Key result
Cardiac involvement in primary (AL) amyloidosis results in progressive heart failure with a spectrum of left ventricular filling abnormalities related to disease progression.
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Warrants attention to evolving LV filling patterns in AL amyloidosis; leaves open prospective validation of progression staging.
CARDIAC involvement in primary (AL) amyloidosis commonly results in progressive heart failure owing to restriction of ventricular filling (restrictive cardiomyopathy).1 2 3 4 5 (AL stands for light chain, describing the protein deposited in tissues in this disorder.) There is considerable variability among patients in the hemodynamic findings associated with this disease, and recent studies using pulsed Doppler echocardiography and radionuclide ventriculography have described a spectrum of left ventricular filling abnormalities that appear to be related to disease progression and severity.6 , 7 In the early stages of cardiac amyloid infiltration, a relative shift of left ventricular filling from early to late diastole with enhancement . . .
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Plehn et al. (1992) studied Primary (AL) amyloidosis. Cardiac involvement in primary (AL) amyloidosis results in progressive heart failure with a spectrum of left ventricular filling abnormalities related to disease progression.
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