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Neurocognitive Outcomes in Young Adults With Early-Onset Type 1 Diabetes: A prospective follow-up study

OBJECTIVE: The aim of this study was to reexamine the neurocognitive function of a cohort of young adults with early-onset type 1 diabetes and compare their cognitive function to a matched control group. We also examined whether cognitive function was related to prospectively obtained severe hypogly...

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Autores principales: Ly, Trang T., Anderson, Mike, McNamara, Kaitrin A., Davis, Elizabeth A., Jones, Timothy W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3177715/
https://www.ncbi.nlm.nih.gov/pubmed/21844288
http://dx.doi.org/10.2337/dc11-0697
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author Ly, Trang T.
Anderson, Mike
McNamara, Kaitrin A.
Davis, Elizabeth A.
Jones, Timothy W.
author_facet Ly, Trang T.
Anderson, Mike
McNamara, Kaitrin A.
Davis, Elizabeth A.
Jones, Timothy W.
author_sort Ly, Trang T.
collection PubMed
description OBJECTIVE: The aim of this study was to reexamine the neurocognitive function of a cohort of young adults with early-onset type 1 diabetes and compare their cognitive function to a matched control group. We also examined whether cognitive function was related to prospectively obtained severe hypoglycemia history, long-term glycemic control, or severe diabetic ketoacidosis. RESEARCH DESIGN AND METHODS: Testing included Wechsler Intelligence Scale for Children and Adults, Wechsler Memory Scale, Cattell Culture Fair Intelligence Test (CCFIT), Wisconsin Card Sorting Test (WCST), youth and adult self-report, and Beck Depression Inventory. We tested 34 control subjects (mean ± SE, age 19.5 ± 0.5 years) and 33 type 1 diabetic subjects (age 19.3 ± 0.5 years, age at type 1 diabetes onset 3.3 ± 0.3 years, A1C from diagnosis 8.7 ± 0.1%, and diabetes duration 16.0 ± 0.5 years). RESULTS: There was no difference in full-scale IQ scores in type 1 diabetic and control subjects (100.7 ± 2.0 vs. 102.5 ± 1.4). There was no difference between groups in memory subtests or in reporting of emotional and behavioral difficulties. The type 1 diabetes group scored lower on the CCFIT for fluid intelligence compared with control subjects (P = 0.028) and also scored lower on WCST with more perseverative errors (P = 0.002) and fewer categories completed (P = 0.022). CONCLUSIONS: These data suggest no difference in general intellectual ability, memory, and emotional difficulties in our cohort of young adults with early-onset type 1 diabetes compared with control subjects and no deterioration over time. There were, however, findings to suggest subtle changes leading to poorer performance on complex tasks of executive function.
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spelling pubmed-31777152012-10-01 Neurocognitive Outcomes in Young Adults With Early-Onset Type 1 Diabetes: A prospective follow-up study Ly, Trang T. Anderson, Mike McNamara, Kaitrin A. Davis, Elizabeth A. Jones, Timothy W. Diabetes Care Original Research OBJECTIVE: The aim of this study was to reexamine the neurocognitive function of a cohort of young adults with early-onset type 1 diabetes and compare their cognitive function to a matched control group. We also examined whether cognitive function was related to prospectively obtained severe hypoglycemia history, long-term glycemic control, or severe diabetic ketoacidosis. RESEARCH DESIGN AND METHODS: Testing included Wechsler Intelligence Scale for Children and Adults, Wechsler Memory Scale, Cattell Culture Fair Intelligence Test (CCFIT), Wisconsin Card Sorting Test (WCST), youth and adult self-report, and Beck Depression Inventory. We tested 34 control subjects (mean ± SE, age 19.5 ± 0.5 years) and 33 type 1 diabetic subjects (age 19.3 ± 0.5 years, age at type 1 diabetes onset 3.3 ± 0.3 years, A1C from diagnosis 8.7 ± 0.1%, and diabetes duration 16.0 ± 0.5 years). RESULTS: There was no difference in full-scale IQ scores in type 1 diabetic and control subjects (100.7 ± 2.0 vs. 102.5 ± 1.4). There was no difference between groups in memory subtests or in reporting of emotional and behavioral difficulties. The type 1 diabetes group scored lower on the CCFIT for fluid intelligence compared with control subjects (P = 0.028) and also scored lower on WCST with more perseverative errors (P = 0.002) and fewer categories completed (P = 0.022). CONCLUSIONS: These data suggest no difference in general intellectual ability, memory, and emotional difficulties in our cohort of young adults with early-onset type 1 diabetes compared with control subjects and no deterioration over time. There were, however, findings to suggest subtle changes leading to poorer performance on complex tasks of executive function. American Diabetes Association 2011-10 2011-09-15 /pmc/articles/PMC3177715/ /pubmed/21844288 http://dx.doi.org/10.2337/dc11-0697 Text en © 2011 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
Ly, Trang T.
Anderson, Mike
McNamara, Kaitrin A.
Davis, Elizabeth A.
Jones, Timothy W.
Neurocognitive Outcomes in Young Adults With Early-Onset Type 1 Diabetes: A prospective follow-up study
title Neurocognitive Outcomes in Young Adults With Early-Onset Type 1 Diabetes: A prospective follow-up study
title_full Neurocognitive Outcomes in Young Adults With Early-Onset Type 1 Diabetes: A prospective follow-up study
title_fullStr Neurocognitive Outcomes in Young Adults With Early-Onset Type 1 Diabetes: A prospective follow-up study
title_full_unstemmed Neurocognitive Outcomes in Young Adults With Early-Onset Type 1 Diabetes: A prospective follow-up study
title_short Neurocognitive Outcomes in Young Adults With Early-Onset Type 1 Diabetes: A prospective follow-up study
title_sort neurocognitive outcomes in young adults with early-onset type 1 diabetes: a prospective follow-up study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3177715/
https://www.ncbi.nlm.nih.gov/pubmed/21844288
http://dx.doi.org/10.2337/dc11-0697
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