Chronic Inflammatory Demyelinating PolyradiculoneuropathyGEARCIDPNCT06325878
Genetic Architecture of Chronic Inflammatory Demyelinating Polyradiculoneuropathy
A study testing Genome-wide association study in people with Chronic Inflammatory Demyelinating Polyradiculoneuropathy, run by Istituto Clinico Humanitas at 1 site in Italy.
Trial summary
The objective of this study is to characterize the genetic architecture of a large cohort of CIDP patients to evaluate whether specific alleles/haplotypes are implicated in the risk of CIDP, in its clinical and immunological variability, severity, therapeutic response, and association with diabetes and other… Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Chronic Inflammatory Demyelinating Polyradiculoneuropathy
- What is being tested?
- Genome-wide association study
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 3,500 participants
- Where
- 1 siteItaly
- Study dates
- 15 Nov 2022to 31 Dec 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
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 Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- Subject with a documented diagnosis of according to the EAN/PNS criteria
Who cannot join
- Subject with an alternative diagnosis for the neuropathy
- Subject without available nerve conduction studies or documented diagnosis of CIDP
Trial locations and contacts
1 site in 1 country.
Italy1 site, 1 recruiting
- Recruiting
IRCCS Istituto Clinico Humanitas
Rozzano
Eduardo Nobile Orazio, Prof, eduardo.nobile@unimi.it
About this study
Official title: Dissecting the Genetic Architecture of Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP)
The objective of this study is to characterize the genetic architecture of a large cohort of CIDP patients to evaluate whether specific alleles/haplotypes are implicated in the risk of CIDP, in its clinical and immunological variability, severity, therapeutic response, and association with diabetes and other autoimmune diseases. We will genotype >700,000 single nucleotide polymorphisms (SNPs) by using the Illumina Global Screening Array (GSA), of approximately 1000 patients with CIDP. About 3500 healthy controls from the Italian population have been already genotyped using GWAS from our genetic department. Alleles/haplotypes will be also compared between patients with typical CIDP and its variants, between CIDP patients with and without specific antibodies, between CIDP patients with and without comorbidities, between CIDP patients with low and high levels of disability and between CIDP patients with and without response to each individual treatment (IVIg, steroids, plasma exchange)
Read the detailed description
- Specific aim 1: Characterize the genetic architecture of CIDP by using a genome-wide association study (GWAS) approach in a large cohort of CIDP patients and healthy controls, thus defining the 1) Specific aim 1: Characterize the genetic architecture of CIDP by using a genome-wide association study (GWAS) approach in a large cohort of CIDP patients and healthy controls, thus defining the spectrum of single common variants or their combinations (in terms of haplotypes or risk score) predisposing to the disease. Hypothesis: The frequency of specific alleles/haplotypes in patients with CIDP is significantly different compared to that of the general population. Approach: We will genotype >700,000 single nucleotide polymorphisms (SNPs) by using the Illumina Global Screening Array (GSA), of approximately 1000 patients with CIDP. About 3500 healthy controls from the Italian population have been already genotyped using GWAS from our genetic department (Prof. Asselta, Humanitas Research Institute, Milan).
- Specific aim 2: Explore the role of specific alleles/haplotypes in determining the clinical and immunological variability, severity, and therapeutic response of CIDP. Hypothesis: The genetic architecture of patients with typical CIDP is -at least in part- distinct from that of the CIDP variants; specific alleles/haplotypes associate with intermediate phenotypes, such as the presence of antibodies anti-NF155, anti-NF186, CNTN1, anti-gangliosides; Specific alleles/haplotypes correlate with severity and treatment-response of CIDP. Approach: Alleles/haplotypes evidence through GWAS will be compared between patients with typical CIDP and its variants, between CIDP patients with and without specific antibodies, between CIDP patients with low and high levels of disability and between CIDP patients with and without response to each individual treatment (IVIg, steroids, plasma exchange) in order to determine whether genetics play a role in determining these phenotypes.
- Specific aim 3: Verify possible overlaps between CIDP and other autoimmune diseases.
Hypothesis: Alleles/haplotypes identified through GWAS play a role in the increased risk of diabetes and other autoimmune disease in CIDP.
Approach: Alleles/haplotypes evidence through GWAS will be compared between CIDP patients with and without diabetes mellitus, and with and without any other autoimmune diseases.
