Literature DB >> 10207273

Urinary indoxyl sulfate is a clinical factor that affects the progression of renal failure.

T Niwa1, I Aoyama, F Takayama, S Tsukushi, T Miyazaki, A Owada, T Shiigai.   

Abstract

We recently demonstrated that indoxyl sulfate is a stimulating factor for the progression of chronic renal failure (CRF). In this study we determined whether the urine or serum levels of indoxyl sulfate are related to the progression rate of CRF in undialyzed uremic patients. Fifty-five CRF patients with a serum creatinine of >2 mg/dl who had not been treated with an oral sorbent (AST-120) were randomly enrolled in the study. We measured the serum and urine levels of indoxyl sulfate, and estimated the recent progression rate of CRF as the slope of the reciprocal serum creatinine versus time (1/S-Cr-time) plot. The mean urinary amount of indoxyl sulfate in the patients was 60 mg/day. Those with indoxyl sulfate urine levels of >60 mg/day had a significantly faster progression rate of CRF than those with <60 mg/day. Especially, those patients with indoxyl sulfate urine levels of >90 mg/day had the highest CRF progression rate and those with indoxyl sulfate urine levels of <30 mg/day had the slowest CRF progression rate. Urinary indoxyl sulfate had a significantly negative correlation with the slope of the 1/S-Cr-time plot. However, the serum level of indoxyl sulfate or the ratio of serum indoxyl sulfate to creatinine was not significantly correlated with the slope of the 1/S-Cr-time plot. In conclusion, high urine levels of indoxyl sulfate are related with a rapid progression of CRF in undialyzed uremic patients. Thus, urinary indoxyl sulfate is one of the clinical factors that affect CRF progression.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10207273     DOI: 10.1159/000057433

Source DB:  PubMed          Journal:  Miner Electrolyte Metab        ISSN: 0378-0392


  6 in total

1.  Hepatic microsomal metabolism of indole to indoxyl, a precursor of indoxyl sulfate.

Authors:  E Banoglu; G G Jha; R S King
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2001 Oct-Dec       Impact factor: 2.441

2.  NMR-based metabolomics of urine for the atherosclerotic mouse model using apolipoprotein-E deficient mice.

Authors:  Gregory C Leo; Andrew L Darrow
Journal:  Magn Reson Chem       Date:  2009-12       Impact factor: 2.447

Review 3.  Uremic toxin and bone metabolism.

Authors:  Yoshiko Iwasaki; Hideyuki Yamato; Tomoko Nii-Kono; Ayako Fujieda; Motoyuki Uchida; Atsuko Hosokawa; Masaru Motojima; Masafumi Fukagawa
Journal:  J Bone Miner Metab       Date:  2006       Impact factor: 2.626

Review 4.  Non-systemic drugs: a critical review.

Authors:  Dominique Charmot
Journal:  Curr Pharm Des       Date:  2012       Impact factor: 3.116

5.  Meprin β metalloproteases associated with differential metabolite profiles in the plasma and urine of mice with type 1 diabetes and diabetic nephropathy.

Authors:  Jessica Gooding; Lei Cao; Courtney Whitaker; Jean-Marie Mwiza; Mizpha Fernander; Faihaa Ahmed; Zach Acuff; Susan McRitchie; Susan Sumner; Elimelda Moige Ongeri
Journal:  BMC Nephrol       Date:  2019-04-25       Impact factor: 2.388

6.  The Carcinogenome Project: In Vitro Gene Expression Profiling of Chemical Perturbations to Predict Long-Term Carcinogenicity.

Authors:  Amy Li; Xiaodong Lu; Ted Natoli; Joshua Bittker; Nisha S Sipes; Aravind Subramanian; Scott Auerbach; David H Sherr; Stefano Monti
Journal:  Environ Health Perspect       Date:  2019-04       Impact factor: 9.031

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.