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Gait abnormalities in older adults with transthyretin cardiac amyloidosis.

Authors :
Petros FE
Santos AM
Adeniyi A
Teruya S
De Los Santos J
Maurer MS
Agrawal SK
Source :
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis [Amyloid] 2024 Jun; Vol. 31 (2), pp. 116-123. Date of Electronic Publication: 2024 Mar 03.
Publication Year :
2024

Abstract

Background: Transthyretin cardiac amyloidosis (ATTR cardiac amyloidosis) is caused by variant (ATTRv) or wild type (ATTRwt) transthyretin. While gait abnormalities have been studied in younger patients with ATTRv amyloidosis, research on gait in older adults with ATTR cardiac amyloidosis is lacking. Given ATTR cardiac amyloidosis' association with neuropathy and orthopedic manifestations, we explore the gait in this population.<br />Methods: Twenty-eight older male ATTR cardiac amyloidosis patients and 11 healthy older male controls walked overground with and without a dual cognitive task. Gait parameters: stride width, length, velocity and stance time percentage were measured using an instrumented mat. ATTR amyloidosis patients were further categorized based on clinical and functional assessments.<br />Results: We found significant gait differences between ATTR cardiac amyloidosis patients and healthy controls; patients had more variable, slower, narrower and shorter strides, with their feet spending more time in contact with the ground as opposed to in swing. However, the observed gait differences did not correlate with clinical and functional measures of ATTR cardiac amyloidosis severity.<br />Conclusions: Our results suggest that gait analysis could be a complementary tool for characterizing ATTR cardiac amyloidosis patients and may inform clinical care as it relates to falls, management of anticoagulation, and functional independence.

Details

Language :
English
ISSN :
1744-2818
Volume :
31
Issue :
2
Database :
MEDLINE
Journal :
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis
Publication Type :
Academic Journal
Accession number :
38433466
Full Text :
https://doi.org/10.1080/13506129.2024.2319133