Value of multilocus genetic risk score for atrial fibrillation in end-stage kidney disease patients in a Polish population

被引:4
作者
Saracyn, Marek [1 ,2 ]
Kisiel, Bartlomiej [3 ]
Bachta, Artur [3 ]
Franaszczyk, Maria [4 ]
Brodowska-Kania, Dorota [1 ]
Zmudzki, Wawrzyniec [1 ]
Szymanski, Konrad [5 ]
Sokalski, Antoni [6 ]
Klatko, Wieslaw [7 ]
Stopinski, Marek [8 ]
Grochowski, Janusz [9 ]
Paplinski, Marek [10 ]
Gozdzik, Zdzislaw [11 ]
Niemczyk, Longin [12 ]
Bober, Barbara [2 ]
Kolodziej, Maciej [2 ]
Tlustochowicz, Witold [3 ]
Kaminski, Grzegorz [2 ]
Ploski, Rafal [5 ]
Niemczyk, Stanislaw [1 ]
机构
[1] Mil Inst Med, Dept Internal Dis Nephrol & Dialysis, Szaserow 128, PL-04141 Warsaw, Poland
[2] Mil Inst Med, Dept Endocrinol & Isotope Therapy, Szaserow 128, PL-04141 Warsaw, Poland
[3] Mil Inst Med, Dept Internal Dis & Rheumatol, Szaserow 128, PL-04141 Warsaw, Poland
[4] Inst Cardiol, Dept Med Biol, Mol Biol Lab, Alpejska 42, PL-04628 Warsaw, Poland
[5] Med Univ Warsaw, Dept Med Genet, Pawinskiego 3c, PL-02106 Warsaw, Poland
[6] Hosp Radom, Nephrol & Dialysis Unit, Lekarska 4, PL-26610 Radom, Poland
[7] Publ Hosp Ciechanow, Dept Nephrol, Powstancow Wielkopolskich 2, PL-06400 Ciechanow, Poland
[8] West Hosp, Daleka 11, PL-05825 Grodzisk Mazowiecki, Poland
[9] Hosp Makow Mazowiecki, Witosa 2, PL-06200 Makow Mazowiecki, Poland
[10] Hosp Sokolow Podlaski, Ks Bosko 5, PL-08300 Sokolow Podlaski, Poland
[11] Hosp Skierniewice, Rybickiego 1, PL-96100 Skierniewice, Poland
[12] Warsaw Med Univ, Dept Nephrol Dialysis & Internal Dis, Warsaw, Poland
关键词
FAMILIAL AGGREGATION; COMMON VARIANTS; RARE VARIANTS; LIFETIME RISK; PREVALENCE; ASSOCIATION; POLYMORPHISM; CHANNELS; MARKERS; PERMEABILITY;
D O I
10.1038/s41598-018-27382-5
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Genetic factors play a key role in the pathogenesis of atrial fibrillation (AF). We would like to establish an association between previously described single-nucleotide polymorphisms (SNPs) and AF in haemodialysed patients with end-stage kidney disease (ESKD HD) as well as to assess the cumulative effect of all genotyped SNPs on AF risk. Sixteen SNPs were genotyped in 113 patients with AF-ESKD-HD and in 157 controls: without AF (NAF) and with ESKD-HD. The distribution of the risk alleles was compared in both groups and between different sub-phenotypes. The multilocus genetic risk score (GRS) was calculated to estimate the cumulative risk conferred by all SNPs. Several loci showed a trend toward an association with permanent AF (perm-AF): CAV1, Cx40 and PITX2. However, GRS was significantly higher in the AF and perm-AF groups, as compared to NAF. Three of the tested variables were independently associated with AF: male sex, history of myocardial infarction (MI) and GRS. The GRS, which combined 13 previously described SNPs, showed a significant and independent association with AF in a Polish population of patients with ESKD-HD and concomitant AF. Further studies on larger groups of patients are needed to confirm the associations.
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页数:8
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