<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li JM</submitter><funding>National Heart, Lung and Blood Institute</funding><funding>Boston University School of Medicine and National Institute on Aging</funding><funding>NCATS NIH HHS</funding><funding>NIA NIH HHS</funding><funding>U.S. National Institutes of Health - National Institute of Aging</funding><funding>NHLBI NIH HHS</funding><funding>National Heart, Lung, and Blood Institute - National Institute of Neurological Disorders and Stroke</funding><funding>NINDS NIH HHS</funding><funding>National Institute for Neurologic Disorders and Stroke</funding><pagination>e71065</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12819166</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>22(1)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Dementia prevalence is associated with modifiable factors. We quantified the contribution of dementia risk factors in midlife (45-64 years) and late life (≥ 65 years) in the United States.&lt;h4>Methods&lt;/h4>Data from six community-based cohorts in the Dementia Risk Prediction Project (DRPP) were used. We estimated risk factor prevalence using nationally representative data. Cohort-specific Cox regression models were used to estimate the association between modifiable risk factors and incident dementia in midlife and late life. Hazard ratios were pooled using meta-analysis then used to calculate population attributable fractions (PAFs) and potential impact fractions.&lt;h4>Results&lt;/h4>Midlife and late-life risk factors contributed to 22.7% and 16.5% of total dementia cases, r</pubmed_abstract><journal>Alzheimer's &amp; dementia : the journal of the Alzheimer's Association</journal><pubmed_title>Midlife and late-life population attributable fractions of risk factors for dementia in the United States: The Dementia Risk Prediction Project.</pubmed_title><pmcid>PMC12819166</pmcid><funding_grant_id>75N92022D00003</funding_grant_id><funding_grant_id>75N92022D00004</funding_grant_id><funding_grant_id>R01AG023629</funding_grant_id><funding_grant_id>75N92022D00001</funding_grant_id><funding_grant_id>75N92022D00002</funding_grant_id><funding_grant_id>1R61NS120245-01/R33NS120245</funding_grant_id><funding_grant_id>UL1-TR-000040</funding_grant_id><funding_grant_id>N01-HC-25195</funding_grant_id><funding_grant_id>R01AG059421</funding_grant_id><funding_grant_id>UF1/UH1NS125513</funding_grant_id><funding_grant_id>75N92022D00005</funding_grant_id><funding_grant_id>R01AG058969</funding_grant_id><funding_grant_id>P30AG072947</funding_grant_id><funding_grant_id>RF1AG066524</funding_grant_id><funding_grant_id>1RF1AG068410-01</funding_grant_id><funding_grant_id>UL1-TR-001420</funding_grant_id><funding_grant_id>U01HL096812</funding_grant_id><funding_grant_id>75N92021D00006</funding_grant_id><funding_grant_id>P30 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SE</pubmed_authors><pubmed_authors>Stephen JJ</pubmed_authors><pubmed_authors>Lopez OL</pubmed_authors><pubmed_authors>Gudnason V</pubmed_authors><pubmed_authors>Peterson EA</pubmed_authors><pubmed_authors>Gross AL</pubmed_authors><pubmed_authors>Helmer C</pubmed_authors><pubmed_authors>Levine DA</pubmed_authors><pubmed_authors>Briceno EM</pubmed_authors><pubmed_authors>Satizabal CL</pubmed_authors><pubmed_authors>Himali J</pubmed_authors><pubmed_authors>Zhao L</pubmed_authors><pubmed_authors>Aiello AE</pubmed_authors><pubmed_authors>Ikram MA</pubmed_authors><pubmed_authors>Hughes TM</pubmed_authors><pubmed_authors>Lloyd-Jones DM</pubmed_authors><pubmed_authors>Mansolf M</pubmed_authors><pubmed_authors>Sedaghat S</pubmed_authors><pubmed_authors>Zmora R</pubmed_authors><pubmed_authors>Li D</pubmed_authors><pubmed_authors>Fohner A</pubmed_authors><pubmed_authors>Debette S</pubmed_authors><pubmed_authors>Seshadri S</pubmed_authors><pubmed_authors>Gauen AM</pubmed_authors><pubmed_authors>Allen NB</pubmed_authors><pubmed_authors>Sorond FA</pubmed_authors><pubmed_authors>Mbangdadji D</pubmed_authors><pubmed_authors>Soumare A</pubmed_authors><pubmed_authors>Wolters FJ</pubmed_authors><pubmed_authors>Singh-Manoux A</pubmed_authors><pubmed_authors>Launer LJ</pubmed_authors><pubmed_authors>Li JM</pubmed_authors><pubmed_authors>Kohli-Lynch C</pubmed_authors><pubmed_authors>Petito LC</pubmed_authors><pubmed_authors>Giorgio K</pubmed_authors><pubmed_authors>Scholtens D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Midlife and late-life population attributable fractions of risk factors for dementia in the United States: The Dementia Risk Prediction Project.</name><description>&lt;h4>Introduction&lt;/h4>Dementia prevalence is associated with modifiable factors. We quantified the contribution of dementia risk factors in midlife (45-64 years) and late life (≥ 65 years) in the United States.&lt;h4>Methods&lt;/h4>Data from six community-based cohorts in the Dementia Risk Prediction Project (DRPP) were used. We estimated risk factor prevalence using nationally representative data. Cohort-specific Cox regression models were used to estimate the association between modifiable risk factors and incident dementia in midlife and late life. Hazard ratios were pooled using meta-analysis then used to calculate population attributable fractions (PAFs) and potential impact fractions.&lt;h4>Results&lt;/h4>Midlife and late-life risk factors contributed to 22.7% and 16.5% of total dementia cases, r</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-06-06T19:22:09.097Z</modification><creation>2026-06-04T03:12:48.804Z</creation></dates><accession>S-EPMC12819166</accession><cross_references><pubmed>41559019</pubmed><doi>10.1002/alz.71065</doi></cross_references></HashMap>