(Circulation. 1999;100:287-291.)
© 1999 American Heart Association, Inc.
Clinical Investigation and Reports |
From the Departments of Surgery (R.G.D., P.J.H.), Medicine (R.A.D., S.J.S.), and Pathology and Laboratory Medicine (J.P.V., A.J.d.B.), University of Ottawa, the Ottawa Heart Institute, and the Ottawa Hospital Civic Site, Ottawa, Ontario, Canada.
Correspondence to Dr Adolfo J. de Bold, University of Ottawa Heart Institute, 40 Ruskin St, Ottawa, Ontario K1Y 4W7, Canada. E-mail adebold{at}ottawaheart.ca
BackgroundIncreased circulating levels of the cardiac polypeptide hormones atrial natriuretic factor (ANF) and brain natriuretic peptide (BNP) may be observed after orthotopic cardiac transplantation. Both the hypertrophic and inflammatory processes in the allograft may contribute to this increase, but no mechanistic explanation has been suggested for this observation.
Methods and ResultsPlasma immunoreactive ANF and BNP
determinations were performed in 10 consecutive transplant patients.
These were correlated with degree of rejection as reflected by
histopathological findings at serial endomyocardial
biopsies. Three patients had associated hemodynamic
measurements and blood samples 24 hours before and after
transplantation. All rejection episodes that received treatment were
accompanied by a marked increase in BNP plasma levels to >
400
pg/mL. Steadily increasing BNP levels preceded overt rejection as
assessed by histopathological criteria. The increase in plasma BNP was
not always accompanied by an increase in ANF, which suggests the
specific upregulation of BNP gene expression during acute rejection
episodes. Treatment of the acute rejection episodes led to a
substantial decrease of BNP plasma levels.
ConclusionsThe significant selective increase in plasma BNP levels found in the present study has not been previously described. This finding provides a new insight into the mechanism of allograft rejection and the modulation of natriuretic peptide synthesis and release. Furthermore, although preliminary, the data suggest that BNP plasma levels could form the basis for a new, noninvasive screening test to predict acute cardiac allograft rejection. Because treatment with the antilymphocyte monoclonal antibody OKT3 (murine monoclonal antibody to the CD3 antigen of the human T-cell) decreased BNP plasma levels, cytokine production by T-cells may mediate the selective increase in circulating BNP.
Key Words: transplantation natriuretic peptides atrial natriuretic factor myocarditis pathology
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