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Transthyretin AmyloidosisBioTRAPNCT02713880

Biomarker for Transthyretin-Related Familial Amyloidotic Polyneuropathy (BioTRAP)

An observational study of Transthyretin Amyloidosis and Transthyretin-Related (ATTR) Familial Amyloid Polyneuropathy, run by CENTOGENE GmbH Rostock at 2 sites in 2 countries.

Withdrawn

Withdrawn. The study stopped before anyone enrolled.

Official record

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Trial summary

International, multicenter, observational, longitudinal study to identify biomarker/s for the development of a new MS-based biomarker for the early and sensitive diagnosis of Transthyretin-Related Familial Amyloidotic Polyneuropathy from blood and number of correctly identified patients with Transthyretin-Related… Read more about this study

Who is it for?
Ages 2 months and older
How many people
0 participants
Where
2 sitesin 2 countries
Study dates
20 Aug 2018to 1 Dec 2019
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 2 months and older
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: Patients with Transthyretin-Related Familial Amyloidotic Polyneuropathy or high-grade suspicion for Transthyretin-Related Familial Amyloidotic Polyneuropathy

Who may be able to join

  • Informed consent will be obtained from the parents before any study related procedures.
  • Patients of both genders older than 2 months
  • The patient has a diagnosis of Transthyretin-Related Familial Amyloidotic Polyneuropathy or a high-grade suspicion for Transthyretin-Related Familial Amyloidotic Polyneuropathy
  • High-grade suspicion present, if one or more inclusion criteria are valid:
  • Positive family anamnesis for Transthyretin-Related Familial Amyloidotic -Polyneuropathy
  • Orthostatic dysregulation
Show all 9Show fewer
  • Acroparaesthesia
  • Dysaesthesia and paraesthesia
  • Muscle paresis and atrophy

Who cannot join

  • No Informed consent from the parents before any study related procedures.
  • Patients of both genders younger than 2 months
  • No diagnosis of Transthyretin-Related Familial Amyloidotic Polyneuropathy or no valid criteria for profound suspicion of Transthyretin-Related Familial Amyloidotic Polyneuropathy

Trial locations and contacts

2 sites in 2 countries.

2 sites in 2 countries

Germany1 site
  • Centogene GmbH

    Rostock, 18055

Other trials in Germany

India1 site
  • Navi Mumbai Institute of Research In Mental And Neurological Handicap (NIRMAN)

    Mumbai, 400705

Other trials in India

About this study

Official title: Biomarker for Transthyretin-Related Familial Amyloidotic Polyneuropathy - An International, Multicenter, Epidemiological Protocol

International, multicenter, observational, longitudinal study to identify biomarker/s for the development of a new MS-based biomarker for the early and sensitive diagnosis of Transthyretin-Related Familial Amyloidotic Polyneuropathy from blood and number of correctly identified patients with Transthyretin-Related Familial Amyloidotic Polyneuropathy

Read the detailed description

Diseases of diverse etiology can be correlated to the term "polyneuropathy"(PNP). The pathogenesis may be of inflammatory, autoimmune, metabolic, toxic or hereditary nature. Careful clinical and electrodiagnostic assessment, with attention to the pattern of involvement and the types of nerve fibers most affected, narrows the differential diagnosis and helps to focus the laboratory evaluation. Beside the frequent genetic etiologies in PNP (pmp22, MFN2) one cause of a polyneuropathy may be a hereditary amyloidosis. This term describes the accumulation of misfolded protein in the interstitial space. The abnormal accumulation of β-fibrils can be detected histologically by Congo pink staining. Aside from acquired amyloidotic neuropathies (e.g. PNP caused by AL-amyloidosis [AL= amyloidosis with light chain immunoglobins]) there are also hereditary amyloidotic neuropathies.

These have been described as endemic in Sweden, Portugal or Japan. More recent studies provided evidence for the presence of hereditary amyloidotic neuropathies amongst the German population and that they are currently underdiagnosed. The most common form of the hereditary familial amyloidotic neuropathy (FAP) is the Transthyretin-related FAP, however two other amyloidogenic proteins have been described: Apolipoprotein A-I and Gelsolin (Ando et al., 2005; Adams et al., 2010).

