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Cohort Study of Insulin Glargine and Risk of Breast, Prostate, and Colorectal Cancer Among Patients With Diabetes
OBJECTIVE: To examine whether use of insulin glargine, compared with another long-acting insulin, is associated with risk of breast, prostate, colorectal cancer, or all cancers combined. RESEARCH DESIGN AND METHODS: Computerized health records from Kaiser Permanente Northern and Southern California...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Diabetes Association
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3836110/ https://www.ncbi.nlm.nih.gov/pubmed/24170756 http://dx.doi.org/10.2337/dc13-0140 |
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author | Habel, Laurel A. Danforth, Kim N. Quesenberry, Charles P. Capra, Angela Van Den Eeden, Stephen K. Weiss, Noel S. Ferrara, Assiamira |
author_facet | Habel, Laurel A. Danforth, Kim N. Quesenberry, Charles P. Capra, Angela Van Den Eeden, Stephen K. Weiss, Noel S. Ferrara, Assiamira |
author_sort | Habel, Laurel A. |
collection | PubMed |
description | OBJECTIVE: To examine whether use of insulin glargine, compared with another long-acting insulin, is associated with risk of breast, prostate, colorectal cancer, or all cancers combined. RESEARCH DESIGN AND METHODS: Computerized health records from Kaiser Permanente Northern and Southern California regions starting in 2001 and ending in 2009 were used to conduct a population-based cohort study among patients with diabetes aged ≥18 years. With use of Cox regression modeling, cancer risk in users of insulin glargine (n = 27,418) was compared with cancer risk in users of NPH (n = 100,757). RESULTS: The cohort had a median follow-up of 3.3 years during which there was a median of 1.2 years of glargine use and 1.4 years of NPH use. Among users of NPH at baseline, there was no clear increase in risk of breast, prostate, colorectal, or all cancers combined associated with switching to glargine. Among those initiating insulin, ever use or ≥2 years of glargine was not associated with increased risk of prostate or colorectal cancer or all cancers combined. Among initiators, the hazard ratio (HR) for breast cancer associated with ever use of glargine was 1.3 (95% CI 1.0–1.8); the HR for breast cancer associated with use of glargine for ≥2 years was 1.6 or 1.7 depending on whether glargine users had also used NPH. CONCLUSIONS: Results of this study should be viewed cautiously, given the relatively short duration of glargine use to date and the large number of potential associations examined. |
format | Online Article Text |
id | pubmed-3836110 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-38361102014-12-01 Cohort Study of Insulin Glargine and Risk of Breast, Prostate, and Colorectal Cancer Among Patients With Diabetes Habel, Laurel A. Danforth, Kim N. Quesenberry, Charles P. Capra, Angela Van Den Eeden, Stephen K. Weiss, Noel S. Ferrara, Assiamira Diabetes Care Original Research OBJECTIVE: To examine whether use of insulin glargine, compared with another long-acting insulin, is associated with risk of breast, prostate, colorectal cancer, or all cancers combined. RESEARCH DESIGN AND METHODS: Computerized health records from Kaiser Permanente Northern and Southern California regions starting in 2001 and ending in 2009 were used to conduct a population-based cohort study among patients with diabetes aged ≥18 years. With use of Cox regression modeling, cancer risk in users of insulin glargine (n = 27,418) was compared with cancer risk in users of NPH (n = 100,757). RESULTS: The cohort had a median follow-up of 3.3 years during which there was a median of 1.2 years of glargine use and 1.4 years of NPH use. Among users of NPH at baseline, there was no clear increase in risk of breast, prostate, colorectal, or all cancers combined associated with switching to glargine. Among those initiating insulin, ever use or ≥2 years of glargine was not associated with increased risk of prostate or colorectal cancer or all cancers combined. Among initiators, the hazard ratio (HR) for breast cancer associated with ever use of glargine was 1.3 (95% CI 1.0–1.8); the HR for breast cancer associated with use of glargine for ≥2 years was 1.6 or 1.7 depending on whether glargine users had also used NPH. CONCLUSIONS: Results of this study should be viewed cautiously, given the relatively short duration of glargine use to date and the large number of potential associations examined. American Diabetes Association 2013-12 2013-11-13 /pmc/articles/PMC3836110/ /pubmed/24170756 http://dx.doi.org/10.2337/dc13-0140 Text en © 2013 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 Habel, Laurel A. Danforth, Kim N. Quesenberry, Charles P. Capra, Angela Van Den Eeden, Stephen K. Weiss, Noel S. Ferrara, Assiamira Cohort Study of Insulin Glargine and Risk of Breast, Prostate, and Colorectal Cancer Among Patients With Diabetes |
title | Cohort Study of Insulin Glargine and Risk of Breast, Prostate, and Colorectal Cancer Among Patients With Diabetes |
title_full | Cohort Study of Insulin Glargine and Risk of Breast, Prostate, and Colorectal Cancer Among Patients With Diabetes |
title_fullStr | Cohort Study of Insulin Glargine and Risk of Breast, Prostate, and Colorectal Cancer Among Patients With Diabetes |
title_full_unstemmed | Cohort Study of Insulin Glargine and Risk of Breast, Prostate, and Colorectal Cancer Among Patients With Diabetes |
title_short | Cohort Study of Insulin Glargine and Risk of Breast, Prostate, and Colorectal Cancer Among Patients With Diabetes |
title_sort | cohort study of insulin glargine and risk of breast, prostate, and colorectal cancer among patients with diabetes |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3836110/ https://www.ncbi.nlm.nih.gov/pubmed/24170756 http://dx.doi.org/10.2337/dc13-0140 |
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