Risk factors of hippocampal sclerosis in the oldest old
The 90+ Study
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Abstract
Objective To examine the risk factors and comorbidities of hippocampal sclerosis (HS) in the oldest-old.
Methods A total of 134 participants with dementia from The 90+ Study with longitudinal evaluations and autopsy were included in this investigation. Participants were divided into 2 groups, one with and one without HS pathology, and differences in clinical and pathologic characteristics were compared.
Results Persons with HS tended to have a longer duration of dementia compared to participants without HS (mean 4.0 years vs 6.7 years, odds ratio [OR] 1.26; 95% confidence interval [CI] 1.11–1.42; p < 0.001). HS was more likely in participants with a history of autoimmune diseases (rheumatoid arthritis or thyroid disease, OR 3.15; 95% CI 1.30–7.62; p = 0.011), high thyroid-stimulating hormone (OR 4.94; 95% CI 1.40–17.46; p = 0.013), or high thyroid antibodies (OR 3.45; 95% CI 1.09–10.88; p = 0.035). Lewy body disease (LBD) pathology was also associated with an increased likelihood of HS (OR 5.70; 95% CI 1.22–26.4; p = 0.027).
Conclusion We identified autoimmune conditions (rheumatoid arthritis and thyroid disease) as potential risk factors for HS in our cohort. LBD was the only pathology that was associated with increased odds of HS and those harboring HS pathology had a longer duration of dementia. This suggests multiple pathways of HS pathology among the oldest-old.
Glossary
- CI=
- confidence interval;
- CVD=
- cerebrovascular disease;
- DSM-IV=
- Diagnostic and Statistical Manual of Mental Disorders, 4th edition;
- H&E=
- hematoxylin & eosin;
- HS=
- hippocampal sclerosis;
- LBD=
- Lewy body disease;
- OR=
- odds ratio;
- RA=
- rheumatoid arthritis;
- TPO=
- thyroid peroxidase;
- TSH=
- thyroid-stimulating hormone
Footnotes
↵* These authors contributed equally to this work.
Go to Neurology.org/N for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.
- Received July 8, 2017.
- Accepted in final form July 31, 2018.
- © 2018 American Academy of Neurology
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