Kinetics of Glucoregulatory Peptide Hormones during Hemodialysis with Cellulose Triacetate and Polysulfone Dialyzers in Patients with Diabetes and End-Stage Kidney Disease
The mechanisms behind reported decreases in plasma insulin and glucagon during hemodialysis (HD) are not clear. Here, we investigated these mechanisms during HD treatment and the characteristics of insulin and glucagon removal when using two super high-flux membranes. In an experimental study, clear...
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description | The mechanisms behind reported decreases in plasma insulin and glucagon during hemodialysis (HD) are not clear. Here, we investigated these mechanisms during HD treatment and the characteristics of insulin and glucagon removal when using two super high-flux membranes. In an experimental study, clearance, adsorption rates, and reduction rates of insulin and glucagon were investigated when using cellulose triacetate (CTA) and polysulfone (PS) membranes in a closed circuit using bovine blood. In a clinical study, 20 diabetes patients with end-stage kidney disease who were stable on HD were randomly selected for two HD sessions with two different membranes. At 1 h after the initiation of HD, insulin and glucagon clearance were measured, and the reduction rates were also investigated. In the experimental study, the PS membrane showed significantly higher clearance, adsorption rates, and reduction rates of insulin and glucagon compared with the CTA membrane. Although glucagon was detected in the ultrafiltration fluids in both membranes, insulin was absent in the PS membrane. In the clinical study, both membranes showed significant reductions in plasma insulin and glucagon at each time point. The PS membrane showed significantly higher insulin clearance and reduction rates compared with the CTA membrane. The two membranes showed no significant difference in glucagon clearance, but the glucagon reduction rate was significantly higher with the PS membrane. Our findings show that HD with the two super high-flux membranes used removes significant amounts of glucoregulatory peptide hormones from plasma in patients with diabetes and end-stage kidney disease, potentially affecting their glucose metabolism. |
doi_str_mv | 10.3390/ijms241310604 |
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Here, we investigated these mechanisms during HD treatment and the characteristics of insulin and glucagon removal when using two super high-flux membranes. In an experimental study, clearance, adsorption rates, and reduction rates of insulin and glucagon were investigated when using cellulose triacetate (CTA) and polysulfone (PS) membranes in a closed circuit using bovine blood. In a clinical study, 20 diabetes patients with end-stage kidney disease who were stable on HD were randomly selected for two HD sessions with two different membranes. At 1 h after the initiation of HD, insulin and glucagon clearance were measured, and the reduction rates were also investigated. In the experimental study, the PS membrane showed significantly higher clearance, adsorption rates, and reduction rates of insulin and glucagon compared with the CTA membrane. Although glucagon was detected in the ultrafiltration fluids in both membranes, insulin was absent in the PS membrane. In the clinical study, both membranes showed significant reductions in plasma insulin and glucagon at each time point. The PS membrane showed significantly higher insulin clearance and reduction rates compared with the CTA membrane. The two membranes showed no significant difference in glucagon clearance, but the glucagon reduction rate was significantly higher with the PS membrane. Our findings show that HD with the two super high-flux membranes used removes significant amounts of glucoregulatory peptide hormones from plasma in patients with diabetes and end-stage kidney disease, potentially affecting their glucose metabolism.