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临床试验/NCT05534139
NCT05534139招募中不适用

Clinicopathological MRI and CSF Correlates of Iron Accumulation, Neurodegeneration and Neuroinflammation in Huntington's Disease.

Leiden University Medical Center1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2021年8月11日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
90
试验地点
1
主要终点
Quantified Susceptibility Mapping

研究概览

简要总结

In this study the investigators will link brain iron levels obtained from quantitative susceptibility maps of HD patients with specific and well-known clinical CSF markers for iron accumulation, neurodegeneration and neuroinflammation. The relationship between iron accumulation and neuroinflammation, and the clinical and genetic characteristics of HD will be investigated. This will provide an important basis for the evaluation of brain iron levels as an imaging biomarker for disease state in HD and their relationship with the salient pathomechanisms of the disease.

详细描述

This investigator-initiated, single-site cross-sectional study looks at iron accumulation using 7T MR-imaging, CSF and blood. This will be achieved in a two-day visit involving clinical assessments, MRI-scanning of the brain, followed by a lumbar puncture the next day, after overnight fasting. Sixty-five volunteers with HD and 25 volunteers without HD will be included. Of these 65 volunteers with HD, 25 will be premanifest, 20 early manifest and 20 moderate manifest, in order to cover the wide-spectrum of Huntington's Disease.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Cross Sectional

入排标准

年龄范围
21 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Native Dutch/Flemish speaker
  • Ability to undergo MRI scanning;
  • Written informed consent must be obtained from the participant.
  • And in addition:
  • If the participant is a pre-manifest HD gene carrier:
  • CAG expansion ≥ 40;
  • UHDRS Total Motor Score (TMS) ≤ 5;
  • Total Functional Capacity (TFC) = 13;
  • Diagnostic Confidence Score <
  • If the participant is an early-manifest HD gene carrier:
  • CAG expansion ≥ 36;
  • Diagnostic Confidence Score = 4;
  • HD stage I: TFC scores between 11 and 13 inclusive.
  • If the participant is a moderate manifest HD gene carrier:
  • CAG expansion ≥ 36;
  • Diagnostic Confidence Score = 4;
  • HD stage II: TFC scores between 7 and 11 inclusive.
  • If the participant is a control subject:
  • Partner/spouse of a patient not at risk of HD OR sibling with genetic test results available that show a normal CAG repeat length for both HTT alleles (<36);
  • No other known cognitive, neurological or psychiatric disorders.

排除标准

  • Additional major comorbidities not related to HD (e.g. cardiovascular diseases, coagulopathy, hypertension, diabetes mellitus, and/or other neurological disorders);
  • History of severe head injury;
  • Status of the participant after brain surgery;
  • Past erythrocyte transfusions;
  • Use of investigational drugs or participation in a clinical drug trial within 30 days prior to study visit;
  • Current intoxication, drug or alcohol abuse or dependence;
  • Pregnancy;
  • Inability to understand the information about the protocol;
  • Severe physical restrictions (completely wheelchair dependent);
  • Severe chorea that, in the investigator's judgment, precludes the patient's participation in and completion of the MRI and/or lumbar puncture.
  • Contra-indication to MRI scanning, such as:
  • Claustrophobia;
  • Pacemakers and defibrillators;
  • Nerve stimulators;
  • Intracranial clips;
  • Intraorbital or intraocular metallic fragments;
  • Cochlear implants;
  • Ferromagnetic implants;
  • Hydrocephalus pump;
  • Intra-utrine device (not all types);
  • Permanent make-up;
  • Tattoos above the shoulders (not all).
  • Contraindications for a lumbar puncture, including:
  • Screening blood test results outside normal ranges(white cell count, neutrophil count, lymphocyte count, hemoglobin, platelets, Prothrombin time (PT), activated partial thromboplastin time (APTT), C-reactive protein (CRP) and serum ferritin) if only marginally decreased or increased this will be decided by the clinical PI;
  • Signs and symptoms of increased intracranial pressure which will be confirmed on the 7T MRI (T1 and FLAIR scan) or by a fundoscopy;
  • Local infections of the skin;
  • Use of anti-coagulant drugs within the last 14 days prior lumbar puncture.

结局指标

主要结局

Quantified Susceptibility Mapping

时间窗: At baseline

MRI analysis to quantify iron accumulation

Iron in CSF

时间窗: At baseline

Amount of iron and ferritin measured in CSF

次要结局

  • Neuroinflammation and neurodegeneration biomarkers in CSF(Baseline)
  • Cognitive score(At baseline)
  • Iron in blood(At baseline)
  • Clinical motor signs(At baseline)
  • Neuropsychiatric symptoms(At baseline)

研究者

发起方
Leiden University Medical Center
申办方类型
Other
责任方
Principal Investigator
主要研究者

Susanne T de Bot, MD, PhD

MD PhD

Leiden University Medical Center

研究点 (1)

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