Rates of obesity are high in adolescents, with these youth at greater risk for developing metabolic complications than their lean peers. Poor metabolic function is associated with worse health outcomes, higher health care costs, and other health comorbidities; however, not all youth with obesity develop metabolic complications. Black youth have fewer metabolic complications compared to White youth, despite having among the highest rates of obesity. Understanding unique protective factors that slow the progression to poor metabolic health is necessary for reducing adverse health outcomes and improving the quality of life of adolescents with obesity. Thus, the specific aims of the proposed research are: 1) to examine differences in weight- and race-based stigma between Black adolescents who have obesity without metabolic complications (OMC-) and matched Black adolescents who have obesity with at least 2 metabolic complications (OMC2+); 2) to evaluate differences in physiological stress and psychological stress between OMC- and OMC2+ adolescents; and 3) to explore differences in resilience between OMC- and OMC2+ adolescents. We will use a case-control cross-sectional design to conduct 100 interviewer-administered surveys with caregivers and Black adolescents with and without metabolic complications in the US Midsouth. We will examine two groups of Black youth (aged 11-17) with obesity (defined as having a waist circumference ?90th percentile). The OMC- group will include 50 adolescents with obesity who have optimal levels of blood pressure, cholesterol, glucose, and liver function. The OMC2+ group will include 50 adolescents with obesity who have two or more metabolic complications (i.e., high blood pressure, elevated triglycerides, low high density lipoprotein (HDL), insulin resistance, and/or impaired liver function) matched to OMC- youth by age and sex. Quantitative surveys will examine caregiver and youth reports of weight- and race-based stigma, psychological stress, and resilience. Physiological stress will be assessed via salivary cortisol (diurnal and awakening response). We will obtain data on metabolic function including: blood pressure, triglycerides, HDL, Homeostatic Model Assessment of Insulin Resistance (HOMA-IR), and liver function. Given known associations with study outcome variables, we will obtain measures of income, physical/mental health, and dietary intake, and as well as measures of physical activity and sleep patterns via actigraphy. This innovative study will contribute to the field's understanding of why some Black youth are not yet exhibiting metabolic complications while others are. While genetic factors may account for ~27% of these variations, biopsychosocial factors have been underexplored. Thus, by studying this rare group of OMC- adolescents, we will obtain data on mutable factors that are relevant to a community most impacted by obesity. Knowledge gained will serve as pilot data for an R01 grant to develop a strength-based, culturally-informed intervention aimed at decreasing health disparities and maintaining metabolic health among Black youth with obesity.

Public Health Relevance

Over the past 30 years, soaring rates of adolescent obesity have become a major public health concern, with many, but not all, of these youth developing metabolic complications. By studying risk and resilience among Black adolescents who have obesity without metabolic complications, we will understand why some youth are able to maintain this lower risk state; thus providing knowledge about modifiable factors that could alter the progression to poor metabolic health. We aim to study differences in physiological stress, psychological stress, weight-based stigma, race-based stigma, and resilience between Black youth with and Black youth without obesity-related metabolic complications; with findings poised to inform the development of strength-based interventions for reducing health disparities and promoting metabolic health among adolescents.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21DK113344-03
Application #
10018865
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Serrano, Katrina Jane
Project Start
2019-07-01
Project End
2021-06-30
Budget Start
2020-07-01
Budget End
2021-06-30
Support Year
3
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Texas A&M University
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
020271826
City
College Station
State
TX
Country
United States
Zip Code
77845