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Published on: September 29, 2014
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
Background:
Muscular dystrophies (MDs), characterized by progressive muscle wasting, are associated with 1 in 2,500 deaths in the United States. Although treatments slow the progression, these disorders lead to early death, usually due to cardiac or respiratory failure.
Methods:
We analyzed death record data from 18,315 MD-associated deaths that occurred in the United States in 1986 through 2005 to assess trends in the age at death of people with MDs.
Results:
From 1986 through 2005, the MD-associated mortality rate did not change among blacks, whites, males, or females. The median age at death among white females with MDs was 12 years higher than among black females. The frequency of reported cardiomyopathy increased among white but not black male decedents with MDs, although cardiomyopathy remained more commonly reported among black males. Among white males, the median age at death increased by 0.2 annually for those with and 1.3 for those without indications of cardiomyopathy. Among black males, the median age at death increased 0.3 years annually among those without reported cardiomyopathy. Among white males, the frequencies of pulmonary failure and pulmonary infection decreased significantly over time.
Conclusions:
Changes in age at death and reported clinical comorbidities reflect improvements in the treatment of MDs. White males with MDs have shown a greater increase in age at death over time than black males. Contributing factors to this difference might include differences in types of MDs, rates of genetic and environmental modifiers, natural history, socioeconomic factors, and access to and use of treatment options.
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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