Lack of Association of the APOL1 G3 Haplotype in African Americans with ESRD
Copyright © 2015 by the American Society of Nephrology..
Apolipoprotein L1 gene (APOL1) G1 and G2 variants are strongly associated with progressive nondiabetic nephropathy in populations with recent African ancestry. Selection for these variants occurred as a result of protection from human African trypanosomiasis (HAT). Resequencing of this region in 10 genetically and geographically distinct African populations residing in HAT endemic regions identified eight single nucleotide polymorphisms (SNPs) in strong linkage disequilibrium and comprising a novel G3 haplotype. To determine whether the APOL1 G3 haplotype was associated with nephropathy, G1, G2, and G3 SNPs and 70 ancestry informative markers spanning the genome were genotyped in 937 African Americans with nondiabetic ESRD, 965 African Americans with type 2 diabetes-associated ESRD, and 1029 non-nephropathy controls. In analyses adjusting for age, sex, APOL1 G1/G2 risk (recessive), and global African ancestry, the G3 haplotype was not significantly associated with ESRD (P=0.05 for nondiabetic ESRD, P=0.57 for diabetes-associated ESRD, and P=0.27 for all-cause ESRD). We conclude that variation in APOL1 G3 makes a nominal, if any, contribution to ESRD in African Americans; G1 and G2 variants explain the vast majority of nondiabetic nephropathy susceptibility.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2015 |
---|---|
Erschienen: |
2015 |
Enthalten in: |
Zur Gesamtaufnahme - volume:26 |
---|---|
Enthalten in: |
Journal of the American Society of Nephrology : JASN - 26(2015), 5 vom: 01. Mai, Seite 1021-5 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Palmer, Nicholette D [VerfasserIn] |
---|
Links: |
---|
Themen: |
APOL1 protein, human |
---|
Anmerkungen: |
Date Completed 20.07.2015 Date Revised 07.12.2022 published: Print-Electronic Citation Status MEDLINE |
---|
doi: |
10.1681/ASN.2014050444 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM242162932 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM242162932 | ||
003 | DE-627 | ||
005 | 20231224125819.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231224s2015 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1681/ASN.2014050444 |2 doi | |
028 | 5 | 2 | |a pubmed24n0807.xml |
035 | |a (DE-627)NLM242162932 | ||
035 | |a (NLM)25249559 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Palmer, Nicholette D |e verfasserin |4 aut | |
245 | 1 | 0 | |a Lack of Association of the APOL1 G3 Haplotype in African Americans with ESRD |
264 | 1 | |c 2015 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 20.07.2015 | ||
500 | |a Date Revised 07.12.2022 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Copyright © 2015 by the American Society of Nephrology. | ||
520 | |a Apolipoprotein L1 gene (APOL1) G1 and G2 variants are strongly associated with progressive nondiabetic nephropathy in populations with recent African ancestry. Selection for these variants occurred as a result of protection from human African trypanosomiasis (HAT). Resequencing of this region in 10 genetically and geographically distinct African populations residing in HAT endemic regions identified eight single nucleotide polymorphisms (SNPs) in strong linkage disequilibrium and comprising a novel G3 haplotype. To determine whether the APOL1 G3 haplotype was associated with nephropathy, G1, G2, and G3 SNPs and 70 ancestry informative markers spanning the genome were genotyped in 937 African Americans with nondiabetic ESRD, 965 African Americans with type 2 diabetes-associated ESRD, and 1029 non-nephropathy controls. In analyses adjusting for age, sex, APOL1 G1/G2 risk (recessive), and global African ancestry, the G3 haplotype was not significantly associated with ESRD (P=0.05 for nondiabetic ESRD, P=0.57 for diabetes-associated ESRD, and P=0.27 for all-cause ESRD). We conclude that variation in APOL1 G3 makes a nominal, if any, contribution to ESRD in African Americans; G1 and G2 variants explain the vast majority of nondiabetic nephropathy susceptibility | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, N.I.H., Extramural | |
650 | 4 | |a FSGS | |
650 | 4 | |a development | |
650 | 4 | |a end stage kidney disease | |
650 | 4 | |a genetics | |
650 | 7 | |a APOL1 protein, human |2 NLM | |
650 | 7 | |a Apolipoprotein L1 |2 NLM | |
650 | 7 | |a Apolipoproteins |2 NLM | |
650 | 7 | |a Lipoproteins, HDL |2 NLM | |
700 | 1 | |a Ng, Maggie C Y |e verfasserin |4 aut | |
700 | 1 | |a Langefeld, Carl D |e verfasserin |4 aut | |
700 | 1 | |a Divers, Jasmin |e verfasserin |4 aut | |
700 | 1 | |a Lea, Janice P |e verfasserin |4 aut | |
700 | 1 | |a Okusa, Mark D |e verfasserin |4 aut | |
700 | 1 | |a Kimberly, Robert P |e verfasserin |4 aut | |
700 | 1 | |a Bowden, Donald W |e verfasserin |4 aut | |
700 | 1 | |a Freedman, Barry I |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Journal of the American Society of Nephrology : JASN |d 1990 |g 26(2015), 5 vom: 01. Mai, Seite 1021-5 |w (DE-627)NLM012606502 |x 1533-3450 |7 nnns |
773 | 1 | 8 | |g volume:26 |g year:2015 |g number:5 |g day:01 |g month:05 |g pages:1021-5 |
856 | 4 | 0 | |u http://dx.doi.org/10.1681/ASN.2014050444 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 26 |j 2015 |e 5 |b 01 |c 05 |h 1021-5 |