Gender differences in developmental programming of cardiovascular diseases

John Henry Dasinger1, Barbara T Alexander2

  • 1Department of Physiology and Biophysics, Center for Women's Health Research, Center for Developmental Disorders Research, University of Mississippi Medical Center, 2500 N State Street, Jackson, MS 39216, U.S.A.

Insights

Low birth weight, influenced by early life growth, increases cardiovascular disease risk. This review explores how sex differences impact this programmed risk, especially with aging.

Area of Science:

  • Developmental biology
  • Cardiovascular health
  • Public health

Background:

  • Hypertension is a major risk factor for cardiovascular disease, a leading global cause of death.
  • The developmental origins of health and disease (DOHaD) hypothesis links early-life growth and environmental exposures to later-life cardiovascular risk.
  • Sex influences cardiovascular risk in experimental models, but its role in programmed hypertension related to early life is understudied.

Purpose of the Study:

  • To review current data on sex differences in the developmental programming of blood pressure.
  • To examine how early-life factors influence cardiovascular risk across the lifespan, considering sex-specific effects.
  • To highlight the impact of aging on sex differences in programmed cardiovascular risk.

Main Methods:

  • Review of epidemiological studies linking early-life influences to later cardiovascular health.
  • Analysis of experimental models demonstrating mechanisms of developmental origins of chronic disease.
  • Synthesis of existing literature on sex differences in blood pressure regulation and cardiovascular outcomes.

Main Results:

  • Early-life growth and adverse exposures are recognized contributors to programmed cardiovascular risk.
  • Sex impacts the severity of cardiovascular risk in response to developmental insults.
  • Limited research exists on sex-specific blood pressure and cardiovascular health in low-birth weight individuals, and the influence of aging on these differences.

Conclusions:

  • Early-life factors significantly influence long-term cardiovascular health, with sex playing a crucial role.
  • Further research is needed to understand sex differences in developmental programming of hypertension and cardiovascular disease, particularly across the lifespan.
  • Investigating sex-specific impacts of aging on programmed cardiovascular risk is essential for targeted prevention strategies.

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