Letter to the editor
Autosomal-dominant transthyretin (TTR)-related amyloidosis usually manifests in the second to over sixth decade with a length-dependent axonal neuropathy with prominent involvement of the small fibers and multi-organ systemic failure.
In Portugal and Sweden where Transthyretin Related Familial Amyloid Polyneuropathy (TTR-FAP) is endemic, disease prevalence ranges from 1 in 1.000 to 1 in 10.000 people. Beyond these endemic regions, the incidence of TTR-FAP is much lower.
Anzeige
More than 130 different mutations of TTR have been identified worldwide, but the first-described Val30Met mutation remains the most common with an early onset phenotype, which is typical in Portuguese population [1]. The prevalence of different mutations varies according to ethnicity and geographic region. In Italy few regions (Sicily, Puglia, Lazio, Piedmont, Tuscan-Emilian Apennines) are endemic for specific mutations.
Early diagnosis is pivotal for effective therapeutic options, but it is hampered by the heterogeneity of the clinical spectrum in not-Portuguese populations, in which the divergences from the canonical phenotype are relevant [2]. In the last years many groups described patients carrying TTR mutations and showing misleading clinical features [3, 4] or mimicking other neurological disorders as ALS [5, 6].
In 2011, Cappellari and colleagues reported atypical presentation of TTR-related familial amyloid polyneuropathy in Italian families. In their sample a relevant percentage of patients (76,4%; 13/17) received no diagnosis or a wrong diagnosis at onset, including Charcot-Marie-Tooth disease (CMT) in 2 patients.
The aim of our study was to search for TTR mutations in a large cohort of selected undiagnosed axonal sensory-motor neuropathy patients, classified as CMT2, to establish if CMT could occasionally mimic TTR-FAP. For this purpose, 98 consecutive patients, referred from all Italian Regions and affected with late onset axonal CMT (≥ 30 y), were enrolled at CMT Clinics of Ospedale Policlinico San Martino. Since we were looking for possible atypical TTR presentation, our selected cases had clinical features quite far from classic TTR phenotype. In particular, the mean age of onset was 46.4 years (SD: ±12,9 y; median 45 y) and the mean disease duration was 8.9 years (median: 4.5; range: some months – 53 years). Main clinical features are summarized in Table 1.
Table 1
Main clinical features
Total patients | 98 |
|---|---|
Male | 51 |
Female | 47 |
Mean age | 55 yr |
Mean onset | 46,4 ± 12,9 yr |
Median onset | 45 yr |
Mean disease duration | 8,9 ± 10,2 yr |
Median disease duration | 4,5 yr |
Prevalent motor neuropathy | 13,20% |
Sensory motor neuropathy | 86,80% |
Hypoacusia | 4% |
Tremor | 1% |
Anzeige
All patients resulted negative for mutations in the most frequently mutated CMT2 genes (MPZ, MNF2, GDAP1, GJB1, NEFL). All patients underwent neurological and neurophysiological evaluation, had regular annual follow up at CMT Clinics and give informed consent to this genetic study.
No pathogenic TTR variants were found in this cohort.
Transthyretin-related amyloidosis is a severe multi-organ disease leading to death within 10 years after the first symptoms occur. Since several pharmacological treatments are now available [7‐10], it is crucial to identify any potential case and to implement diagnostic strategies to reach an early diagnosis and plan a tailored therapy. In the early stages, a possible misdiagnosis with CIDP has been often reported and different authors recommend to consider TTR-related amyloidosis in cases presenting as immune-mediated neuropathies not responding to immunomodulant therapies [3].
Coincident Diabetes Mellitus and Monoclonal Gammopathy of Undetermined Significance, both frequent particularly in elder population, could also mask a TTR-related amyloidosis [11].
Charcot-Marie-Tooth disease is the most frequent inherited neuromuscular disorder and, in spite of a huge genetic heterogeneity, has peculiar clinical hallmarks as distal weakness and atrophy and pes cavus. The subgroup of patients presenting with a late onset axonal CMT2 could share some clinical features with TTR related amyloidosis, even if the course is often slowly instead of rapidly progressing.
Since Cappellari and colleagues identified a TTR mutation in two patients previously classified as CMT2 patients, we decided to screen a cohort of late onset CMT2 patients in which mutations in major CMT2-related genes have been excluded.
The study has some limitations. The number of CMT2 patients with a late onset, screened in this project, were referred from many Italian Regions in which TTR amyloidosis is not endemic and limited to 98 subjects, thus affecting the diagnostic yield.
However, although in a small sample, misdiagnosis of TTR-FAP in CMT2 patients seems not to be common.
Anzeige
In conclusion, our study shows that TTR testing not should be recommended in CMT2 patients but only when “red flags” TTR’s features are present, such as a rapid progressive course, carpal tunnel syndrome particularly in males, cardiologic involvement or signs suggesting autonomic nervous system impairment.
Funding
The present study was supported by a Research Grant from Pfizer Inc. Pfizer Inc. had no role in the study design, data analysis, and results interpretation of the present study.
Availability of data and materials
The datasets used for the current study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
All patients signed an informed consent to genetic study approved by ethical committee of IRCCS Policinico San Martino, Genova, Italy.
Anzeige
Consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.