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The Alternative Complement Pathway Is Activated Without a Corresponding Terminal Pathway Activation in Patients With Heart Failure.
Holt, Margrethe Flesvig; Michelsen, Annika E; Shahini, Negar; Bjørkelund, Elisabeth; Bendz, Christina Holt; Massey, Richard J; Schjalm, Camilla; Halvorsen, Bente; Broch, Kaspar; Ueland, Thor; Gullestad, Lars; Nilsson, Per H; Aukrust, Pål; Mollnes, Tom Eirik; Louwe, Mieke C.
Afiliación
  • Holt MF; Research Institute of Internal Medicine, Oslo University Hospital, Oslo, Norway.
  • Michelsen AE; Department of Cardiology, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
  • Shahini N; Research Institute of Internal Medicine, Oslo University Hospital, Oslo, Norway.
  • Bjørkelund E; Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.
  • Bendz CH; Research Institute of Internal Medicine, Oslo University Hospital, Oslo, Norway.
  • Massey RJ; Department of Cardiology, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
  • Schjalm C; Department of Cardiology, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
  • Halvorsen B; Department of Cardiology, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
  • Broch K; Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.
  • Ueland T; Department of Immunology, Oslo University Hospital Rikshospitalet and University of Oslo, Oslo, Norway.
  • Gullestad L; Research Institute of Internal Medicine, Oslo University Hospital, Oslo, Norway.
  • Nilsson PH; Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.
  • Aukrust P; Department of Cardiology, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
  • Mollnes TE; K.G. Jebsen Cardiac Research Center, Center for Heart Failure Research, Faculty of Medicine, University of Oslo, Oslo, Norway.
  • Louwe MC; Research Institute of Internal Medicine, Oslo University Hospital, Oslo, Norway.
Front Immunol ; 12: 800978, 2021.
Article en En | MEDLINE | ID: mdl-35003128
ABSTRACT

Objective:

Dysregulation of the complement system has been described in patients with heart failure (HF). However, data on the alternative pathway are scarce and it is unknown if levels of factor B (FB) and the C3 convertase C3bBbP are elevated in these patients. We hypothesized that plasma levels of FB and C3bBbP would be associated with disease severity and survival in patients with HF.

Methods:

We analyzed plasma levels of FB, C3bBbP, and terminal C5b-9 complement complex (TCC) in 343 HF patients and 27 healthy controls.

Results:

Compared with controls, patients with HF had elevated levels of circulating FB (1.6-fold, p < 0.001) and C3bBbP (1.3-fold, p < 0.001). In contrast, TCC, reflecting the terminal pathway, was not significantly increased (p = 0.15 vs controls). FB was associated with NT-proBNP, troponin, eGFR, and i.e., C-reactive protein. FB, C3bBbP and TCC were not associated with mortality in HF during a mean follow up of 4.3 years.

Conclusion:

Our findings suggest that in patients with HF, the alternative pathway is activated. However, this is not accompanied by activation of the terminal pathway.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Vía Alternativa del Complemento / Insuficiencia Cardíaca Límite: Female / Humans / Male Idioma: En Revista: Front Immunol Año: 2021 Tipo del documento: Article País de afiliación: Noruega

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Vía Alternativa del Complemento / Insuficiencia Cardíaca Límite: Female / Humans / Male Idioma: En Revista: Front Immunol Año: 2021 Tipo del documento: Article País de afiliación: Noruega