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Statin use and cognitive function in middle-aged adults with type 1 diabetes
AIM: To test associations between statin use and cognitive impairment in adults with childhood-onset type 1 diabetes (T1D). METHODS: In 2010-13, n = 108 middle-aged participants from ongoing observational Pittsburgh Epidemiology of Diabetes Complications Study underwent neurocognitive assessment (me...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5483427/ https://www.ncbi.nlm.nih.gov/pubmed/28694929 http://dx.doi.org/10.4239/wjd.v8.i6.286 |
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author | Nunley, Karen A Orchard, Trevor J Ryan, Christopher M Miller, Rachel Costacou, Tina Rosano, Caterina |
author_facet | Nunley, Karen A Orchard, Trevor J Ryan, Christopher M Miller, Rachel Costacou, Tina Rosano, Caterina |
author_sort | Nunley, Karen A |
collection | PubMed |
description | AIM: To test associations between statin use and cognitive impairment in adults with childhood-onset type 1 diabetes (T1D). METHODS: In 2010-13, n = 108 middle-aged participants from ongoing observational Pittsburgh Epidemiology of Diabetes Complications Study underwent neurocognitive assessment (mean age and T1D duration of 49 and 41 years, respectively). All were diagnosed with childhood-onset (i.e., prior to age 18) T1D between 1950 and 1980 and were seen within one year of diagnosis at Children’s Hospital of Pittsburgh. Self-reported statin use (yes/no and if yes, name of statin) was collected biennially from parent study baseline (1986-1988) to time of neurocognitive testing. Logistic regression models tested associations between statin use groups and cognitive impairment (defined as having two or more cognitive test scores 1.5SD or worse than published norms) while linear regression models tested associations between statin use groups and cognitive domain z-scores (domains: Verbal IQ, memory, executive function, psychomotor speed, and visuo-construction). All models controlled for education and age. To address confounding by indication, models were repeated using a propensity score for statin use. RESULTS: Of the 108 participants, 51 reported never using statins. Median duration of statin use among the 57 ever users was 6 years. These 57 ever statin users were split to create two groups (≤ or > median years of statin use): 1-6 years (n = 25), and 7-12 years (n = 32). Compared with never users, using statins 1-6 years tripled the odds of cognitive impairment (OR = 3.16; 95%CI: 0.93-10.72; P = 0.06) and using statins 7-12 years almost quintupled the odds of cognitive impairment (OR = 4.84; 95%CI: 1.63-14.44; P = 0.005). Compared with never users, using statins 1-6 or 7-12 years was related to worse performance in the memory domain (β = -0.52; P = 0.003, and -0.39; P = 0.014, respectively). Adjusting for coronary artery disease, low density lipoprotein cholesterol, and Apo E4 status did not substantially alter results, and none of these covariates were significantly related to cognitive outcomes (all P > 0.05). Propensity score analyses support that associations between poor cognitive outcomes and statin use were not due merely to confounding by indication. CONCLUSION: Statin use was associated with cognitive impairment, particularly affecting memory, in these middle-aged adults with childhood-onset T1D, whom at this age, should not yet manifest age-related memory deficits. |
format | Online Article Text |
id | pubmed-5483427 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-54834272017-07-10 Statin use and cognitive function in middle-aged adults with type 1 diabetes Nunley, Karen A Orchard, Trevor J Ryan, Christopher M Miller, Rachel Costacou, Tina Rosano, Caterina World J Diabetes Observational Study AIM: To test associations between statin use and cognitive impairment in adults with childhood-onset type 1 diabetes (T1D). METHODS: In 2010-13, n = 108 middle-aged participants from ongoing observational Pittsburgh Epidemiology of Diabetes Complications Study underwent neurocognitive assessment (mean age and T1D duration of 49 and 41 years, respectively). All were diagnosed with childhood-onset (i.e., prior to age 18) T1D between 1950 and 1980 and were seen within one year of diagnosis at Children’s Hospital of Pittsburgh. Self-reported statin use (yes/no and if yes, name of statin) was collected biennially from parent study baseline (1986-1988) to time of neurocognitive testing. Logistic regression models tested associations between statin use groups and cognitive impairment (defined as having two or more cognitive test scores 1.5SD or worse than published norms) while linear regression models tested associations between statin use groups and cognitive domain z-scores (domains: Verbal IQ, memory, executive function, psychomotor speed, and visuo-construction). All models controlled for education and age. To address confounding by indication, models were repeated using a propensity score for statin use. RESULTS: Of the 108 participants, 51 reported never using statins. Median duration of statin use among the 57 ever users was 6 years. These 57 ever statin users were split to create two groups (≤ or > median years of statin use): 1-6 years (n = 25), and 7-12 years (n = 32). Compared with never users, using statins 1-6 years tripled the odds of cognitive impairment (OR = 3.16; 95%CI: 0.93-10.72; P = 0.06) and using statins 7-12 years almost quintupled the odds of cognitive impairment (OR = 4.84; 95%CI: 1.63-14.44; P = 0.005). Compared with never users, using statins 1-6 or 7-12 years was related to worse performance in the memory domain (β = -0.52; P = 0.003, and -0.39; P = 0.014, respectively). Adjusting for coronary artery disease, low density lipoprotein cholesterol, and Apo E4 status did not substantially alter results, and none of these covariates were significantly related to cognitive outcomes (all P > 0.05). Propensity score analyses support that associations between poor cognitive outcomes and statin use were not due merely to confounding by indication. CONCLUSION: Statin use was associated with cognitive impairment, particularly affecting memory, in these middle-aged adults with childhood-onset T1D, whom at this age, should not yet manifest age-related memory deficits. Baishideng Publishing Group Inc 2017-06-15 2017-06-15 /pmc/articles/PMC5483427/ /pubmed/28694929 http://dx.doi.org/10.4239/wjd.v8.i6.286 Text en ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Observational Study Nunley, Karen A Orchard, Trevor J Ryan, Christopher M Miller, Rachel Costacou, Tina Rosano, Caterina Statin use and cognitive function in middle-aged adults with type 1 diabetes |
title | Statin use and cognitive function in middle-aged adults with type 1 diabetes |
title_full | Statin use and cognitive function in middle-aged adults with type 1 diabetes |
title_fullStr | Statin use and cognitive function in middle-aged adults with type 1 diabetes |
title_full_unstemmed | Statin use and cognitive function in middle-aged adults with type 1 diabetes |
title_short | Statin use and cognitive function in middle-aged adults with type 1 diabetes |
title_sort | statin use and cognitive function in middle-aged adults with type 1 diabetes |
topic | Observational Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5483427/ https://www.ncbi.nlm.nih.gov/pubmed/28694929 http://dx.doi.org/10.4239/wjd.v8.i6.286 |
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