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多发性硬化症患者中的拉丁裔、非裔美国人和白种人的比较。

Comparisons of Latinos, African Americans, and Caucasians with multiple sclerosis.

机构信息

Department of Political Science and Public Administration, Mississippi State University, PO Box PC, Mississippi State, MS, 39762, USA.

出版信息

Ethn Dis. 2010 Autumn;20(4):451-7.

Abstract

OBJECTIVE

Identify racial/ethnic differences among people with multiple sclerosis (MS) in demographics, MS disease characteristics, and health services received.

PARTICIPANTS

We analyzed enrollment data from the Registry of the North American Research Committee on Multiple Sclerosis (NARCOMS) Project to compare 26,967 Caucasians, 715 Latinos, and 1,313 African Americans with MS.

DESIGN

Racial/ethnic analyses of NARCOMS data focused on descriptive characteristics, using ANOVA and chi-square tests to identify significant differences in means and frequencies among Caucasians, Latinos, and African Americans.

RESULTS

We identified significant racial/ethnic differences in demographics, MS disease characteristics, and treatments. Caucasians were older when first MS symptoms were experienced (30.1 years) and at MS diagnosis (37.4 years) than Latinos (28.6 years and 34.5 years) or African Americans (29.8 years and 35.8 years). Larger proportions of Latinos reported normal function for mobility and bladder/bowel function compared to Caucasians. Larger proportions of Latinos (44.2 percent) and African Americans (45.8 percent) reported at least mild depression compared to only 38.7 percent of Caucasians. Larger proportions of Latinos never received mental health care or care from rehabilitation specialists than Caucasians or African Americans. A larger proportion of African Americans had never been treated by a neurologist specializing in MS and a smaller proportion of African Americans received care at a MS clinic than Caucasians or Latinos.

CONCLUSIONS

Our findings highlight the need for future analyses to determine if age, disease duration, MS symptoms, and disability levels provide additional insights into racial/ethic differences in the use of MS-related providers.

摘要

目的

确定多发性硬化症(MS)患者在人口统计学、MS 疾病特征和所接受的医疗服务方面的种族/民族差异。

参与者

我们分析了北美多发性硬化症研究委员会(NARCOMS)项目注册表的入组数据,以比较 26967 名白种人、715 名拉丁裔和 1313 名非裔美国人的多发性硬化症患者。

设计

NARCOMS 数据的种族/民族分析侧重于描述性特征,使用方差分析和卡方检验来确定白种人、拉丁裔和非裔美国人之间均值和频率的显著差异。

结果

我们发现人口统计学、MS 疾病特征和治疗方面存在显著的种族/民族差异。首次出现 MS 症状时(30.1 岁)和诊断为 MS 时(37.4 岁),白种人比拉丁裔(28.6 岁和 34.5 岁)或非裔美国人(29.8 岁和 35.8 岁)年龄更大。与白种人相比,更多的拉丁裔报告在移动和膀胱/肠道功能方面的正常功能。与白种人相比,更多的拉丁裔(44.2%)和非裔美国人(45.8%)报告至少有轻度抑郁,而白种人只有 38.7%。与白种人和非裔美国人相比,更多的拉丁裔从未接受过心理健康护理或康复专家护理。与白种人和拉丁裔相比,更多的非裔美国人从未接受过专门治疗 MS 的神经科医生的治疗,而且接受 MS 诊所治疗的非裔美国人比例较小。

结论

我们的研究结果强调需要进一步分析,以确定年龄、疾病持续时间、MS 症状和残疾程度是否为 MS 相关提供者使用方面的种族/民族差异提供更多见解。

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