Latent autoimmune diabetes in adults differs genetically from classical type 1 diabetes diagnosed after the age of 35 years

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Latent autoimmune diabetes in adults differs genetically from classical type 1 diabetes diagnosed after the age of 35 years. / Andersen, Mette K.; Lundgren, Virve; Turunen, Joni A.; Forsblom, Carol; Isomaa, Bo; Groop, Per Henrik; Groop, Leif; Tuomi, Tiinamaija.

In: Diabetes Care, Vol. 33, No. 9, 01.09.2010, p. 2062-2064.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Andersen, MK, Lundgren, V, Turunen, JA, Forsblom, C, Isomaa, B, Groop, PH, Groop, L & Tuomi, T 2010, 'Latent autoimmune diabetes in adults differs genetically from classical type 1 diabetes diagnosed after the age of 35 years', Diabetes Care, vol. 33, no. 9, pp. 2062-2064. https://doi.org/10.2337/dc09-2188

APA

Andersen, M. K., Lundgren, V., Turunen, J. A., Forsblom, C., Isomaa, B., Groop, P. H., Groop, L., & Tuomi, T. (2010). Latent autoimmune diabetes in adults differs genetically from classical type 1 diabetes diagnosed after the age of 35 years. Diabetes Care, 33(9), 2062-2064. https://doi.org/10.2337/dc09-2188

Vancouver

Andersen MK, Lundgren V, Turunen JA, Forsblom C, Isomaa B, Groop PH et al. Latent autoimmune diabetes in adults differs genetically from classical type 1 diabetes diagnosed after the age of 35 years. Diabetes Care. 2010 Sep 1;33(9):2062-2064. https://doi.org/10.2337/dc09-2188

Author

Andersen, Mette K. ; Lundgren, Virve ; Turunen, Joni A. ; Forsblom, Carol ; Isomaa, Bo ; Groop, Per Henrik ; Groop, Leif ; Tuomi, Tiinamaija. / Latent autoimmune diabetes in adults differs genetically from classical type 1 diabetes diagnosed after the age of 35 years. In: Diabetes Care. 2010 ; Vol. 33, No. 9. pp. 2062-2064.

Bibtex

@article{17438f3db49045b985bc12a50abdbf55,
title = "Latent autoimmune diabetes in adults differs genetically from classical type 1 diabetes diagnosed after the age of 35 years",
abstract = "OBJECTIVE - We studied differences between patients with latent autoimmune diabetes in adults (LADA), type 2 diabetes, and classical type 1 diabetes diagnosed after age 35 years. RESEARCH DESIGN AND METHODS - Polymorphisms in HLA-DQB1, INS, PTPN22, and CTLA4 were genotyped in patients with LADA (n = 213), type 1 diabetes diagnosed at >35 years of age (T1D>35y; n = 257) or <20 years of age (T1D<20y; n = 158), and type 2 diabetes. RESULTS - Although patients with LADA had an increased frequency of HLA-DQB1 and PTPN22 risk genotypes and alleles compared with type 2 diabetic subjects, the frequency was significantly lower compared with T1D >35y patients. Genotype frequencies, measures of insulin secretion, and metabolic traits within LADA differed according to GAD antibody (GADA) quartiles, but even the highest quartile differed from type 1 diabetes. Having two or more risk genotypes was associated with lower C-peptide concentrations in LADA. CONCLUSIONS - LADA patients differed genetically and phenotypically from both T1D>35y and type 2 diabetic patients in a manner dependent on GADA levels.",
author = "Andersen, {Mette K.} and Virve Lundgren and Turunen, {Joni A.} and Carol Forsblom and Bo Isomaa and Groop, {Per Henrik} and Leif Groop and Tiinamaija Tuomi",
year = "2010",
month = sep,
day = "1",
doi = "10.2337/dc09-2188",
language = "English",
volume = "33",
pages = "2062--2064",
journal = "Diabetes Care",
issn = "0149-5992",
publisher = "American Diabetes Association",
number = "9",

}

RIS

TY - JOUR

T1 - Latent autoimmune diabetes in adults differs genetically from classical type 1 diabetes diagnosed after the age of 35 years

AU - Andersen, Mette K.

AU - Lundgren, Virve

AU - Turunen, Joni A.

AU - Forsblom, Carol

AU - Isomaa, Bo

AU - Groop, Per Henrik

AU - Groop, Leif

AU - Tuomi, Tiinamaija

PY - 2010/9/1

Y1 - 2010/9/1

N2 - OBJECTIVE - We studied differences between patients with latent autoimmune diabetes in adults (LADA), type 2 diabetes, and classical type 1 diabetes diagnosed after age 35 years. RESEARCH DESIGN AND METHODS - Polymorphisms in HLA-DQB1, INS, PTPN22, and CTLA4 were genotyped in patients with LADA (n = 213), type 1 diabetes diagnosed at >35 years of age (T1D>35y; n = 257) or <20 years of age (T1D<20y; n = 158), and type 2 diabetes. RESULTS - Although patients with LADA had an increased frequency of HLA-DQB1 and PTPN22 risk genotypes and alleles compared with type 2 diabetic subjects, the frequency was significantly lower compared with T1D >35y patients. Genotype frequencies, measures of insulin secretion, and metabolic traits within LADA differed according to GAD antibody (GADA) quartiles, but even the highest quartile differed from type 1 diabetes. Having two or more risk genotypes was associated with lower C-peptide concentrations in LADA. CONCLUSIONS - LADA patients differed genetically and phenotypically from both T1D>35y and type 2 diabetic patients in a manner dependent on GADA levels.

AB - OBJECTIVE - We studied differences between patients with latent autoimmune diabetes in adults (LADA), type 2 diabetes, and classical type 1 diabetes diagnosed after age 35 years. RESEARCH DESIGN AND METHODS - Polymorphisms in HLA-DQB1, INS, PTPN22, and CTLA4 were genotyped in patients with LADA (n = 213), type 1 diabetes diagnosed at >35 years of age (T1D>35y; n = 257) or <20 years of age (T1D<20y; n = 158), and type 2 diabetes. RESULTS - Although patients with LADA had an increased frequency of HLA-DQB1 and PTPN22 risk genotypes and alleles compared with type 2 diabetic subjects, the frequency was significantly lower compared with T1D >35y patients. Genotype frequencies, measures of insulin secretion, and metabolic traits within LADA differed according to GAD antibody (GADA) quartiles, but even the highest quartile differed from type 1 diabetes. Having two or more risk genotypes was associated with lower C-peptide concentrations in LADA. CONCLUSIONS - LADA patients differed genetically and phenotypically from both T1D>35y and type 2 diabetic patients in a manner dependent on GADA levels.

UR - http://www.scopus.com/inward/record.url?scp=79951607479&partnerID=8YFLogxK

U2 - 10.2337/dc09-2188

DO - 10.2337/dc09-2188

M3 - Journal article

C2 - 20805278

AN - SCOPUS:79951607479

VL - 33

SP - 2062

EP - 2064

JO - Diabetes Care

JF - Diabetes Care

SN - 0149-5992

IS - 9

ER -

ID: 200858529