This is a multicenter, international, observational study where a large number of CIDP patients will be screened using GWAS. About 3500 healthy controls from the Italian population have been already genotyped using GWAS. Patients with a diagnosis of CIDP according to the current diagnostic criteria will be included. Patients with autoimmune nodopathies will be also included. Patients must give informed consent to participate. For all the patients, the diagnosis at enrollment will be revised by the coordinating Center, according to the European Academy of Neurology/Peripheral Nerve Society (EAN/PNS) diagnostic criteria.
All included patients will undergo a detailed clinical history including time of clinical onset, presence - distribution and date of onset of motor and sensory symptoms, ataxia, pain, tremor, cramps, fatigue, autonomic dysfunction, and cranial nerve involvement using a specific questionnaire. This information will be integrated with the data reported in the medical records. Disease course will be defined as progressive, relapsing or monophasic by the treating neurologist. The clinical evaluation at enrolment will include assessment of muscle strength using the Medical Research Council (MRC) sumscore on 12 muscles (range 0-60). Neurological disability will be evaluated at enrollment with the Inflammatory-Rash Overall Built Disability Scale (I-RODS), and the Inflammatory Neuropathy Cause and Treatment (INCAT) disability scale, while Quality of life (QoL) will be assessed with the EuroQol-5D-3L scale. Response to treatment will be defined as a subjective improvement that was objectively confirmed by I-RODS: + ≥ 4 centile points, or INCAT disability scale (≥ 1 point), or MRC sum score (0-60) (≥ 2-4 points), or grip strength using Martin Vigorimeter (≥ 8 -14 kPa).6 Results of previously performed examinations including cerebrospinal fluid (CSF) analysis, nerve ultrasound or brachial/lumbosacral plexus MR (magnetic resonance) examination and sural nerve biopsy, will be included when available. The results of nerve conduction studies performed during the course of the disease will be included. Sensory nerve conduction studies will be performed bilaterally in median, ulnar and sural nerves and included evaluation of sensory nerve action potential amplitude, distal latency and sensory conduction velocity. Motor nerve conduction studies will be also performed bilaterally in median, ulnar, common peroneal and tibial nerves and included distal and proximal compound muscle action potential amplitude and duration, motor conduction velocity, distal and proximal motor latency and in most patients F-wave latency. Abnormalities of motor and sensory nerve conduction studies consistent with demyelination will be defined according to the EAN/PNS criteria. In all the patients, the diagnosis at entry will be revised by the coordinating Center according to the above-mentioned diagnostic criteria.
Patient's data will be shared under pseudonymised form using the patients' code among the centres.
Enrollment in the study will be offered to all patients included in the Italian CIDP database. Enrollment will then be extended to other Italian and European centers
- Being tested
- Genome-wide association study
- Keywords
- Chronic Inflammatory Polyradiculoneuropathy, Polyneuropathy, Inflammatory Demyelinating, Chronic, Chronic Inflammatory Demyelinating Polyradiculoneuropathy, cidp
- Medical subject headings
- Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Genome-wide association studyGenetic
Alleles/haplotypes evidence through GWAS will be compared between patients with CIDP and control subjects without CIDP
| Study group | Role | What they receive |
|---|---|---|
| Chronic inflammatory demyelinating polyneuropathy (CIDP) | Experimental | Single nucleotide polymorphisms (SNPs) of 1000 patients with chronic inflammatory demyelinating polyneuropathy will be genotyped using the Illumina Global Screening Array Receives: Genetic: Genome-wide association study |
| Control Subjects | Experimental | Single nucleotide polymorphisms (SNPs) of 2500 control subjects without chronic inflammatory demyelinating polyneuropathy will be genotyped using the Illumina Global Screening Array Receives: Genetic: Genome-wide association study |
What is being measured
The primary outcome is the main question the study is designed to answer.
single nucleotide polymorphisms (SNPs)
Differences in single nucleotide polymorphisms (SNPs) between CIDP patients and controls
Measured: 3 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Mar 2024
- Study start15 Nov 2022
- Primary completion31 Dec 2025 (estimated)
- Study completion31 Dec 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Chronic Inflammatory Demyelinating PolyradiculoneuropathyStudies of the same condition, open and under way.
