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Familial Risks for Type 2 Diabetes in Sweden
OBJECTIVE: Our aim was to characterize familial risks for type 2 diabetes by the type and number of affected family members, including half-siblings, adoptees, and spouses, to quantify risks and estimate the contribution of environmental effect. RESEARCH DESIGN AND METHODS: Families were identified...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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American Diabetes Association
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2809269/ https://www.ncbi.nlm.nih.gov/pubmed/19903751 http://dx.doi.org/10.2337/dc09-0947 |
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author | Hemminki, Kari Li, Xinjun Sundquist, Kristina Sundquist, Jan |
author_facet | Hemminki, Kari Li, Xinjun Sundquist, Kristina Sundquist, Jan |
author_sort | Hemminki, Kari |
collection | PubMed |
description | OBJECTIVE: Our aim was to characterize familial risks for type 2 diabetes by the type and number of affected family members, including half-siblings, adoptees, and spouses, to quantify risks and estimate the contribution of environmental effect. RESEARCH DESIGN AND METHODS: Families were identified from the Multigeneration Register, and type 2 diabetic patients were obtained from the Hospital Discharge Register. Standardized incidence ratios were calculated for offspring with type 2 diabetes whose family members were hospitalized for type 2 diabetes at ages >39 years compared with those lacking affected family members. RESULTS: The number of hospitalized type 2 diabetic patients was 157,549. Among 27,895 offspring, 27.9% had a parent or sibling also hospitalized for type 2 diabetes. The familial relative risk (RR) ranged from 2.0 to >30, depending on the number and type of probands. The highest RRs of type 2 diabetes were found in individuals who had at least two siblings affected by type 2 diabetes, irrespective of the parental disease. Adoptees showed no risk from adopted parents. CONCLUSIONS: The study, the largest yet published, showed that familial RRs varied by the number and type of affected family member. However, much of the familial clustering remains yet to be genetically explained. The high risk should be recognized in clinical genetic counseling. The data from adoptees confirmed the genetic basis of the familial associations, but those from half siblings and spouses suggested that a smaller part of familial clustering may be accounted for by environmental factors. |
format | Text |
id | pubmed-2809269 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-28092692011-02-01 Familial Risks for Type 2 Diabetes in Sweden Hemminki, Kari Li, Xinjun Sundquist, Kristina Sundquist, Jan Diabetes Care Original Research OBJECTIVE: Our aim was to characterize familial risks for type 2 diabetes by the type and number of affected family members, including half-siblings, adoptees, and spouses, to quantify risks and estimate the contribution of environmental effect. RESEARCH DESIGN AND METHODS: Families were identified from the Multigeneration Register, and type 2 diabetic patients were obtained from the Hospital Discharge Register. Standardized incidence ratios were calculated for offspring with type 2 diabetes whose family members were hospitalized for type 2 diabetes at ages >39 years compared with those lacking affected family members. RESULTS: The number of hospitalized type 2 diabetic patients was 157,549. Among 27,895 offspring, 27.9% had a parent or sibling also hospitalized for type 2 diabetes. The familial relative risk (RR) ranged from 2.0 to >30, depending on the number and type of probands. The highest RRs of type 2 diabetes were found in individuals who had at least two siblings affected by type 2 diabetes, irrespective of the parental disease. Adoptees showed no risk from adopted parents. CONCLUSIONS: The study, the largest yet published, showed that familial RRs varied by the number and type of affected family member. However, much of the familial clustering remains yet to be genetically explained. The high risk should be recognized in clinical genetic counseling. The data from adoptees confirmed the genetic basis of the familial associations, but those from half siblings and spouses suggested that a smaller part of familial clustering may be accounted for by environmental factors. American Diabetes Association 2010-02 2009-11-10 /pmc/articles/PMC2809269/ /pubmed/19903751 http://dx.doi.org/10.2337/dc09-0947 Text en © 2010 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 Hemminki, Kari Li, Xinjun Sundquist, Kristina Sundquist, Jan Familial Risks for Type 2 Diabetes in Sweden |
title | Familial Risks for Type 2 Diabetes in Sweden |
title_full | Familial Risks for Type 2 Diabetes in Sweden |
title_fullStr | Familial Risks for Type 2 Diabetes in Sweden |
title_full_unstemmed | Familial Risks for Type 2 Diabetes in Sweden |
title_short | Familial Risks for Type 2 Diabetes in Sweden |
title_sort | familial risks for type 2 diabetes in sweden |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2809269/ https://www.ncbi.nlm.nih.gov/pubmed/19903751 http://dx.doi.org/10.2337/dc09-0947 |
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