Racial-Ethnic Inequity in Young Adults With Type 1 Diabetes

Abstract Context Minority young adults (YA) currently represent the largest growing population with type 1 diabetes (T1D) and experience very poor outcomes. Modifiable drivers of disparities need to be identified, but are not well-studied. Objective To describe racial-ethnic disparities among YA wit...

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Vydáno v:The journal of clinical endocrinology and metabolism Ročník 105; číslo 8; s. e2960 - e2969
Hlavní autoři: Agarwal, Shivani, Kanapka, Lauren G, Raymond, Jennifer K, Walker, Ashby, Gerard-Gonzalez, Andrea, Kruger, Davida, Redondo, Maria J, Rickels, Michael R, Shah, Viral N, Butler, Ashley, Gonzalez, Jeffrey, Verdejo, Alandra S, Gal, Robin L, Willi, Steven, Long, Judith A
Médium: Journal Article
Jazyk:angličtina
Vydáno: US Oxford University Press 01.08.2020
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ISSN:0021-972X, 1945-7197, 1945-7197
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Abstract Abstract Context Minority young adults (YA) currently represent the largest growing population with type 1 diabetes (T1D) and experience very poor outcomes. Modifiable drivers of disparities need to be identified, but are not well-studied. Objective To describe racial-ethnic disparities among YA with T1D and identify drivers of glycemic disparity other than socioeconomic status (SES). Design Cross-sectional multicenter collection of patient and chart-reported variables, including SES, social determinants of health, and diabetes-specific factors, with comparison between non-Hispanic White, non-Hispanic Black, and Hispanic YA and multilevel modeling to identify variables that account for glycemic disparity apart from SES. Setting Six diabetes centers across the United States. Participants A total of 300 YA with T1D (18-28 years: 33% non-Hispanic White, 32% non-Hispanic Black, and 34% Hispanic). Main Outcome Racial-ethnic disparity in HbA1c levels. Results Non-Hispanic Black and Hispanic YA had lower SES, higher HbA1c levels, and much lower diabetes technology use than non-Hispanic White YA (P < 0.001). Non-Hispanic Black YA differed from Hispanic, reporting higher diabetes distress and lower self-management (P < 0.001). After accounting for SES, differences in HbA1c levels disappeared between non-Hispanic White and Hispanic YA, whereas they remained for non-Hispanic Black YA (+ 2.26% [24 mmol/mol], P < 0.001). Diabetes technology use, diabetes distress, and disease self-management accounted for a significant portion of the remaining non-Hispanic Black–White glycemic disparity. Conclusion This study demonstrated large racial-ethnic inequity in YA with T1D, especially among non-Hispanic Black participants. Our findings reveal key opportunities for clinicians to potentially mitigate glycemic disparity in minority YA by promoting diabetes technology use, connecting with social programs, and tailoring support for disease self-management and diabetes distress to account for social contextual factors.
