Effect of sucroferric oxyhydroxide on gastrointestinal microbiome and uremic toxins in patients with chronic kidney disease undergoing hemodialysis.


Journal

Clinical and experimental nephrology
ISSN: 1437-7799
Titre abrégé: Clin Exp Nephrol
Pays: Japan
ID NLM: 9709923

Informations de publication

Date de publication:
Aug 2020
Historique:
received: 07 11 2019
accepted: 03 04 2020
pubmed: 15 4 2020
medline: 7 7 2021
entrez: 15 4 2020
Statut: ppublish

Résumé

In patients with chronic kidney disease (CKD), dysbiosis in the gastrointestinal microbiome is thought to be associated with increased production of uremic toxins, such as indoxyl sulfate (IS) and p-cresyl sulfate (PCS). Sucroferric oxyhydroxide (SFO), an iron-based phosphate binder, may affect the gastrointestinal microbiome and the production of uremic toxins. We aimed to examine whether SFO administration affected distribution of gastrointestinal microbiome and serum uremic toxin levels in CKD patients undergoing hemodialysis. In this single-center, open-label, interventional study, 18 maintenance hemodialysis patients with hyperphosphatemia were prescribed with SFO. We collected serum samples before and after 3 months of administration, and serum levels of IS and PCS were measured. A control group of 20 hemodialysis patients without SFO was evaluated. We evaluated gastrointestinal microbiome of patients pre- and post-SFO administration by 16S rDNA sequencing and bioinformatics analysis. Serum IS and PCS levels were significantly elevated after administration of SFO (IS before 2.52 ± 1.60 mg/dl vs. after 3.13 ± 1.51 mg/dl, P = 0.008; PCS before 2.32 ± 2.44 mg/dl vs. after 3.45 ± 2.11 mg/dl, P = 0.002), while serum IS and PCS levels did not change in the control group. Microbiome analysis in the SFO group showed no significant change in diversity and major components in phylum, class, order, family, gene, and species. Administration of SFO increased the serum levels of IS and PCS with no change of major components of gastrointestinal microbiome.

Sections du résumé

BACKGROUND BACKGROUND
In patients with chronic kidney disease (CKD), dysbiosis in the gastrointestinal microbiome is thought to be associated with increased production of uremic toxins, such as indoxyl sulfate (IS) and p-cresyl sulfate (PCS). Sucroferric oxyhydroxide (SFO), an iron-based phosphate binder, may affect the gastrointestinal microbiome and the production of uremic toxins. We aimed to examine whether SFO administration affected distribution of gastrointestinal microbiome and serum uremic toxin levels in CKD patients undergoing hemodialysis.
METHODS METHODS
In this single-center, open-label, interventional study, 18 maintenance hemodialysis patients with hyperphosphatemia were prescribed with SFO. We collected serum samples before and after 3 months of administration, and serum levels of IS and PCS were measured. A control group of 20 hemodialysis patients without SFO was evaluated. We evaluated gastrointestinal microbiome of patients pre- and post-SFO administration by 16S rDNA sequencing and bioinformatics analysis.
RESULTS RESULTS
Serum IS and PCS levels were significantly elevated after administration of SFO (IS before 2.52 ± 1.60 mg/dl vs. after 3.13 ± 1.51 mg/dl, P = 0.008; PCS before 2.32 ± 2.44 mg/dl vs. after 3.45 ± 2.11 mg/dl, P = 0.002), while serum IS and PCS levels did not change in the control group. Microbiome analysis in the SFO group showed no significant change in diversity and major components in phylum, class, order, family, gene, and species.
CONCLUSION CONCLUSIONS
Administration of SFO increased the serum levels of IS and PCS with no change of major components of gastrointestinal microbiome.

Identifiants

pubmed: 32285213
doi: 10.1007/s10157-020-01892-x
pii: 10.1007/s10157-020-01892-x
doi:

Substances chimiques

Cresols 0
Drug Combinations 0
Ferric Compounds 0
Sulfuric Acid Esters 0
sucroferric oxyhydroxide 0
4-cresol sulfate 56M34ZQY1S
Sucrose 57-50-1
Indican N187WK1Y1J

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

725-733

Subventions

Organisme : Kidney Foundation, Japan
ID : JKFB16-25

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Auteurs

Akira Iguchi (A)

Department of Internal Medicine, Nagaoka Red-Cross Hospital, 2-297-1 Sensyu, Nagaoka, Niigata, 940-2085, Japan. igucci4444@yahoo.co.jp.

Suguru Yamamoto (S)

Division of Blood Purification Therapy, Niigata University Medical and Dental Hospital, 1-757 Asahimachi-dori, Chuo-ku, Niigata, Niigata, 951-8510, Japan.

Akira Oda (A)

Department of Nephrology and Hypertension, Fukushima Medical University, 1 Hikariga-oka, Fukushima, Fukushima, 960-1295, Japan.

Kenichi Tanaka (K)

Department of Nephrology and Hypertension, Fukushima Medical University, 1 Hikariga-oka, Fukushima, Fukushima, 960-1295, Japan.

Junichiro James Kazama (JJ)

Department of Nephrology and Hypertension, Fukushima Medical University, 1 Hikariga-oka, Fukushima, Fukushima, 960-1295, Japan.

Takako Saeki (T)

Department of Internal Medicine, Nagaoka Red-Cross Hospital, 2-297-1 Sensyu, Nagaoka, Niigata, 940-2085, Japan.

Hajime Yamazaki (H)

Department of Internal Medicine, Nagaoka Red-Cross Hospital, 2-297-1 Sensyu, Nagaoka, Niigata, 940-2085, Japan.

Ken Ishioka (K)

Department of Microbiology, Fukushima Medical University, 1 Hikariga-oka, Fukushima, Fukushima, 960-1295, Japan.

Tatsuo Suzutani (T)

Department of Microbiology, Fukushima Medical University, 1 Hikariga-oka, Fukushima, Fukushima, 960-1295, Japan.

Ichiei Narita (I)

Division of Clinical Nephrology and Rheumatology, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachi-dori, Chuo-ku, Niigata, Niigata, 951-8510, Japan.

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Classifications MeSH