How renal toxins respond to renal function deterioration and oral toxic adsorbent in pH‐controlled releasing capsule

Author:

Liu Wen‐Sheng12345,Liang Shih‐Shin67,Cheng Mei‐Mei8,Wu Ming‐Tsan9,Li Szu‐Yuan210,Cheng Tien‐Tien4,Liu Tsung‐Yun4ORCID,Tsai Ching‐Yao111213,Lai Yen‐Ting141516,Lin Chien‐Hung2317,Wang Hsiang‐Tsui18,Tsou Han‐Hsing419ORCID

Affiliation:

1. Division of Nephrology, Department of Medicine Taipei City Hospital Taipei Taiwan

2. School of Medicine National Yang Ming Chiao Tung University Hsinchu Taiwan

3. College of Science and Engineering Fu Jen Catholic University New Taipei City Taiwan

4. Institute of Food Safety and Health Risk Assessment National Yang Ming Chiao Tung University Hsinchu Taiwan

5. Department of Special Education University of Taipei Taipei Taiwan

6. Institute of Biomedical Science, College of Medicine National Sun Yat‐sen University Kaohsiung Taiwan

7. Department of Biotechnology College of Life Science, Kaohsiung Medical University Kaohsiung Taiwan

8. Division of nephrology, Department of internal medicine West Garden Hospital Taipei Taiwan

9. Department of internal medicine Fu‐Ling clinic New Taipei City Taiwan

10. Division of Nephrology, and Department of Medicine Taipei Veterans General Hospital Taipei Taiwan

11. Institute of Public Health, Department of Public Health, College of Medicine National Yang Ming Chiao Tung University Hsinchu Taiwan

12. Department of Ophthalmology Taipei City Hospital Taipei Taiwan

13. Department of Business Administration Fu Jen Catholic University New Taipei City Taiwan

14. Department of Physical Medicine and Rehabilitation National Taiwan University College of Medicine Taipei Taiwan

15. Department of Physical Medicine and Rehabilitation National Taiwan University Hospital Hsin‐Chu Branch Hsinchu Taiwan

16. Department of Nursing College of Medical Technology and Nursing, Yuanpei University of Medical Technology Hsinchu Taiwan

17. Division of Pediatric Immunology and Nephrology, Department of Pediatrics Taipei Veterans General Hospital Taipei Taiwan

18. Department of Pharmacology National Yang Ming Chiao Tung University Hsinchu Taiwan

19. Kim Forest Enterprise Co., Ltd. New Taipei City Taiwan

Abstract

AbstractThe number of patients with chronic kidney disease (CKD) is increasing. Oral toxin adsorbents may provide some value. Several uremic toxins, including indoxyl sulfate (IS), p‐cresol (PCS), acrolein, per‐ and poly‐fluoroalkyl substances (PFAS), and inflammation markers (interleukin 6 [IL‐6] and tumor necrosis factor [TNF]‐alpha) have been shown to be related to CKD progression. A total of 81 patients taking oral activated charcoal toxin adsorbents (AC‐134), which were embedded in capsules that dissolved in the terminal ileum, three times a day for 1 month, were recruited. The renal function, hemoglobulin (Hb), inflammation markers, three PFAS (PFOA, PFOS, and PFNA), and acrolein were quantified. Compared with the baseline, an improved glomerular filtration rate (GFR) and significantly lower acrolein were noted. Furthermore, the CKD stage 4 and 5 group had significantly higher concentrations of IS, PCS, IL‐6, and TNF but lower levels of Hb and PFAS compared with the CKD Stage 3 group at baseline and after the intervention. Hb was increased only in the CKD Stage 3 group after the trial (p = .032). Acrolein did not differ between the different CKD stage groups. Patients with improved GFR (responders) (about 77%) and nonresponders had similar baseline GFR. Responders had higher acrolein and PFOA levels throughout the study and a more significant reduction in acrolein, indicating a better digestion function. Both the higher PFOA and lower acrolein may be related to improved eGFR (and possibly to improvements in proteinuria, which we did not measure. Proteinuria is associated with PFAS loss in the urine), AC‐134 showed the potential to improve the GFR and decrease acrolein, which might better indicate renal function change. Future studies are needed with longer follow‐ups.

Funder

Taipei City Hospital

Publisher

Wiley

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