of Middle Eastern/Arab Americans and Latinos living in Michigan to our PRPs. Assessment tools and community advisory board feedback identified missteps and culturally sensitive solutions.

MAIN FINDINGS

In the first year of MCCFAD activities, 100 Middle Eastern/Arab Americans and 117 Latinos joined the MCCFAD PRPs. Comparisons to state-level data showed that PRP participants were on average older and more likely to be female than the Middle Eastern/Arab American and Latino populations in Michigan. Further, Middle Eastern/Arab Americans in the PRP reported higher education levels while Latinos reported lower education levels than their respective statewide populations. Community partnerships/feedback identified the importance of connecting with community leaders, attending to matters of within-group diversity, as well as language and semantics.

CONCLUSION

Partnership with communities to develop culturally targeted and sensitive community health events can fill a significant gap in addressing ADRD health disparities by establishing sustainable relationships to increase participation in ADRD research.

摘要

目的

美国传统上代表性不足的族裔群体在研究中的招募和保留仍然是一个挑战。密歇根州阿尔茨海默病情境因素研究中心(MCCFAD)与密歇根州的两个服务不足的移民社区合作,招募和保留两个参与者资源池(PRP)。

程序

我们采用现有的社区参与式研究(CBPR)方法,招募中东/阿拉伯裔美国人和拉丁裔成年人参与阿尔茨海默病和相关痴呆症(ADRD)研究。利用美国社区调查(2014-2018 年)的数据,我们将居住在密歇根州的中东/阿拉伯裔美国人和拉丁裔的社会人口统计学特征与我们的 PRP 进行比较。评估工具和社区咨询委员会的反馈意见确定了失误和需要文化敏感处理的解决方案。

主要发现

在 MCCFAD 活动的第一年,有 100 名中东/阿拉伯裔美国人和 117 名拉丁裔加入了 MCCFAD PRP。与州级数据的比较表明,PRP 参与者的平均年龄较大,女性比例高于密歇根州的中东/阿拉伯裔美国人和拉丁裔人口。此外,PRP 中的中东/阿拉伯裔美国人的受教育程度高于其各自的全州人口,而拉丁裔的受教育程度则低于其各自的全州人口。社区伙伴关系/反馈意见表明,与社区领导人建立联系、关注群体内多样性问题以及语言和语义问题非常重要。

结论

与社区合作开展针对特定文化和敏感问题的社区健康活动,可以通过建立可持续的关系来增加 ADRD 研究的参与度,从而显著缩小 ADRD 健康差异。