Abstract | INTRODUCTION: High indoxyl sulfate (IS) concentration is a serious problem for patients with CKD increasing the risk of cardiovascular diseases and CKD progression. Thus, the methods of decreasing the toxin concentrations are highly desired. The study aimed to discover the role of selected intestine-related factors on IS concentration. METHODS: We evaluated the impact of ABCG2 and ABCC2 polymorphisms influencing activity and protein intake by normalized protein catabolic rate. Additionally, we examined the relation of IS and uric acid (UA) that can share common elimination transporters. A monocentric, prospective, open cohort pilot study was performed on 108 patients undergoing dialysis treatment. RESULTS: The positive effect of residual diuresis on the reduction of IS levels was confirmed (p = 0.005). Also, an increase in IS depending on the dietary protein intake was confirmed (p = 0.040). No significant correlation between ABC gene polymorphisms was observed either, suggesting the negligible role of ABCG2 and ABCC2 in the elimination of IS in small bowel. The significant difference was observed for UA where ABCG2 421C>A (rs72552713) gene polymorphism was higher (505.3 μmol/L) in comparison with a wild-type genotype (360.5 μmol/L). CONCLUSION:
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Authors | Adéla Tomášová, Alena Tichá, Sylvie Dusilová Sulková, Roman Šafránek, Petr Moučka, Marcela Chmelařová, Ivana Baranová, Helena Párová, Zora Nývltová, Karolína Štochlová, Vladimír Palička, Ladislava Pavlíková, Zdeněk Zadák, Radomír Hyšpler |
Journal | Kidney & blood pressure research
(Kidney Blood Press Res)
Vol. 48
Issue 1
Pg. 28-34
( 2023)
ISSN: 1423-0143 [Electronic] Switzerland |
PMID | 36423594
(Publication Type: Journal Article)
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Copyright | © 2022 The Author(s). Published by S. Karger AG, Basel. |
Chemical References |
- Indican
- Uremic Toxins
- Dietary Proteins
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Topics |
- Humans
- Indican
- Uremic Toxins
- Renal Dialysis
(methods)
- Prospective Studies
- Dietary Proteins
- Intestinal Elimination
- Pilot Projects
- Renal Insufficiency, Chronic
(therapy, etiology)
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