Plasmatic osteopontin and vascular access dysfunction in hemodialysis patients: a cross-sectional, case–control study (The OSMOSIS Study)

Background and aims Despite close follow-up of patients with native arteriovenous fistulas (AVFs), up to 10% experience thrombosis each year. The OSMOSIS Study (Osteopontin as a Marker of Stenosis) tested the hypothesis that the systemic osteopontin level, a pro-inflammatory mediator related to vasc...

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Published inJournal of nephrology Vol. 35; no. 2; pp. 527 - 534
Main Authors Contenti, Julie, Durand, Matthieu, Vido, Sandor, Declemy, Serge, Raffort, Juliette, Carboni, Joseph, Bonnet, Sophie, Koelsch, Christophe, Hassen-Khodja, Réda, Gual, Philippe, Mazure, Nathalie M., Sadaghianloo, Nirvana
Format Journal Article
LanguageEnglish
Published Cham Springer International Publishing 01.03.2022
Italian Society of Nephrology/Springer
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Online AccessGet full text
ISSN1121-8428
1724-6059
1724-6059
DOI10.1007/s40620-021-01129-4

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Abstract Background and aims Despite close follow-up of patients with native arteriovenous fistulas (AVFs), up to 10% experience thrombosis each year. The OSMOSIS Study (Osteopontin as a Marker of Stenosis) tested the hypothesis that the systemic osteopontin level, a pro-inflammatory mediator related to vascular remodelling and intimal hyperplasia, increases in AVF stenosis, and may be used in clinical surveillance. Methods Our cross-sectional study compared the level of plasmatic osteopontin (pOPN) between patients with a well-functioning AVF (control group) and patients who required revision of their AVF due to stenosis (stenosis group). Blood samples were collected before dialysis (control group) or before intervention (stenosis group) from the AVF arm, and from the opposite arm as a within-subject control. pOPN level was measured by enzyme-linked immunosorbent assay. Results A total of 76 patients were included in the study. Baseline characteristics were similar between the groups (mean age, 70 years; men, 63%; AVF duration, 39 months), apart from prevalence of type 2 diabetes (T2D) (control group, 33%; stenosis group, 57%; p  = 0.04). pOPN levels were similar between the AVF arm and the contralateral arm (551 ± 42 ng/mL vs. 521 ± 41 ng/mL, respectively, p  = 0.11, paired t-test). Patients in the stenosis group displayed a higher pOPN level than patients in the control group (650.2 ± 59.8 ng/mL vs. 460.5 ± 61.2, respectively, p  = 0.03; two-way ANOVA). T2D was not identified as an associated factor in a multivariate analysis ( p  = 0.50). Conclusions The level of pOPN in hemodialysis patients was associated with the presence of AVF stenosis requiring intervention. Thus, its potential as a diagnostic biomarker should be assessed in a vascular access surveillance program. Graphic abstract
AbstractList Despite close follow-up of patients with native arteriovenous fistulas (AVFs), up to 10% experience thrombosis each year. The OSMOSIS Study (Osteopontin as a Marker of Stenosis) tested the hypothesis that the systemic osteopontin level, a pro-inflammatory mediator related to vascular remodelling and intimal hyperplasia, increases in AVF stenosis, and may be used in clinical surveillance.BACKGROUND AND AIMSDespite close follow-up of patients with native arteriovenous fistulas (AVFs), up to 10% experience thrombosis each year. The OSMOSIS Study (Osteopontin as a Marker of Stenosis) tested the hypothesis that the systemic osteopontin level, a pro-inflammatory mediator related to vascular remodelling and intimal hyperplasia, increases in AVF stenosis, and may be used in clinical surveillance.Our cross-sectional study compared the level of plasmatic osteopontin (pOPN) between patients with a well-functioning AVF (control group) and patients who required revision of their AVF due to stenosis (stenosis group). Blood samples were collected before dialysis (control group) or before intervention (stenosis group) from the AVF arm, and from the opposite arm as a within-subject control. pOPN level was measured by enzyme-linked immunosorbent assay.METHODSOur cross-sectional study compared the level of plasmatic osteopontin (pOPN) between patients with a well-functioning AVF (control group) and patients who required revision of their AVF due to stenosis (stenosis group). Blood samples were collected before dialysis (control group) or before intervention (stenosis group) from the AVF arm, and from the opposite arm as a within-subject control. pOPN level was measured by enzyme-linked immunosorbent assay.A total of 76 patients were included in the study. Baseline characteristics were similar between the groups (mean age, 70 years; men, 63%; AVF duration, 39 months), apart from prevalence of type 2 diabetes (T2D) (control group, 33%; stenosis group, 57%; p = 0.04). pOPN levels were similar between the AVF arm and the contralateral arm (551 ± 42 ng/mL vs. 521 ± 41 ng/mL, respectively, p = 0.11, paired t-test). Patients in the stenosis group displayed