Why the study?
CMR is often obtained early in suspected cardiac amyloidosis but currently cannot differentiate between AL and ATTR subtypes.
Does a diagnostic algorithm combining typical LGE and Look-Locker pattern on CMR with negative light chains accurately diagnose ATTR-CA in patients with suspected cardiac amyloidosis?
Does a diagnostic algorithm combining typical LGE and Look-Locker pattern on CMR with negative light chains accurately diagnose ATTR-CA in patients with suspected cardiac amyloidosis?
A diagnostic algorithm combining typical LGE and Look-Locker pattern on CMR with negative light chains is highly specific (98%) for diagnosing ATTR-CA, potentially reducing the need for invasive biopsy.
May support ATTR diagnosis without scintigraphy in typical-CMR cases; leaves open prospective validation and should not yet change practice.
AIMS: While cardiac magnetic resonance (CMR) is often obtained early in the evaluation of suspected cardiac amyloidosis (CA), it currently cannot be utilized to differentiate immunoglobulin (AL) and transthyretin (ATTR) CA. We aimed to determine whether a novel CMR and light-chain biomarker-based algorithm could accurately diagnose ATTR-CA. METHODS AND RESULTS: Patients with confirmed AL or ATTR-CA with typical late gadolinium enhancement (LGE) and Look-Locker pattern for CA on CMR were retrospectively identified at three academic medical centres. Comprehensive light-chain analysis including free light chains, serum, and urine electrophoresis/immunofixation was performed. The diagnostic accuracy of the typical CMR pattern for CA in combination with negative light chains for the diagnosis of ATTR-CA was determined both in the entire cohort and in the subset of patients with invasive tissue biopsy as the gold standard. A total of 147 patients (age 70 ± 11, 76% male, 51% black) were identified: 89 ATTR-CA and 58 AL-CA. Light-chain biomarkers were abnormal in 81 (55%) patients. Within the entire cohort, the sensitivity and specificity of a typical LGE and Look-Locker CMR pattern and negative light chains for ATTR-CA was 73 and 98%, respectively. Within the subset with biopsy-confirmed subtype, the CMR and light-chain algorithm were 69% sensitive and 98% specific. CONCLUSION: The combination of a typical LGE and Look-Locker pattern on CMR with negative light chains is highly specific for ATTR-CA. The successful non-invasive diagnosis of ATTR-CA using CMR has the potential to reduce diagnostic and therapeutic delays and healthcare costs for many patients.
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Slivnick et al. (2022) studied this question.
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