Energy Homeostasis Gene Nucleotide Variants and Survival of Hemodialysis Patients-A Genetic Cohort Study

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Energy Homeostasis Gene Nucleotide Variants and Survival of Hemodialysis Patients-A Genetic Cohort Study. / Świderska, Monika Katarzyna; Mostowska, Adrianna; Skrypnik, Damian; Jagodziński, Paweł Piotr; Bogdański, Paweł; Grzegorzewska, Alicja Ewa.

In: J CLIN MED, Vol. 11, No. 18, 5477, 18.09.2022.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Świderska, MK, Mostowska, A, Skrypnik, D, Jagodziński, PP, Bogdański, P & Grzegorzewska, AE 2022, 'Energy Homeostasis Gene Nucleotide Variants and Survival of Hemodialysis Patients-A Genetic Cohort Study', J CLIN MED, vol. 11, no. 18, 5477. https://doi.org/10.3390/jcm11185477

APA

Świderska, M. K., Mostowska, A., Skrypnik, D., Jagodziński, P. P., Bogdański, P., & Grzegorzewska, A. E. (2022). Energy Homeostasis Gene Nucleotide Variants and Survival of Hemodialysis Patients-A Genetic Cohort Study. J CLIN MED, 11(18), [5477]. https://doi.org/10.3390/jcm11185477

Vancouver

Bibtex

@article{530fb64c8fd84698b7bdb85bc885cac0,
title = "Energy Homeostasis Gene Nucleotide Variants and Survival of Hemodialysis Patients-A Genetic Cohort Study",
abstract = "BACKGROUND: Patients undergoing hemodialysis (HD) therapy have an increased risk of death compared to the general population. We investigated whether selected single nucleotide variants (SNVs) involved in glucose and lipid metabolism are associated with mortality risk in HD patients.METHODS: The study included 805 HD patients tested for 11 SNVs in FOXO3, IGFBP3, FABP1, PCSK9, ANGPTL6, and DOCK6 using HRM analysis and TaqMan assays. FOXO3, IGFBP3, L-FABP, PCSK9, ANGPTL6, and ANGPTL8 plasma concentrations were measured by ELISA in 86 individuals. The Kaplan-Meier method and Cox proportional hazards models were used for survival analyses.RESULTS: We found out that the carriers of a C allele in ANGPTL6 rs8112063 had an increased risk of all-cause, cardiovascular, and cardiac mortality. In addition, the C allele of DOCK6 rs737337 was associated with all-cause and cardiac mortality. The G allele of DOCK6 rs17699089 was correlated with the mortality risk of patients initiating HD therapy. The T allele of FOXO3 rs4946936 was negatively associated with cardiac and cardiovascular mortality in HD patients. We observed no association between the tested proteins' circulating levels and the survival of HD patients.CONCLUSIONS: The ANGPTL6 rs8112063, FOXO3 rs4946936, DOCK6 rs737337, and rs17699089 nucleotide variants are predictors of survival in patients undergoing HD.",
author = "{\'S}widerska, {Monika Katarzyna} and Adrianna Mostowska and Damian Skrypnik and Jagodzi{\'n}ski, {Pawe{\l} Piotr} and Pawe{\l} Bogda{\'n}ski and Grzegorzewska, {Alicja Ewa}",
year = "2022",
month = sep,
day = "18",
doi = "10.3390/jcm11185477",
language = "English",
volume = "11",
journal = "J CLIN MED",
issn = "2077-0383",
publisher = "MDPI AG",
number = "18",

}

RIS

TY - JOUR

T1 - Energy Homeostasis Gene Nucleotide Variants and Survival of Hemodialysis Patients-A Genetic Cohort Study

AU - Świderska, Monika Katarzyna

AU - Mostowska, Adrianna

AU - Skrypnik, Damian

AU - Jagodziński, Paweł Piotr

AU - Bogdański, Paweł

AU - Grzegorzewska, Alicja Ewa

PY - 2022/9/18

Y1 - 2022/9/18

N2 - BACKGROUND: Patients undergoing hemodialysis (HD) therapy have an increased risk of death compared to the general population. We investigated whether selected single nucleotide variants (SNVs) involved in glucose and lipid metabolism are associated with mortality risk in HD patients.METHODS: The study included 805 HD patients tested for 11 SNVs in FOXO3, IGFBP3, FABP1, PCSK9, ANGPTL6, and DOCK6 using HRM analysis and TaqMan assays. FOXO3, IGFBP3, L-FABP, PCSK9, ANGPTL6, and ANGPTL8 plasma concentrations were measured by ELISA in 86 individuals. The Kaplan-Meier method and Cox proportional hazards models were used for survival analyses.RESULTS: We found out that the carriers of a C allele in ANGPTL6 rs8112063 had an increased risk of all-cause, cardiovascular, and cardiac mortality. In addition, the C allele of DOCK6 rs737337 was associated with all-cause and cardiac mortality. The G allele of DOCK6 rs17699089 was correlated with the mortality risk of patients initiating HD therapy. The T allele of FOXO3 rs4946936 was negatively associated with cardiac and cardiovascular mortality in HD patients. We observed no association between the tested proteins' circulating levels and the survival of HD patients.CONCLUSIONS: The ANGPTL6 rs8112063, FOXO3 rs4946936, DOCK6 rs737337, and rs17699089 nucleotide variants are predictors of survival in patients undergoing HD.

AB - BACKGROUND: Patients undergoing hemodialysis (HD) therapy have an increased risk of death compared to the general population. We investigated whether selected single nucleotide variants (SNVs) involved in glucose and lipid metabolism are associated with mortality risk in HD patients.METHODS: The study included 805 HD patients tested for 11 SNVs in FOXO3, IGFBP3, FABP1, PCSK9, ANGPTL6, and DOCK6 using HRM analysis and TaqMan assays. FOXO3, IGFBP3, L-FABP, PCSK9, ANGPTL6, and ANGPTL8 plasma concentrations were measured by ELISA in 86 individuals. The Kaplan-Meier method and Cox proportional hazards models were used for survival analyses.RESULTS: We found out that the carriers of a C allele in ANGPTL6 rs8112063 had an increased risk of all-cause, cardiovascular, and cardiac mortality. In addition, the C allele of DOCK6 rs737337 was associated with all-cause and cardiac mortality. The G allele of DOCK6 rs17699089 was correlated with the mortality risk of patients initiating HD therapy. The T allele of FOXO3 rs4946936 was negatively associated with cardiac and cardiovascular mortality in HD patients. We observed no association between the tested proteins' circulating levels and the survival of HD patients.CONCLUSIONS: The ANGPTL6 rs8112063, FOXO3 rs4946936, DOCK6 rs737337, and rs17699089 nucleotide variants are predictors of survival in patients undergoing HD.

U2 - 10.3390/jcm11185477

DO - 10.3390/jcm11185477

M3 - SCORING: Journal article

C2 - 36143124

VL - 11

JO - J CLIN MED

JF - J CLIN MED

SN - 2077-0383

IS - 18

M1 - 5477

ER -