4.7 Article Proceedings Paper

The Impact of Racial and Ethnic Health Disparities in Diabetes Management on Clinical Outcomes: A Reinforcement Learning Analysis of Health Inequity Among Youth and Young Adults in the SEARCH for Diabetes in Youth Study

Journal

DIABETES CARE
Volume 45, Issue 1, Pages 108-118

Publisher

AMER DIABETES ASSOC
DOI: 10.2337/dc21-0496

Keywords

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Funding

  1. National Institutes of Health (NIH), National Institute of Diabetes and Digestive and Kidney Diseases [1R01DK127208-01, 1UC4DK108173]
  2. Centers for Disease Control and Prevention [1U18DP006131, U18DP006133, U18DP006134, U18DP006136, U18DP006138, U18DP006139, DP-15-002, 00097, DP-05-069, DP-10-001]
  3. National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases [1U18DP006131, U18DP006133, U18DP006134, U18DP006136, U18DP006138, U18DP006139]
  4. National Institute of Diabetes and Digestive and Kidney Diseases
  5. Kaiser Permanente Southern California [U48/CCU919219, U01 DP000246, U18DP002714]
  6. University of Colorado Denver [U48/CCU819241-3, U01 DP000247, U18DP000247-06A1]
  7. Cincinnati Children's Hospital Medical Center [U48/CCU519239, U01 DP000248, 1U18DP002709]
  8. University of North Carolina at Chapel Hill [U48/CCU419249, U01 DP000254, U18DP002708]
  9. Seattle Children's Hospital [U58/CCU019235-4, U01 DP000244, U18DP002710-01]
  10. Wake Forest University School of Medicine [U48/CCU919219, U01 DP000250, 200-201035171]
  11. Kaiser Permanente Southern California's Clinical Research Center ( Kaiser Foundation Health Plan)
  12. Kaiser Permanente Southern California's Clinical Research Center (Southern California Permanente Medical Group)
  13. South Carolina Clinical & Translational Research Institute at the Medical University of South Carolina (NIH/National Center for Advancing Translational Sciences [NCATS]) [UL1 TR000062, UL1 TR001450]
  14. Seattle Children's Hospital
  15. University of Washington (NIH/NCATS grant) [UL1 TR00423]
  16. University of Colorado Pediatric Clinical and Translational Research Center (NIH/NCATS grant) [UL1 TR000154]
  17. Barbara Davis Center at the University of Colorado at Denver (DERC NIH) [P30 DK57516]
  18. University of Cincinnati (NIH/NCATS) [UL1 TR000077, UL1 TR001425]
  19. Children with Medical Handicaps program
  20. National Institute of Diabetes and Digestive and Kidney Diseases of the NIH [F30DK113728]
  21. NIH/National Center for Advancing Translational Sciences [NCATS] [UL1 TR002489]

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Mathematically modeling an equalized distribution of T1D self-management tools and technology accounted for part of but not all disparities in glycemic control between non-White and White YYA, underscoring the complexity of race and ethnicity-based health inequity.
OBJECTIVE To estimate difference in population-level glycemic control and the emergence of diabetes complications given a theoretical scenario in which non-White youth and young adults (YYA) with type 1 diabetes (T1D) receive and follow an equivalent distribution of diabetes treatment regimens as non-Hispanic White YYA. RESEARCH DESIGN AND METHODS Longitudinal data from YYA diagnosed 2002-2005 in the SEARCH for Diabetes in Youth Study were analyzed. Based on self-reported race/ethnicity, YYA were classified as non-White race or Hispanic ethnicity (non-White subgroup) versus non-Hispanic White race (White subgroup). In the White versus non-White subgroups, the propensity score models estimated treatment regimens, including patterns of insulin modality, self-monitored glucose frequency, and continuous glucose monitoring use. An analysis based on policy evaluation techniques in reinforcement learning estimated the effect of each treatment regimen on mean hemoglobin A(1c) (HbA(1c)) and the prevalence of diabetes complications for non-White YYA. RESULTS The study included 978 YYA. The sample was 47.5% female and 77.5% non-Hispanic White, with a mean age of 12.8 +/- 2.4 years at diagnosis. The estimated population mean of longitudinal average HbA(1c) over visits was 9.2% and 8.2% for the non-White and White subgroup, respectively (difference of 0.9%). Within the non-White subgroup, mean HbA(1c) across visits was estimated to decrease by 0.33% (95% CI -0.45, -0.21) if these YYA received the distribution of diabetes treatment regimens of the White subgroup, explaining similar to 35% of the estimated difference between the two subgroups. The non-White subgroup was also estimated to have a lower risk of developing diabetic retinopathy, diabetic kidney disease, and peripheral neuropathy with the White youth treatment regimen distribution (P < 0.05), although the low proportion of YYA who developed complications limited statistical power for risk estimations. CONCLUSIONS Mathematically modeling an equalized distribution of T1D self-management tools and technology accounted for part of but not all disparities in glycemic control between non-White and White YYA, underscoring the complexity of race and ethnicity-based health inequity.

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