- More trials run by Istituto Clinico HumanitasThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Basic science
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 3,500 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Istituto Clinico Humanitas
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Pietro Emiliano Doneddu, MD, Principal investigator, Humanitas Research Institute
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06325878
- Sponsor's protocol ID
- NEU2-OSS-2022-001
- Acronym
- GEARCIDP
- Status last verified
- Mar 2024
- First submitted
- 16 Mar 2024
- Last updated
- 26 Mar 2024
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 26 Mar 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Dissecting the Genetic Architecture of Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP)
- ClinicalTrials.gov ID
- NCT06325878
- Acronym / sponsor ID
- GEARCIDP / NEU2-OSS-2022-001
- Keywords
- Chronic Inflammatory Polyradiculoneuropathy, Polyneuropathy, Inflammatory Demyelinating, Chronic, Chronic Inflammatory Demyelinating Polyradiculoneuropathy, cidp
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 3,500 participants (estimated)
- Lead sponsor
- Istituto Clinico HumanitasUniversity, hospital or other
- Study start
- 15 Nov 2022 (actual)
- Primary completion
- 31 Dec 2025 (estimated)
- Study completion
- 31 Dec 2025 (estimated)
- First posted
- 22 Mar 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The objective of this study is to characterize the genetic architecture of a large cohort of CIDP patients to evaluate whether specific alleles/haplotypes are implicated in the risk of CIDP, in its clinical and immunological variability, severity, therapeutic response, and association with diabetes and other autoimmune diseases. We will genotype >700,000 single nucleotide polymorphisms (SNPs) by using the Illumina Global Screening Array (GSA), of approximately 1000 patients with CIDP. About 3500 healthy controls from the Italian population have been already genotyped using GWAS from our genetic department. Alleles/haplotypes will be also compared between patients with typical CIDP and its variants, between CIDP patients with and without specific antibodies, between CIDP patients with and without comorbidities, between CIDP patients with low and high levels of disability and between CIDP patients with and without response to each individual treatment (IVIg, steroids, plasma exchange)
Detailed description
- Specific aim 1: Characterize the genetic architecture of CIDP by using a genome-wide association study (GWAS) approach in a large cohort of CIDP patients and healthy controls, thus defining the 1) Specific aim 1: Characterize the genetic architecture of CIDP by using a genome-wide association study (GWAS) approach in a large cohort of CIDP patients and healthy controls, thus defining the spectrum of single common variants or their combinations (in terms of haplotypes or risk score) predisposing to the disease. Hypothesis: The frequency of specific alleles/haplotypes in patients with CIDP is significantly different compared to that of the general population. Approach: We will genotype >700,000 single nucleotide polymorphisms (SNPs) by using the Illumina Global Screening Array (GSA), of approximately 1000 patients with CIDP. About 3500 healthy controls from the Italian population have been already genotyped using GWAS from our genetic department (Prof. Asselta, Humanitas Research Institute, Milan).
- Specific aim 2: Explore the role of specific alleles/haplotypes in determining the clinical and immunological variability, severity, and therapeutic response of CIDP. Hypothesis: The genetic architecture of patients with typical CIDP is -at least in part- distinct from that of the CIDP variants; specific alleles/haplotypes associate with intermediate phenotypes, such as the presence of antibodies anti-NF155, anti-NF186, CNTN1, anti-gangliosides; Specific alleles/haplotypes correlate with severity and treatment-response of CIDP. Approach: Alleles/haplotypes evidence through GWAS will be compared between patients with typical CIDP and its variants, between CIDP patients with and without specific antibodies, between CIDP patients with low and high levels of disability and between CIDP patients with and without response to each individual treatment (IVIg, steroids, plasma exchange) in order to determine whether genetics play a role in determining these phenotypes.
- Specific aim 3: Verify possible overlaps between CIDP and other autoimmune diseases.
Hypothesis: Alleles/haplotypes identified through GWAS play a role in the increased risk of diabetes and other autoimmune disease in CIDP.
Approach: Alleles/haplotypes evidence through GWAS will be compared between CIDP patients with and without diabetes mellitus, and with and without any other autoimmune diseases.
