<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jain L</submitter><funding>NIA NIH HHS</funding><funding>NINDS NIH HHS</funding><pagination>549-562</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10840643</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(1)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>The National Institute on Aging - Alzheimer's Association (NIA-AA) ATN research framework proposes to use biomarkers for amyloid (A), tau (T), and neurodegeneration (N) to stage individuals with AD pathological features and track changes longitudinally. The overall aim was to utilize this framework to characterize pre-mortem ATN status longitudinally in a clinically diagnosed cohort of dementia with Lewy bodies (DLB) and to correlate it with the post mortem diagnosis.&lt;h4>Methods&lt;/h4>The cohort was subtyped by cerebrospinal fluid (CSF) ATN category. A subcohort had longitudinal data, and a subgroup was neuropathologically evaluated.&lt;h4>Results&lt;/h4>We observed a significant difference in Aβ&lt;sub>42/40&lt;/sub> after 12 months in the A+T- group. Post mortem neuropathologic analyses indicated that most of the p-Tau 181 positive (T+) cases also had a high Braak stage.&lt;h4>Discussion&lt;/h4>This suggests that DLB patients who are A+ but T- may need to be monitored to determine whether they remain A+ or ever progress to T positivity.&lt;h4>Highlights&lt;/h4>Some A+T- DLB subjects transition from A+ to negative after 12-months. Clinically diagnosed DLB with LBP-AD (A+T+) maintain their positivity. Clinically diagnosed DLB with LBP-AD (A+T+) maintain their positivity. Monitoring of the A+T- sub-type of DLB may be necessary.</pubmed_abstract><journal>Alzheimer's &amp; dementia : the journal of the Alzheimer's Association</journal><pubmed_title>ATN cerebrospinal fluid biomarkers in dementia with Lewy bodies: Initial results from the United States Dementia with Lewy Bodies Consortium.</pubmed_title><pmcid>PMC10840643</pmcid><funding_grant_id>U01 NS100610</funding_grant_id><funding_grant_id>P30 AG062428</funding_grant_id><funding_grant_id>R01 AG022304</funding_grant_id><funding_grant_id>P30 AG066468</funding_grant_id><funding_grant_id>R56 AG022304</funding_grant_id><funding_grant_id>R56 AG063870</funding_grant_id><funding_grant_id>P30 AG062429</funding_grant_id><funding_grant_id>P30 AG072959</funding_grant_id><pubmed_authors>Marder KS</pubmed_authors><pubmed_authors>Rao S</pubmed_authors><pubmed_authors>Lippa CF</pubmed_authors><pubmed_authors>Formica S</pubmed_authors><pubmed_authors>Jain L</pubmed_authors><pubmed_authors>Pillai JA</pubmed_authors><pubmed_authors>Fleisher JE</pubmed_authors><pubmed_authors>Khrestian M</pubmed_authors><pubmed_authors>Lopez OL</pubmed_authors><pubmed_authors>Tuason ED</pubmed_authors><pubmed_authors>Oguh O</pubmed_authors><pubmed_authors>Zabetian CP</pubmed_authors><pubmed_authors>Berman SB</pubmed_authors><pubmed_authors>Galvin JE</pubmed_authors><pubmed_authors>Litvan I</pubmed_authors><pubmed_authors>Irwin DJ</pubmed_authors><pubmed_authors>Honig LS</pubmed_authors><pubmed_authors>Tsuang DW</pubmed_authors><pubmed_authors>Leverenz JB</pubmed_authors><pubmed_authors>Bekris LM</pubmed_authors><pubmed_authors>Sabbagh MN</pubmed_authors><pubmed_authors>Taylor AS</pubmed_authors><pubmed_authors>Galasko DR</pubmed_authors><pubmed_authors>Bozoki AC</pubmed_authors></additional><is_claimable>false</is_claimable><name>ATN cerebrospinal fluid biomarkers in dementia with Lewy bodies: Initial results from the United States Dementia with Lewy Bodies Consortium.</name><description>&lt;h4>Introduction&lt;/h4>The National Institute on Aging - Alzheimer's Association (NIA-AA) ATN research framework proposes to use biomarkers for amyloid (A), tau (T), and neurodegeneration (N) to stage individuals with AD pathological features and track changes longitudinally. The overall aim was to utilize this framework to characterize pre-mortem ATN status longitudinally in a clinically diagnosed cohort of dementia with Lewy bodies (DLB) and to correlate it with the post mortem diagnosis.&lt;h4>Methods&lt;/h4>The cohort was subtyped by cerebrospinal fluid (CSF) ATN category. A subcohort had longitudinal data, and a subgroup was neuropathologically evaluated.&lt;h4>Results&lt;/h4>We observed a significant difference in Aβ&lt;sub>42/40&lt;/sub> after 12 months in the A+T- group. Post mortem neuropathologic analyses indicated that most of the p-Tau 181 positive (T+) cases also had a high Braak stage.&lt;h4>Discussion&lt;/h4>This suggests that DLB patients who are A+ but T- may need to be monitored to determine whether they remain A+ or ever progress to T positivity.&lt;h4>Highlights&lt;/h4>Some A+T- DLB subjects transition from A+ to negative after 12-months. Clinically diagnosed DLB with LBP-AD (A+T+) maintain their positivity. Clinically diagnosed DLB with LBP-AD (A+T+) maintain their positivity. Monitoring of the A+T- sub-type of DLB may be necessary.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jan</publication><modification>2025-08-17T03:06:07.834Z</modification><creation>2025-08-17T03:06:07.834Z</creation></dates><accession>S-EPMC10840643</accession><cross_references><pubmed>37740924</pubmed><doi>10.1002/alz.13398</doi></cross_references></HashMap>