Racial/ethnic variations in the prevalence of selected major birth defects, metropolitan Atlanta, 1994-2005

James E Kucik1, Clinton J Alverson, Suzanne M Gilboa

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

Insights

Racial and ethnic disparities exist in the prevalence of many birth defects. These differences may stem from genetics, environmental exposures, or variations in diagnosis and reporting. Addressing these disparities is crucial for reducing infant mortality and morbidity.

Area of Science:

  • Public Health
  • Epidemiology
  • Genetics

Background:

  • Birth defects are a primary cause of infant mortality and significant source of child and adult morbidity.
  • Understanding racial/ethnic variations in birth defect prevalence is essential for identifying disparities in diagnosis, case ascertainment, and risk factors.

Purpose of the Study:

  • To investigate racial/ethnic variations in the prevalence of 46 major birth defects.
  • To examine the influence of socioeconomic status (SES) as a potential modifier of these disparities.

Main Methods:

  • Utilized data from the Metropolitan Atlanta Congenital Defects Program (MACDP), a population-based registry.
  • Analyzed prevalence of 46 major birth defects among live births, stillbirths, and pregnancy terminations (gestation >20 weeks) from 1994-2005.
  • Adjusted for infant sex, maternal age, gravidity, and SES; explored SES as an effect modifier.

Main Results:

  • Significant racial/ethnic disparities were observed in the prevalence of numerous birth defects.
  • Compared to non-Hispanic white women, non-Hispanic black women had higher prevalence of 5 defects and lower prevalence of 10 defects.
  • Hispanic women showed higher prevalence of 4 defects and lower prevalence of 6 defects; some disparities varied by SES without a clear pattern.

Conclusions:

  • Racial/ethnic disparities were identified in 57% of the studied birth defects.
  • Potential causes include genetic susceptibility, differential exposure to risk factors, and variations in diagnosis or reporting.
  • Policies enhancing early birth defect diagnosis can mitigate associated morbidity and mortality.
Abstract

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