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms241310604</identifier><identifier>PMID: 37445782</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Adsorption ; Animals ; Care and treatment ; Cattle ; Cellulose ; Cellulose triacetate ; Chronic kidney failure ; Dextrose ; Diabetes ; Diabetes Mellitus ; Diabetes therapy ; Diabetics ; Dialyzers ; End-stage renal disease ; Glucagon ; Glucose ; Glucose metabolism ; Hemodialysis ; Hormones ; Humans ; Insulin ; Insulin, Regular, Human ; Kidney diseases ; Kidney Failure, Chronic - therapy ; Kinetics ; Medical research ; Medicine, Experimental ; Membranes ; Membranes, Artificial ; Molecular weight ; Patients ; Peptide hormones ; Peptides ; Physiological aspects ; Plasma ; Pore size ; Proteins ; Renal Dialysis ; Ultrafiltration</subject><ispartof>International journal of molecular sciences, 2023-06, Vol.24 (13), p.10604</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c439t-4a7bf04a9828aee9d30d59ca6247035fda554b65398591da022c0b6aaf50ceb73</cites><orcidid>0000-0002-9156-5415 ; 0000-0002-9674-0374</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10341656/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10341656/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37445782$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Takao, Nobuteru</creatorcontrib><creatorcontrib>Maruyama, Takashi</creatorcontrib><creatorcontrib>Kobayashi, Hiroki</creatorcontrib><creatorcontrib>Kitai, Maki</creatorcontrib><creatorcontrib>Yoshida, Yoshinori</creatorcontrib><creatorcontrib>Takashima, Hiroyuki</creatorcontrib><creatorcontrib>Abe, Masanori</creatorcontrib><title>Kinetics of Glucoregulatory Peptide Hormones during Hemodialysis with Cellulose Triacetate and Polysulfone Dialyzers in Patients with Diabetes and End-Stage Kidney Disease</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>The mechanisms behind reported decreases in plasma insulin and glucagon during hemodialysis (HD) are not clear. Here, we investigated these mechanisms during HD treatment and the characteristics of insulin and glucagon removal when using two super high-flux membranes. In an experimental study, clearance, adsorption rates, and reduction rates of insulin and glucagon were investigated when using cellulose triacetate (CTA) and polysulfone (PS) membranes in a closed circuit using bovine blood. In a clinical study, 20 diabetes patients with end-stage kidney disease who were stable on HD were randomly selected for two HD sessions with two different membranes. At 1 h after the initiation of HD, insulin and glucagon clearance were measured, and the reduction rates were also investigated. In the experimental study, the PS membrane showed significantly higher clearance, adsorption rates, and reduction rates of insulin and glucagon compared with the CTA membrane. Although glucagon was detected in the ultrafiltration fluids in both membranes, insulin was absent in the PS membrane. In the clinical study, both membranes showed significant reductions in plasma insulin and glucagon at each time point. The PS membrane showed significantly higher insulin clearance and reduction rates compared with the CTA membrane. The two membranes showed no significant difference in glucagon clearance, but the glucagon reduction rate was significantly higher with the PS membrane. Our findings show that HD with the two super high-flux membranes used removes significant amounts of glucoregulatory peptide hormones from plasma in patients with diabetes and end-stage kidney disease, potentially affecting their glucose metabolism.</description><subject>Adsorption</subject><subject>Animals</subject><subject>Care and treatment</subject><subject>Cattle</subject><subject>Cellulose</subject><subject>Cellulose triacetate</subject><subject>Chronic kidney failure</subject><subject>Dextrose</subject><subject>Diabetes</subject><subject>Diabetes Mellitus</subject><subject>Diabetes therapy</subject><subject>Diabetics</subject><subject>Dialyzers</subject><subject>End-stage renal disease</subject><subject>Glucagon</subject><subject>Glucose</subject><subject>Glucose metabolism</subject><subject>Hemodialysis</subject><subject>Hormones</subject><subject>Humans</subject><subject>Insulin</subject><subject>Insulin, Regular, Human</subject><subject>Kidney diseases</subject><subject>Kidney Failure, Chronic - therapy</subject><subject>Kinetics</subject><subject>Medical research</subject><subject>Medicine, Experimental</subject><subject>Membranes</subject><subject>Membranes, Artificial</subject><subject>Molecular weight</subject><subject>Patients</subject><subject>Peptide