This discussion summarizes the various factors that lead to the disparity of patient care in African American and Hispanic populations compared with the non-Hispanic white population. Dr. Mitzi Williams, Dr. Shiv Saidha, and Dr. Megan Weigel discuss reasons for these disparities in patient care and how to overcome them.
Critical Management of Multiple Sclerosis in African American and Hispanic Populations
Disparities in Multiple Sclerosis: Optimizing Care of African American and Hispanic American Populations
Historically, multiple sclerosis (MS) has been considered a disease seen largely in the non-Hispanic white population, but more recent research has proven that is not the case.1 A 2013 study showed that in US patients newly diagnosed with MS, the incidence rate was 10.2 in African Americans versus 6.9 in non-Hispanic whites and 2.9 in Hispanics.2 Further, in the United States, the incidence of MS in African Americans and Hispanic Americans has been demonstrated to be higher than in the ancestral countries of origin of these individuals.3 Research also shows that in minority populations, MS is distinguished by differences in disease onset, presentation, and course. Disease onset is more common in African Americans at a later age and in Hispanic Americans at a younger age than in non-Hispanic whites.2 Disease course may be more aggressive in African Americans, and opticospinal MS is more common in both African American and Hispanic patients with the disease.4,5
The clinical picture for minority patients is also complicated by the fact that optimization of their care is difficult because these populations are underrepresented in clinical trials, resulting in limited evidence on which clinicians can base decisions about treatment and follow-up.4 Barriers to clinical trial participation are multiple, including differential response to first-line treatments, socioeconomic issues, and cultural influences.1 This article summarizes data on the epidemiology of MS in African Americans and Hispanic Americans, disabilities associated with the disease in these two populations, the reasons for ethnic disparities in treatment of MS, and results of recent randomized clinical trials targeting specific ethnicities.
Epidemiology of MS in African American and Hispanic Populations
Two large multiethnic cohorts indicate that in recent years, the demographics of MS in the United States have changed drastically, in tandem with overall nationwide population shifts influenced by factors such as immigration.6-8 Incidence of MS may be increased in African Americans and up to 47% higher in African American women compared to non-Hispanic white women.1
Higher rates of disability are seen in both African Americans and Hispanics than in non-Hispanic whites with MS, and there are suggestions that African Americans may reach step 6 on the Expanded Disability Status Scale (EDSS) up to 6 to 10 years earlier than their white counterparts.1 Potential challenges in treatment and care of MS in Hispanic Americans include population changes, delayed diagnosis, immigration, acculturation, and lack of culturally relevant MS materials and programs.9
Demographics and Clinical Characteristics
MS across EDSS Grades
A longitudinal study that tracked 15 African Americans and 115 non-Hispanic whites with MS using optical coherence tomography (OCT) found that, regardless of treatment status, African Americans tended to have increased rates of degeneration of retinal tissue and of brain and brain structure atrophy compared with their white counterparts.10 Gray matter, white matter, and nuclear thalamic atrophy rates were approximately twice as fast in the African Americans.10 These results underscore the need for future research in African Americans to identify individual differences in treatment responses in MS.
While the incidence of MS is lower in Hispanic Americans than in African Americans, their disease patterns also differ from that seen in non-Hispanic whites. Research is lacking in this population, but in a single-institution study based on medical chart review, initiation of symptoms occurred at a median age of 28.4 years in Hispanics versus 32.5 years in non-Hispanic whites.9 Compared with whites, Hispanic Americans were more likely to have a relapsing-remitting form of MS with presenting symptoms of optic neuritis and transverse myelitis and lower levels of vitamin D.9 Optic neuritis was also more common in Hispanics with MS from western parts of the United States than in non-Hispanic whites.6,11,12
Overall, ambulatory disability does not appear to differ between Hispanic whites and non-Hispanic whites.9 However, an analysis of Hispanics from the USC Hispanic MS registry, presented at ECTRIMS 2019, showed that cardiovascular comorbidities were common in the cohort.13 A strong association was found between hypertension and ambulatory disability defined as EDSS ≥ 6. Timing of immigration to the United States, too, appears to be a significant determinant of ambulatory disability in the Hispanic population, according to a survey-based study of low-income minority patients with MS. Risk was more than 3-fold higher in Hispanic patients who were older than age 15 when they migrated to the United States than in those born in the United States.9
Little information exists about imaging for MS in the Hispanic population. In one study done of Hispanics with MS in California, 25% of patients with adult-onset disease had complete transverse myelitis at presentation compared with 13% of non-Hispanic whites.12 In another study, cervical spinal cord lesions were seen on magnetic resonance imaging (MRI) in more than 75% of Hispanic patients with MS, with a median time of diagnosis of 2 years at the time MRI was collected.11
Disparities in MS Care Among Minority Populations
Factors that prevent minority populations from accessing care for MS and receiving adequate treatment include personal risk factors, economic factors, accessibility issues, cultural and religious beliefs, and distrust of the medical system. An analysis of data from the 2006-2013 Medical Expenditure Panel Survey (MEPS) showed that, compared with whites, Hispanic participants were 40% less likely to see an outpatient neurologist (odds ratio [OR] 0.61, confidence interval [CI] 0.54-0.69) and blacks were nearly 30% less likely to see an outpatient neurologist (OR 0.72, CI 0.64-0.81), even after adjusting for other factors that could affect access to care.14
Research shows that Medicaid’s home- and community-based services to support African Americans and Hispanic Americans with MS are underutilized by those populations.15 As a result, these populations are less likely to receive case management, equipment, technology, and home modifications compared to whites, even though programs to provide assistance are available.