AbstractList Context: Minority young adults (YA) currently represent the largest growing population with type 1 diabetes (T1D) and experience very poor outcomes. Modifiable drivers of disparities need to be identified, but are not well-studied. Objective: To describe racial-ethnic disparities among YA with T1D and identify drivers of glycemic disparity other than socioeconomic status (SES). Design: Cross-sectional multicenter collection of patient and chart-reported variables, including SES, social determinants of health, and diabetes-specific factors, with comparison between non-Hispanic White, non-Hispanic Black, and Hispanic YA and multilevel modeling to identify variables that account for glycemic disparity apart from SES. Setting: Six diabetes centers across the United States. Participants: A total of 300 YA with T1D (18-28 years: 33% non-Hispanic White, 32% nonHispanic Black, and 34% Hispanic). Main Outcome: Racial-ethnic disparity in HbA1c levels. Results: Non-Hispanic Black and Hispanic YA had lower SES, higher HbA1c levels, and much lower diabetes technology use than non-Hispanic White YA (P < 0.001). Non-Hispanic Black YA differed from Hispanic, reporting higher diabetes distress and lower self-management (P < 0.001). After accounting for SES, differences in HbA1c levels disappeared between nonHispanic White and Hispanic YA, whereas they remained for non-Hispanic Black YA (+ 2.26% [24 mmol/mol], P < 0.001). Diabetes technology use, diabetes distress, and disease self-management accounted for a significant portion of the remaining non-Hispanic Black-White glycemic disparity. Conclusion: This study demonstrated large racial-ethnic inequity in YA with T1D, especially among non-Hispanic Black participants. Our findings reveal key opportunities for clinicians to potentially mitigate glycemic disparity in minority YA by promoting diabetes technology use, connecting with social programs, and tailoring support for disease self-management and diabetes distress to account for social contextual factors. (J Clin Endocrinol Metab 105: 1-10, 2020) Key Words: type 1 diabetes, young adults, healthcare disparities, inequity, social determinants of health
Abstract Context Minority young adults (YA) currently represent the largest growing population with type 1 diabetes (T1D) and experience very poor outcomes. Modifiable drivers of disparities need to be identified, but are not well-studied. Objective To describe racial-ethnic disparities among YA with T1D and identify drivers of glycemic disparity other than socioeconomic status (SES). Design Cross-sectional multicenter collection of patient and chart-reported variables, including SES, social determinants of health, and diabetes-specific factors, with comparison between non-Hispanic White, non-Hispanic Black, and Hispanic YA and multilevel modeling to identify variables that account for glycemic disparity apart from SES. Setting Six diabetes centers across the United States. Participants A total of 300 YA with T1D (18-28 years: 33% non-Hispanic White, 32% non-Hispanic Black, and 34% Hispanic). Main Outcome Racial-ethnic disparity in HbA1c levels. Results Non-Hispanic Black and Hispanic YA had lower SES, higher HbA1c levels, and much lower diabetes technology use than non-Hispanic White YA (P < 0.001). Non-Hispanic Black YA differed from Hispanic, reporting higher diabetes distress and lower self-management (P < 0.001). After accounting for SES, differences in HbA1c levels disappeared between non-Hispanic White and Hispanic YA, whereas they remained for non-Hispanic Black YA (+ 2.26% [24 mmol/mol], P < 0.001). Diabetes technology use, diabetes distress, and disease self-management accounted for a significant portion of the remaining non-Hispanic Black–White glycemic disparity. Conclusion This study demonstrated large racial-ethnic inequity in YA with T1D, especially among non-Hispanic Black participants. Our findings reveal key opportunities for clinicians to potentially mitigate glycemic disparity in minority YA by promoting diabetes technology use, connecting with social programs, and tailoring support for disease self-management and diabetes distress to account for social contextual factors.
Minority young adults (YA) currently represent the largest growing population with type 1 diabetes (T1D) and experience very poor outcomes. Modifiable drivers of disparities need to be identified, but are not well-studied. To describe racial-ethnic disparities among YA with T1D and identify drivers of glycemic disparity other than socioeconomic status (SES). Cross-sectional multicenter collection of patient and chart-reported variables, including SES, social determinants of health, and diabetes-specific factors, with comparison between non-Hispanic White, non-Hispanic Black, and Hispanic YA and multilevel modeling to identify variables that account for glycemic disparity apart from SES. Six diabetes centers across the United States. A total of 300 YA with T1D (18-28 years: 33% non-Hispanic White, 32% non-Hispanic Black, and 34% Hispanic). Racial-ethnic disparity in HbA1c levels. Non-Hispanic Black and Hispanic YA had lower SES, higher HbA1c levels, and much lower diabetes technology use than non-Hispanic White YA (P < 0.001). Non-Hispanic Black YA differed from Hispanic, reporting higher diabetes distress and lower self-management (P < 0.001). After accounting for SES, differences in HbA1c levels disappeared between non-Hispanic White and Hispanic YA, whereas they remained for non-Hispanic Black YA (+ 2.26% [24 mmol/mol], P < 0.001). Diabetes technology use, diabetes distress, and disease self-management accounted for a significant portion of the remaining non-Hispanic Black-White glycemic disparity. This study demonstrated large racial-ethnic inequity in YA with T1D, especially among non-Hispanic Black participants. Our findings reveal key opportunities for clinicians to potentially mitigate glycemic disparity in minority YA by promoting diabetes technology use, connecting with social programs, and tailoring support for disease self-management and diabetes distress to account for social contextual factors.
