Retina Microvascular Remodeling and Cognitive Function In Hypertension (EYEBRAIN)

Retina Microvascular Remodeling and Cognitive Function In Hypertension : Eyebrain

This study aims to determine the relationships between retina micro-vascular remodeling and cognitive function in hypertensive patients.

The study plans to enrol 160 patients (100 patients with mild cognitive impairment -MCI- and 60 without MCI).

Study Overview

Detailed Description

Our project stands on physiopathological and cognitive angles, and is mainly based on the major role of large and small arteries elasticity on cognitive aging. It will benefit from the recent innovative accurate and non invasive techniques such as MRI for central large arteries and adaptative optics for retina arterioles imaging.

Study population is the following:

  • 60 patients with hypertension and no MCI,
  • 50 patients with hypertension and stable MCI, without dementia
  • 50 patients with hypertension and progressive MCI, without dementia

Every patients will perform a medical interview and examination, an MRI (brain + aorta), adaptative optics imaging, a cognitive tests and a blood test.

Primary outcome is to determine the relationships between retina micro-vascular remodeling and cognitive function in this population.

Study Type

Observational

Enrollment (Anticipated)

160

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Paris, France, 75013
        • Recruiting
        • Unité de prévention des maladies cardiovasculaires Pôle Cardiologie/Métabolisme Hôpital Pitié-Salpétriêre, APHP, 83 bd de l'hôpital,
        • Contact:
          • David Rosenbaum, Dr

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

65 years and older (OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Patients' recruitment will be carried out in two centers to ensure inclusion of both patients: 1) with hypertension and without cognitive impairment, 2) with hypertension and with mild cognitive impairment (without dementia) including patients with stable MCI and converters.

Population size: 160 patients:

  • 60 patients with hypertension and no MCI,
  • 50 patients with hypertension and stable MCI, without dementia
  • 50 patients with hypertension and progressive MCI, without dementia

Description

Inclusion Criteria:

  1. Aged 65 or more
  2. hypertension (BP ≥140/90 mmHg and/or antihypertensive treatment)
  3. Signed informed consent by the patient
  4. Sufficient mastery of the French language to perform neuropsychological tests

Exclusion Criteria:

  1. Impossibility to visualize the retinal : severe cataract
  2. Dementia (defined by MMSE<20)
  3. Clinical stroke
  4. Severe or resistant Hypertension
  5. Hypertension treated with more than 3 different pharmacological classes
  6. any other disease that may interfere with the assessment of cognitive disorders (epilepsy, Parkinson's disease, major depression, schizophrenia, manic-depressive)
  7. Enrolment in a therapeutic trial that could interfere with the main objective
  8. Less than 4 years of formal education
  9. Illiterate, unable to read, write or count
  10. major physical problems that may interfere with the tests (sight, hearing, ...)
  11. Short term life threatening disease
  12. Non-affiliation to a healthcare system
  13. Consent refusal
  14. Contraindication to MRI including claustrophobia, metallic devices, pacemaker, mechanical valve implanted before 1985, and nursing, as well as technical contra-indication: patient diameter > 70 cm or/and weight > 250 kg

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Hypertension and progressive MCI
50 subjects will perform brain and aorta RMI, blood test, cognitive tests and adaptative optics.

Cognitive tests include:

  • The MMSE (Mini Mental State Examination)
  • Free and Cued Selective Recall Reminding Test (FCSRT).
  • Executive functions (fluencies, TMT A and B, span).
  • Tests of verbal fluency (literal and category)
  • Digit symbol substitution test or Wechsler adult intelligence scale (W.A.I.S)
  • The Clinical Dementia Rating Scale
  • The IADL scale evaluates autonomy.
  • Geriatric Depression screening Scale (GDS)
A blood test will be performed in order to collect following parameters: Urea, BUN, Creatinine, Potassium, Sodium, hematocrit, hsCRP, NFS, Pq, LDL-C, HDL-C, Triglycerides, Lp(a), Lp-PLA2 as well as fasting glucose, HbA1C and microalbuminuria
A magnetic resonance imaging exam will be performed at the Neuroimaging Research Center of the Pitié-Salpêtrière Hospital. This exam will be optimized to fit in 30 minutes. Indeed brain 3D T1 and T2 FLAIR imaging lasts 15 minutes while cine and velocity encoded imaging of the aorta lasts 15 minutes.
The retina adaptative optic imaging will be performed at the "Unité de prevention des maladies cardiovasculaires" Pitié Salpetrière Hospital. This exam lasts 10 minutes including patient positioning and imaging.
Hypertension and stable MCI
50 subjects will perform brain and aorta RMI, blood test, cognitive tests and adaptative optics.

