Detail
Článek
Článek online
FT
Medvik - BMČ
  • Je něco špatně v tomto záznamu ?

Genetic risk factors for diabetic nephropathy on chromosomes 6p and 7q identified by the set-association approach

K Kankova, A Stejskalova, L Pacal, S Tschoplova, M Hertlova, D Krusova, L Izakovicova-Holla, M Beranek, A Vasku, S Barral, J Ott

. 2007 ; 50 (5) : 990-999.

Jazyk angličtina Země Německo

Perzistentní odkaz   https://www.medvik.cz/link/bmc10010736
E-zdroje Online

NLK SpringerLink Journals od 1997-01-01 do 2012-08-31
ProQuest Central od 1999-01-01 do Před 1 rokem
Medline Complete (EBSCOhost) od 2000-01-01 do Před 1 rokem
Health & Medicine (ProQuest) od 1999-01-01 do Před 1 rokem
Public Health Database (ProQuest) od 1999-01-01 do Před 1 rokem

AIMS/HYPOTHESIS: In the present study we investigated potential associations of a set of 45 single nucleotide polymorphisms (SNP) in 20 candidate genes on eight chromosomes with diabetic nephropathy (DN) in type 2 diabetes mellitus. We aimed to compare two methodological approaches suitable for analysing susceptibility to complex traits: single- and multi-locus analyses. MATERIALS AND METHODS: The study comprised a total of 647 subjects in one of three groups: diabetes with or without DN, or no diabetes. Genotypes were detected by PCR-based methodology (PCR only, PCR plus RFLP, or allele-specific PCR). Haplotypes were inferred in silico. Set association (tested using SUMSTAT software) was used for multilocus analysis. RESULTS: After correction for multiple comparisons, only one SNP, in the gene encoding the receptor of advanced glycation end products, AGER 2184A/G (gene symbol formerly known as RAGE) showed a significant association with DN (p = 0.0006) in single-locus analysis. In multi-locus analysis, six SNPs exhibited a significant association with DN: four SNPs on chromosome 6p (AGER 2184A/G, LTA 252A/G, EDN1 8002G/A and AGER -429T/C) and two SNPs on chromosome 7q (NOS3 774C/T and NOS3 E298D), omnibus p = 0.033. Haplotype analysis revealed significant differences between DN and control groups in haplotype frequencies on chromosome 6 (p = 0.0002); however, there were no significant difference in the frequencies of the NOS3 haplotypes on chromosome 7. Logistic regression analysis identified SNPs AGER 2184A/G and NOS3 774C/T, together with diabetes duration and HbA1c, as significant predictors of DN. Testing for interactions between SNPs on chromosomes 6 and 7 did not provide significant evidence for epistatic interaction. CONCLUSIONS/INTERPRETATION: Using the set-association approach we identified significant associations of several SNPs on chromosomes 6 and 7 with DN. The single- and multi-locus analyses represent complementary methods.

