<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Saltiel N</submitter><funding>National Institute of Neurological Disorders and Stroke</funding><funding>BLRD VA</funding><funding>NCATS NIH HHS</funding><funding>NIA NIH HHS</funding><funding>U.S. Department of Defense</funding><funding>NINDS NIH HHS</funding><funding>Concussion Legacy Foundation</funding><funding>Andlinger Family Foundation</funding><funding>U.S. Department of Veterans Affairs</funding><funding>National Institute on Aging</funding><pagination>314-324</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10842014</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>95(2)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>Exposure to repetitive head impacts (RHI) is associated with later-life cognitive symptoms and neuropathologies, including chronic traumatic encephalopathy (CTE). Cognitive decline in community cohorts is often due to multiple pathologies; however, the frequency and contributions of these pathologies to cognitive impairment in people exposed to RHI are unknown. Here, we examined the relative contributions of 13 neuropathologies to cognitive symptoms and dementia in RHI-exposed brain donors.&lt;h4>Methods&lt;/h4>Neuropathologists examined brain tissue from 571 RHI-exposed donors and assessed for the presence of 13 neuropathologies, including CTE, Alzheimer disease (AD), Lewy body disease (LBD), and transactive response DNA-binding protein 43 (TDP-43) inclusions. Cognitive status</pubmed_abstract><journal>Annals of neurology</journal><pubmed_title>Relative Contributions of Mixed Pathologies to Cognitive and Functional Symptoms in Brain Donors Exposed to Repetitive Head Impacts.</pubmed_title><pmcid>PMC10842014</pmcid><funding_grant_id>PRARP #13267017</funding_grant_id><funding_grant_id>U01NS086659</funding_grant_id><funding_grant_id>U54NS115266</funding_grant_id><funding_grant_id>RF1AG054156</funding_grant_id><funding_grant_id>K23NS102399</funding_grant_id><funding_grant_id>UL1 TR001430</funding_grant_id><funding_grant_id>R01 AG075876</funding_grant_id><funding_grant_id>RF1AG057768</funding_grant_id><funding_grant_id>I01BX005933</funding_grant_id><funding_grant_id>RF1 NS122854</funding_grant_id><funding_grant_id>I01 BX005933</funding_grant_id><funding_grant_id>RF1 AG057902</funding_grant_id><funding_grant_id>K23AG046377</funding_grant_id><funding_grant_id>RF1 AG054156</funding_grant_id><funding_grant_id>RF1 AG062348</funding_grant_id><funding_grant_id>K23 NS102399</funding_grant_id><funding_grant_id>U54 NS115266</funding_grant_id><funding_grant_id>R01 AG062348</funding_grant_id><funding_grant_id>U19AG068753</funding_grant_id><funding_grant_id>P30 AG072978</funding_grant_id><funding_grant_id>P30AG072978</funding_grant_id><funding_grant_id>I01 BX005161</funding_grant_id><pubmed_authors>Mez J</pubmed_authors><pubmed_authors>Nair E</pubmed_authors><pubmed_authors>Saltiel N</pubmed_authors><pubmed_authors>McKee AC</pubmed_authors><pubmed_authors>Alosco ML</pubmed_authors><pubmed_authors>Huber B</pubmed_authors><pubmed_authors>Nowinski C</pubmed_authors><pubmed_authors>Baucom Z</pubmed_authors><pubmed_authors>Abdolmohammadi B</pubmed_authors><pubmed_authors>Olaniyan A</pubmed_authors><pubmed_authors>Dwyer B</pubmed_authors><pubmed_authors>Alvarez VE</pubmed_authors><pubmed_authors>Palmisano JN</pubmed_authors><pubmed_authors>Stern RA</pubmed_authors><pubmed_authors>Martin B</pubmed_authors><pubmed_authors>Uretsky M</pubmed_authors><pubmed_authors>Stein TD</pubmed_authors><pubmed_authors>Menzin T</pubmed_authors><pubmed_authors>Shah A</pubmed_authors><pubmed_authors>Schneider JA</pubmed_authors><pubmed_authors>Boyle PA</pubmed_authors><pubmed_authors>Cantu RC</pubmed_authors><pubmed_authors>Tripodis Y</pubmed_authors><pubmed_authors>Nicks R</pubmed_authors><pubmed_authors>Daneshvar DH</pubmed_authors><pubmed_authors>Yhang E</pubmed_authors><pubmed_authors>Katz DI</pubmed_authors></additional><is_claimable>false</is_claimable><name>Relative Contributions of Mixed Pathologies to Cognitive and Functional Symptoms in Brain Donors Exposed to Repetitive Head Impacts.</name><description>&lt;h4>Objective&lt;/h4>Exposure to repetitive head impacts (RHI) is associated with later-life cognitive symptoms and neuropathologies, including chronic traumatic encephalopathy (CTE). Cognitive decline in community cohorts is often due to multiple pathologies; however, the frequency and contributions of these pathologies to cognitive impairment in people exposed to RHI are unknown. Here, we examined the relative contributions of 13 neuropathologies to cognitive symptoms and dementia in RHI-exposed brain donors.&lt;h4>Methods&lt;/h4>Neuropathologists examined brain tissue from 571 RHI-exposed donors and assessed for the presence of 13 neuropathologies, including CTE, Alzheimer disease (AD), Lewy body disease (LBD), and transactive response DNA-binding protein 43 (TDP-43) inclusions. Cognitive status</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Feb</publication><modification>2025-04-21T23:55:19.826Z</modification><creation>2025-04-05T19:20:28.121Z</creation></dates><accession>S-EPMC10842014</accession><cross_references><pubmed>37921042</pubmed><doi>10.1002/ana.26823</doi></cross_references></HashMap>