a higher pOPN level than patients in the control group (650.2 ± 59.8 ng/mL vs. 460.5 ± 61.2, respectively, p = 0.03; two-way ANOVA). T2D was not identified as an associated factor in a multivariate analysis (p = 0.50).RESULTSA total of 76 patients were included in the study. Baseline characteristics were similar between the groups (mean age, 70 years; men, 63%; AVF duration, 39 months), apart from prevalence of type 2 diabetes (T2D) (control group, 33%; stenosis group, 57%; p = 0.04). pOPN levels were similar between the AVF arm and the contralateral arm (551 ± 42 ng/mL vs. 521 ± 41 ng/mL, respectively, p = 0.11, paired t-test). Patients in the stenosis group displayed a higher pOPN level than patients in the control group (650.2 ± 59.8 ng/mL vs. 460.5 ± 61.2, respectively, p = 0.03; two-way ANOVA). T2D was not identified as an associated factor in a multivariate analysis (p = 0.50).The level of pOPN in hemodialysis patients was associated with the presence of AVF stenosis requiring intervention. Thus, its potential as a diagnostic biomarker should be assessed in a vascular access surveillance program.CONCLUSIONSThe level of pOPN in hemodialysis patients was associated with the presence of AVF stenosis requiring intervention. Thus, its potential as a diagnostic biomarker should be assessed in a vascular access surveillance program.
Despite close follow-up of patients with native arteriovenous fistulas (AVFs), up to 10% experience thrombosis each year. The OSMOSIS Study (Osteopontin as a Marker of Stenosis) tested the hypothesis that the systemic osteopontin level, a pro-inflammatory mediator related to vascular remodelling and intimal hyperplasia, increases in AVF stenosis, and may be used in clinical surveillance. Our cross-sectional study compared the level of plasmatic osteopontin (pOPN) between patients with a well-functioning AVF (control group) and patients who required revision of their AVF due to stenosis (stenosis group). Blood samples were collected before dialysis (control group) or before intervention (stenosis group) from the AVF arm, and from the opposite arm as a within-subject control. pOPN level was measured by enzyme-linked immunosorbent assay. A total of 76 patients were included in the study. Baseline characteristics were similar between the groups (mean age, 70 years; men, 63%; AVF duration, 39 months), apart from prevalence of type 2 diabetes (T2D) (control group, 33%; stenosis group, 57%; p = 0.04). pOPN levels were similar between the AVF arm and the contralateral arm (551 ± 42 ng/mL vs. 521 ± 41 ng/mL, respectively, p = 0.11, paired t-test). Patients in the stenosis group displayed a higher pOPN level than patients in the control group (650.2 ± 59.8 ng/mL vs. 460.5 ± 61.2, respectively, p = 0.03; two-way ANOVA). T2D was not identified as an associated factor in a multivariate analysis (p = 0.50). The level of pOPN in hemodialysis patients was associated with the presence of AVF stenosis requiring intervention. Thus, its potential as a diagnostic biomarker should be assessed in a vascular access surveillance program.
Background and aims Despite close follow-up of patients with native arteriovenous fistulas (AVFs), up to 10% experience thrombosis each year. The OSMOSIS Study (Osteopontin as a Marker of Stenosis) tested the hypothesis that the systemic osteopontin level, a pro-inflammatory mediator related to vascular remodelling and intimal hyperplasia, increases in AVF stenosis, and may be used in clinical surveillance. Methods Our cross-sectional study compared the level of plasmatic osteopontin (pOPN) between patients with a well-functioning AVF (control group) and patients who required revision of their AVF due to stenosis (stenosis group). Blood samples were collected before dialysis (control group) or before intervention (stenosis group) from the AVF arm, and from the opposite arm as a within-subject control. pOPN level was measured by enzyme-linked immunosorbent assay. Results A total of 76 patients were included in the study. Baseline characteristics were similar between the groups (mean age, 70 years; men, 63%; AVF duration, 39 months), apart from prevalence of type 2 diabetes (T2D) (control group, 33%; stenosis group, 57%; p  = 0.04). pOPN levels were similar between the AVF arm and the contralateral arm (551 ± 42 ng/mL vs. 521 ± 41 ng/mL, respectively, p  = 0.11, paired t-test). Patients in the stenosis group displayed a higher pOPN level than patients in the control group (650.2 ± 59.8 ng/mL vs. 460.5 ± 61.2, respectively, p  = 0.03; two-way ANOVA). T2D was not identified as an associated factor in a multivariate analysis ( p  = 0.50). Conclusions The level of pOPN in hemodialysis patients was associated with the presence of AVF stenosis requiring intervention. Thus, its potential as a diagnostic biomarker should be assessed in a vascular access surveillance program. Graphic abstract
Author Declemy, Serge
Bonnet, Sophie
Carboni, Joseph
Hassen-Khodja, Réda
Sadaghianloo, Nirvana
Vido, Sandor
Gual, Philippe
Contenti, Julie
Durand, Matthieu
Raffort, Juliette
Koelsch, Christophe
Mazure, Nathalie M.