Therapeutic Approaches for MS in African Americans and Hispanics
One of the largest gaps that exists in knowledge about therapy for MS is regarding specific ways to make treatment decisions based on an individual’s ethnicity. In part, this stems from a lack of MS clinical trials with minority patient enrollment. However, new data are emerging in this area.
Two interim analyses from ESTEEM, an ongoing, Phase IV, 5-year observational study of the safety and efficacy of delayed-release dimethyl fumarate, were presented at the 2019 meeting of the Consortium of Multiple Sclerosis Centers (CMSC). Both reflect real-world evidence with the drug, one in black or African American patients and one in Hispanics.16,17 These post hoc analyses included patients newly prescribed dimethyl fumarate in routine practice at approximately 380 sites globally. An 82% lower unadjusted absolute risk reduction (ARR) was seen in black or African American patients at 24 months after initiation of dimethyl fumarate than 12 months before.17 Results were similar in the Hispanic patients with 76% lower unadjusted ARR for the same time periods.16
Also presented at the 2019 CMSC meeting was a post hoc analysis of treatment retention and satisfaction in Hispanic and Latino patients from the PREFERMS study. The trial was a 12-month, phase IV, open-label multicenter study of fingolimod versus injectable disease-modifying therapies (DMTs) for relapsing-remitting MS. Although the Hispanic and Latino subgroup was small, the post hoc analysis showed that treatment satisfaction was higher with fingolimod (75%) versus intravenous (IV) DMTs (63.6%) as was retention (91.7% and 50%, respectively).18 In a previous subgroup analysis from PREFERMS, retention was studied in African American patients.19 As in Hispanics, retention was significantly higher for fingolimod than for IV DMTs (80.6% vs 30.4%). The most common treatment switch was from an IV DMT to fingolimod for injection-related reasons.
Presented at ECTRIMS 2018, a subgroup analysis of the efficacy of ocrelizumab versus interferon β-1a from the OPERA I and OPERA II studies showed that treatment benefit on MRI and composite efficacy outcomes in African American patients with relapsing-remitting MS were similar to those in the overall study populations.20
Data from a retrospective analysis presented at ECTRIMs 2018 showed no difference in treatment outcomes between African Americans and whites in the CombiRx study.21 African Americans did, however, have worse disability (P = 0.007), higher total lesion burden (P < 0.0001), and a trend toward lower normalized brain volume (P = 0.055) than their white counterparts. CombiRx was a multicenter, randomized controlled trial of the combined use of interferon β-1a weekly and glatiramer acetate daily versus individual use in relapsing-remitting MS.
To enrich the data on MS in minority populations, diversification of participants in clinical trials is crucial. Registries of multi-institutional studies are also needed to help clinicians better understand these patients. Increasing efforts to educate patients with MS who are members of minority communities is another area for improvement. One such initiative is the MS Minority Research Partnership Engagement Network.22 This group is composed of multiple parties and includes industry partners, advocacy group representatives, physicians, clinicians, researchers, and people living with MS. The Network has produced several toolkits to improve cultural competency, including one for people living with MS to help them understand clinical research and another for researchers to ensure that the way they address minority populations is culturally appropriate.
Progress is being made in improving care for African American and Hispanic patients with MS, and while the understanding of these populations has improved significantly, gaps in knowledge remain. More research is needed about the impact of the disease in minority populations, how to make individualized treatment decisions based on an individual’s ethnicity, and on disparities in response to therapy. For their part, clinicians should seek resources for African American and Hispanic American patients with MS that will encourage these individuals to trust the healthcare system and increase their adherence so that they will have better outcomes throughout their disease course.
