Quantification of muscle involvement in familial amyloid polyneuropathy using MRI

Author:

Durelle Clémence1ORCID,Delmont Emilien1ORCID,Michel Constance2,Trabelsi Amira3,Hostin Marc‐Adrien2,Ogier Augustin4ORCID,Bendahan David2ORCID,Attarian Shahram1

Affiliation:

1. Centre de référence des maladies neuromusculaires et de la SLA, hôpitaux universitaires de Marseille Marseille France

2. Centre de résonance magnétique biologique et médicale (Crmbm) Marseille France

3. Aix‐Marseille Univ, CNRS, Centrale Marseille Institute Fresnel Marseille France

4. Department of Radiology Lausanne University Hospital (CHUV) and University of Lausanne (UNIL) Lausanne Switzerland

Abstract

AbstractBackground and purposeTransthyretin familial amyloid polyneuropathy (TTR‐FAP) is a rare genetic disease with autosomal‐dominant inheritance. In this study, we aimed to quantify fatty infiltration (fat fraction [FF]) and magnetization transfer ratio (MTR) in individual muscles of patients with symptomatic and asymptomatic TTR‐FAP using magnetic resonance imaging. Secondarily, we aimed to assess correlations with clinical and electrophysiological variables.MethodsA total of 39 patients with a confirmed mutation in the TTR gene (25 symptomatic and 14 asymptomatic) and 14 healthy volunteers were included. A total of 16 muscles were manually delineated in the nondominant lower limb from T1‐weighted anatomical images. The corresponding masks were propagated on the MTR and FF maps. Detailed neurological and electrophysiological examinations were conducted in each group.ResultsThe MTR was decreased (42.6 AU; p = 0.001) and FF was elevated (14%; p = 0.003) in the lower limbs of the symptomatic group, with preferential posterior and lateral involvement. In the asymptomatic group, elevated FF was quantified in the gastrocnemius lateralis muscle (11%; p = 0.021). FF was significantly correlated with disease duration (r = 0.49, p = 0.015), neuropathy impairment score for the lower limb (r = 0.42, p = 0.041), Overall Neuropathy Limitations Scale score (r = 0.49, p = 0.013), polyneuropathy disability score (r = 0.57, p = 0.03) and the sum of compound muscle action potential (r = 0.52, p = 0.009). MTR was strongly correlated to FF (r = 0.78, p < 0.0001), and a few muscles with an FF within the normal range had a reduced MTR.ConclusionThese observations suggest that FF and MTR could be interesting biomarkers in TTR‐FAP. In asymptomatic patients, FF in the gastrocnemius lateralis muscle could be a good indicator of the transition from an asymptomatic to a symptomatic form of the disease. MTR could be an early biomarker of muscle alterations.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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