A pathway linking pulse pressure to dementia in adults with Down syndrome
Brain Communications, ISSN: 2632-1297, Vol: 6, Issue: 3, Page: fcae157
2024
- 12Captures
- 2Mentions
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Metrics Details
- Captures12
- Readers12
- 12
- Mentions2
- News Mentions2
- News2
Most Recent News
Data from University of California Update Knowledge in Down Syndrome (A pathway linking pulse pressure to dementia in adults with Down syndrome)
2024 MAY 24 (NewsRx) -- By a News Reporter-Staff News Editor at Mental Health News Daily -- Researchers detail new data in down syndrome. According
Article Description
Adults with Down syndrome are less likely to have hypertension than neurotypical adults. However, whether blood pressure measures are associated with brain health and clinical outcomes in this population has not been studied in detail. Here, we assessed whether pulse pressure is associated with markers of cerebrovascular disease and is linked to a diagnosis of dementia in adults with Down syndrome via structural imaging markers of cerebrovascular disease and atrophy. The study included participants with Down syndrome from the Alzheimer's Disease - Down Syndrome study (n = 195, age = 50.6 ± 7.2 years, 44% women, 18% diagnosed with dementia). Higher pulse pressure was associated with greater global, parietal and occipital white matter hyperintensity volume but not with enlarged perivascular spaces, microbleeds or infarcts. Using a structural equation model, we found that pulse pressure was associated with greater white matter hyperintensity volume, which in turn was related to increased neurodegeneration, and subsequent dementia diagnosis. Pulse pressure is an important determinant of brain health and clinical outcomes in individuals with Down syndrome despite the low likelihood of frank hypertension.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85193741806&origin=inward; http://dx.doi.org/10.1093/braincomms/fcae157; http://www.ncbi.nlm.nih.gov/pubmed/38764776; https://academic.oup.com/braincomms/article/doi/10.1093/braincomms/fcae157/7667845; https://dx.doi.org/10.1093/braincomms/fcae157; https://academic.oup.com/braincomms/article/6/3/fcae157/7667845
Oxford University Press (OUP)
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