Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Thursday, November 7, 2024

Personality and Biomarkers of Neurodegeneration and Alzheimer’s Disease in Swedish Older Adults

I have no neuroticism and lots of conscientiousness.

 Personality and Biomarkers of Neurodegeneration and
Alzheimer’s Disease in Swedish Older Adults

Jonas Molinder
J Molinder1 , D Vetrano 2,3 , H Zetterberg1,4,5 , K Blennow 1,4 , M Waern 1,6 ,
L Johansson 1 , H Falk Erhag 1 , R Sigström 1,7 , I Skoog1,7
1 Department of Psychiatry and Neurochemistry, Sahlgrenska Academy at University
of Gothenburg, Gothenburg, Sweden
2 Aging Research Center, Karolinska Institutet and Stockholm University,
Stockholm, Sweden
3 Stockholm Gerontology, Research Center, Stockholm, Sweden
4 Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital,
Gothenburg, Sweden
5 Department of Neurodegenerative Disease, University College London, London, UK
6 Psychosis Department, Sahlgrenska University Hospital, Region Västr,
Gothenburg, Sweden
7 Department of Cognition, and Old Age Psychiatry, Sahlgrenska University,
Gothenburg, Sweden
Contact: jonas.molinder@gu.se
Background: 

Personality is associated with dementia risk.
Neuroticism and conscientiousness may be involved in resistance
and resilience to Alzheimer’s Disease (AD) pathology (ADP). These
traits have also been associated with unspecific biomarkers of neuro-
degeneration; glial fibrillary acidic protein (GFAP) and neurofila-
ment light (NfL). This study explores the role of personality in
cognitive ageing.
Methods: 

We used data from the Swedish population-based studies
H70 (individuals age 70 years only), and SNAC-K (individuals ages
60-104). Personality was assessed with the NEO-five-factor inven-
tory. In H70, biomarkers of ADP were measured in cerebrospinal
fluid (CSF, N ¼ 305), except NfL which was also available in plasma
(N ¼ 1082). In SNAC-K (N ¼ 1754), all biomarkers were measured
in serum. We used multivariable regression models to evaluate the
association between personality traits and ADP biomarkers, GFAP
and NfL among individuals without dementia. We further examined
if associations differed by age (SNAC-K only) and sex.

Results: 

In H70, higher neuroticism and was associated with lower
Ab42/Ab40 ratio (B¼-0.01, p ¼ 0.02). In SNAC-K, higher openness
was associated with lower NfL (B¼-0.04, p ¼ 0.03). For age 60-66,
higher openness was associated with lower NfL (B¼-0.09, p ¼ 0.01),
higher neuroticism was associated with higher GFAP (B ¼ 0.09,
p ¼ 0.01), and NfL (B ¼ 0.10, p ¼ 0.003). For age >80, higher open-
ness was associated with higher ptau-181, (B ¼ 0.14, p ¼ 0.01), and
ptau-181/Ab42 ratio (B ¼ 0.15, p ¼ 0.003).

Conclusions: 

Higher neuroticism and lower openness are associated
with neurodegeneration. Higher openness may also be associated
with resilience to AD-pathology.
Key messages:
• Neuroticism may contribute to neurodegeneration in people <70.
• Openness may contribute to cognitive resilience to ADP in peo-
ple >80.

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