Kidney Diseases
|
0.100 |
GeneticVariation
|
group |
BEFREE |
The Apolipoprotein L1 (APOL1) risk variants G1 and G2 are associated with high rates of kidney disease in African Americans in genetic studies.
|
31611067 |
2019 |
Kidney Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
No evidence for association between APOL1 kidney disease risk alleles and Human African Trypanosomiasis in two Ugandan populations.
|
29470556 |
2018 |
Kidney Diseases
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Some of the most striking findings relate to APOL1 genetic variants, seen exclusively in individuals of sub-Saharan African descent, that create a predisposition to particular renal disorders, including focal segmental glomerulosclerosis and arterionephrosclerosis.
|
30082052 |
2018 |
Kidney Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
Since HIVAN has the strongest association with APOL1 genotype of any of the APOL1-associated nephropathies, studies to determine the mechanisms by which HIV and APOL1 risk variants together promote kidney injury hold great promise to improve our understanding of the pathogenesis of APOL1-mediated kidney diseases.
|
29930940 |
2018 |
Kidney Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
Transcript analysis of mouse kidney disease models, including folic-acid (FA)-induced nephropathy, unilateral ureteral obstruction (UUO), or apolipoprotein L1 (APOL1)-associated kidney disease, indicated that Jag1 and Notch2 levels were higher in all analyzed kidney fibrosis models.
|
30226866 |
2018 |
Kidney Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
Detection of APOL1 associations with kidney diseases and delineation of injury pathways brings hope for effective treatment for these kidney diseases.
|
30343724 |
2018 |
Kidney Diseases
|
0.100 |
GeneticVariation
|
group |
BEFREE |
APOL1 genotypes are associated with kidney diseases in African American individuals and may influence cardiovascular disease and mortality risk, but findings have been inconsistent.
|
29971324 |
2018 |
Kidney Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
Thus, although variants with small individual effects cannot be ruled out and are likely to exist, our results suggest that APOL1-environment interactions may be of greater clinical importance in triggering nephropathy in African Americans than APOL1 interactions with other single nucleotide polymorphisms.
|
29885931 |
2018 |
Kidney Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
An evolving understanding of the pathogenesis of APOL1-mediated kidney damage may aid in personalized medicine approaches to APOL1 attributable kidney disease.
|
29406442 |
2018 |
Kidney Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
Expanding the spectrum of APOL1-related renal disease: de novo collapsing glomerulopathy following kidney transplant.
|
30466562 |
2018 |
Kidney Diseases
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Apolipoprotein L1 ( ApoL1) genetic variants are strongly associated with kidney diseases.
|
29357411 |
2018 |
Kidney Diseases
|
0.100 |
GeneticVariation
|
group |
BEFREE |
The Natural History of APOL1-Associated Nephropathy Study (NHAANS) reported that urine JC polyomavirus (JCPyV) associated with a lower risk of APOL1-associated nephropathy in African Americans.
|
29420808 |
2018 |
Kidney Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
In the era of precision medicine, these findings should translate into improved longitudinal risk assessment for this high-risk population and might also provide additional insights regarding sites and mechanisms of APOL1 nephropathy.
|
29792270 |
2018 |
Kidney Diseases
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Genetic variants in apolipoprotein L1 (APOL1) account for much of the increased risk for kidney disease in blacks.
|
30173819 |
2018 |
Kidney Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
APOL1 nephropathy risk variants do not associate with subclinical atherosclerosis or left ventricular mass in middle-aged black adults.
|
29042080 |
2018 |
Kidney Diseases
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Further evidence supports risk modifiers in APOL1-associated nephropathy; some studies demonstrate that heterozygotes possess excess risk for ESKD or show earlier age at ESKD, relative to those with zero risk alleles.
|
28339911 |
2018 |
Kidney Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
In this review, we will describe the intriguing interplay between microbiology, genetics, and kidney disease as revealed in APOL1-associated kidney disease, discuss APOL1-induced cytotoxicity and its therapeutic implications.
|
29886044 |
2018 |
Kidney Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
Apolipoprotein L1 nephropathies: 2017 in review.
|
29389775 |
2018 |
Kidney Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
Here, we discuss the possibility that abnormal efflux of cellular potassium or other cations may be relevant to the pathogenesis of APOL1 nephropathy.
|
29110762 |
2017 |
Kidney Diseases
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Genome-wide association studies have identified a substantial signal at 22q13, now assigned to variation at apolipoprotein L1 (APOL1), which has associated with progressive nondiabetic nephropathy, cardiovascular disease, and many immune-associated renal diseases, including lupus nephritis.
|
28265848 |
2017 |
Kidney Diseases
|
0.100 |
GeneticVariation
|
group |
BEFREE |
For example, the G1 and G2 variants of the APOL1 gene supporting control of Trypanosoma infection come with the trade-off that they promote the progression of kidney disease.
|
28481398 |
2017 |
Kidney Diseases
|
0.100 |
GeneticVariation
|
group |
BEFREE |
In populations of African ancestry, two <i>apolipoprotein-L1 (APOL1</i>) variants with a recessive kidney disease risk, named G1 and G2, occur at high frequency.
|
28537557 |
2017 |
Kidney Diseases
|
0.100 |
Biomarker
|
group |
BEFREE |
Uncontrolled or poorly controlled human immunodeficiency virus (HIV) infection is the most potent susceptibility factor for APOL1 nephropathy that has been identified to date.
|
29110758 |
2017 |
Kidney Diseases
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Variants of the APOL1 gene, found primarily in individuals of African descent, are associated with various forms of kidney disease and kidney disease progression.
|
29110759 |
2017 |
Kidney Diseases
|
0.100 |
GeneticVariation
|
group |
BEFREE |
The presence of two APOL1 renal risk variants markedly increases an individual's risk for kidney disease.
|
29110760 |
2017 |