hormones</subject><subject>Peptides</subject><subject>Physiological aspects</subject><subject>Plasma</subject><subject>Pore size</subject><subject>Proteins</subject><subject>Renal Dialysis</subject><subject>Ultrafiltration</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptkk1vEzEQhlcIREvhyBVZ4sJli9cf-3FCVSgNaiUiUc7WrD2bOtq1g-0Fhb_En8RRQ5Ui5IMtz_O-4xlPUbyu6DnnHX1vN1NkouIVral4UpxWgrGS0rp5enQ-KV7EuKGUcSa758UJb4SQTctOi9_X1mGyOhI_kKtx1j7geh4h-bAjK9wma5AsfZi8w0jMHKxbkyVO3lgYd9FG8tOmO7LAcZxHH5HcBgsaEyQk4AxZ-UzN45Dl5ONe8gtDJNaRFSSLLh30OdRjyhn2mktnyq8J1kiurXG4y9GIEPFl8WyAMeKrw35WfPt0ebtYljdfrj4vLm5KLXiXSgFNP1ABXctaQOwMp0Z2GmomGsrlYEBK0deSd63sKgOUMU37GmCQVGPf8LPiw73vdu4nNDo_M8CotsFOEHbKg1WPI87eqbX_oSrKRVXLOju8OzgE_33GmNRko849Aod-joq1vGWCVVRk9O0_6MbPweX69lQt6vytR9QaRlTWDT4n1ntTddHIllcN522mzv9D5WVwsjp_wWDz_SNBeS_QwccYcHgosqJqP17q0Xhl_s1xZx7ov_PE_wA7ac42</recordid><startdate>20230625</startdate><enddate>20230625</enddate><creator>Takao, Nobuteru</creator><creator>Maruyama, Takashi</creator><creator>Kobayashi, Hiroki</creator><creator>Kitai, Maki</creator><creator>Yoshida, Yoshinori</creator><creator>Takashima, Hiroyuki</creator><creator>Abe, Masanori</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-9156-5415</orcidid><orcidid>https://orcid.org/0000-0002-9674-0374</orcidid></search><sort><creationdate>20230625</creationdate><title>Kinetics of Glucoregulatory Peptide Hormones during Hemodialysis with Cellulose Triacetate and Polysulfone Dialyzers in Patients with Diabetes and End-Stage Kidney Disease</title><author>Takao, Nobuteru ; 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Here, we investigated these mechanisms during HD treatment and the characteristics of insulin and glucagon removal when using two super high-flux membranes. In an experimental study, clearance, adsorption rates, and reduction rates of insulin and glucagon were investigated when using cellulose triacetate (CTA) and polysulfone (PS) membranes in a closed circuit using bovine blood. In a clinical study, 20 diabetes patients with end-stage kidney disease who were stable on HD were randomly selected for two HD sessions with two different membranes. At 1 h after the initiation of HD, insulin and glucagon clearance were measured, and the reduction rates were also investigated. In the experimental study, the PS membrane showed significantly higher clearance, adsorption rates, and reduction rates of insulin and glucagon compared with the CTA membrane. Although glucagon was detected in the ultrafiltration fluids in both membranes, insulin was absent in the PS membrane. In the clinical study, both membranes showed significant reductions in plasma insulin and glucagon at each time point. The PS membrane showed significantly higher insulin clearance and reduction rates compared with the CTA membrane. The two membranes showed no significant difference in glucagon clearance, but the glucagon reduction rate was significantly higher with the PS membrane. Our findings show that HD with the two super high-flux membranes used removes significant amounts of glucoregulatory peptide hormones from plasma in patients with diabetes and end-stage kidney disease, potentially affecting their glucose metabolism.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>37445782</pmid><doi>10.3390/ijms241310604</doi><orcidid>https://orcid.org/0000-0002-9156-5415</orcidid><orcidid>https://orcid.org/0000-0002-9674-0374</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adsorption Animals Care and treatment Cattle Cellulose Cellulose triacetate Chronic kidney failure Dextrose Diabetes Diabetes Mellitus Diabetes therapy Diabetics Dialyzers End-stage renal disease Glucagon Glucose Glucose metabolism Hemodialysis Hormones Humans Insulin Insulin, Regular, Human Kidney diseases Kidney Failure, Chronic - therapy Kinetics Medical research Medicine, Experimental Membranes Membranes, Artificial Molecular weight Patients Peptide hormones Peptides Physiological aspects Plasma Pore size Proteins Renal Dialysis Ultrafiltration |
title | Kinetics of Glucoregulatory Peptide Hormones during Hemodialysis with Cellulose Triacetate and Polysulfone Dialyzers in Patients with Diabetes and End-Stage Kidney Disease |
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