Widening gap in age at muscular dystrophy-associated death between blacks and whites, 1986-2005

Aileen Kenneson1, Ajay Vatave, Richard Finkel

  • 1National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA. cconstantin@cdc.gov

Neurology
|September 15, 2010
PubMed
Abstract

Insights

Improvements in muscular dystrophy (MD) treatment have increased survival rates, particularly for white males. However, disparities in age at death persist between racial groups, highlighting the need for further research and equitable care.

Area of Science:

  • Neurology
  • Genetics
  • Public Health

Background:

  • Muscular dystrophies (MDs) are progressive muscle-wasting disorders causing early mortality, often from cardiac or respiratory failure.
  • MDs affect approximately 1 in 2,500 deaths in the United States.

Purpose of the Study:

  • To analyze trends in age at death for individuals with muscular dystrophies in the United States.
  • To assess changes in clinical comorbidities and their association with mortality over time.

Main Methods:

  • Analysis of death record data for 18,315 MD-associated deaths from 1986 to 2005.
  • Examination of mortality rates, age at death, and reported comorbidities (cardiomyopathy, pulmonary failure/infection) across racial and sex demographics.

Main Results:

  • Overall MD-associated mortality rates remained stable. White females with MDs had a median age at death 12 years higher than black females.
  • Cardiomyopathy reporting increased in white males but not black males; it remained more common in black males.
  • Significant increases in median age at death were observed, especially in white males without cardiomyopathy. Pulmonary failure and infection decreased in white males.

Conclusions:

  • Observed changes in age at death and comorbidities suggest improvements in muscular dystrophy treatment.
  • White males with MDs experienced a greater increase in age at death compared to black males.
  • Disparities may stem from differences in MD types, genetic/environmental factors, disease progression, socioeconomic status, and treatment access.

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