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Clinical Trial
. 2021 Apr 2;22(7):3732.
doi: 10.3390/ijms22073732.

The Effect of Far-Infrared Therapy on the Peritoneal Expression of Glucose Degradation Products in Diabetic Patients on Peritoneal Dialysis

Affiliations
Clinical Trial

The Effect of Far-Infrared Therapy on the Peritoneal Expression of Glucose Degradation Products in Diabetic Patients on Peritoneal Dialysis

Chia-Ning Chang et al. Int J Mol Sci. .

Abstract

Peritoneal dialysis (PD) is a treatment modality for end-stage renal disease (ESRD) patients. Dextrose is a common osmotic agent used in PD solutions and its absorption may exacerbate diabetes mellitus, a common complication of ESRD. PD solutions also contain glucose degradation products (GDPs) that may lead to encapsulating peritoneal sclerosis (EPS), a severe complication of PD. A previous study showed that far-infrared (FIR) therapy improved a patient's gastrointestinal symptoms due to EPS. Due to limited literature on the matter, this study aims to investigate dialysate GDPs and peritoneal function in diabetic patients on PD. Thirty-one PD patients were enrolled and underwent 40 min of FIR therapy twice daily for six months. We demonstrated the effect of FIR therapy on the following: (1) decrease of methylglyoxal (p = 0.02), furfural (p = 0.005), and 5-hydroxymethylfurfural (p = 0.03), (2) increase of D/D0 glucose ratio (p = 0.03), and (3) decrease of potassium levels (p = 0.008) in both DM and non-DM patients, as well as (4) maintenance and increase of peritoneal Kt/V in DM and non-DM patients, respectively (p = 0.03). FIR therapy is a non-invasive intervention that can decrease dialysate GDPs in PD patients by improving peritoneal transport rate and solute removal clearance, while also maintaining dialysis adequacy.

Keywords: diabetes mellitus; far-infrared therapy; glucose degradation products; peritoneal dialysis.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Flow chart of study participants to compare the effect of FIR therapy on DM and non-DM patients. Abbreviations: FIR: far-infrared; DM: diabetes mellitus; GDP: glucose degradation products.
Figure 2
Figure 2
Chromatograms of GDP-DNPH hydrazone derivatives using UPLC-PDA method. The x-axis represents retention time and the y-axis represents UV absorption. (A) GDP-DNPH standard solution at UV absorption 360 nm. (B) GDP-DNPH standard solution at UV absorption 430 nm. (C) GDP-DNPH in dialysate samples at UV absorption 360 nm. (D) GDP-DNPH in dialysate samples at UV absorption 430 nm. Abbreviations: GDP: glucose degradation products; DNPH: 2,4-dinitrophenylhydrazine; UPLC-PDA: ultra-performance liquid chromatography photodiode array; UV: ultraviolet.
Figure 2
Figure 2
Chromatograms of GDP-DNPH hydrazone derivatives using UPLC-PDA method. The x-axis represents retention time and the y-axis represents UV absorption. (A) GDP-DNPH standard solution at UV absorption 360 nm. (B) GDP-DNPH standard solution at UV absorption 430 nm. (C) GDP-DNPH in dialysate samples at UV absorption 360 nm. (D) GDP-DNPH in dialysate samples at UV absorption 430 nm. Abbreviations: GDP: glucose degradation products; DNPH: 2,4-dinitrophenylhydrazine; UPLC-PDA: ultra-performance liquid chromatography photodiode array; UV: ultraviolet.
Figure 3
Figure 3
FIR therapy set-up during a PD exchange. Abbreviation: FIR: far-infrared; PD: peritoneal dialysis.

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References

    1. Sowinski K.M., Churchwell M.D., Decker B.S. Hemodialysis and Peritoneal Dialysis. In: DiPiro J.T., Yee G.C., Posey L.M., Haines S.T., Nolin T.D., Ellingrod V., editors. Pharmacotherapy: A Pathophysiologic Approach. 11th ed. McGraw-Hill Education; New York, NY, USA: 2020.
    1. Mehrotra R. Metabolic Effects of Peritoneal Dialysis. In: Nissenson A.R., Fine R.N., editors. Handbook of Dialysis Therapy. 5th ed. Elsevier; New York, NY, USA: 2017. - DOI
    1. Haybrard J., Simon N., Danel C., Pinçon C., Barthélémy C., Tessier F.J., Décaudin B., Boulanger E., Odou P. Factors Generating Glucose Degradation Products In Sterile Glucose Solutions For Infusion: Statistical Relevance Determination of Their Impacts. Sci. Rep. 2017;7:11932. doi: 10.1038/s41598-017-12296-5. - DOI - PMC - PubMed
    1. Hodge J.E. Dehydrated Foods, Chemistry of Browning Reactions in Model Systems. J. Agric. Food Chem. 1953;1:928–943. doi: 10.1021/jf60015a004. - DOI
    1. Wieslander A.P., Nordin M.K., Kjellstrand P.T., Boberg U.C. Toxicity of Peritoneal Dialysis Fluids on Cultured Fibroblasts, L-929. Kidney Int. 1991;40:77–79. doi: 10.1038/ki.1991.182. - DOI - PubMed

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