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Early Detection of Mild Cognitive Impairment in Individual Patients

2 de setembro de 2011 atualizado por: James C. Patterson, II, MD. Ph, Louisiana State University Health Sciences Center Shreveport
Our central hypothesis is that the early metabolic lesions of MCI can be reliably detected in individual subjects by objective analysis of [18]F-fluorodeoxyglucose (FDG) positron-emission tomography (PET) brain images, earlier and more accurately than by subjective clinician rating.

Visão geral do estudo

Status

Concluído

Intervenção / Tratamento

Descrição detalhada

Our goal with this proposal is a prospective, longitudinal study that will examine subjects over a three-year span to establish the presence of MCI, evaluate progression of disease, and determine the validity of this method in detecting early MCI. Specifically, we predict that by using our Cognitive Decline Index (CDI) method of objective examination of FDG PET brain images from patients diagnosed with MCI or mild AD, we can accurately discriminate very early abnormalities in cerebral metabolism, and that this research method can be validated and translated into a clinically useful tool for the early detection of MCI. Our long-range goals are the development of methods and tools that enable the detection of pathology in individual patients at risk for cognitive impairment.

Tipo de estudo

Observacional

Inscrição (Antecipado)

34

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

    • Louisiana
      • Shreveport, Louisiana, Estados Unidos, 71103
        • Louisiana State University Health Sciences Center

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

55 anos a 85 anos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Sim

Gêneros Elegíveis para o Estudo

Tudo

Método de amostragem

Amostra Não Probabilística

População do estudo

Subjects must have a diagnosis of MCI or mild AD.

Descrição

MCI Inclusion Criteria (patients):

MCI criteria met:

  1. Memory complaint, preferably corroborated by an informant.
  2. Objective memory impairment (based on cognitive test scores).
  3. Normal general cognitive function.
  4. Intact ADL.
  5. Not demented.

    • At least 10 years of education, or GED, or equivalent.
    • Patients with ApoE4 positive homozygous or heterozygous status and/or first-degree relative with probable AD are preferred, but patients who meet all other criteria including well-defined MCI criteria will be accepted.
    • Age: 55-85
    • Have normal or clinically unimportant physical exam, beyond those consistent with a diagnosis of MCI.
    • Able to give informed consent, or assent and informed consent from a legal representative.
    • Centrally acting medications will be closely tracked, patients on any such medications will be PET-scanned only after a 24-hour washout, with meds restarted immediately after the scan.
    • Because depression and depressive pseudodementia are often prodromal to cognitive decline, these diagnoses will not be exclusive.
    • MRI findings must be normal or unremarkable for the age of the patient. Examples of abnormal (exclusory) findings are occult lacunar infarct, arteriovenous malformation) Examples of non-exclusory findings include mild atrophy, mild to moderate periventricular white matter changes. Other MRI findings will be evaluated in consultation with coinvestigator neuroradiologists and clinical judgment will be used to determine if the subject can continue in the study.

MCI Exclusion Criteria (patients):

  • Other neuropsychiatric diagnoses (e.g., stroke, head trauma, any psychotic disorder, Parkinson's) other than MCI.
  • Major medical illness (e.g., diabetes, severe or uncontrolled hypertension), especially potential secondary causes of cognitive decline (e.g., hypothyroidism).
  • Disease, combination of disease, or presentation that, in the clinician's judgment, could introduce intolerable variance into the PET brain scan image (example: coronary artery disease, hypercholesterolemia, on 5 medications, HTN 2 yrs controlled with meds, random glucose of 125, but no Dx of DM, Hx of ?TIA).
  • Current substance or alcohol dependence or history of same, and no alcohol or substance abuse within the last eight weeks.

Mild Alzheimer's Disease (AD) Inclusion criteria (patients):

  1. You must have a Mini Mental State Examination score of greater than 20.
  2. You must have one or more of these signs and symptoms of mild AD:

Cognitive impairment manifested as memory problems, problems with language, difficulty carrying out motor activities, difficulty naming things, and/or problems planning or organizing, all of which impair function and are worsening over time.

