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Lavretsky, Helen

0000-0001-9990-5085

Mayo Clinic

University of California, Los Angeles

Citations 2

Alzheimer Disease as a Clinical-Biological Construct—An International Working Group Recommendation
Dubois, Bruno , Villain, Nicolas , Schneider, Lon S. , Galasko, Douglas, Kivipelto, Miia , Jessen, Frank , Boada, Merçé , Barkhof, Frederik , Frederiksen, Kristian Steen , Planche, Vincent , Bejanin, Alexandre , Ibáñez, Agustín , Blennow, Kaj , Agronin, Marc , Lopera, Francisco, Delano‐Wood, Lisa , Bombois, Stéphanie , Lévy, Richard, Thambisetty, Madhav , Swantek, Sandra, Newhouse, Paul , Feldman, Howard , Frisoni, Giovanni B. , Bejanin, Alexandre , Barkhof, Frederik , Ibañez, Agustín , Boada, Merce , Feldman, Howard H , Fox, Nick C. , Campbell, Noll L. , Hanseeuw, Bernard , Nordberg, Agneta , Froelich, Lutz , Waldemar, Gunhild , Padovani, Alessandro , Rowe, Christopher Cleon , Cappa, Stefano F. , Caramelli, Paulo , Nitríni, Ricardo , Allegri, Ricardo , Slachevsky, Andrea , Souza, Leonardo Cruz de , Bozoki, Andrea C , Widera, Eric , Ritchie, Craig , Lopera, Francisco, Georges, Jean , Jones, David T. , Lavretsky, Helen , Schott, Jonathan M. , Gatchel, Jennifer R.

JAMA Neurology | November 1, 2024 | Volume: 81 | Issue: 12 | Pages: 1304

10.1001/jamaneurol.2024.3770 Get It

Importance Since 2018, a movement has emerged to define Alzheimer disease (AD) as a purely biological entity based on biomarker findings. The recent revision of the Alzheimer’s Association (AA) criteria for AD furthers this direction. However, concerns about a purely biological definition of AD being applied clinically, the understanding of AD by society at large, and the translation of blood-based biomarkers into clinical practice prompt these International Working Group (IWG) updated recommendations. Objective To consider the revised AA criteria and to offer an alternative definitional view of AD as a clinical-biological construct for clinical use. The recommendations of the 2021 IWG diagnostic criteria are updated for further elaborating at-risk and presymptomatic states. Evidence Review PubMed was searched for articles published between July 1, 2020, and March 1, 2024, using the terms “biomarker” OR “amyloid” OR “tau” OR “neurodegeneration” OR “preclinical” OR “CSF” OR “PET” OR “plasma” AND “Alzheimer’s disease.” The references of relevant articles were also searched. Findings In the new AA diagnostic criteria, AD can be defined clinically as encompassing cognitively normal people having a core 1 AD biomarker. However, recent literature shows that the majority of biomarker-positive cognitively normal individuals will not become symptomatic along a proximate timeline. In the clinical setting, disclosing a diagnosis of AD to cognitively normal people with only core 1 AD biomarkers represents the most problematic implication of a purely biological definition of the disease. Conclusions and Relevance The ultimate aim of the field was to foster effective AD treatments, including preventing symptoms and dementia. The approach of diagnosing AD without a clinical and biological construct would be unwarranted and potentially concerning without a clear knowledge of when or whether symptoms will ever develop. It is recommended that those who are amyloid-positive only and, more generally, most biomarker-positive cognitively normal individuals, should not be labeled as having AD. Rather, they should be considered as being at risk for AD. The expansion of presymptomatic AD is viewed as a better diagnostic construct for those with a specific pattern of biomarkers, indicating that they are proximate to the expression of symptoms in the near future.
Status of Cardiovascular Health in US Adults and Children Using the American Heart Association’s New “Life’s Essential 8” Metrics: Prevalence Estimates From the National Health and Nutrition Examination Survey (NHANES), 2013 Through 2018
Lloyd‐Jones, Donald M. , Labarthe, Darwin R. , Brewer, LaPrincess C. , Sharma, Garima , Rosamond, Wayne D. , Foraker, Randi E. , Black, Terrie , Anderson, Cheryl A.M. , Brewer, LaPrincess C , Sharma, Garima , Rosamond, Wayne , Foraker, Randi , Anderson, Cheryl , Lloyd-Jones, Donald M , Ning, Hongyan , Grandner, Michael A. , Allen, Norrina B. , Lavretsky, Helen , Perak, Amanda Marma

Circulation | June 29, 2022 | Volume: 146 | Issue: 11 | Pages: 822-835

10.1161/circulationaha.122.060911 Get It

Background: The American Heart Association recently published an updated algorithm for quantifying cardiovascular health (CVH)—the Life’s Essential 8 score. We quantified US levels of CVH using the new score. Methods: We included individuals ages 2 through 79 years (not pregnant or institutionalized) who were free of cardiovascular disease from the National Health and Nutrition Examination Surveys in 2013 through 2018. For all participants, we calculated the overall CVH score (range, 0 [lowest] to 100 [highest]), as well as the score for each component of diet, physical activity, nicotine exposure, sleep duration, body mass index, blood lipids, blood glucose, and blood pressure, using published American Heart Association definitions. Sample weights and design were incorporated in calculating prevalence estimates and standard errors using standard survey procedures. CVH scores were assessed across strata of age, sex, race and ethnicity, family income, and depression. Results: There were 23 409 participants, representing 201 728 000 adults and 74 435 000 children. The overall mean CVH score was 64.7 (95% CI, 63.9–65.6) among adults using all 8 metrics and 65.5 (95% CI, 64.4–66.6) for the 3 metrics available (diet, physical activity, and body mass index) among children and adolescents ages 2 through 19 years. For adults, there were significant differences in mean overall CVH scores by sex (women, 67.0; men, 62.5), age (range of mean values, 62.2–68.7), and racial and ethnic group (range, 59.7–68.5). Mean scores were lowest for diet, physical activity, and body mass index metrics. There were large differences in mean scores across demographic groups for diet (range, 23.8–47.7), nicotine exposure (range, 63.1–85.0), blood glucose (range, 65.7–88.1), and blood pressure (range, 49.5–84.0). In children, diet scores were low (mean 40.6) and were progressively lower in higher age groups (from 61.1 at ages 2 through 5 to 28.5 at ages 12 through 19); large differences were also noted in mean physical activity (range, 63.1–88.3) and body mass index (range, 74.4–89.4) scores by sociodemographic group. Conclusions: The new Life’s Essential 8 score helps identify large group and individual differences in CVH. Overall CVH in the US population remains well below optimal levels and there are both broad and targeted opportunities to monitor, preserve, and improve CVH across the life course in individuals and the population.