Author_xml – sequence: 1
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  givenname: Matthieu
  surname: Durand
  fullname: Durand, Matthieu
  organization: Department of Urology and Andrology and Renal Transplantation, Centre Hospitalier Universiatire de Nice, Institute of Research on Cancer and Aging of Nice, INSERM U1081-CNRS, UMR 7284, Université Côte d’Azur
– sequence: 3
  givenname: Sandor
  surname: Vido
  fullname: Vido, Sandor
  organization: Department of Nephrology and Hemodialysis, Centre Hospitalier Universitaire de Nice
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  surname: Declemy
  fullname: Declemy, Serge
  organization: Department of Vascular Surgery, Centre Hospitalier Universitaire de Nice
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  organization: Department of Vascular Surgery, Centre Hospitalier Universitaire de Nice
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  givenname: Sophie
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  fullname: Bonnet, Sophie
  organization: Department of Vascular Surgery, Centre Hospitalier Universitaire de Nice, Department of Clinical Research and Innovation, Centre Hospitalier Universitaire de Nice
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  givenname: Christophe
  surname: Koelsch
  fullname: Koelsch, Christophe
  organization: Department of Anesthesiology, Centre Hospitalier Universitaire de Nice
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  givenname: Réda
  surname: Hassen-Khodja
  fullname: Hassen-Khodja, Réda
  organization: Centre Méditerranéen de Médecine Moléculaire, INSERM U1065, Université Côte d’Azur, Department of Vascular Surgery, Centre Hospitalier Universitaire de Nice
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  givenname: Philippe
  surname: Gual
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  organization: Centre Méditerranéen de Médecine Moléculaire, INSERM U1065, Université Côte d’Azur
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  givenname: Nathalie M.
  surname: Mazure
  fullname: Mazure, Nathalie M.
  organization: Centre Méditerranéen de Médecine Moléculaire, INSERM U1065, Université Côte d’Azur
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  givenname: Nirvana
  orcidid: 0000-0003-3394-8458
  surname: Sadaghianloo
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  email: sadaghianloo.n@chu-nice.fr
  organization: Centre Méditerranéen de Médecine Moléculaire, INSERM U1065, Université Côte d’Azur, Department of Vascular Surgery, Centre Hospitalier Universitaire de Nice
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CitedBy_id crossref_primary_10_3390_biomedicines11051356
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crossref_primary_10_4236_ojneph_2021_114039
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Issue 2
Keywords Biomarkers
Osteopontin
Surgical arteriovenous shunt
Hemodialysis access
Language English
License 2021. Italian Society of Nephrology.
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  publication-title: Eur J Cardiothorac Surg
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  publication-title: Cardiovasc Diabetol
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Snippet Background and aims Despite close follow-up of patients with native arteriovenous fistulas (AVFs), up to 10% experience thrombosis each year. The OSMOSIS Study...
Despite close follow-up of patients with native arteriovenous fistulas (AVFs), up to 10% experience thrombosis each year. The OSMOSIS Study (Osteopontin as a...
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SubjectTerms Aged
Arteriovenous Shunt, Surgical - adverse effects
Case-Control Studies
Cross-Sectional Studies
Diabetes Mellitus, Type 2
Humans
Life Sciences
Male
Medicine
Medicine & Public Health
Nephrology
Original Article
Osmosis
Osteopontin
Renal Dialysis - adverse effects
Retrospective Studies
Time Factors
Treatment Outcome
Urology
Vascular Patency
Title Plasmatic osteopontin and vascular access dysfunction in hemodialysis patients: a cross-sectional, case–control study (The OSMOSIS Study)
URI https://link.springer.com/article/10.1007/s40620-021-01129-4
https://www.ncbi.nlm.nih.gov/pubmed/34468976
https://www.proquest.com/docview/2568249834
https://hal.science/hal-03429114
Volume 35
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