  • You must have at least 10 years of education, or a GED, or its equivalent.
  • We will be drawing blood to determine your ApoE genotype. ApoE4 is a risk factor for Alzheimer's disease. We will share these results with you, if you desire to know the results. ApoE4 is only a risk factor. That means it is possible to get Alzheimer's without being ApoE4 positive, and it is possible to be ApoE4 positive and not get Alzheimer's. If you are positive for the ApoE4 genetic marker, you can be included. If you do NOT have the ApoE4 genetic marker, then you must have all other criteria.
  • Age: 55-85.
  • Normal or clinically unimportant physical exam, beyond those consistent with a diagnosis of mild AD.
  • Able to give informed consent, or assent and informed consent from a legal representative. You will be assessed for capacity and assent/consent obtained as appropriate based on the Consensus Recommendations for Research Consent for Cognitively Impaired Adults (2004, Alzheimer's Disease Association Disorder, 18 (3):171-175).
  • If you take medications that have an effect on the brain, they will be closely monitored. You will be PET-scanned only after a 24-hour washout of this medication(s), but this medication(s) will be restarted immediately after the scan.

Mild Alzheimer's Disease (AD) Exclusion Criteria:

  • Any problems related to the brain or mental disorders (e.g., stroke, head trauma, any psychotic disorder, Parkinson's) other than mild AD. Some mood disorders will be acceptable because depression is often a precursor to mild AD.
  • You will get an MRI of your brain taken on the second visit, and a radiologist will read it. If there are any abnormal findings, you will be told, and these findings will be forwarded to your medical doctor. These findings may or may not result in your exclusion from the study.
  • Any major medical illness (e.g., diabetes, severe or uncontrolled hypertension), especially potential secondary causes of cognitive decline (e.g., hypothyroidism).
  • Any disease, combination of disease, or presentation that, in the clinician's judgment, could introduce intolerable variance into the PET brain scan image.
  • Current diagnosis of substance or alcohol dependence or a history of same, and no alcohol or substance abuse within the last eight weeks.

MCI Inclusion criteria (controls)

  • Normal cognitive screening exam.
  • Age: 55-85.
  • At least 10 years of education or GED, or equivalent.
  • Socioeconomic status, age, and sex matched. Able to give informed consent, or assent and informed consent from a legal representative.
  • Centrally acting medications will be closely tracked, patients on any such medications will be PET-scanned only after a 24-hour washout, with meds restarted immediately after the scan.

MCI Exclusion criteria (controls)

  • First-degree relative with dementia or clinically relevant memory problems.
  • Neuropsychiatric diagnoses (e.g., stroke, head trauma, depression, any psychoses).
  • Major medical illness (e.g., diabetes, severe /uncontrolled hypertension, hypothyroidism).
  • Current substance or alcohol dependence or history of same, and no alcohol or substance abuse within the last eight weeks.
  • MRI findings must be normal or unremarkable for the age of the patient. Examples of abnormal (exclusory) findings are occult lacunar infarct, arteriovenous malformation) Examples of non-exclusory findings include mild atrophy, mild to moderate periventricular white matter changes. Other MRI findings will be evaluated in consultation with coinvestigator neuroradiologists and clinical judgment will be used to determine if the subject can continue in the study.

    • Disease, combination of disease, or presentation that, in the clinician's judgment, could introduce intolerable variance into the PET brain scan image (example: coronary artery disease, hypercholesterolemia, on 5 medications, HTN 2 yrs controlled with meds, random glucose of 125, but no Dx of DM, Hx of ?TIA).

Dropout criteria (all):

Subjects that begin the study and are not able to finish the study will be tracked. Ongoing criteria for termination from the study will include:

  • Adverse events intolerable to the patient that prevent continued involvement in the study.
  • New onset medical disorder of such significance as to prohibit further involvement.
  • Initiation or recurrence of alcohol or substance abuse/dependence.
  • Subject withdraws consent for any reason.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Prazo
Determine if the Cognitive Decline Index will discriminate subtle lesions earlier than the standard analysis of the Nuclear Medicine physician.
Prazo: within the next 3 years
within the next 3 years

Medidas de resultados secundários

Medida de resultado
Prazo
Determine if sensitivity, specificity, receiver-operator characteristics, and predictive value of our method are appropriate for translation into a clinically useful tool.
Prazo: within the next three years
within the next three years

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

  • Investigador principal: James Patterson, MD PhD, Louisiana State University Health Sciences Center

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo

1 de setembro de 2003

Conclusão Primária (Real)

1 de julho de 2011

Conclusão do estudo (Real)

1 de julho de 2011

Datas de inscrição no estudo

Enviado pela primeira vez

13 de setembro de 2005

Enviado pela primeira vez que atendeu aos critérios de CQ

20 de outubro de 2005

Primeira postagem (Estimativa)

24 de outubro de 2005

Atualizações de registro de estudo

Última Atualização Postada (Estimativa)

7 de setembro de 2011

Última atualização enviada que atendeu aos critérios de controle de qualidade

2 de setembro de 2011

Última verificação

1 de setembro de 2011

Mais Informações

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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