A high-throughput population screening system for the estimation of genetic risk for type 1 diabetes:: An application for the TEDDY (The environmental determinants of diabetes in the young) study

被引:59
作者
Kiviniemi, Minna
Hermann, Robert
Nurmi, Fussi
Ziegler, Anette G.
Knip, Mikael
Simell, Olli
Veijola, Riitta
Loevgren, Timo
Ilonen, Jorma
机构
[1] Univ Turku, MediCity Res Lab, FIN-20520 Turku, Finland
[2] Univ Turku, Immunogenet Lab, FIN-20520 Turku, Finland
[3] Univ Turku, Dept Pediat, FIN-20520 Turku, Finland
[4] Univ Turku, Dept Biotechnol, FIN-20520 Turku, Finland
[5] Abacus Diagnost Oy, Turku, Finland
[6] Diabet Res Inst, Munich, Germany
[7] Hosp Munchen Schwabing, Munich, Germany
[8] Univ Helsinki, Hosp Children & Adolescents, Helsinki, Finland
[9] Tampere Univ Hosp, Dept Pediat, Tampere, Finland
[10] Univ Oulu, Dept Pediat, SF-90100 Oulu, Finland
[11] Univ Kuopio, Dept Clin Microbiol, FIN-70211 Kuopio, Finland
关键词
D O I
10.1089/dia.2007.0229
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: In the TEDDY (The Environmental Determinants of Diabetes in the Young) study patient eligibility is based on the presence of some selected type 1 diabetes risk-associated human leukocyte antigen DR-DQ genotypes. A practical screening strategy was needed with efficient exclusion of ineligible patients at an early stage. Also, a simple, low-cost, and fast screening system was essential for the primary step of the risk assessment including thousands of samples. Methods: A homogeneous genotyping system utilizing an asymmetric polymerase chain reaction (PCR) and subsequent hybridization of allele-specific probes was designed to be used as the first screening step. This assay was combined with methods further elucidating the genetic risk of type 1 diabetes to screen for high-risk individuals. Results: The homogeneous assay platform allows the typing of hundreds of samples within one working day. The costs of the assay are minimal, and the reduction in hands-on time provides considerable improvements compared to the heterogeneous genotyping methods comprising separate PCR and hybridization steps. The primary selection criteria used in the first step proved to be efficient since the numbers of samples typed in subsequent stages were markedly reduced. Conclusions: The presented assay system provides a practical approach to the rapid screening of thousands of samples at low cost, a general starting point for large-scale screening studies.
引用
收藏
页码:460 / 472
页数:13
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