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Completed

NCT Number: NCT01303133

Natural History of Amyloid Deposition in Adults With Down Syndrome

The primary objective of this study is to assess the presence of amyloid in non-demented/functionally stable adults with DS as a function of age, dividing the sample into amyloid-positive and amyloid-negative groups. We will also obtain baseline cognitive measures across a range of areas that are often affected by AD.

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Key information

About this study

Specific Aim 1: To assess and compare amyloid deposition (with PiB PET) in non-demented/functionally stable adults with DS across three age cohorts (30-39, 40-49, and >50 years of age).

Primary Hypothesis 1: At initial assessment, there will be a significantly higher prevalence of amyloid-positive (PiB+) subjects in each succeeding age cohort.

In addition, we will test the following secondary hypothesis:

Secondary Aim 1: To compare the presence or absence of the apolipoprotein-E4 allele to the retention of PiB in various brain areas of the DS subjects.

Secondary Hypothesis 1: At baseline, subjects who carry at least one Apolipoprotein-E4 (ApoE4) allele will show a higher prevalence of being PiB+.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participant IQ at least 47 (based upon Stanford-Binet V Abbrev. Test Battery)
  • Participant at least 30 years of age
  • DSDS score indicating participant is asymptomatic for AD
  • Reliable caregiver who is capable of providing correct information about the participant's clinical symptoms and history
  • Agreement of caregiver and clinician that participant is able to cooperate with the protocol tasks
  • Participant has provided assent (or consent) and/or parent/caregiver has provided informed consent

Exclusion criteria

  • Participant is non-verbal or has extremely limited language skills
  • Score within the "symptomatic" range on the DSDS
  • Any significant disease or unstable medical condition that could affect neuropsychological testing
  • Any problems with vision or hearing that could affect neuropsychological testing
  • Participants in whom MRI is contraindicated
  • Claustrophobia or prior failed experiences of completing MRI scans or blood draws
  • Participant is pregnant or breast feeding
  • History or other evidence of severe illness or other condition that would make the participant, in the opinion of the investigator, unsuitable for the study?

Treatment and study plan

Primary outcomes

  1. Amyloid deposition

    Time frame: every 36 months for 9 years

    Obtained via PiB PET scan

Sponsors and collaborators

Lead sponsor

University of Pittsburgh

Other

Collaborators

  • National Institute on Aging (NIA)

Registry information

Important dates

Study start
2009
Primary completion
2018
Study completion
2018
First posted
Feb 24, 2011
Registry last updated
Jan 9, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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