Minority young adults (YA) currently represent the largest growing population with type 1 diabetes (T1D) and experience very poor outcomes. Modifiable drivers of disparities need to be identified, but are not well-studied.CONTEXTMinority young adults (YA) currently represent the largest growing population with type 1 diabetes (T1D) and experience very poor outcomes. Modifiable drivers of disparities need to be identified, but are not well-studied.To describe racial-ethnic disparities among YA with T1D and identify drivers of glycemic disparity other than socioeconomic status (SES).OBJECTIVETo describe racial-ethnic disparities among YA with T1D and identify drivers of glycemic disparity other than socioeconomic status (SES).Cross-sectional multicenter collection of patient and chart-reported variables, including SES, social determinants of health, and diabetes-specific factors, with comparison between non-Hispanic White, non-Hispanic Black, and Hispanic YA and multilevel modeling to identify variables that account for glycemic disparity apart from SES.DESIGNCross-sectional multicenter collection of patient and chart-reported variables, including SES, social determinants of health, and diabetes-specific factors, with comparison between non-Hispanic White, non-Hispanic Black, and Hispanic YA and multilevel modeling to identify variables that account for glycemic disparity apart from SES.Six diabetes centers across the United States.SETTINGSix diabetes centers across the United States.A total of 300 YA with T1D (18-28 years: 33% non-Hispanic White, 32% non-Hispanic Black, and 34% Hispanic).PARTICIPANTSA total of 300 YA with T1D (18-28 years: 33% non-Hispanic White, 32% non-Hispanic Black, and 34% Hispanic).Racial-ethnic disparity in HbA1c levels.MAIN OUTCOMERacial-ethnic disparity in HbA1c levels.Non-Hispanic Black and Hispanic YA had lower SES, higher HbA1c levels, and much lower diabetes technology use than non-Hispanic White YA (P < 0.001). Non-Hispanic Black YA differed from Hispanic, reporting higher diabetes distress and lower self-management (P < 0.001). After accounting for SES, differences in HbA1c levels disappeared between non-Hispanic White and Hispanic YA, whereas they remained for non-Hispanic Black YA (+ 2.26% [24 mmol/mol], P < 0.001). Diabetes technology use, diabetes distress, and disease self-management accounted for a significant portion of the remaining non-Hispanic Black-White glycemic disparity.RESULTSNon-Hispanic Black and Hispanic YA had lower SES, higher HbA1c levels, and much lower diabetes technology use than non-Hispanic White YA (P < 0.001). Non-Hispanic Black YA differed from Hispanic, reporting higher diabetes distress and lower self-management (P < 0.001). After accounting for SES, differences in HbA1c levels disappeared between non-Hispanic White and Hispanic YA, whereas they remained for non-Hispanic Black YA (+ 2.26% [24 mmol/mol], P < 0.001). Diabetes technology use, diabetes distress, and disease self-management accounted for a significant portion of the remaining non-Hispanic Black-White glycemic disparity.This study demonstrated large racial-ethnic inequity in YA with T1D, especially among non-Hispanic Black participants. Our findings reveal key opportunities for clinicians to potentially mitigate glycemic disparity in minority YA by promoting diabetes technology use, connecting with social programs, and tailoring support for disease self-management and diabetes distress to account for social contextual factors.CONCLUSIONThis study demonstrated large racial-ethnic inequity in YA with T1D, especially among non-Hispanic Black participants. Our findings reveal key opportunities for clinicians to potentially mitigate glycemic disparity in minority YA by promoting diabetes technology use, connecting with social programs, and tailoring support for disease self-management and diabetes distress to account for social contextual factors.
