Inclusion Criteria:
For the Healthy Control group, participants eligible are persons who meet the following criteria:
1. Are capable of providing informed consent and
2. Are capable of complying with study procedures and
3. Are aged between 18-47 years old and
4. Have no known family history of HD (gene negative); or
5. Have known family history of HD but have been tested for the huntingtin gene CAG expansion and are not at genetic risk for HD (CAG \< 36\*) (family control or community control)
For the Young Adult Premanifest HD group, participants eligible are persons who meet the following criteria:
1. Are capable of providing informed consent and
2. Are capable of complying with study procedures and
3. Are aged between 18-47 years old and
4. Have CAG expansion ≥ 40;
5. New participants must have a DBS \<240
Exclusion Criteria:
Current use of investigational drugs or participation in a clinical drug trial within 30 days prior to study visit; or b. Current intoxication, drug or alcohol abuse or dependence; or c. If using any antidepressant, psychoactive, psychotropic or other medications or nutraceuticals used to treat HD, the use of inappropriate (e.g., non-therapeutically high) or unstable dose within 30 days prior to study visit; or d. Significant medical, neurological or psychiatric co-morbidity likely, in the judgment of the Principal Investigator, to impair participant's ability to complete essential study procedures; or e. Predictable non-compliance as assessed by the Principal Investigator; or f. Inability or unwillingness to undertake any of the essential study procedures; or g. Needle phobia: or h. Contraindication to MRI, including, but not limited to, MR-incompatible pacemakers, recent metallic implants, foreign body in the eye or other indications, as assessed by a standard pre-MRI questionnaire;or i. Pregnant (as confirmed by urine pregnancy test); or j. Claustrophobia, or any other condition that would make the subject incapable of undergoing an MRI.
For CSF collection:
1. Needle phobia, frequent headache, significant lower spinal deformity or major surgery; or
2. Antiplatelet or anticoagulant therapy within the 14 days prior to sampling visit, including but not limited to: aspirin, clopidogrel, dipyridamole, warfarin, dabigatran, rivaroxaban and apixaban; or
3. Clotting or bruising disorder; or
4. Screening blood test results outside the clinical laboratory's normal range for the following: white cell count, neutrophil count, lymphocyte count, haemoglobin (Hb), platelets, prothrombin time (PT) or activated partial thromboplastin time (APTT); or
5. Screening blood test results for C-reactive protein (CRP)\>2× upper limit of normal; or
6. Exclusion during history or physical examination, final decision to be made by the Principal Investigator; including but not limited to:
i any reason to suspect abnormal bleeding tendency, e.g. easy bruising, petechial rash; or ii any reason to suspect new focal neurological lesion, e.g. new headache, optic disc swelling, asymmetric focal long tract signs; or iii any other reason that, in the clinical judgment of the operator or the Principal Investigator, it is felt that lumbar puncture is unsafe.
For Optional 7T MRI and MEG
1. Contraindication to MRI, including, but not limited to, MR-incompatible pacemakers, recent metallic implants, foreign body in the eye or other indications, as assessed by a standard pre-MRI questionnaire; or
2. Pregnant (as confirmed by urine pregnancy test); or
3. Claustrophobia, or any other condition that would make the subject incapable of undergoing an MRI; or
4. Tattoos that fall above the line defined by the crease of the elbow or on the genitals.
