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Neurology

Does Race or Geography Affect Which MSA Subtype You Get?

At a Glance

The overall risk of developing multiple system atrophy (MSA) is similar worldwide, but genetic and geographic background strongly influence the specific subtype. People of Western descent are more likely to develop MSA-P, while those of East Asian descent are more likely to develop MSA-C.

Receiving a diagnosis of multiple system atrophy (MSA) can be incredibly overwhelming, and you may find yourself wondering why this happened or if certain people are more likely to get it. While MSA affects populations worldwide at roughly equal rates, the specific subtype a person develops is strongly linked to their geographic and genetic background [1]. People of Western descent (like North America and Europe) are much more likely to develop the parkinsonian subtype (MSA-P), whereas people of East Asian descent (particularly in Japan) are significantly more likely to develop the cerebellar subtype (MSA-C) [2].

How Subtypes Differ by Region

MSA is typically divided into two main subtypes based on which symptoms are most prominent when the disease begins. Both subtypes involve autonomic dysfunction (issues with automatic body processes like blood pressure and bladder control), but they differ in their primary movement symptoms [3].

  • Western Populations and MSA-P: In North America and Europe, the parkinsonian subtype (MSA-P) is the most common form [2][4]. MSA-P is characterized primarily by symptoms similar to Parkinson’s disease, such as stiffness, slowed movements, and tremors. This occurs because the disease affects the striatonigral system, a brain network that helps control smooth, voluntary muscle movement [4]. If you have MSA-P, your daily management will likely focus heavily on maintaining mobility and managing muscle stiffness.
  • Asian Populations and MSA-C: In East Asian populations, particularly in Japan and China, the cerebellar subtype (MSA-C) is significantly more prevalent [2]. MSA-C primarily causes ataxia, which includes problems with balance, coordination, and walking. This subtype involves changes in the olivopontocerebellar network, the part of the brain responsible for coordinating your balance and precise movements [4][5]. For those with MSA-C, physical therapy often focuses on fall prevention and coordination exercises.

Interestingly, recent data from Japan suggests that as the population ages and doctors get better at distinguishing MSA from Parkinson’s disease, the proportion of MSA-P diagnoses may be slightly larger than historically reported, though MSA-C remains the dominant subtype there [6].

Why Do Geography and Genetic Background Matter?

The distinct differences in how MSA presents across the globe are believed to be partly driven by genetics [2]. Researchers have found that certain genetic variations are more common in specific populations.

For example, variants in the COQ2 gene have been identified as a susceptibility factor for developing MSA [7]. These genetic variants are particularly associated with the MSA-C subtype and are found more frequently in East Asian populations than in Western populations [8][9]. This demonstrates that ethnic variation in genetic risk plays a role in determining which parts of the brain are most vulnerable to the disease.

However, it is crucial to understand that despite these genetic susceptibility factors, the vast majority of MSA cases are sporadic [10][11]. This means the disease occurs randomly and is not considered a condition that is directly passed down from parent to child.

Overall Global Incidence

While the subtypes of MSA are heavily influenced by a person’s ancestry and geographic origins, the overall likelihood of getting MSA is roughly equal around the world [1].

Sometimes, reported rates of MSA seem to vary from one country to another. However, experts believe this is mostly due to differences in how the disease is studied, diagnosed, and recorded rather than true differences in how often the disease occurs [1]. Diagnostic criteria, the average age of the population, and how healthcare systems track rare diseases all make direct country-to-country comparisons difficult [1].

Understanding your background can help your care team anticipate which symptoms might be most prominent. Regardless of where you live or what subtype you have, your care team will work with you to manage your specific symptoms and preserve your quality of life.

Common questions in this guide

Is multiple system atrophy (MSA) inherited from my parents?
The vast majority of MSA cases occur sporadically, meaning they happen randomly and are not directly passed down from parent to child. While certain genetic variations may increase susceptibility, MSA is not considered an inherited condition.
What is the main difference between MSA-P and MSA-C?
Both subtypes involve autonomic issues like blood pressure drops or bladder control problems, but their movement symptoms differ. MSA-P primarily causes stiffness, slowed movements, and tremors, while MSA-C primarily causes balance and coordination problems known as ataxia.
Are certain races more likely to get MSA overall?
No, the overall global likelihood of developing MSA is roughly equal regardless of race or geography. However, your ethnic and genetic background strongly influences which specific subtype (MSA-P or MSA-C) you are more likely to develop.
Why is MSA-P more common in North America and Europe?
Yes, genetic background plays a major role in how the disease presents. People of Western descent have genetic susceptibilities that make the brain's striatonigral system more vulnerable, leading to the parkinsonian symptoms of MSA-P.

