{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,13]],"date-time":"2026-10-13T22:09:07Z","timestamp":1791929347701,"version":"4.3.4"},"reference-count":56,"publisher":"Oxford University Press (OUP)","issue":"6","license":[{"start":{"date-parts":[[2024,4,30]],"date-time":"2024-04-30T00:00:00Z","timestamp":1714435200000},"content-version":"vor","delay-in-days":1,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"}],"funder":[{"name":"Niercentrum aan de Amstel, Amstelveen, The\n                                Netherlands"},{"name":"B. Braun Avitum AG, Melsungen"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2024,6,3]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n               <jats:sec>\n                  <jats:title>Background<\/jats:title>\n                  <jats:p>Intradialytic hypotension (IDH) and subsequent tissue damage may contribute to the poor outcome of chronic haemodialysis (HD) patients. While the IDH-incidence is lower in high-volume haemodiafiltration (HV-HDF) than in standard HD (S-HD), survival is better in HV-HDF. Tissue injury, as measured by extracellular vesicle (EV)-release, was compared between four modalities.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Methods<\/jats:title>\n                  <jats:p>Forty chronic patients were cross-over randomized to S-HD, cool-HD (C-HD), low-volume HDF (LV-HDF), and HV-HDF. Blood pressure was recorded every 15 minutes. EVs from circulating blood-cell-elements (bio-incompatibility-related) and cardiovascular (CV) tissues (CV-related), were measured before and after dialysis. The influence of modalities and IDH on the rate of change of EVs was assessed. Both crude and haemoconcentration-adjusted analyses were performed.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Results<\/jats:title>\n                  <jats:p>Leukocyte and erythrocyte-derived EVs increased in all modalities. Platelet-derived EVs increased more in LV-HDF and HV-HDF (68.4 respectively 56.1\u00a0\u00d7\u00a0106\/ml) than in S-HD (27.5\u00a0\u00d7\u00a0106\/ml), P values for interaction were &amp;lt;.01 respectively .06. Endothelial-derived CD144+ (2.3\u00a0\u00d7\u00a0106\/ml in HV-HDF and 9.8\u00a0\u00d7\u00a0106\/ml in S-HD) and cardiomyocyte-derived Connexin-43+ (12.0 respectively 31.9\u00a0\u00d7\u00a0106\/ml) EVs increased less in HV-HDF than in S-HD (P for interaction .03 respectively .06). Correction for haemoconcentration attenuated all changes, although the increase in platelet-derived EVs remained significant in LV-HDF and HV-HDF, and CD144+ and Connexin-43+ EVs increased most in S-HD. EV release was similar in patients with varying IDH susceptibility and in sessions with and without IDH.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Conclusions<\/jats:title>\n                  <jats:p>Most EVs increase during HD and HDF. Regarding platelet-derived EVs, HDF appears less biocompatible than HD. Considering CV-related EVs, tissue injury seems less pronounced in HV-HDF. The finding that EV release is IDH-independent needs confirmation.<\/jats:p>\n               <\/jats:sec>","DOI":"10.1093\/ckj\/sfae134","type":"journal-article","created":{"date-parts":[[2024,4,30]],"date-time":"2024-04-30T02:46:46Z","timestamp":1714445206000},"source":"Crossref","is-referenced-by-count":5,"title":["Intradialytic cardiovascular injury is lowest in high-volume\n                    haemodiafiltration: a randomized cross-over trial in four intermittent dialysis\n                    strategies"],"prefix":"10.1093","volume":"17","author":[{"given":"Peiyun","family":"Liu","sequence":"first","affiliation":[{"name":"Department of Nephrology, Amsterdam UMC, location Vrije Universiteit Amsterdam , Amsterdam ,","place":["the Netherlands"]},{"name":"Department of Renal Medicine, Singapore General Hospital, Singapore ,","place":["Singapore"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3693-5268","authenticated-orcid":false,"given":"Paul A","family":"Rootjes","sequence":"additional","affiliation":[{"name":"Department of Nephrology, Amsterdam UMC, location Vrije Universiteit Amsterdam , Amsterdam ,","place":["the Netherlands"]},{"name":"Department of Internal Medicine, Gelre Hospitals , Apeldoorn ,","place":["the Netherlands"]},{"name":"Amsterdam Cardiovascular Sciences (ACS), Diabetes & Metabolism , Amsterdam ,","place":["the Netherlands"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-6369-8341","authenticated-orcid":false,"given":"Camiel L M","family":"de Roij van Zuijdewijn","sequence":"additional","affiliation":[{"name":"Department of Nephrology, Amsterdam UMC, location Vrije Universiteit Amsterdam , Amsterdam ,","place":["the Netherlands"]},{"name":"Amsterdam Cardiovascular Sciences (ACS), Diabetes & Metabolism , Amsterdam ,","place":["the Netherlands"]},{"name":"Department of Internal Medicine , Spaarne Gasthuis, Haarlem ,","place":["the\n                            Netherlands"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Chi M","family":"Hau","sequence":"additional","affiliation":[{"name":"Laboratory of Experimental Clinical Chemistry, Amsterdam University Medical Center, University of Amsterdam , Amsterdam ,","place":["the\n                            Netherlands"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Menso J","family":"Nub\u00e9","sequence":"additional","affiliation":[{"name":"Department of Nephrology, Amsterdam UMC, location Vrije Universiteit Amsterdam , Amsterdam ,","place":["the Netherlands"]},{"name":"Amsterdam Cardiovascular Sciences (ACS), Diabetes & Metabolism , Amsterdam ,","place":["the Netherlands"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-5671-3400","authenticated-orcid":false,"given":"Rienk","family":"Nieuwland","sequence":"additional","affiliation":[{"name":"Laboratory of Experimental Clinical Chemistry, Amsterdam University Medical Center, University of Amsterdam , Amsterdam ,","place":["the\n                            Netherlands"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gertrude","family":"Wijngaarden","sequence":"additional","affiliation":[{"name":"Department of Nephrology, Amsterdam UMC, location Vrije Universiteit Amsterdam , Amsterdam ,","place":["the Netherlands"]},{"name":"Amsterdam Cardiovascular Sciences (ACS), Diabetes & Metabolism , Amsterdam ,","place":["the Netherlands"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Muriel P C","family":"Grooteman","sequence":"additional","affiliation":[{"name":"Department of Nephrology, Amsterdam UMC, location Vrije 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