1. Khan O, Williams MJ, Amezcua L, Javed A, Larsen KE, Smrtka JM. Multiple sclerosis in US minority populations: clinical practice insights. Neurol Clin Pract. 2015;5(2):132-142.
2. Langer-Gould A, Brara SM, Beaber BE, Zhang JL. Incidence of multiple sclerosis in multiple racial and ethnic groups. Neurology. 2013;80(19):1734-1739.
3. Amezcua L, Lund BT, Weiner LP, Islam T. Multiple sclerosis in Hispanics: a study of clinical disease expression. Mult Scler. 2011;17(8):1010-1016.
4. Cree BA, Reich DE, Khan O, et al. Modification of multiple sclerosis phenotypes by African ancestry at HLA. Arch Neurol. 2009;66(2):226-233.
5. Reich DS, Lucchinetti CF, Calabresi PA. Multiple sclerosis. N Engl J Med. 2018;378(2):169-180.
6. Langer-Gould A, Brara SM, Beaber BE, Zhang JL. The incidence of clinically isolated syndrome in a multi-ethnic cohort. J Neurol. 2014;261(7):1349-1355.
7. Wallin MT, Culpepper WJ, Campbell JD, et al. The prevalence of MS in the United States: a population-based estimate using health claims data. Neurology. 2019;92(10):e1029-e1040.
8. Rivas-Rodriguez E, Amezcua L. Ethnic considerations and multiple sclerosis disease variability in the United States. Neurol Clin. 2018;36(1):151-162.
9. Amezcua L, Oksenberg JR, McCauley JL. MS in self-identified Hispanic/Latino individuals living in the US. Mult Scler J Exp Transl Clin. 2017;3(3):2055217317725103.
10. Caldito NG, Saidha S, Sotirchos ES, et al. Brain and retinal atrophy in African-Americans versus Caucasian-Americans with multiple sclerosis: a longitudinal study. Brain. 2018;141(11):3115-3129.
11. Amezcua L, Lerner A, Ledezma K, et al. Spinal cord lesions and disability in Hispanics with multiple sclerosis. J Neurol. 2013;260(11):2770-2776.
12. Langille MM, Islam T, Burnett M, Amezcua L. Clinical characteristics of pediatric-onset and adult-onset multiple sclerosis in Hispanic Americans. J Child Neurol. 2016;31(8):1068-1073.
13. Robers M, Chan C, Martinez A, Ramanathan M, Amezcua L. The association of cardiovascular disease and ambulatory disability is driven by hypertension in Hispanic-American patients with multiple sclerosis. Paper presented at 2019 ECTRIMS Congress; 2019; Stockholm, Sweden. P1635.
14. Saadi A, Himmelstein DU, Woolhandler S, Mejia NI. Racial disparities in neurologic health care access and utilization in the United States. Neurology. 2017;88(24):2268-2275.
15. Fabius CD, Thomas KS, Zhang T, Ogarek J, Shireman TI. Racial disparities in Medicaid home and community-based service utilization and expenditures among persons with multiple sclerosis. BMC Health Serv Res. 2018;18(1):773.
16. Chinea A, Amezcua L, Vargas W, et al. Real-world safety and effectiveness of dimethyl fumarate in Hispanic or Latino patients with multiple sclerosis: 3-year results from ESTEEM [published online ahead of print 2020 May 29]. Neurol Ther. doi:10.1007/s40120-020-00192-6
17. Williams MJ, Johnson K, Trenz HM, et al. Adherence, persistence, and discontinuation among Hispanic and African American patients with multiple sclerosis treated with fingolimod or glatiramer acetate. Curr Med Res Opin. 2018;34(1):107-115.
18. Martinez ARC, Amezcua L, Lund BT, Meng X, Schofield L, Tenenbaum N. Post hoc analysis of treatment retention and satisfaction in the subgroup of Hispanic/Latino patients from the PREFERMS study. Paper presented at: 2019 CMSC Annual Meeting; Seattle, Washington.
19. Cascione M, Tenenbaum N, Wendt J, et al. Treatment retention on fingolimod compared with injectable multiple sclerosis therapies in African-American patients: a subgroup analysis of a randomized phase 4 study. Mult Scler Relat Disord. 2018;25:50-56.
20. Cree BAC, Han J, Pradhan A, Masterman D, Williams MJ. Subgroup analysis to evaluate the efficacy of ocrelizumab versus interferon β-1a in African-descended patients with relapsing multiple sclerosis in the OPERA 1 and OPERA II studies. Paper presented at: 2018 ECTRIMS Congress; 2018; Berlin, Germany. P639.
