Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3122
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
Background: Mild behavioral impairment (MBI) is associated with all-cause dementia. Little is known about MBI's effects on cognitive function among individuals in earlier disease stages, particularly in racially diverse samples. We examined relationships between MBI and cognitive decline in a richly characterized sample of white and African American (AA) older-middle aged adults. AA participants were enrolled in African Americans Fighting Alzheimer's in Midlife (AA-FAIM), an ancillary study of the Wisconsin Disease Research Center's (WADRC) Clinical Core.
Method: Analytic sample included participants without dementia, with ≥1 study visits and measures of cognitive/clinical function. A baseline MBI rating (present/absent) was derived using study partners' report of neuropsychiatric symptoms at two consecutive visits, (i.e., two consecutive positive MBI scores = MBI present). Cognitive outcomes included measures of speed, mental flexibility and memory.
Result: Table 1 provides characteristics by MBI status for white (N = 450), AA (N = 100), and other underrepresented group (URG) (N = 34) participants. In the full sample, baseline MBI significantly moderated cognitive trajectory on Trails B, though not on any other tasks. Participants with MBI displayed worse trajectory of decline on Trails B relative to those without MBI (Figure 1). Additionally, MBI at baseline significantly predicted progression to cognitive impairment CDR >0 (HR est: 2.84; HR 95% CI: 1.68 - 4.81; p = 0.0001) (Figure 2). Stratified analysis in a smaller AA subgroup showed a similar pattern but was not significant.
Conclusion: MBI associated with more adverse cognitive trajectory and predicted incident cognitive decline in older, middle aged participants without dementia. Our findings highlight the importance of identifying MBI as a possible target for intervention in early disease stages. A fifth of our sample (21.5%) identified as Black/URG. Still, ongoing work in inclusive cohorts is needed to better understand MBI in under-represented groups.
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Source |
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http://dx.doi.org/10.1002/alz.089933 | DOI Listing |
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