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Fine, Lawrence J.

Mayo Clinic

National Institutes of Health

Citations 2

Vascular contributions to cognitive impairment and dementia (VCID): A report from the 2018 National Heart, Lung, and Blood Institute and National Institute of Neurological Disorders and Stroke Workshop
McKee, Ann C. , Snyder, Heather M. , Greenberg, Steven M. , Yaffe, Kristine , Schaffer, Chris B. , Yuan, Chun , Hughes, Timothy M. , Williamson, Jeff D. , González, Héctor M. , Wellington, Cheryl L. , Katušić, Zvonimir S. , Stoeckel, Luke E. , Corriveau, Roderick A. , Fine, Lawrence J., Galis, Zorina S. , Reis, Jared P. , Wright, Jacqueline D. , Chen, Jue , Galis, Zorina S , Gonzalez, Hector M , Zloković, Berislav V. , Gottesman, Rebecca F. , Bernstein, Kenneth E. , Seshadri, Sudha , Daemen, Mat J.A.P. , Schneider, Julie A. , Koenig, James I. , Chen, Jue

Alzheimer's & Dementia | October 8, 2020 | Volume: 16 | Issue: 12 | Pages: 1714-1733

10.1002/alz.12157 Get It

Abstract Vascular contributions to cognitive impairment and dementia (VCID) are characterized by the aging neurovascular unit being confronted with and failing to cope with biological insults due to systemic and cerebral vascular disease, proteinopathy including Alzheimer's biology, metabolic disease, or immune response, resulting in cognitive decline. This report summarizes the discussion and recommendations from a working group convened by the National Heart, Lung, and Blood Institute and the National Institute of Neurological Disorders and Stroke to evaluate the state of the field in VCID research, identify research priorities, and foster collaborations. As discussed in this report, advances in understanding the biological mechanisms of VCID across the wide spectrum of pathologies, chronic systemic comorbidities, and other risk factors may lead to potential prevention and new treatment strategies to decrease the burden of dementia. Better understanding of the social determinants of health that affect risks for both vascular disease and VCID could provide insight into strategies to reduce racial and ethnic disparities in VCID.
Effect of Intensive Blood Pressure Lowering on the Risk of Atrial Fibrillation
Soliman, Elsayed Z. , Rahman, AKM F., Zhang, Zhu-Ming , Chang, Tara I. , Bates, Jeffrey T. , Ghazi, Lama , Blackshear, Joseph L., Chonchol, Michel , Fine, Lawrence J., Ambrosius, Walter T. , Lewis, Cora E. , Rahman, AKM F., Rodríguez, Carlos J. , Ghazi, Lama

Hypertension | May 4, 2020 | Volume: 75 | Issue: 6 | Pages: 1491-1496

10.1161/hypertensionaha.120.14766 Get It

It remains uncertain whether intensive control of blood pressure (BP) results in a lower risk of atrial fibrillation (AF) in patients with hypertension. Using data from SPRINT (Systolic Blood Pressure Intervention Trial), which enrolled participants with hypertension at increased risk of cardiovascular disease, we examined whether intensive BP lowering (target systolic BP [SBP] <120 mm Hg), compared with standard BP lowering (target SBP<140 mm Hg), results in a lower risk of AF. This analysis included 8022 participants (4003 randomized to the intensive arm and 4019 to standard BP arm) who were free of AF at the time of enrollment and with available baseline and follow-up electrocardiographic data. AF was ascertained from standard 12-lead electrocardiograms recorded at biannual study examinations and an exit visit. During up to 5.2 years of follow-up and a total of 28 322 person-years, 206 incident AF cases occurred; 88 in the intensive BP-lowering arm and 118 in the standard BP-lowering arm. Intensive BP lowering was associated with a 26% lower risk of developing new AF (hazard ratio, 0.74 [95% CI, 0.56–0.98]; P =0.037). This effect was consistent among prespecified subgroups of SPRINT participants stratified by age, sex, race, SBP tertiles, prior cardiovascular disease, and prior chronic kidney disease when interactions between treatment effect and these subgroups were assessed using Hommel adjusted P values. In conclusion, intensive treatment to a target of SBP <120 mm Hg in patients with hypertension at high risk of cardiovascular disease has the potential to reduce the risk of AF. Registration— URL: https://www.clinicaltrials.gov ; Unique identifier: NCT01206062.