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GAD Antibody Positivity Predicts Type 2 Diabetes in an Adult Population
OBJECTIVE: To evaluate the significance of GAD antibodies (GADAs) and family history for type 1 diabetes (FH(T1)) or type 2 diabetes (FH(T2)) in nondiabetic subjects. RESEARCH DESIGN AND METHODS: GADAs were analyzed in 4,976 nondiabetic relatives of type 2 diabetic patients or control subjects from...
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Formato: | Texto |
Lenguaje: | English |
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American Diabetes Association
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2809967/ https://www.ncbi.nlm.nih.gov/pubmed/19864397 http://dx.doi.org/10.2337/db09-0747 |
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author | Lundgren, Virve M. Isomaa, Bo Lyssenko, Valeriya Laurila, Esa Korhonen, Pasi Groop, Leif C. Tuomi, Tiinamaija |
author_facet | Lundgren, Virve M. Isomaa, Bo Lyssenko, Valeriya Laurila, Esa Korhonen, Pasi Groop, Leif C. Tuomi, Tiinamaija |
author_sort | Lundgren, Virve M. |
collection | PubMed |
description | OBJECTIVE: To evaluate the significance of GAD antibodies (GADAs) and family history for type 1 diabetes (FH(T1)) or type 2 diabetes (FH(T2)) in nondiabetic subjects. RESEARCH DESIGN AND METHODS: GADAs were analyzed in 4,976 nondiabetic relatives of type 2 diabetic patients or control subjects from Finland. Altogether, 289 (5.9%) were GADA(+)—a total of 253 GADA(+) and 2,511 GADA(−) subjects participated in repeated oral glucose tolerance tests during a median time of 8.1 years. The risk of progression to diabetes was assessed using Cox regression analysis. RESULTS: Subjects within the highest quartile of GADA(+) (GADA(+)(high)) had more often first-degree FH(T1) (29.2 vs. 7.9%, P < 0.00001) and GADA(+) type 2 diabetic (21.3 vs. 13.7%, P = 0.002) or nondiabetic (26.4 vs. 13.3%, P = 0.010) relatives than GADA(−) subjects. During the follow-up, the GADA(+) subjects developed diabetes significantly more often than the GADA(−) subjects (36/253 [14.2%] vs. 134/2,511 [5.3%], P < 0.00001). GADA(+)(high) conferred a 4.9-fold increased risk of diabetes (95% CI 2.8–8.5) compared with GADA(−)—seroconversion to positive during the follow-up was associated with 6.5-fold (2.8–15.2) and first-degree FH(T1) with 2.2-fold (1.2–4.1) risk of diabetes. Only three subjects developed type 1 diabetes, and others had a non–insulin-dependent phenotype 1 year after diagnosis. GADA(+) and GADA(−) subjects did not clinically differ at baseline, but they were leaner and less insulin resistant after the diagnosis of diabetes. CONCLUSIONS: GADA positivity clusters in families with type 1 diabetes or latent autoimmune diabetes in adults. GADA positivity predicts diabetes independently of family history of diabetes, and this risk was further increased with high GADA concentrations. |
format | Text |
id | pubmed-2809967 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-28099672011-02-01 GAD Antibody Positivity Predicts Type 2 Diabetes in an Adult Population Lundgren, Virve M. Isomaa, Bo Lyssenko, Valeriya Laurila, Esa Korhonen, Pasi Groop, Leif C. Tuomi, Tiinamaija Diabetes Original Article OBJECTIVE: To evaluate the significance of GAD antibodies (GADAs) and family history for type 1 diabetes (FH(T1)) or type 2 diabetes (FH(T2)) in nondiabetic subjects. RESEARCH DESIGN AND METHODS: GADAs were analyzed in 4,976 nondiabetic relatives of type 2 diabetic patients or control subjects from Finland. Altogether, 289 (5.9%) were GADA(+)—a total of 253 GADA(+) and 2,511 GADA(−) subjects participated in repeated oral glucose tolerance tests during a median time of 8.1 years. The risk of progression to diabetes was assessed using Cox regression analysis. RESULTS: Subjects within the highest quartile of GADA(+) (GADA(+)(high)) had more often first-degree FH(T1) (29.2 vs. 7.9%, P < 0.00001) and GADA(+) type 2 diabetic (21.3 vs. 13.7%, P = 0.002) or nondiabetic (26.4 vs. 13.3%, P = 0.010) relatives than GADA(−) subjects. During the follow-up, the GADA(+) subjects developed diabetes significantly more often than the GADA(−) subjects (36/253 [14.2%] vs. 134/2,511 [5.3%], P < 0.00001). GADA(+)(high) conferred a 4.9-fold increased risk of diabetes (95% CI 2.8–8.5) compared with GADA(−)—seroconversion to positive during the follow-up was associated with 6.5-fold (2.8–15.2) and first-degree FH(T1) with 2.2-fold (1.2–4.1) risk of diabetes. Only three subjects developed type 1 diabetes, and others had a non–insulin-dependent phenotype 1 year after diagnosis. GADA(+) and GADA(−) subjects did not clinically differ at baseline, but they were leaner and less insulin resistant after the diagnosis of diabetes. CONCLUSIONS: GADA positivity clusters in families with type 1 diabetes or latent autoimmune diabetes in adults. GADA positivity predicts diabetes independently of family history of diabetes, and this risk was further increased with high GADA concentrations. American Diabetes Association 2010-02 2009-10-28 /pmc/articles/PMC2809967/ /pubmed/19864397 http://dx.doi.org/10.2337/db09-0747 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 Article Lundgren, Virve M. Isomaa, Bo Lyssenko, Valeriya Laurila, Esa Korhonen, Pasi Groop, Leif C. Tuomi, Tiinamaija GAD Antibody Positivity Predicts Type 2 Diabetes in an Adult Population |
title | GAD Antibody Positivity Predicts Type 2 Diabetes in an Adult Population |
title_full | GAD Antibody Positivity Predicts Type 2 Diabetes in an Adult Population |
title_fullStr | GAD Antibody Positivity Predicts Type 2 Diabetes in an Adult Population |
title_full_unstemmed | GAD Antibody Positivity Predicts Type 2 Diabetes in an Adult Population |
title_short | GAD Antibody Positivity Predicts Type 2 Diabetes in an Adult Population |
title_sort | gad antibody positivity predicts type 2 diabetes in an adult population |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2809967/ https://www.ncbi.nlm.nih.gov/pubmed/19864397 http://dx.doi.org/10.2337/db09-0747 |
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