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Active NON-SBIR/STTR RPGS NIH (US)

Genes, neighborhoods, and alcohol misuse from adolescence to mid-adulthood in the Add Health study

$3.15M USD

Funder NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM
Recipient Organization University of Wisconsin-Madison
Country United States
Start Date Sep 15, 2024
End Date May 31, 2027
Duration 988 days
Number of Grantees 1
Roles Principal Investigator
Data Source NIH (US)
Grant ID 10940119
Grant Description

PROJECT SUMMARY Where one lives is an important contributor to disparities in health behaviors and outcomes, but it has been difficult to draw firm conclusions on the relations between regional/neighborhood context and alcohol use and misuse. This may be because (a) the influence of alcohol use and misuse (and genetic risk for alcohol use and

misuse) on where one lives is rarely considered, and (b) the effects of regional/neighborhood contexts may only be relevant for certain genetically vulnerable individuals. Incorporating genetic information into a prospective longitudinal study of the relation between regional/neighborhood context and alcohol use and

misuse might resolve inconsistencies in the literature. The proposed research will involve secondary analyses of data from the National Longitudinal Study of Adolescent to Adult Health (AH), which included 20,745 adolescents in 1994-95 and has since conducted four follow-up waves. All five waves of data collection

gathered extensive health and behavior information, including alcohol use and misuse; administrative data from the census and other sources were linked to the participants’ home addresses to provide information about the region/neighborhoods in which they lived. Importantly, 9,974 participants provided DNA samples for

genotyping, allowing for the quantification of alcohol-related genetic risk by aggregating the effect of individual measured polymorphisms into polygenic risk scores. The inclusion of 1,962 (289 monozygotic twin, 452 dizygotic twin, and 1,251 full sibling pairs) in the sample allows for the control of genetic factors when

examining associations between alcohol involvement and regional/neighborhood context and can provide evidence consistent with a potentially causal relation. The three main goals of this proposal are to: (1) examine prospectively the relation between regional/neighborhood contexts and later alcohol use and misuse, and (in

adulthood) the prospective relation between alcohol use and misuse and later regional/neighborhood contexts, (2) examine prospectively, within exposure-discordant adult twin and sibling pairs, the relation between regional/neighborhood contexts and later alcohol use and misuse, and the prospective relation between

alcohol use and misuse and later regional/neighborhood contexts, (3) examine whether alcohol-related polygenic risk is associated with moving to or remaining in a high-risk neighborhood context and whether alcohol-related polygenic risk amplifies the associations between neighborhood context and alcohol use and

misuse. The proposed research has the potential to provide critical insights into how alcohol-related genetic propensities may exacerbate health disparities by influencing whether individuals reside in a high-risk neighborhood context. It will also inform prevention and intervention efforts by clarifying whether the relation

between neighborhood context and alcohol misuse involves a direct causal relation. Evidence consistent with such a causal relation would point to neighborhood-level interventions; evidence of a non-causal relation would suggest that interventions delivered directly to individuals or families might prove more effective.

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University of Wisconsin-Madison

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