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Metabolic and Inflammatory Links to Depression in Youth With Diabetes

OBJECTIVE: Youth with diabetes are at increased risk for depression. The objectives of this study were to provide preliminary evidence that this at-risk status for depression is associated with metabolic and inflammatory markers and to inform future, more stringent examinations of the directionality...

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Autores principales: Hood, Korey K., Lawrence, Jean M., Anderson, Andrea, Bell, Ronny, Dabelea, Dana, Daniels, Stephen, Rodriguez, Beatriz, Dolan, Lawrence M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3507554/
https://www.ncbi.nlm.nih.gov/pubmed/23033243
http://dx.doi.org/10.2337/dc11-2329
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author Hood, Korey K.
Lawrence, Jean M.
Anderson, Andrea
Bell, Ronny
Dabelea, Dana
Daniels, Stephen
Rodriguez, Beatriz
Dolan, Lawrence M.
author_facet Hood, Korey K.
Lawrence, Jean M.
Anderson, Andrea
Bell, Ronny
Dabelea, Dana
Daniels, Stephen
Rodriguez, Beatriz
Dolan, Lawrence M.
author_sort Hood, Korey K.
collection PubMed
description OBJECTIVE: Youth with diabetes are at increased risk for depression. The objectives of this study were to provide preliminary evidence that this at-risk status for depression is associated with metabolic and inflammatory markers and to inform future, more stringent examinations of the directionality of these associations. RESEARCH DESIGN AND METHODS: Data from SEARCH for Diabetes in Youth (SEARCH), an observational study of U.S. children diagnosed with diabetes at <20 years of age, were used for these analyses. SEARCH participants were drawn from four geographically defined populations in Ohio, Washington, South Carolina, and Colorado; health plan enrollees in Hawaii and California; and Indian Health Service beneficiaries from four Native American populations. Participants were 2,359 youth with diabetes from the 2001 prevalent and 2002–2004 incident SEARCH cohorts. Depression was measured with the Center for Epidemiologic Studies Depression scale. Eight metabolic and inflammatory markers were measured: adiponectin, leptin, C-reactive protein, serum amyloid A, apolipoprotein B (apoB), lipoprotein A, interleukin-6, and LDL. RESULTS: Six of eight markers were significantly (P < 0.006) associated with depression in youth with diabetes in bivariate analyses. In general, higher levels of depression were associated with indicators of worse metabolic or inflammatory functioning. In regression models stratified by diabetes type and accounting for demographic and clinical characteristics, only higher levels of apoB remained associated with higher levels of depression in youth with type 1 diabetes. CONCLUSIONS: These data suggest that depression reported by youth with diabetes is partially associated with metabolic abnormalities and systemic inflammation.
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spelling pubmed-35075542013-12-01 Metabolic and Inflammatory Links to Depression in Youth With Diabetes Hood, Korey K. Lawrence, Jean M. Anderson, Andrea Bell, Ronny Dabelea, Dana Daniels, Stephen Rodriguez, Beatriz Dolan, Lawrence M. Diabetes Care Original Research OBJECTIVE: Youth with diabetes are at increased risk for depression. The objectives of this study were to provide preliminary evidence that this at-risk status for depression is associated with metabolic and inflammatory markers and to inform future, more stringent examinations of the directionality of these associations. RESEARCH DESIGN AND METHODS: Data from SEARCH for Diabetes in Youth (SEARCH), an observational study of U.S. children diagnosed with diabetes at <20 years of age, were used for these analyses. SEARCH participants were drawn from four geographically defined populations in Ohio, Washington, South Carolina, and Colorado; health plan enrollees in Hawaii and California; and Indian Health Service beneficiaries from four Native American populations. Participants were 2,359 youth with diabetes from the 2001 prevalent and 2002–2004 incident SEARCH cohorts. Depression was measured with the Center for Epidemiologic Studies Depression scale. Eight metabolic and inflammatory markers were measured: adiponectin, leptin, C-reactive protein, serum amyloid A, apolipoprotein B (apoB), lipoprotein A, interleukin-6, and LDL. RESULTS: Six of eight markers were significantly (P < 0.006) associated with depression in youth with diabetes in bivariate analyses. In general, higher levels of depression were associated with indicators of worse metabolic or inflammatory functioning. In regression models stratified by diabetes type and accounting for demographic and clinical characteristics, only higher levels of apoB remained associated with higher levels of depression in youth with type 1 diabetes. CONCLUSIONS: These data suggest that depression reported by youth with diabetes is partially associated with metabolic abnormalities and systemic inflammation. American Diabetes Association 2012-12 2012-11-14 /pmc/articles/PMC3507554/ /pubmed/23033243 http://dx.doi.org/10.2337/dc11-2329 Text en © 2012 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
spellingShingle Original Research
Hood, Korey K.
Lawrence, Jean M.
Anderson, Andrea
Bell, Ronny
Dabelea, Dana
Daniels, Stephen
Rodriguez, Beatriz
Dolan, Lawrence M.
Metabolic and Inflammatory Links to Depression in Youth With Diabetes
title Metabolic and Inflammatory Links to Depression in Youth With Diabetes
title_full Metabolic and Inflammatory Links to Depression in Youth With Diabetes
title_fullStr Metabolic and Inflammatory Links to Depression in Youth With Diabetes
title_full_unstemmed Metabolic and Inflammatory Links to Depression in Youth With Diabetes
title_short Metabolic and Inflammatory Links to Depression in Youth With Diabetes
title_sort metabolic and inflammatory links to depression in youth with diabetes
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3507554/
https://www.ncbi.nlm.nih.gov/pubmed/23033243
http://dx.doi.org/10.2337/dc11-2329
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