000      
03852naa 2200529 a 4500
001      
bmc10010736
003      
CZ-PrNML
005      
20121030121749.0
008      
100505s2007 gw e eng||
009      
AR
040    __
$a ABA008 $b cze $c ABA008 $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a gw
100    1_
$a Kaňková, Kateřina, $d 1971- $7 mzk2003190820
245    10
$a Genetic risk factors for diabetic nephropathy on chromosomes 6p and 7q identified by the set-association approach / $c K Kankova, A Stejskalova, L Pacal, S Tschoplova, M Hertlova, D Krusova, L Izakovicova-Holla, M Beranek, A Vasku, S Barral, J Ott
314    __
$a Faculty of Medicine, Department of Pathophysiology, Masaryk University Brno, Komenskeho nam. 2, 662 43 Brno, Czech Republic. kankov@med.muni.cz
520    9_
$a AIMS/HYPOTHESIS: In the present study we investigated potential associations of a set of 45 single nucleotide polymorphisms (SNP) in 20 candidate genes on eight chromosomes with diabetic nephropathy (DN) in type 2 diabetes mellitus. We aimed to compare two methodological approaches suitable for analysing susceptibility to complex traits: single- and multi-locus analyses. MATERIALS AND METHODS: The study comprised a total of 647 subjects in one of three groups: diabetes with or without DN, or no diabetes. Genotypes were detected by PCR-based methodology (PCR only, PCR plus RFLP, or allele-specific PCR). Haplotypes were inferred in silico. Set association (tested using SUMSTAT software) was used for multilocus analysis. RESULTS: After correction for multiple comparisons, only one SNP, in the gene encoding the receptor of advanced glycation end products, AGER 2184A/G (gene symbol formerly known as RAGE) showed a significant association with DN (p = 0.0006) in single-locus analysis. In multi-locus analysis, six SNPs exhibited a significant association with DN: four SNPs on chromosome 6p (AGER 2184A/G, LTA 252A/G, EDN1 8002G/A and AGER -429T/C) and two SNPs on chromosome 7q (NOS3 774C/T and NOS3 E298D), omnibus p = 0.033. Haplotype analysis revealed significant differences between DN and control groups in haplotype frequencies on chromosome 6 (p = 0.0002); however, there were no significant difference in the frequencies of the NOS3 haplotypes on chromosome 7. Logistic regression analysis identified SNPs AGER 2184A/G and NOS3 774C/T, together with diabetes duration and HbA1c, as significant predictors of DN. Testing for interactions between SNPs on chromosomes 6 and 7 did not provide significant evidence for epistatic interaction. CONCLUSIONS/INTERPRETATION: Using the set-association approach we identified significant associations of several SNPs on chromosomes 6 and 7 with DN. The single- and multi-locus analyses represent complementary methods.
650    _2
$a senioři $7 D000368
650    _2
$a Bayesova věta $7 D001499
650    _2
$a mapování chromozomů $7 D002874
650    _2
$a lidské chromozomy, pár 6 $7 D002896
650    _2
$a lidské chromozomy, pár 7 $7 D002897
650    _2
$a diabetické nefropatie $x epidemiologie $x genetika $7 D003928
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a genotyp $7 D005838
650    _2
$a lidé $7 D006801
650    _2
$a mužské pohlaví $7 D008297
650    _2
$a lidé středního věku $7 D008875
650    _2
$a polymerázová řetězová reakce $7 D016133
650    _2
$a polymorfismus genetický $7 D011110
650    _2
$a referenční hodnoty $7 D012016
650    _2
$a rizikové faktory $7 D012307
650    _2
$a financování organizované $7 D005381
651    _2
$a Česká republika $7 D018153
700    1_
$a Stejskalová, Andrea $7 xx0097181
700    1_
$a Pácal, Lukáš $7 xx0084072
700    1_
$a Tschöplová, Svatava. $7 _AN033174
700    1_
$a Hertlová, Miluše, $d 1946- $7 xx0073987
700    1_
$a Krusová, Darja $7 xx0143317
700    1_
$a Izakovičová Hollá, Lydie, $d 1971- $7 nlk19990074300
700    1_
$a Beránek, Michal. $7 xx0193695
700    1_
$a Vašků, Anna, $d 1954- $7 mzk2006356130
700    1_
$a Barral, Sandra
700    1_
$a Ott, Jurg
773    0_
$t Diabetologia $w MED00001391 $g Roč. 50, č. 5 (2007), s. 990-999 $x 0012-186X
910    __
$a ABA008 $b x $y 8
990    __
$a 20100521124211 $b ABA008
991    __
$a 20121030121752 $b ABA008
999    __
$a ok $b bmc $g 724593 $s 587737
BAS    __
$a 3
BMC    __
$a 2007 $b 50 $c 5 $d 990-999 $i 0012-186X $m Diabetologia (Berlin) $n Diabetologia $x MED00001391
LZP    __
$a 2010-B2/dkme

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...