Audience Academic
Author Gonzalez, Jeffrey
Gal, Robin L
Walker, Ashby
Kanapka, Lauren G
Gerard-Gonzalez, Andrea
Kruger, Davida
Shah, Viral N
Verdejo, Alandra S
Agarwal, Shivani
Redondo, Maria J
Long, Judith A
Rickels, Michael R
Raymond, Jennifer K
Willi, Steven
Butler, Ashley
AuthorAffiliation 2 Jaeb Center for Health Research , Tampa, FL
3 Children’s Hospital Los Angeles , Los Angeles, CA
6 Henry Ford Medical Center , Detroit, MI
7 Baylor College of Medicine, Texas Children’s Hospital , Houston, TX
8 Institute for Diabetes, Obesity & Metabolism, University of Pennsylvania Perelman School of Medicine , Philadelphia, PA
9 Ferkauf Graduate School of Psychology, Yeshiva University , Bronx, NY
5 Barbara Davis Center for Diabetes, University of Colorado Anschutz Medical Campus , Aurora, CO
1 Fleischer Institute for Diabetes and Metabolism, New York-Regional Center for Diabetes Translational Research, Division of Endocrinology, Albert Einstein College of Medicine , Bronx, NY
10 Children’s Hospital of Philadelphia , Philadelphia, PA
4 University of Florida , Gainesville, FL
11 Corporal Michael J. Crescenz VA Medical Center , Philadelphia, PA
AuthorAffiliation_xml – name: 3 Children’s Hospital Los Angeles , Los Angeles, CA
– name: 6 Henry Ford Medical Center , Detroit, MI
– name: 8 Institute for Diabetes, Obesity & Metabolism, University of Pennsylvania Perelman School of Medicine , Philadelphia, PA
– name: 11 Corporal Michael J. Crescenz VA Medical Center , Philadelphia, PA
– name: 1 Fleischer Institute for Diabetes and Metabolism, New York-Regional Center for Diabetes Translational Research, Division of Endocrinology, Albert Einstein College of Medicine , Bronx, NY
– name: 2 Jaeb Center for Health Research , Tampa, FL
– name: 5 Barbara Davis Center for Diabetes, University of Colorado Anschutz Medical Campus , Aurora, CO
– name: 4 University of Florida , Gainesville, FL
– name: 10 Children’s Hospital of Philadelphia , Philadelphia, PA
– name: 7 Baylor College of Medicine, Texas Children’s Hospital , Houston, TX
– name: 9 Ferkauf Graduate School of Psychology, Yeshiva University , Bronx, NY
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  givenname: Shivani
  orcidid: 0000-0003-4506-3702
  surname: Agarwal
  fullname: Agarwal, Shivani
  email: Shivani.Agarwal@einsteinmed.org
  organization: Fleischer Institute for Diabetes and Metabolism, New York-Regional Center for Diabetes Translational Research, Division of Endocrinology, Albert Einstein College of Medicine, Bronx, NY
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  surname: Kanapka
  fullname: Kanapka, Lauren G
  organization: Jaeb Center for Health Research, Tampa, FL
– sequence: 3
  givenname: Jennifer K
  surname: Raymond
  fullname: Raymond, Jennifer K
  organization: Children’s Hospital Los Angeles, Los Angeles, CA
– sequence: 4
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  surname: Walker
  fullname: Walker, Ashby
  organization: University of Florida, Gainesville, FL
– sequence: 5
  givenname: Andrea
  surname: Gerard-Gonzalez
  fullname: Gerard-Gonzalez, Andrea
  organization: Barbara Davis Center for Diabetes, University of Colorado Anschutz Medical Campus, Aurora, CO
– sequence: 6
  givenname: Davida
  surname: Kruger
  fullname: Kruger, Davida
  organization: Henry Ford Medical Center, Detroit, MI
– sequence: 7
  givenname: Maria J
  surname: Redondo
  fullname: Redondo, Maria J
  organization: Baylor College of Medicine, Texas Children’s Hospital, Houston, TX
– sequence: 8
  givenname: Michael R
  surname: Rickels
  fullname: Rickels, Michael R
  organization: Institute for Diabetes, Obesity & Metabolism, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA
– sequence: 9
  givenname: Viral N
  surname: Shah
