Prevalence of Neurologic Disease Among Those in Same-Sex Relationships: Evidence from the Medical Expenditure Panel Survey.

IF 2.3 Q3 CLINICAL NEUROLOGY Neurology. Clinical practice Pub Date : 2025-02-01 Epub Date: 2024-10-08 DOI:10.1212/CPJ.0000000000200385
Lennox Byer, Elan L Guterman, Nicole Rosendale
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Abstract

Background and objectives: Prior research has shown several health disparities affecting sexual minority people. Research on the neurologic health of sexual minority people has been limited. Our objective was to characterize the prevalence of neurologic disease and utilization of a neurologist among a population of sexual minority people.

Methods: We conducted a cross-sectional analysis of sexual minority people, using people in same-sex relationships as a proxy for sexual minority status, from the Medical Expenditure Panel Survey (MEPS) from 2016 to 2020. The MEPS is a government-run survey that uses complex sampling to obtain a nationally representative sample. Our primary outcome was a diagnosis of any neurologic disease. We also completed stratified analyses by sex, race, and ethnicity. Our secondary outcome was visit to a neurologist within the past year. Logistic regression was used to compare the odds of both outcomes in those in same-sex relationships and those in different-sex relationships.

Results: Among 153,313 MEPS participants, there were 61,645 (40.2%) participants in relationships who were included in our sample. Of those, 822 (1.33%) participants were in same-sex relationships. Participants were, on average, aged 51 years (median 50 years, IQR 38-63); nearly 50% reported female sex and mostly non-Hispanic White (67.81%). Among those in same-sex relationships, 22.7% reported a neurologic diagnosis compared with 18.1% of those in different-sex relationships (OR 1.33; 95% CI 1.04-1.71). This difference was maintained with adjustment for age, sex, education, and insurance (OR 1.48; 95% CI 1.15-1.91). There was no significant difference in visit to a neurologist (adjusted OR 1.38; 95% CI 0.91-2.10).

Discussion: In this nationally representative sample, neurologic disease was more prevalent among those in same-sex relationships compared with those in different-sex relationships. Limited sample size and absent measurements of minority stress limited the etiologic search for factors driving this disparity. There was no significant difference in visit to a neurologist, and both groups reported their overall health as being similar. There is a need for more routine measurement of sexual orientation in neurologic research. This will allow us to detail differences in neurologic disease risk factors, prevalence, and outcomes. The end goal is the identification of opportunities for intervention and advancement of neurologic health equity.

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同性关系人群中神经系统疾病的患病率:来自医疗支出小组调查的证据。
背景和目标:先前的研究表明,性少数群体在健康方面存在一些差异。有关性少数群体神经系统健康的研究还很有限。我们的目的是了解性少数人群中神经系统疾病的患病率和神经科医生的使用情况:我们从 2016 年至 2020 年的医疗支出面板调查(MEPS)中对性少数人群进行了横截面分析,并将同性关系人群作为性少数人群的替代身份。MEPS是一项由政府管理的调查,采用复杂的抽样方法获得具有全国代表性的样本。我们的主要结果是任何神经系统疾病的诊断。我们还按性别、种族和民族进行了分层分析。我们的次要结果是在过去一年内就诊于神经科医生。我们使用逻辑回归法比较了同性关系者和异性关系者出现这两种结果的几率:在 153,313 名 MEPS 参与者中,有 61,645 名(40.2%)有恋爱关系的参与者被纳入样本。其中,822 人(1.33%)处于同性关系中。参与者的平均年龄为 51 岁(中位数为 50 岁,IQR 为 38-63);近 50%的参与者报告性别为女性,大部分为非西班牙裔白人(67.81%)。在同性关系中,22.7%的人报告了神经系统诊断,而在异性关系中,18.1%的人报告了神经系统诊断(OR 1.33; 95% CI 1.04-1.71)。在对年龄、性别、教育程度和保险进行调整后,这一差异依然存在(OR 1.48; 95% CI 1.15-1.91)。在看神经科医生方面没有明显差异(调整后 OR 为 1.38;95% CI 为 0.91-2.10):讨论:在这一具有全国代表性的样本中,神经系统疾病在同性关系者中的发病率高于异性关系者。有限的样本量和缺乏对少数群体压力的测量限制了对造成这种差异的因素的病因学研究。两组人在看神经科医生方面没有明显差异,他们报告的总体健康状况相似。在神经病学研究中,有必要对性取向进行更常规的测量。这将使我们能够详细了解神经系统疾病风险因素、发病率和结果的差异。最终目标是找到干预和促进神经系统健康公平的机会。
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来源期刊
Neurology. Clinical practice
Neurology. Clinical practice CLINICAL NEUROLOGY-
CiteScore
4.00
自引率
0.00%
发文量
77
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.
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