This is a multicenter, international, observational study where a large number of CIDP patients will be screened using GWAS. About 3500 healthy controls from the Italian population have been already genotyped using GWAS. Patients with a diagnosis of CIDP according to the current diagnostic criteria will be included. Patients with autoimmune nodopathies will be also included. Patients must give informed consent to participate. For all the patients, the diagnosis at enrollment will be revised by the coordinating Center, according to the European Academy of Neurology/Peripheral Nerve Society (EAN/PNS) diagnostic criteria.
All included patients will undergo a detailed clinical history including time of clinical onset, presence - distribution and date of onset of motor and sensory symptoms, ataxia, pain, tremor, cramps, fatigue, autonomic dysfunction, and cranial nerve involvement using a specific questionnaire. This information will be integrated with the data reported in the medical records. Disease course will be defined as progressive, relapsing or monophasic by the treating neurologist. The clinical evaluation at enrolment will include assessment of muscle strength using the Medical Research Council (MRC) sumscore on 12 muscles (range 0-60). Neurological disability will be evaluated at enrollment with the Inflammatory-Rash Overall Built Disability Scale (I-RODS), and the Inflammatory Neuropathy Cause and Treatment (INCAT) disability scale, while Quality of life (QoL) will be assessed with the EuroQol-5D-3L scale. Response to treatment will be defined as a subjective improvement that was objectively confirmed by I-RODS: + ≥ 4 centile points, or INCAT disability scale (≥ 1 point), or MRC sum score (0-60) (≥ 2-4 points), or grip strength using Martin Vigorimeter (≥ 8 -14 kPa).6 Results of previously performed examinations including cerebrospinal fluid (CSF) analysis, nerve ultrasound or brachial/lumbosacral plexus MR (magnetic resonance) examination and sural nerve biopsy, will be included when available. The results of nerve conduction studies performed during the course of the disease will be included. Sensory nerve conduction studies will be performed bilaterally in median, ulnar and sural nerves and included evaluation of sensory nerve action potential amplitude, distal latency and sensory conduction velocity. Motor nerve conduction studies will be also performed bilaterally in median, ulnar, common peroneal and tibial nerves and included distal and proximal compound muscle action potential amplitude and duration, motor conduction velocity, distal and proximal motor latency and in most patients F-wave latency. Abnormalities of motor and sensory nerve conduction studies consistent with demyelination will be defined according to the EAN/PNS criteria. In all the patients, the diagnosis at entry will be revised by the coordinating Center according to the above-mentioned diagnostic criteria.
Patient's data will be shared under pseudonymised form using the patients' code among the centres.
Enrollment in the study will be offered to all patients included in the Italian CIDP database. Enrollment will then be extended to other Italian and European centers
Study design
- Primary purpose
- Basic science
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Chronic inflammatory demyelinating polyneuropathy (CIDP) | Experimental | Genetic: Genome-wide association studySingle nucleotide polymorphisms (SNPs) of 1000 patients with chronic inflammatory demyelinating polyneuropathy will be genotyped using the Illumina Global Screening Array |
| Control Subjects | Experimental | Genetic: Genome-wide association studySingle nucleotide polymorphisms (SNPs) of 2500 control subjects without chronic inflammatory demyelinating polyneuropathy will be genotyped using the Illumina Global Screening Array |
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (1 listed)
- Subject with a documented diagnosis of according to the EAN/PNS criteria
Key exclusion criteria (2 listed)
- Subject with an alternative diagnosis for the neuropathy
- Subject without available nerve conduction studies or documented diagnosis of CIDP
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Genome-wide association studyAlleles/haplotypes evidence through GWAS will be compared between patients with CIDP and control subjects without CIDP | Genetic | Chronic inflammatory demyelinating polyneuropathy (CIDP), Control Subjects |
Primary outcome
single nucleotide polymorphisms (SNPs)
Time frame: 3 years
Differences in single nucleotide polymorphisms (SNPs) between CIDP patients and controls
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 Mar 2024.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Pietro Emiliano Doneddu, MD principal investigator
Humanitas Research Institute
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Genome-wide association study in people with Chronic Inflammatory Demyelinating Polyradiculoneuropathy, run by Istituto Clinico Humanitas at 1 site in Italy.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 26 Mar 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Pietro Emiliano Emiliano Doneddu, MD (00390282247761, pietro.doneddu@hunimed.eu), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
single nucleotide polymorphisms (SNPs) (time frame: 3 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Mar 2024.