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Active NON-SBIR/STTR RPGS NIH (US)

Childhood Adversity and Biological Mechanisms of Accelerated Aging

$2.75M USD

Funder EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT
Recipient Organization Emma Pendleton Bradley Hospital
Country United States
Start Date Sep 04, 2024
End Date Aug 31, 2026
Duration 726 days
Number of Grantees 2
Roles Co-Investigator; Principal Investigator
Data Source NIH (US)
Grant ID 10905770
Grant Description

Project Summary/Abstract Early life adversity, including childhood maltreatment and other traumas, is a major risk factor for a host of health conditions, including psychiatric disorders, obesity, diabetes, and cardiovascular disease. Health behaviors, such as diet, sleep, and activity, are linked to childhood adversity and can further contribute to risk

for these conditions. These effects compound over time and poor health outcomes are most evident in adults when biological effects of stress and health behaviors combine with age-related decline to produce frank disease. There is now evidence that these processes begin early in life and that some of the health outcomes

can be observed in childhood. Converging evidence from animal models and recent human studies indicate that mitochondria play a key role in coordinating the stress response and in the aging process. Here we hypothesize that early stress alters mitochondrial DNA and mitochondrial function and that this may be a

mechanism of risk for stress- and age-related disorders. The proposed study leverages data and specimens available in a longitudinal developmental study of childhood maltreatment that includes rich data on exposures, biomarkers of aging, and health outcomes. Results of this study are expected to provide insight into the

biological mechanisms of adversity-related risk for accelerated aging and risk for disease, and provide targets for new treatment and prevention approaches.

All Grantees

Emma Pendleton Bradley Hospital

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