Extended reports
111Indium antimyosin antibody imaging of primary
myocardial invovement in systemic diseases
a Departments of
Nuclear Medicine, b Cardiology, c and Rheumatology, d Hôpital
Bichat, Paris, France Department of
Internal Medicine, Hôpital Avicenne, Bobigny, France
Correspondence to: Dr L Sarda, Nuclear Medicine Department, Hôpital Bichat, 46 rue Henri Huchard, 75018 Paris, France.
Accepted for publication 12 October 1998
OBJECTIVE
The
diagnosis of primary myocardial involvement in systemic diseases is
clinically relevant but difficult in the absence of specific criteria.
Whatever the underlying disease, myocytes degeneration is observed
during the active phase of myocardial damage. The aim of this study was
to assess the diagnostic value of scintigraphic imaging with
111Indium antimyosin antibody (AM), a specific marker of
the damaged myocyte, for ongoing myocardial damage related to systemic diseases.
METHODS
40 patients
with histologically confirmed systemic diseases were studied. They were
classified into two groups according to the presence (group 1, n=30),
or the absence (group 2, n=10) of clinical, electrocardiographic (ECG)
or echocardiographic signs suggestive of myocardial involvement. Planar
and tomographic acquisitions were obtained 48 hours after injection of
AM (90 MBq). Rest 201thallium (Tl) scintigraphy was also
performed to assess myocardial perfusion and scarring. Clinical, ECG,
and echocardiographic ± scintigraphic evaluations were repeated
during follow up (17 ±19 months) in 36 of 40 patients.
RESULTS
In group 1, 13 of 30 patients (43%) showed diffuse significant AM uptake throughout
the left ventricle (LV), and no or mild Tl abnormality. Two of these
were asymptomatic, four had normal ECG, and two had no clinical or
echographic LV dysfunction. All patients in group 2 had negative AMA
scintigraphy and normal Tl scintigraphy. During follow up of 12 AM
positive patients, cardiac status improved after immunosuppressive
treatment was intensified in nine cases, worsened in two cases, and
remained stable in one. During follow up of 24 AM negative patients,
cardiac status remained stable in 23 cases despite treatment not being
increased in 20, including two patients with sequellary myocardial
involvement. The last patient developed mild LV dysfunction after 36 months.
CONCLUSION
AM
scintigraphy allows detection of active myocardial damage related to
systemic diseases, with increased specificity compared with
conventional methods, and increased sensitivity in some cases. Further
studies are needed to assess the potential value of AM scintigraphy as
a therapeutic guide.
© 1999 by Annals of the Rheumatic Diseases
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