| Literature DB >> 28906148 |
Jonah Rubin1, Julissa Alvarez1, Sergio Teruya1, Adam Castano1, Ronald A Lehman2, Mark Weidenbaum2, Jeffrey A Geller2, Stephen Helmke1, Mathew S Maurer1.
Abstract
Transthyretin cardiac amyloidosis (ATTR-CA) causes a restrictive cardiomyopathy in older adults, often diagnosed at advanced stages when emerging therapies in late phase clinical trials may not have clinical benefit. This investigation aimed to detect clinical entities that may provide more advanced warning of ATTR-CA. Since ATTR preferentially deposits in ligaments, tendons, and articular cartilage, we hypothesized that ATTR-CA patients have a greater prevalence of total hip (THA) and knee (TKA) arthroplasties compared with the general population, and that arthroplasty occurs significantly before ATTR-CA diagnosis. Three-hundred and thirteen patients with cardiac amyloidosis (172 with ATTR-CA, 141 with light-chain) from our institutional database were analyzed and compared to published data in over 300 million patients. Overall, 23.3% of patients with ATTR-CA and 9.2% of patients with light-chain cardiac amyloidosis (AL-CA) underwent lower extremity arthroplasty. Compared to the general population, both THA and TKA were significantly more common among patients with ATTR-CA (THA: RR 5.61, 95% CI 2.25-4.64; TKA: RR 3.32, 95% CI 2.25-4.64) but not those with AL-CA (THA: RR 1.87, 95% CI 0.85-4.08; TKA: RR 1.42, 95% CI 0.73-2.84). On an average, arthroplasty occurred 7.2 years before ATTR-CA diagnosis.Entities:
Keywords: Cardiac amyloidosis; arthroplasty; light-chain; transthyretin
Mesh:
Year: 2017 PMID: 28906148 DOI: 10.1080/13506129.2017.1375908
Source DB: PubMed Journal: Amyloid ISSN: 1350-6129 Impact factor: 7.141