  fullname: Shah, Viral N
  organization: Barbara Davis Center for Diabetes, University of Colorado Anschutz Medical Campus, Aurora, CO
– sequence: 10
  givenname: Ashley
  surname: Butler
  fullname: Butler, Ashley
  organization: Baylor College of Medicine, Texas Children’s Hospital, Houston, TX
– sequence: 11
  givenname: Jeffrey
  surname: Gonzalez
  fullname: Gonzalez, Jeffrey
  organization: Fleischer Institute for Diabetes and Metabolism, New York-Regional Center for Diabetes Translational Research, Division of Endocrinology, Albert Einstein College of Medicine, Bronx, NY
– sequence: 12
  givenname: Alandra S
  surname: Verdejo
  fullname: Verdejo, Alandra S
  organization: Jaeb Center for Health Research, Tampa, FL
– sequence: 13
  givenname: Robin L
  surname: Gal
  fullname: Gal, Robin L
  organization: Jaeb Center for Health Research, Tampa, FL
– sequence: 14
  givenname: Steven
  surname: Willi
  fullname: Willi, Steven
  organization: Children’s Hospital of Philadelphia, Philadelphia, PA
– sequence: 15
  givenname: Judith A
  surname: Long
  fullname: Long, Judith A
  organization: Institute for Diabetes, Obesity & Metabolism, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA
BackLink https://www.ncbi.nlm.nih.gov/pubmed/32382736$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright Endocrine Society 2020. 2020
Endocrine Society 2020.
COPYRIGHT 2020 Oxford University Press
Copyright_xml – notice: Endocrine Society 2020. 2020
– notice: Endocrine Society 2020.
– notice: COPYRIGHT 2020 Oxford University Press
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Issue 8
Keywords type 1 diabetes
social determinants of health
healthcare disparities
inequity
young adults
Language English
License This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
http://creativecommons.org/licenses/by/4.0
Endocrine Society 2020.
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  article-title: Supplemental tables for “Racial-Ethnic Inequity in Young Adults With Type 1 Diabetes.”
  publication-title: Dryad
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Snippet Abstract Context Minority young adults (YA) currently represent the largest growing population with type 1 diabetes (T1D) and experience very poor outcomes....
Minority young adults (YA) currently represent the largest growing population with type 1 diabetes (T1D) and experience very poor outcomes. Modifiable drivers...
Context: Minority young adults (YA) currently represent the largest growing population with type 1 diabetes (T1D) and experience very poor outcomes. Modifiable...
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SubjectTerms Analysis
Blood Glucose Self-Monitoring - instrumentation
Blood Glucose Self-Monitoring - statistics & numerical data
Continental Population Groups - statistics & numerical data
Cross-Sectional Studies
Diabetes Mellitus, Type 1 - blood
Diabetes Mellitus, Type 1 - diagnosis
Diabetes Mellitus, Type 1 - epidemiology
Diabetes Mellitus, Type 1 - therapy
Discrimination in medical care
Ethnic Groups - statistics & numerical data
Female
Glycated Hemoglobin A - analysis
Glycosylated hemoglobin
Health care disparities
Health Status Disparities
Humans
Male
Minority Groups - statistics & numerical data
Online Only
Patient Compliance - statistics & numerical data
Self-care, Health
Self-Management - statistics & numerical data
Social Class
Social Determinants of Health - statistics & numerical data
Teenagers
Type 1 diabetes
United States
Young Adult
Youth
Title Racial-Ethnic Inequity in Young Adults With Type 1 Diabetes
URI https://www.ncbi.nlm.nih.gov/pubmed/32382736
https://www.proquest.com/docview/2400546179
https://pubmed.ncbi.nlm.nih.gov/PMC7457963
Volume 105
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