| Literature DB >> 31865797 |
Mohammad R Ostovaneh1,2, Kasra Moazzami1,3, Kihei Yoneyama1,4, Bharath A Venkatesh1, Susan R Heckbert5, Colin O Wu6, Steven Shea7,8, Wendy S Post1, Annette L Fitzpatrick9,10, Gregory L Burke11, Hossein Bahrami12, Otto A Sanchez13, Lori B Daniels14, Erin D Michos1, David A Bluemke15, João A C Lima1.
Abstract
Cross-sectionally measured NT-proBNP (N-terminal pro-B-type natriuretic peptide) is related to incident dementia. However, data linking changes in NT-proBNP to risk of future dementia are lacking. We aimed to examine the association of change in NT-proBNP over 3.2 years with incident dementia. We included 4563 participants in MESA (Multi-Ethnic Study of Atherosclerosis) prospective cohort who were free of cardiovascular disease at enrollment, had NT-proBNP level measured at MESA exams 1 (baseline, 2000-2002) and 3 (2004-2005), and had no diagnosis of dementia before exam 3. The association of change in NT-proBNP level between MESA exams 1 through 3 and all-cause hospitalized dementia (by International Classification of Diseases, Ninth Revision, codes) after MESA exam 3 (2004-2005) through 2015 was assessed using competing-risks Cox proportional hazard regression analysis. During 45 522 person-years of follow-up, 223 dementia cases were documented. Increase in log-NT-proBNP from MESA exams 1 through 3 was positively associated with incidence of dementia (multivariable hazard ratio, 1.28 [95% CI, 1.001-1.64]; P=0.049). An increase of at least 25% in NT-proBNP level from MESA exam 1 through 3 was associated with a 55% (P=0.02) increase in the risk of dementia in multivariable analysis. Addition of temporal NT-proBNP change to a model including risk factors and baseline NT-proBNP improved the prediction of dementia (Harrell C statistic from 0.85 to 0.87, P=0.049). Increase in NT-proBNP is independently associated with future all-cause hospitalized dementia and offers a moderately better predictive performance for risk of dementia compared with risk factors and baseline NT-proBNP. Clinical Trial Registration- URL: https://www.clinicaltrials.gov. Unique identifier: NCT00005487.Entities:
Keywords: cardiovascular diseases; cognition disorders; cohort studies; dementia; risk factors
Mesh:
Substances:
Year: 2019 PMID: 31865797 PMCID: PMC7482429 DOI: 10.1161/HYPERTENSIONAHA.119.13952
Source DB: PubMed Journal: Hypertension ISSN: 0194-911X Impact factor: 10.190