Genetic Architecture of Chronic Inflammatory Demyelinating Polyradiculoneuropathy
NCT06325878 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 3500
Last updated 2024-03-26
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 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)
Conditions
- Chronic Inflammatory Demyelinating Polyradiculoneuropathy
Interventions
- GENETIC
-
Genome-wide association study
Alleles/haplotypes evidence through GWAS will be compared between patients with CIDP and control subjects without CIDP
Sponsors & Collaborators
-
Istituto Clinico Humanitas
lead OTHER
Principal Investigators
-
Pietro Emiliano Doneddu, MD · Humanitas Research Institute
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- BASIC_SCIENCE
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-11-15
- Primary Completion
- 2025-12-31
- Completion
- 2025-12-31
Countries
- Italy
Study Locations
More Related Trials
-
Genotype-phenotype Characterization Study on Genetic Diseases With Immune and Neurological Dysfunctions
NCT06235580 ·Status: RECRUITING
-
Genetic Profile In Patients With Ruptured and Unruptured Intracranial Aneurysms
NCT07233915 ·Status: RECRUITING
-
Blood Sample Donations to Study the Role of Genes in Pain
NCT00341367 ·Status: COMPLETED
-
Observational Study of the Impact of Genetic Testing on Healthcare Decisions and Care in Interventional Pain Management
NCT02485795 ·Status: UNKNOWN
-
Protective Genetic Factors Against Neurological Diseases
NCT03914599 ·Status: COMPLETED
-
Functional Genomics of Rare Genetic Diseases: Realization of Innovative Tools With High Diagnostic Power
NCT04152876 ·Status: UNKNOWN
-
Genetics in the Progression of Nephropathies
NCT06416761 ·Status: RECRUITING
-
Genetics of Rheumatoid Arthritis
NCT00001678 ·Status: COMPLETED
-
Search for Phenotype-modifying Genes in Patients With Intellectual Disabilities.
NCT06706934 ·Status: NOT_YET_RECRUITING
-
Clinical and Genetic Evaluation of Individuals With Undiagnosed Disorders Through the Undiagnosed Diseases Network
NCT02450851 ·Status: RECRUITING
-
A Genetic Linkage Study of Schizophrenia
NCT00155688 ·Status: COMPLETED
-
A Study of the Impact of Genetic Testing on Clinical Decision Making and Patient Care
NCT02487888 ·Status: UNKNOWN ·Phase: NA
-
Genetic Analysis to Predict the Development of Paget's Disease
NCT05309954 ·Status: ACTIVE_NOT_RECRUITING
-
Study of Inherited Neurological Disorders
NCT00004568 ·Status: RECRUITING
-
Studies of Heritable Disorders of Connective Tissue
NCT00270686 ·Status: COMPLETED
-
Genomics of Fibrin Clot Structure in Patients With Constitutional Dysfibrinogenemia
NCT05233384 ·Status: ACTIVE_NOT_RECRUITING
-
Genetic Predictors of Lithium Response in Bipolar Disorder
NCT00252577 ·Status: COMPLETED
-
Pain Predict Genetics
NCT02383342 ·Status: RECRUITING
-
Genetic and Blood Biomarkers in Neurological and Neuromuscular Diseases
NCT02780531 ·Status: COMPLETED
-
Nephronophthisis : Clinical and Genetic Study
NCT01022957 ·Status: COMPLETED ·Phase: NA
-
Study to Identify the Genetic Variations Associated With Phantom Limb Pain
NCT01462448 ·Status: COMPLETED
-
Study of the Genetic Factors Involved in Autism and Related Disorders
NCT04727489 ·Status: RECRUITING
-
Prevalence Of Germline Gene Mutations In Patients With Myeloproliferative Neoplasms With Family History
NCT06923670 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Pharmacogenetic Testing and Chronic Pain
NCT05259865 ·Status: SUSPENDED
-
Longitudinal Study of Neurogenetic Disorders
NCT03492060 ·Status: RECRUITING