Podcast on Identifying and Understanding Barriers to Care in Underserved Populations With MS in the United States

Sandra Parawira1, Victoria Reese2

  • 1Department of Neurology, University of Cincinnati, Waddell Center for Multiple Sclerosis, 3113 Bellevue Ave, Cincinnati, OH, 45219, USA. parawisa@ucmail.uc.edu.

Neurology and Therapy
|November 20, 2023
PubMed

Insights

Multiple sclerosis (MS) affects diverse populations differently. Black or African American and Hispanic or Latino individuals experience unique disease characteristics and face significant barriers to care, necessitating increased awareness and improved access.

Area of Science:

  • Neurology
  • Epidemiology
  • Health Disparities

Background:

  • Historically, multiple sclerosis (MS) incidence was considered highest in White populations in the U.S.
  • Recent data indicate comparable MS incidence in Black or African American individuals versus White individuals.
  • Hispanic or Latino individuals show lower MS incidence but potentially earlier age of onset.

Purpose of the Study:

  • To discuss the characteristics of MS in Black or African American and Hispanic or Latino populations.
  • To identify barriers to accessing care for these underrepresented groups.
  • To propose solutions for improving MS care access and outcomes.

Main Methods:

  • The study is based on a podcast discussion.
  • Key discussion points include disease characteristics, barriers to care, and potential solutions.
  • Data presented reflects current understanding of MS epidemiology and clinical presentation in diverse populations.

Main Results:

  • Black or African American and Hispanic or Latino individuals exhibit distinct MS disease severity, progression, and mortality compared to White individuals.
  • Specific neurological impacts include accelerated tissue loss in Black or African American individuals and optic neuritis in Hispanic individuals.
  • These groups often face more aggressive disease courses, earlier disability, and greater need for assistance.

Conclusions:

  • Genetic factors, systemic racism, and healthcare access barriers contribute to MS health disparities.
  • Underrepresentation in clinical trials poses a risk for detecting population-specific drug efficacy and safety.
  • Increasing awareness and addressing care barriers are crucial for improving MS outcomes in non-White communities.

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