The TTR-FAP is an autosomal dominant disease, the exact prevalence of which is unknown but estimated to be around 1:100,000 to 1:1,000,000 in the normal population. By limiting the study population to patients with PNP of unknown etiology it should be possible to gain evidence for the prevalence of the disease in Germany by investigating fewer patients.

While the diagnosis of the amyloidotic neuropathy can be conducted histologically, a molecular genetic approach is necessary to diagnose TTR-FAP. Even though more than 100 point mutations are known to cause the disease, the most common amino acid change is V30M.

The mutation in the TTR gene causes the destabilization of the physiologically tetrameric protein. Usually transthyretin consists of four identical monomeric subunits and binds the thyroxin circulating in the blood plasma. The monomeric subunits exhibit a pronounced β- sheet structure which leads to the accumulation of unsoluble β-fibrils when they are destabilised as in TTR-FAP.

This accumulation of misfolded TTR can lead to three phenotypes known as:

  • cardiac TTR amyloidosis
  • leptomeningeal TTR amyloidosis and the
  • TTR-FAP

The TTR-FAP has a very heterogeneous phenotype which can manifest starting at the age of 18 and may lead to death within 10 years. The symptoms can be categorized in three groups (Ando et al. 2005):

Dysfunction of peripheral nerves:

  • Dissociated anesthesia
  • Muscle paresis and atrophy
  • Dysaesthesia and paraesthesia
  • Reduced skin temperature
  • Coldness
  • Hoarseness

Autonomic dysfunction:

  • Dysuria
  • Diarrhea
  • Constipation
  • Orthostatic dysregulation
  • Erectile dysfunction
  • Nausea

Constitutional conditions

  • Anemia
  • Weight loss
  • Arrhythmia
  • Edema
  • Acroparaesthesia

The currently available therapeutic approaches are either liver transplantation (as the liver mainly produces transthyretin this is a feasible approach) or as of more recently also a TTR- tetramer stabilizing agent (Tafamidis). Tafamidis (Vyndaqel®) gained the European approval under "exceptional circumstances"in November 2011 for treating FAP in adults with a symptomatic polyneuropathy. In light of the potential therapy of this very rare disease, this study aims to determine the prevalence of TTR-FAP in a selected, clinical subpopulation. New methods, like mass-spectrometry give a good chance to characterize specific metabolic alterations in the blood (plasma) of affected patients that allow diagnosing in the future the disease earlier, with a higher sensitivity and specificity.

Therefore it is the goal of the study to identify and validate a new biochemical marker from the plasma of the affected patients helping to benefit other patients by an early diagnose and thereby with an earlier treatment.

Keywords
Amyloid Neuropathies, Biomarker
Medical subject headings
Amyloidosis, Hereditary, Transthyretin-Related, Amyloid Neuropathies, Familial, Amyloid Neuropathies

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT02713880
Study groupRoleWhat they receive
Patients with Transthyretin-Related FamilialPatients with Transthyretin-Related Familial Amyloidotic Polyneuropathy or high-grade suspicion for Transthyretin-Related Familial Amyloidotic Polyneuropathy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Development of a new MS-based biomarker for the early and sensitive diagnosis of Transthyretin-Related Familial Amyloidotic Polyneuropathy from blood

    Measured: 36 months

Secondary outcomes (1)
  1. Number of correctly identified patients with Transthyretin-Related Familial Amyloidotic Polyneuropathy

    Measured: 36 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 Mar 2016 (estimated)
  2. Study start20 Aug 2018
  3. Primary completion1 Dec 2019
  4. Study completion1 Dec 2019

Why it stopped: University of Rostock terminated participation in the study conduct; Study Sponsorship is moved to Centogene AG

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
0 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02713880
Sponsor's protocol ID
BTR 06-2018
Acronym
BioTRAP
Status last verified
Feb 2023
First submitted
13 Jan 2016
Last updated
10 Feb 2023
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

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