To assess the association between baseline blood pressure and change in neurocognitive functioning after four years, and to assess whether baseline MRI phenotypes are predictive for changes in neurocognitive functioning after four years in the DANTEā¦
ID
Source
Brief title
Condition
- Other condition
- Central nervous system vascular disorders
- Dementia and amnestic conditions
Synonym
Health condition
depressie, apathie, dagelijks functioneren en kwaliteit van leven
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
The main study parameters are blood pressure, (domains of) cognitive
functioning, symptoms of depression and apathy, general daily functioning and
quality of life.
Secondary outcome
Secondary study parameters are antihypertensive medications, occurrence of
(cardiovascular) events, as well as (new) medical diseases such as dementia,
and death.
Background summary
High blood pressure at mid-life is a well-known risk factor for cognitive
decline in old age. Nevertheless, the effect of late-life blood pressure on
cognition remains ambiguous. Observational studies suggested that in old age a
lower rather than a higher blood pressure is associated with an increased risk
of cognitive decline .The DANTE Study Leiden, was a community-based randomized
controlled trial designed to explore whether discontinuation of
antihypertensive treatment for four months would improve cognitive and
psychological functioning. In the DANTE population (n=398) of older persons
aged 75 years and over, blood pressure as well as cognition, symptoms of
depression and apathy, general daily functioning and quality of life were
assessed at baseline and at four-month follow-up. The results of the DANTE
study Leiden indicated that discontinuation of antihypertensive treatment
indeed increased the blood pressure. However, the four-month discontinuation of
antihypertensive treatment did not improve cognitive, psychological, and
general daily functioning.
In a subset (n=220) of the DANTE population, MRI was performed at baseline.
These data showed that in persons with a relatively low BP, specific features
of neurodegeneration were present, such as increased subcortical atrophy and a
diminished microstructural integrity. On baseline, these changes were
cross-sectionally associated with a lower cognitive performance. Interestingly,
similar neurodegenerative changes, were predictive for a steeper decline in
cognitive ability in a slightly younger population (mean age 73y). The
hypothesis of the present research proposal is that older persons with a
relatively low blood pressure at baseline will show a steeper decline in
neurocognitive functioning at four-year follow up than persons with a
relatively high BP at baseline. We also think that certain MRI phenotypes,
including subcortical atrophy and a diminished microstructural integrity, are
predictive for a decline in cognitive functioning after four years.
Study objective
To assess the association between baseline blood pressure and change in
neurocognitive functioning after four years, and to assess whether baseline MRI
phenotypes are predictive for changes in neurocognitive functioning after four
years in the DANTE population.
Study design
Observational follow-up study
Study burden and risks
Persons who wish to participate will receive a one-time home visit. Within a
maximum of 90 minutes the researcher will measure blood pressure and assess
neurocognitive functioning, general daily functioning and quality of life using
above mentioned tests and questionnaires. There are no risks associated with
participation in this study. The burden associated with participation is mostly
the demands on the subjects* time and energy.
Ablinusdreef 2
Leiden 2300 RC
NL
Ablinusdreef 2
Leiden 2300 RC
NL
Listed location countries
Age
Inclusion criteria
This is a follow-up study of the DANTE study Leiden. Therefore, inclusion criteria are:
(1) previous participation in the DANTE study Leiden.
(2) agreement on the informed consent form of the DANTE study Leiden that the subject may be contacted for future studies associated with the DANTE study Leiden.
(3) a confirmation of the subjects* general practitioner that the subject is able to participate in the follow-up study.
Exclusion criteria
Judgement by the subject*s general practitioner that the subject is not able to participate in the follow-up study
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL56159.058.16 |