{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,31]],"date-time":"2026-10-31T06:00:59Z","timestamp":1793426459165,"version":"4.5.0"},"reference-count":48,"publisher":"American Medical Association (AMA)","issue":"6","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA Netw Open"],"abstract":"<jats:sec id=\"ab-zoi240536-4\"><jats:title>Importance<\/jats:title><jats:p>Several clinical practice guidelines advise race- and ethnicity-based screening for youth-onset type 2 diabetes (T2D) due to a higher prevalence among American Indian and Alaska Native, Asian, Black, and Hispanic youths compared with White youths. However, rather than a biological risk, this disparity likely reflects the inequitable distribution of adverse social determinants of health (SDOH), a product of interpersonal and structural racism.<\/jats:p><\/jats:sec><jats:sec id=\"ab-zoi240536-5\"><jats:title>Objective<\/jats:title><jats:p>To evaluate prediabetes prevalence by presence or absence of adverse SDOH in adolescents eligible for T2D screening based on weight status.<\/jats:p><\/jats:sec><jats:sec id=\"ab-zoi240536-6\"><jats:title>Design, Setting, and Participants<\/jats:title><jats:p>This cross-sectional study and analysis used data from the 2011 to 2018 cycles of the National Health and Nutrition Examination Survey. Data were analyzed from June 1, 2023, to April 5, 2024. Participants included youths aged 12 to 18 years with body mass index (BMI) at or above the 85th percentile without known diabetes.<\/jats:p><\/jats:sec><jats:sec id=\"ab-zoi240536-7\"><jats:title>Main Outcomes and Measures<\/jats:title><jats:p>The main outcome consisted of an elevated hemoglobin A<jats:sub>1c<\/jats:sub> (HbA<jats:sub>1c<\/jats:sub>) level greater than or equal to 5.7% (prediabetes or undiagnosed presumed T2D). Independent variables included race, ethnicity, and adverse SDOH (food insecurity, nonprivate health insurance, and household income &amp;amp;lt;130% of federal poverty level). Survey-weighted logistic regression was used to adjust for confounders of age, sex, and BMI <jats:italic>z<\/jats:italic> score and to determine adjusted marginal prediabetes prevalence by race, ethnicity, and adverse SDOH.<\/jats:p><\/jats:sec><jats:sec id=\"ab-zoi240536-8\"><jats:title>Results<\/jats:title><jats:p>The sample included 1563 individuals representing 10\u202f178\u202f400 US youths aged 12 to 18 years (mean age, 15.5 [95% CI, 15.3-15.6] years; 50.5% [95% CI, 47.1%-53.9%] female; Asian, 3.0% [95% CI, 2.2%-3.9%]; Black, 14.9% [95% CI, 11.6%-19.1%]; Mexican American, 18.8% [95% CI, 15.4%-22.9%]; Other Hispanic, 8.1% [95% CI, 6.5%-10.1%]; White, 49.1% [95% CI, 43.2%-55.0%]; and &amp;amp;gt;1 or other race, 6.1% [95% CI, 4.6%-8.0%]). Food insecurity (4.1% [95% CI, 0.7%-7.5%]), public insurance (5.3% [95% CI, 1.6%-9.1%]), and low income (5.7% [95% CI, 3.0%-8.3%]) were each independently associated with higher prediabetes prevalence after adjustment for race, ethnicity, and BMI <jats:italic>z<\/jats:italic> score. While Asian, Black, and Hispanic youths had higher prediabetes prevalence overall, increasing number of adverse SDOH was associated with higher prevalence among White youths (8.3% [95% CI, 4.9%-11.8%] for 3 vs 0.6% [95% CI, \u22120.7% to 2.0%] for 0 adverse SDOH).<\/jats:p><\/jats:sec><jats:sec id=\"ab-zoi240536-9\"><jats:title>Conclusions and Relevance<\/jats:title><jats:p>Adverse SDOH were associated with higher prediabetes prevalence, across and within racial and ethnic categories. Consideration of adverse SDOH may offer a more actionable alternative to race- and ethnicity-based screening to evaluate T2D risk in youth.<\/jats:p><\/jats:sec>","DOI":"10.1001\/jamanetworkopen.2024.16088","type":"journal-article","created":{"date-parts":[[2024,6,11]],"date-time":"2024-06-11T16:37:04Z","timestamp":1718123824000},"page":"e2416088","source":"Crossref","is-referenced-by-count":21,"title":["Prediabetes Prevalence by Adverse Social Determinants of Health in Adolescents"],"prefix":"10.1001","volume":"7","author":[{"given":"Caleb","family":"Harrison","sequence":"first","affiliation":[{"name":"Center for Pediatric Research in Obesity and Metabolism, UPMC Children\u2019s Hospital of Pittsburgh, Pittsburgh, Pennsylvania"},{"name":"Division of Pediatric Endocrinology, Diabetes, and Metabolism, University of Pittsburgh School of Medicine, Pittsburgh, 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