Questions to Ask Your Doctor

Curated prompts to bring to your next appointment.

  1. 1.Based on my symptoms, which subtype of MSA (MSA-P or MSA-C) do my clinical signs align with most closely?
  2. 2.How does my specific subtype change what we should prioritize in my physical therapy and daily symptom management?
  3. 3.Are there specific signs of autonomic dysfunction I should monitor at home to help us better track my disease progression?
  4. 4.Are there any clinical trials for my specific subtype of MSA that I might be eligible for?

Questions For You

Tap a prompt to share your answer — we'll use it plus this page's context to start a tailored conversation.

References

References (11)
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    Prevalence of multiple system atrophy: A literature review.

    Kaplan S

    Revue neurologique 2024; (180(5)):438-450 doi:10.1016/j.neurol.2023.11.013.

    PMID: 38453600
  2. 2

    Multiple system atrophy: clinicopathological characteristics in Japanese patients.

    Ozawa T, Onodera O

    Proceedings of the Japan Academy. Series B, Physical and biological sciences 2017; (93(5)):251-258 doi:10.2183/pjab.93.016.

    PMID: 28496050
  3. 3

    A historical review of multiple system atrophy with a critical appraisal of cellular and animal models.

    Marmion DJ, Peelaerts W, Kordower JH

    Journal of neural transmission (Vienna, Austria : 1996) 2021; (128(10)):1507-1527 doi:10.1007/s00702-021-02419-8.

    PMID: 34613484
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    Quantitative cellular changes in multiple system atrophy brains.

    Andersen AM, Kaalund SS, Marner L, et al.

    Neuropathology and applied neurobiology 2023; (49(6)):e12941 doi:10.1111/nan.12941.

    PMID: 37812040
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    Cellular iron deposition patterns predict clinical subtypes of multiple system atrophy.

    Lee S, Martinez-Valbuena I, Lang AE, Kovacs GG

    Neurobiology of disease 2024; (197()):106535 doi:10.1016/j.nbd.2024.106535.

    PMID: 38761956
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    Changes in clinical features of multiple system atrophy in Japan.

    Tokuhara Y, Watanabe S, Yoshikawa H

    Clinical parkinsonism & related disorders 2020; (3()):100054 doi:10.1016/j.prdoa.2020.100054.

    PMID: 34316637
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    Association of the COQ2 V393A variant with risk of multiple system atrophy in East Asians: a case-control study and meta-analysis of the literature.

    Zhao Q, Yang X, Tian S, et al.

    Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2016; (37(3)):423-30 doi:10.1007/s10072-015-2414-8.

    PMID: 26590992
  8. 8

    Mutation Analysis of COQ2 in Chinese Patients with Cerebellar Subtype of Multiple System Atrophy.

    Wen XD, Li HF, Wang HX, et al.

    CNS neuroscience & therapeutics 2015; (21(8)):626-30 doi:10.1111/cns.12412.

    PMID: 26096180
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    COQ2 V393A confers high risk susceptibility for multiple system atrophy in East Asian population.

    Porto KJ, Hirano M, Mitsui J, et al.

    Journal of the neurological sciences 2021; (429()):117623 doi:10.1016/j.jns.2021.117623.

    PMID: 34455210
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    Occupational histories in neuropathologically confirmed multiple system atrophy.

    Cheshire WP, Tipton PW, Koga S, et al.

    Clinical autonomic research : official journal of the Clinical Autonomic Research Society 2025; (35(3)):421-430 doi:10.1007/s10286-025-01109-9.

    PMID: 39847196
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    Multiple system atrophy.

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This page provides educational information about MSA subtypes and global prevalence. It is not a substitute for professional medical advice, diagnosis, or treatment from a qualified neurologist.

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