Cognitive tests include:

  • The MMSE (Mini Mental State Examination)
  • Free and Cued Selective Recall Reminding Test (FCSRT).
  • Executive functions (fluencies, TMT A and B, span).
  • Tests of verbal fluency (literal and category)
  • Digit symbol substitution test or Wechsler adult intelligence scale (W.A.I.S)
  • The Clinical Dementia Rating Scale
  • The IADL scale evaluates autonomy.
  • Geriatric Depression screening Scale (GDS)
A blood test will be performed in order to collect following parameters: Urea, BUN, Creatinine, Potassium, Sodium, hematocrit, hsCRP, NFS, Pq, LDL-C, HDL-C, Triglycerides, Lp(a), Lp-PLA2 as well as fasting glucose, HbA1C and microalbuminuria
A magnetic resonance imaging exam will be performed at the Neuroimaging Research Center of the Pitié-Salpêtrière Hospital. This exam will be optimized to fit in 30 minutes. Indeed brain 3D T1 and T2 FLAIR imaging lasts 15 minutes while cine and velocity encoded imaging of the aorta lasts 15 minutes.
The retina adaptative optic imaging will be performed at the "Unité de prevention des maladies cardiovasculaires" Pitié Salpetrière Hospital. This exam lasts 10 minutes including patient positioning and imaging.
Hypertension, without MCI
60 subjects will perform brain and aorta RMI, blood test, cognitive tests and adaptative optics.

Cognitive tests include:

  • The MMSE (Mini Mental State Examination)
  • Free and Cued Selective Recall Reminding Test (FCSRT).
  • Executive functions (fluencies, TMT A and B, span).
  • Tests of verbal fluency (literal and category)
  • Digit symbol substitution test or Wechsler adult intelligence scale (W.A.I.S)
  • The Clinical Dementia Rating Scale
  • The IADL scale evaluates autonomy.
  • Geriatric Depression screening Scale (GDS)
A blood test will be performed in order to collect following parameters: Urea, BUN, Creatinine, Potassium, Sodium, hematocrit, hsCRP, NFS, Pq, LDL-C, HDL-C, Triglycerides, Lp(a), Lp-PLA2 as well as fasting glucose, HbA1C and microalbuminuria
A magnetic resonance imaging exam will be performed at the Neuroimaging Research Center of the Pitié-Salpêtrière Hospital. This exam will be optimized to fit in 30 minutes. Indeed brain 3D T1 and T2 FLAIR imaging lasts 15 minutes while cine and velocity encoded imaging of the aorta lasts 15 minutes.
The retina adaptative optic imaging will be performed at the "Unité de prevention des maladies cardiovasculaires" Pitié Salpetrière Hospital. This exam lasts 10 minutes including patient positioning and imaging.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Relationships between retina micro-vascular remodeling and cognitive function in hypertensive patients.
Time Frame: September 2017
September 2017

Secondary Outcome Measures

Outcome Measure
Time Frame
• Associations between cognitive function and proximal aortic stiffness indices estimated from MRI images.
Time Frame: September 2017
September 2017
• Associations between retina arteriolar remodelling and cerebrovascular lesions (infarcts, lacuna, and white matter lesions) quantified from MRI images.
Time Frame: September 2017
September 2017
• Associations between retina arteriolar remodelling and neurodegenerative lesions (hippocampus atrophy) quantified from MRI images.
Time Frame: September 2017
September 2017
• Associations between proximal aortic stiffness and cerebrovascular lesions (infarcts, lacuna, and white matter lesions) quantified from MRI images.
Time Frame: September 2017
September 2017
• Associations between proximal aortic stiffness and neurodegenerative lesions (hippocampus atrophy) quantified from MRI images.
Time Frame: September 2017
September 2017
• Associations between retina arteriolar remodelling and proximal aortic stiffness indices.
Time Frame: September 2017
September 2017

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

October 1, 2014

Primary Completion (ANTICIPATED)

September 1, 2017

Study Completion (ANTICIPATED)

December 1, 2017

Study Registration Dates

First Submitted

August 4, 2015

First Submitted That Met QC Criteria

March 2, 2016

First Posted (ESTIMATE)

March 8, 2016

Study Record Updates

Last Update Posted (ESTIMATE)

March 8, 2016

Last Update Submitted That Met QC Criteria

March 2, 2016

Last Verified

March 1, 2016

More Information

Terms related to this study

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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