Tf. Muller et al., NONINVASIVE MONITORING USING SERUM AMYLOID-A AND SERUM NEOPTERIN IN CARDIAC TRANSPLANTATION, Clinica chimica acta, 276(1), 1998, pp. 63-74
The monitoring of allograft function for cardiac transplant patients s
till relies on endomyocardial routine biopsies. We investigated the di
agnostic value of noninvasive monitoring using the parameters serum am
yloid A protein and serum neopterin. The circulating levels of the acu
te phase reactant, amyloid A protein, and the macrophage product, neop
terin, were measured serially in 13 patients after cardiac transplanta
tion. The mean period of observation was 240 days. Nine acute cardiac
allograft rejections, five cases of viral infection and eight cases of
bacterial infection occurred. The levels of serum amyloid A protein a
nd serum neopterin remained low ((x) over tilde = 6.0 mg/dL and 12.6 n
mol/L, respectively) during the periods of stable graft function. In c
ontrast, both parameters were significantly elevated (p < 0.01) during
the rejection episodes ((x) over tilde = 12.7 mg/dL and 38.0 nmol/L f
or serum amyloid A protein and serum neopterin, respectively). For a r
eliable differentiation between rejection and stable graft function, s
erum amyloid A protein had a diagnostic accuracy of 84% (with a cut-of
f level of 10 mg/dL) and serum neopterin had one of 75% (with a cut-of
f level of 23 nmol/L). However, significant increases in the circulati
ng levels of serum amyloid A protein and serum neopterin were also obs
erved during bacterial ((x) over tilde = 14.9 and 88 nmol/L, respectiv
ely) and viral ((x) over tilde = 6.2 mg/dL and 44 nmol/L, respectively
) infections. The detection of immunological complications after cardi
ac transplantation using serial measurements of serum amyloid A protei
n and serum neopterin is possible. These parameters can be used to hel
p in judging both the need and the optimal timing for the otherwise fr
equent endomyocardial biopsies. (C) 1998 Elsevier Science BN. All righ
ts reserved.