Axonal excitability as an early biomarker of nerve involvement in hereditary transthyretin amyloidosis.
Clin Neurophysiol
; 159: 81-95, 2024 03.
Article
en En
| MEDLINE
| ID: mdl-38377648
ABSTRACT
OBJECTIVES:
The treatment of hereditary transthyretin amyloidosis polyneuropathy (ATTRv-PN) has been revolutionised by genetic therapies, with dramatic improvements in patient outcomes. Whilst the optimal timing of treatment initiation remains unknown, early treatment is desirable. Consequently, the aim of the study was to develop biomarkers of early nerve dysfunction in ATTRv-PN.METHODS:
Ulnar motor and sensory axonal excitability studies were prospectively undertaken on 22 patients with pathogenic hereditary transthyretin amyloid (ATTRv) gene variants, 12 with large fibre neuropathy (LF+) and 10 without (LF-), with results compared to age- and sex-matched healthy controls.RESULTS:
In motor axons we identified a continuum of change from healthy controls, to LF- and LF+ ATTRv with progressive reduction in hyperpolarising threshold electrotonus (TEh40(10-20 ms) p = 0.04, TEh40(20-40 ms) p = 0.01 and TEh40(90-10 ms) p = 0.01), suggestive of membrane depolarisation. In sensory axons lower levels of subexcitability were observed on single (SubEx) and double pulse (SubEx2) recovery cycle testing in LF+ (SubEx p = 0.015, SubEx2 p = 0.015, RC(2-1) p = 0.04) suggesting reduced nodal slow potassium conductance, which promotes sensory hyperexcitability, paraesthesia and pain. There were no differences in sensory or motor excitability parameters when comparing different ATTRv variants.CONCLUSIONS:
These progressive changes seen across the disease spectrum in ATTRv-PN suggest that axonal excitability has utility to identify early and progressive nerve dysfunction in ATTRv, regardless of genotype.SIGNIFICANCE:
Axonal excitability is a promising early biomarker of nerve dysfunction in ATTRv-PN.Palabras clave
Texto completo:
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Base de datos:
MEDLINE
Asunto principal:
Polineuropatías
/
Neuropatías Amiloides Familiares
Idioma:
En
Revista:
Clin Neurophysiol
/
Clin. neurophysiol
/
Clinical neurophysiology
Asunto de la revista:
NEUROLOGIA
/
PSICOFISIOLOGIA
Año:
2024
Tipo del documento:
Article