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Cognitive Function in Children With Type 1 Diabetes: A meta-analysis
OBJECTIVE—To quantify the magnitude and pattern of cognitive difficulties in pediatric type 1 diabetes as well as the effects associated with earlier disease onset and severe hypoglycemia. RESEARCH DESIGN AND METHODS—Pediatric studies of cognitive function since 1985 were identified for study inclus...
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Formato: | Texto |
Lenguaje: | English |
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American Diabetes Association
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2518367/ https://www.ncbi.nlm.nih.gov/pubmed/18753668 http://dx.doi.org/10.2337/dc07-2132 |
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author | Gaudieri, Patricia A. Chen, Rusan Greer, Tammy F. Holmes, Clarissa S. |
author_facet | Gaudieri, Patricia A. Chen, Rusan Greer, Tammy F. Holmes, Clarissa S. |
author_sort | Gaudieri, Patricia A. |
collection | PubMed |
description | OBJECTIVE—To quantify the magnitude and pattern of cognitive difficulties in pediatric type 1 diabetes as well as the effects associated with earlier disease onset and severe hypoglycemia. RESEARCH DESIGN AND METHODS—Pediatric studies of cognitive function since 1985 were identified for study inclusion using MEDLINE and PsycInfo. Effect size (ES, Cohen's d) between the diabetic and control groups, expressed in SD units, were calculated within cognitive domains to standardize meta-analysis test performance. RESULTS—The meta-analysis sample of 2,144 children consisted of 1,393 study subjects with type 1 diabetes and 751 control subjects from 19 studies. Overall, type 1 diabetes was associated with slightly lower overall cognition (ES −0.13), with small differences compared with control subjects across a broad range of domains, excluding learning and memory, which were similar for both groups. Learning and memory skills, both verbal and visual (−0.28 and −0.25), were more affected for children with early-onset diabetes (EOD) than late-onset diabetes (LOD), along with attention/executive function skills (−0.27). Compared with nondiabetic control subjects, EOD effects were larger, up to one-half SD lower, particularly for learning and memory (−0.49). Generally, seizures were associated with a negligible overall cognition ES of −0.06, with slight and inconsistent cognitive effects found on some measures, possibly reflecting the opposing effects of poorer versus better metabolic control. CONCLUSIONS—Pediatric diabetes generally relates to mildly lower cognitive scores across most cognitive domains. Cognitive effects are most pronounced and pervasive for EOD, with moderately lower performance compared with control subjects. Seizures are generally related to nominal, inconsistent performance differences. |
format | Text |
id | pubmed-2518367 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-25183672009-09-01 Cognitive Function in Children With Type 1 Diabetes: A meta-analysis Gaudieri, Patricia A. Chen, Rusan Greer, Tammy F. Holmes, Clarissa S. Diabetes Care Reviews/Commentaries/ADA Statements OBJECTIVE—To quantify the magnitude and pattern of cognitive difficulties in pediatric type 1 diabetes as well as the effects associated with earlier disease onset and severe hypoglycemia. RESEARCH DESIGN AND METHODS—Pediatric studies of cognitive function since 1985 were identified for study inclusion using MEDLINE and PsycInfo. Effect size (ES, Cohen's d) between the diabetic and control groups, expressed in SD units, were calculated within cognitive domains to standardize meta-analysis test performance. RESULTS—The meta-analysis sample of 2,144 children consisted of 1,393 study subjects with type 1 diabetes and 751 control subjects from 19 studies. Overall, type 1 diabetes was associated with slightly lower overall cognition (ES −0.13), with small differences compared with control subjects across a broad range of domains, excluding learning and memory, which were similar for both groups. Learning and memory skills, both verbal and visual (−0.28 and −0.25), were more affected for children with early-onset diabetes (EOD) than late-onset diabetes (LOD), along with attention/executive function skills (−0.27). Compared with nondiabetic control subjects, EOD effects were larger, up to one-half SD lower, particularly for learning and memory (−0.49). Generally, seizures were associated with a negligible overall cognition ES of −0.06, with slight and inconsistent cognitive effects found on some measures, possibly reflecting the opposing effects of poorer versus better metabolic control. CONCLUSIONS—Pediatric diabetes generally relates to mildly lower cognitive scores across most cognitive domains. Cognitive effects are most pronounced and pervasive for EOD, with moderately lower performance compared with control subjects. Seizures are generally related to nominal, inconsistent performance differences. American Diabetes Association 2008-09 /pmc/articles/PMC2518367/ /pubmed/18753668 http://dx.doi.org/10.2337/dc07-2132 Text en Copyright © 2008, DIABETES CARE 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 | Reviews/Commentaries/ADA Statements Gaudieri, Patricia A. Chen, Rusan Greer, Tammy F. Holmes, Clarissa S. Cognitive Function in Children With Type 1 Diabetes: A meta-analysis |
title | Cognitive Function in Children With Type 1 Diabetes: A meta-analysis |
title_full | Cognitive Function in Children With Type 1 Diabetes: A meta-analysis |
title_fullStr | Cognitive Function in Children With Type 1 Diabetes: A meta-analysis |
title_full_unstemmed | Cognitive Function in Children With Type 1 Diabetes: A meta-analysis |
title_short | Cognitive Function in Children With Type 1 Diabetes: A meta-analysis |
title_sort | cognitive function in children with type 1 diabetes: a meta-analysis |
topic | Reviews/Commentaries/ADA Statements |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2518367/ https://www.ncbi.nlm.nih.gov/pubmed/18753668 http://dx.doi.org/10.2337/dc07-2132 |
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