Abstract

Patients with chronic kidney disease have a greater risk of cognitive impairment. Cerebral uremic solute accumulation causes uremic encephalopathy; however, the association of protein-bound uremic toxins on cognitive function remains unclear. The present study aimed to investigate the association of two protein-bound uremic toxins, namely indoxyl sulfate (IS) and p-cresyl sulfate (PCS), on cognitive function in patients receiving hemodialysis (HD) for at least 90 days. Circulating free form IS and PCS were quantified by liquid chromatography/mass spectrometry. Mini-Mental State Examination (MMSE) and Cognitive Abilities Screening Instrument (CASI) were used to evaluate cognitive function. In total, 260 HD patients were recruited with a mean age of 58.1 ± 11.3 years, of which, 53.8% were men, 40% had diabetes, and 75.4% had hypertension. The analysis revealed that both free IS and free PCS were negatively associated with the CASI score and MMSE. After controlling for confounders, circulating free IS levels persisted to be negatively associated with MMSE scores [β = −0.62, 95% confidence interval (CI): −1.16 to −0.08] and CASI scores (β = −1.97, 95% CI: −3.78 to −0.16), mainly in the CASI domains of long-term memory, mental manipulation, language ability, and spatial construction. However, there was no correlation between free PCS and total MMSE or total CASI scores after controlling for confounders. In conclusion, circulating free form IS, but not PCS is associated with lower cognitive function test scores in HD patients. Thus, a further study is needed to evaluate whether a decrease in free IS levels can slow down cognitive decline in HD patients.

Highlights

  • Patients with chronic kidney disease have a greater risk of cognitive impairment

  • Peritoneal dialysis clearance of protein-bound uremic toxins is lower than the clearance of small solutes[9,10,11,12], with residual renal function accounting for most protein-bound uremic toxin removal in peritoneal dialysis patients[9,10]

  • Indoxyl sulfate (IS) and p-cresyl sulfate (PCS), known as protein-bound uremic toxins, are difficult to eliminate via dialysis because they tightly bind to albumin in the blood; the indoxyl sulfate (IS) level in brain and plasma in patients with chronic kidney disease (CKD) is high compared with control subjects[13]

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Summary

Introduction

Cerebral uremic solute accumulation causes uremic encephalopathy; the association of protein-bound uremic toxins on cognitive function remains unclear. The present study aimed to investigate the association of two protein-bound uremic toxins, namely indoxyl sulfate (IS) and p-cresyl sulfate (PCS), on cognitive function in patients receiving hemodialysis (HD) for at least 90 days. Previous studies have addressed the role of cerebrovascular disease, anemia, and hyperparathyroidism in dementia development in patients with CKD or ESKD4,5, but the association of uremic toxins on cognitive function remains unclear. Indoxyl sulfate (IS) and p-cresyl sulfate (PCS), known as protein-bound uremic toxins, are difficult to eliminate via dialysis because they tightly bind to albumin in the blood; the IS level in brain and plasma in patients with CKD is high compared with control subjects[13]. We investigated the association of IS and PCS with cognitive function in HD patients

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