Sensitive and rapid assessment of amyloid by oligothiophene fluorescence in subcutaneous fat tissue

Abstract

Systemic amyloidosis (SA) is often diagnosed late. Combining clinical and biochemical biomarkers is necessary for raising suspicion of disease. Fine needle aspiration (FNA) of subcutaneous fat enables SA detection by Congo red staining. The luminescent conjugated probe heptameric formic thiophene acetic acid (h-FTAA) is a sensitive alternative to Congo red-staining of tissue samples. Our objective was to compare h-FTAA fluorescence with the Congo red stain for amyloid detection in FNA-obtained fat tissue. Herein, we studied samples from 57 patients with established SA (19 with AA, 20 with AL, and 18 with ATTR) and 17 age-matched controls (34–75 years). Positivity for h-FTAA was graded according to a Congo red-based grading scale ranging from 0 to 4+. Amyloid grading by both methods correlated strongly (r = 0.87). Here h-FTAA was positive in 53 of 54 Congo red-positive cases (sensitivity 98%) and h-FTAA was negative in 7 of 17 Congo red-negative controls (specificity 41%), but was also positive for 3 Congo red-negative SA cases. We conclude that h-FTAA fluorescence is more sensitive than Congo red staining in this small exploratory study of fat tissue samples, implicating potential sensitivity for prodromal amyloidosis, but is less specific for clinical amyloidosis defined by Congo red positivity. Given its simplicity h-FTAA staining may therefore be the most appropriate method for rapid screening of fat tissue samples but should presently treat grade 1+ as only suggestive, whereas 2+ or higher as positive for amyloidosis. Parallel assessment of h-FTAA and Congo red staining appears highly promising for clinical applications.

• AA amyloidosis
• amyloid light chain
• hyper spectral imaging
• systemic amyloidosis
• transthyretin

Declarations of interest

The authors have no conflicts of interest to declare. Our work was supported by the European Commission FP-7 Health project LUPAS (D. S., P. H, K. P. R. N.), The Swedish Foundation for Strategic Research (K. P. R. N.), the Swedish Research Council (P. H., K. P. R. N.) and the Linköping University Center for Neuroscience (D. S.). K. P. R. N is financed by an ERC Starting Independent Researcher Grant (Project: MUMID) from the European Research Council.

Supplementary information available online

Supplementary Figures S1–S4.