A genonte-wide search for genes involved in type 2 diabetes in a recently genetically isolated population from the Netherlands

被引:19
作者
Aulchenko, YS
Vaessen, N
Heutink, P
Pullen, J
Snijders, PJLM
Hofman, A
Sandkuijl, LA
Honwin-Duistermaat, JJ
Edwards, M
Bennett, S
Oostra, BA
van Duijn, CM
机构
[1] Erasmus Med Ctr Rotterdam, Genet Epidemiol Unit, Dept Epidemiol & Biostat, NL-3000 DR Rotterdam, Netherlands
[2] RAS, Inst Cytol & Genet, SD, Novosibirsk, Russia
[3] Erasmus Med Ctr, Dept Clin Genet, Rotterdam, Netherlands
[4] Oxagen Ltd, Abingdon, Oxon, England
[5] Leiden Univ, Ctr Med, Leiden, Netherlands
关键词
D O I
10.2337/diabetes.52.12.3001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Multiple genes, interacting with the environment, contribute to the susceptibility to type 2 diabetes. We performed a genome-wide search to localize type 2 diabetes susceptibility genes in a recently genetically isolated population in the Netherlands. We identified 79 nuclear families with type 2 diabetes who were related within 13 generations and performed a 770-marker genome-wide scan search for shared founder alleles. Twenty-six markers yielded a logarithm of odds (LOD) score > 0.59 (nominal P < 0.05), of which 7 reached LOD scores >1.11 (nominal P < 0.01). The.strongest evidence for a type 2 diabetes locus was at marker D18S63 on chromosome 18p (LOD 2.3, F = 0.0006). This region was investigated further using additional markers. For one of these markers (D18S1105), we found a significant association with type 2 diabetes (odds ratio 6.7 [95% CI 1.5-30.7], P = 0.005 for the 97-bp allele, assuming a dominant model), which increased when limiting the analysis to patients with high BMI (12.25 [2.1-71], P = 0.003). A locus on chromosome 18p in patients with high BMI was suggested earlier by Parker et al. Our study is the first to confirm this locus.
引用
收藏
页码:3001 / 3004
页数:4
相关论文
共 16 条
  • [1] Merlin-rapid analysis of dense genetic maps using sparse gene flow trees
    Abecasis, GR
    Cherny, SS
    Cookson, WO
    Cardon, LR
    [J]. NATURE GENETICS, 2002, 30 (01) : 97 - 101
  • [2] Novel genes for familial combined hyperlipidemia
    Aouizerat, BE
    Allayee, H
    Bodnar, J
    Krass, KL
    Peltonen, L
    de Bruin, TWA
    Rotter, JI
    Lusis, AJ
    [J]. CURRENT OPINION IN LIPIDOLOGY, 1999, 10 (02) : 113 - 122
  • [3] Assessing the feasibility of linkage disequilibrium methods for mapping complex traits: An initial screen for bipolar disorder loci on chromosome 18
    Escamilla, MA
    McInnes, LA
    Spesny, M
    Reus, VI
    Service, SK
    Shimayoshi, N
    Tyler, DJ
    Silva, S
    Molina, J
    Gallegos, A
    Meza, L
    Cruz, ML
    Batki, S
    Vinogradov, S
    Neylan, T
    Nguyen, JB
    Fournier, E
    Araya, C
    Barondes, SH
    Leon, P
    Sandkuijl, LA
    Freimer, NB
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 64 (06) : 1670 - 1678
  • [4] *EXP COMM DIAGN CL, 1997, DIABETES CARE, V20, P183
  • [5] Molecular genetics of maturity-onset diabetes of the young
    Froguel, P
    Velho, G
    [J]. TRENDS IN ENDOCRINOLOGY AND METABOLISM, 1999, 10 (04) : 142 - 146
  • [6] A genome-wide search for human non-insulin dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2
    Hanis, CL
    Boerwinkle, E
    Chakraborty, R
    Ellsworth, DL
    Concannon, P
    Stirling, B
    Morrison, VA
    Wapelhorst, B
    Spielman, RS
    GogolinEwens, KJ
    Shephard, JM
    Williams, SR
    Risch, N
    Hinds, D
    Iwasaki, N
    Ogata, M
    Omori, Y
    Petzold, C
    Rietzsch, H
    Schroder, HE
    Schulze, J
    Cox, NJ
    Menzel, S
    Boriraj, VV
    Chen, X
    Lim, LR
    Lindner, T
    Mereu, LE
    Wang, YQ
    Xiang, K
    Yamagata, K
    Yang, Y
    Bell, GI
    [J]. NATURE GENETICS, 1996, 13 (02) : 161 - 166
  • [7] Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus
    Horikawa, Y
    Oda, N
    Cox, NJ
    Li, XQ
    Orho-Melander, M
    Hara, M
    Hinokio, Y
    Lindner, TH
    Mashima, H
    Schwarz, PEH
    del Bosque-Plata, L
    Horikawa, Y
    Oda, Y
    Yoshiuchi, I
    Colilla, S
    Polonsky, KS
    Wei, S
    Concannon, P
    Iwasaki, N
    Schulze, T
    Baier, LJ
    Bogardus, C
    Groop, L
    Boerwinkle, E
    Hanis, CL
    Bell, GI
    [J]. NATURE GENETICS, 2000, 26 (02) : 163 - 175
  • [8] Genomewide scan of multiple sclerosis in Finnish multiplex families
    Kuokkanen, S
    Gschwend, M
    Rioux, JD
    Daly, MJ
    Terwilliger, JD
    Tienari, PJ
    Wikström, J
    Palo, J
    Stein, LD
    Hudson, TJ
    Lander, ES
    Peltonen, L
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (06) : 1379 - 1387
  • [9] Genome scan for predisposing loci for distal interphalangeal joint osteoarthritis:: Evidence for a locus on 2q
    Leppävuori, J
    Kujala, U
    Kinnunen, J
    Kaprio, J
    Nissilä, M
    Heliövaara, M
    Klinger, N
    Partanen, J
    Terwilliger, JD
    Peltonen, L
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : 1060 - 1067
  • [10] Genetic approaches to the molecular understanding of type 2 diabetes
    McCarthy, MI
    Froguel, P
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2002, 283 (02): : E217 - E225