21. Ayeni O, Sumowski J, Cutter G, et al. Outcomes of African-Americans compared to Caucasian-Americans in the CombiRx study. Paper presented at: 2018 ECTRIMS Congress; 2018; Berlin, Germany. P675.
22. Patient-Centered Outcomes Research Institute. The MS Minority Research Engagement Partnership Network. Accessed June 17, 2020. https://www.pcori.org/research-results/2016/ms-minority-research-engagement-partnership-network
In accordance with the ACCME Standards for Commercial Support, Global Learning Collaborative (GLC) requires that individuals in a position to control the content of an educational activity disclose all relevant financial relationships with any commercial interest. GLC resolves all conflicts of interest to ensure independence, objectivity, balance, and scientific rigor in all its educational programs.
Shiv Saidha MBBCh, MD, MRCPI
Associate Professor of Neurology,
Division of Neuroimmunology and Neurological Infections
Johns Hopkins University School of Medicine
Consulting Fees: Biogen, Celgene, EMD Serono, Genentech
Research Funding: Biogen, Genentech
Equity: June Brain (retinal imaging device developer/manufacturer)
Megan R. Weigel, DNP, ARNP-c, MSCN
First Coast Integrative Medicine
Consulting Fees: Biogen, Celgen (BMS), Novartis, Sanofi Genzyme, Viela Bio
Speakers Bureau: Celgene (BMS), Novartis, Sanofi Genzyme, Viela Bio
Mitzi Joi Williams, MD
Neurologist, MS Specialist
Joi Life Wellness Group
Consulting Fees: Biogen, BMS,Genentech, Merck, Novartis, Sanofi
Speakers Bureau: Abbvie, Biogen, BMS, Genentech, Merck, Novartis, Sanofi, TEVA
- Cathy Aubel has nothing to disclose.
- Ann Early has nothing to disclose.
- Nick Lombardi discloses Ownership Interest in Vertex Pharmaceuticals.
- Libby Lurwick has nothing to disclose.
- Brian P. McDonough, MD FAAP has nothing to disclose.
- Tricia O’Leary has nothing to disclose.
After participating in this educational activity, participants should be better able to:
- Explain differences in MS epidemiology among African American, Hispanic, and non-Hispanic white populations
- Describe the key risk factors for MS in African American and Hispanic populations and the complications for which these populations are at risk
- Review the safety and efficacy of current and emerging agents for MS, with particular attention to African American and Hispanic populations
This activity is designed to meet the educational needs of neurologists, nurse practitioners, physician assistants, and neurology nurses who treat patients with multiple sclerosis.
Global Learning Collaborative is accredited by the Accreditation Council for Continuing Medical Education (ACCME) to provide continuing medical education for physicians.
Global Learning Collaborative designates this enduring material for a maximum of .25 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
Prova Education, designs and executes continuing education founded on evidence-based medicine, clinical need, gap analysis, learner feedback, and more. Our mission is to serve as an inventive and relevant resource for clinical content and educational interventions across a broad spectrum of specialties.
Prova Education's methodology demonstrates a commitment to continuing medical education and the innovative assessment of its effects. Our goal is clear—to develop and deliver the very best education in the most impactful manner and to verify its results with progressive outcomes research.
This activity is supported by independent educational grants from Biogen, and Celgene Corporation, a Bristol Myers Squibb company.
The views and opinions expressed in this educational activity are those of the faculty and do not necessarily represent the views of GLC and Prova Education. This presentation is not intended to define an exclusive course of patient management; the participant should use his/her clinical judgment, knowledge, experience, and diagnostic skills in applying or adopting for professional use any of the information provided herein. Any procedures, medications, or other courses of diagnosis or treatment discussed or suggested in this activity should not be used by clinicians without evaluation of their patients’ conditions and possible contraindications or dangers in use, review of any applicable manufacturer’s product information, and comparison with recommendations of other authorities. Links to other sites may be provided as additional sources of information. Once you elect to link to a site outside of Prova Education you are subject to the terms and conditions of use, including copyright and licensing restriction, of that site.
Reproduction of this material is not permitted without written permission from the copyright owner.
Our site requires a computer, tablet or mobile device and a connection to the Internet. For best results, a high-speed Internet connection is recommended (DSL/cable). We also recommend using the latest version of your favorite browser to ensure compliance with W3C standards, such as Internet Explorer, Microsoft Edge, Chrome, Firefox or Safari. Users accustomed to IE8, IE9 IE10 are advised to update their browsers for the best experience.
Sharon L. Hillier, PhDPeer