2021
DOI: 10.1016/j.kint.2021.05.037
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A genome-wide association study suggests correlations of common genetic variants with peritoneal solute transfer rates in patients with kidney failure receiving peritoneal dialysis

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Cited by 16 publications
(16 citation statements)
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“…And this is exactly what a recent study by Mehrotra et al investigated [10]. The authors performed a GWAS in a cohort of over 2000 European PD patients to search for associations between any of > 2.3 million genetic variants and PSTR.…”
Section: Predicting Pore Performancementioning
confidence: 63%
See 1 more Smart Citation
“…And this is exactly what a recent study by Mehrotra et al investigated [10]. The authors performed a GWAS in a cohort of over 2000 European PD patients to search for associations between any of > 2.3 million genetic variants and PSTR.…”
Section: Predicting Pore Performancementioning
confidence: 63%
“…Even the genetically most advantageous "Ubermembrane" will not transport sufficiently, if scarred by infections. As discussed above, Mehrotra et al calculate that roughly one fifth of the variability in PSTR is inherited, yet that this is driven by numerous variants, each with rather small effects [10]. In this regard, it is unfortunate that the study on UF only assessed variants in the candidate gene AQP1, rather than performing a GWAS.…”
Section: Discussionmentioning
confidence: 99%
“…Among patients starting treatment with peritoneal dialysis, there is a broad variability in water and solute transport across the peritoneal membrane, which influences dialysis prescriptions and outcomes [ 37 , 38 , 39 , 40 ]. A recent genome-wide study showed that the peritoneal small-solute transport rate was associated with a polygenic risk score and with 17% heritability; these findings support a genetic influence on solute transport across the peritoneal membrane [ 41 ]. It was recently demonstrated that a common promoter variant rs2075574 in AQP1 was associated with decreased ultrafiltration and with an increased risk of death or technique failure among peritoneal dialysis patients [ 42 ].…”
Section: Molecular and Genetic Studiesmentioning
confidence: 98%
“…It was recently demonstrated that a common promoter variant rs2075574 in AQP1 was associated with decreased ultrafiltration and with an increased risk of death or technique failure among peritoneal dialysis patients [ 42 ]. The translation of genetic and molecular insights to precision medicine would help to understand better the dialysis process and to improve dialysis care [ 41 , 43 ].…”
Section: Molecular and Genetic Studiesmentioning
confidence: 99%
“…Mehrotra et al [17] collected blood samples from 2850 PD patients in different regions for Genome-wide association study (GWAS) analysis, and found that genetic variation was an important factor influencing inter-individual variation of PSTR. Morelle et al [18] performed Aquaporin 1 (AQP1) genotyping in 1851 PD patients and found that the AQP1 rs2075574 genotype was associated with ultrafiltration and prognosis in PD patients: T allele of rs2075574 carriers had a lower mean net ultrafiltration than C allele carriers and had a higher risk of all-cause mortality and technique failure. Further basic studies confirmed that this locus was associated with AQP1 promoter activity and AQP1 expression.…”
mentioning
confidence: 99%