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Inflammation in the early phase after kidney transplantation is associated with increased long-term all-cause mortality.
Heldal, Torbjørn Fossum; Åsberg, Anders; Ueland, Thor; Reisaeter, Anna Varberg; Pischke, Søren E; Mollnes, Tom Eirik; Aukrust, Pål; Hartmann, Anders; Heldal, Kristian; Jenssen, Trond.
Afiliação
  • Heldal TF; Department of Internal Medicine, Telemark Hospital Trust, Skien, Norway.
  • Åsberg A; Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
  • Ueland T; Department of Transplantation Medicine, Oslo University Hospital - Rikshospitalet, Oslo, Norway.
  • Reisaeter AV; Department of Transplantation Medicine, Oslo University Hospital - Rikshospitalet, Oslo, Norway.
  • Pischke SE; Norwegian Renal Registry, Oslo University Hospital - Rikshospitalet, Oslo, Norway.
  • Mollnes TE; Department of Pharmacy, University of Oslo, Oslo, Norway.
  • Aukrust P; Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
  • Hartmann A; K.G. Jebsen Thrombosis Research and Expertise Center, University of Tromsø, Tromsø, Norway.
  • Heldal K; Research Institute of Internal Medicine, Oslo University Hospital - Rikshospitalet, Oslo, Norway.
  • Jenssen T; Department of Transplantation Medicine, Oslo University Hospital - Rikshospitalet, Oslo, Norway.
Am J Transplant ; 22(8): 2016-2027, 2022 08.
Article em En | MEDLINE | ID: mdl-35352462
ABSTRACT
In the general population, low-grade inflammation has been established as a risk factor for all-cause mortality. We hypothesized that an inflammatory milieu beyond the time of recovery from the surgical trauma could be associated with increased long-term mortality in kidney transplant recipients (KTRs). This cohort study included 1044 KTRs. Median follow-up time post-engraftment was 10.3 years. Inflammation was assessed 10 weeks after transplantation by different composite inflammation scores based on 21 biomarkers. We constructed an overall inflammation score and five pathway-specific inflammation scores (fibrogenesis, vascular inflammation, metabolic inflammation, growth/angiogenesis, leukocyte activation). Mortality was assessed with Cox regression models adjusted for traditional risk factors. A total of 312 (29.9%) patients died during the follow-up period. The hazard ratio (HR) for death was 4.71 (95% CI 2.85-7.81, p < .001) for patients in the highest quartile of the overall inflammation score and HRs 2.35-2.54 (95% CI 1.40-3.96, 1.52-4.22, p = .001) for patients in the intermediate groups. The results were persistent when the score was analyzed as a continuous variable (HR 1.046, 95% CI 1.033-1.056, p < .001). All pathway-specific analyses showed the same pattern with HRs ranging from 1.19 to 2.70. In conclusion, we found a strong and consistent association between low-grade systemic inflammation 10 weeks after kidney transplantation and long-term mortality.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Obtenção de Tecidos e Órgãos / Transplante de Rim Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Obtenção de Tecidos e Órgãos / Transplante de Rim Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article