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      Associations of Change in Body Size With All-Cause and Cause-Specific Mortality Among Healthy Older Adults

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          Key Points

          Question

          Is change in body size associated with increased mortality risk among healthy older adults?

          Findings

          In this cohort study of 16 523 community-dwelling healthy participants, 1256 died over a mean (SD) of 4.4 (1.7) years of follow-up. Among men, loss of 5% to 10% of body weight and loss of more than 10% of body weight were associated with a 33% and 289% increase in mortality, respectively; among women, loss of 5% to 10% of body weight and loss of more than 10% of body weight were associated with a 26% and 114% increase in mortality, respectively.

          Meaning

          This study suggests that weight loss was associated with an increase in mortality, particularly among men, highlighting the need to monitor and investigate weight loss in older adults.

          Abstract

          Importance

          The association between weight change and subsequent cause-specific mortality among older adults is not well described. The significance of changes in waist circumference (WC) has also not been compared with weight change for this purpose.

          Objective

          To examine the associations of changes in body weight and WC with all-cause and cause-specific mortality.

          Design, Setting, and Participants

          This cohort study is a post hoc analysis of data from the Aspirin in Reducing Events in the Elderly (ASPREE) randomized clinical trial, which recruited participants between March 1, 2010, and December 31, 2014. The study included community-based older adults (16 703 Australian participants aged ≥70 years and 2411 US participants aged ≥65 years) without evident cardiovascular disease (CVD), dementia, physical disability, or life-limiting chronic illness. Data analysis was performed from April to September 2022.

          Exposures

          Body weight and WC were measured at baseline and at annual visit 2. Analysis models were adjusted for baseline body mass index because height and weight were measured at baseline, allowing for calculation of body mass index and other variables. Both body weight and WC changes were categorized as change within 5% (stable), decrease by 5% to 10%, decrease by more than 10%, increase by 5% to 10%, and increase by more than 10%.

          Main Outcomes and Measures

          All-cause, cancer-specific, CVD-specific, and noncancer non-CVD–specific mortality. Mortality events were adjudicated by an expert review panel. Cox proportional hazards regression and competing risk analyses were used to calculate hazard ratios (HRs) and 95% CIs.

          Results

          Among 16 523 participants (mean [SD] age, 75.0 [4.3] years; 9193 women [55.6%]), 1256 deaths were observed over a mean (SD) of 4.4 (1.7) years. Compared with men with stable weight, those with a 5% to 10% weight loss had a 33% higher (HR, 1.33; 95% CI, 1.07-1.66) risk of all-cause mortality, and those with more than a 10% decrease in body weight had a 289% higher (HR, 3.89; 95% CI, 2.93-5.18) risk. Compared with women with stable weight, those with a 5% to 10% weight loss had a 26% higher (HR, 1.26; 95% CI, 1.00-1.60) risk of all-cause mortality, and those with more than a 10% decrease in body weight had a 114% higher (HR, 2.14; 95% CI, 1.58-2.91) risk. Weight loss was associated with a higher cancer-specific mortality (>10% decrease among men: HR, 3.49; 95% CI, 2.26-5.40; 5%-10% decrease among women: HR, 1.44; 95% CI, 1.46-2.04; >10% decrease among women: HR, 2.78; 95% CI, 1.82-4.26), CVD-specific mortality (>10% decrease among men: HR, 3.14; 95% CI, 1.63-6.04; >10% decrease among women: HR, 1.92; 95% CI, 1.05-3.51), and noncancer non-CVD–specific mortality (>10% decrease among men: HR, 4.98; 95% CI, 3.14-7.91). A decrease in WC was also associated with mortality.

          Conclusions and Relevance

          This cohort study of healthy older adults suggests that weight loss was associated with an increase in all-cause and cause-specific mortality, including an increased risk of cancer, CVD, and other life-limiting conditions. Physicians should be aware of the significance of weight loss, especially among older men.

          Abstract

          This cohort study uses data from the Aspirin in Reducing Events in the Elderly clinical trial to examine the associations of changes in body weight and waist circumference with all-cause and cause-specific mortality.

          Related collections

          Most cited references35

          • Record: found
          • Abstract: found
          • Article: found
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          Waist circumference as a vital sign in clinical practice: a Consensus Statement from the IAS and ICCR Working Group on Visceral Obesity

          Despite decades of unequivocal evidence that waist circumference provides both independent and additive information to BMI for predicting morbidity and risk of death, this measurement is not routinely obtained in clinical practice. This Consensus Statement proposes that measurements of waist circumference afford practitioners with an important opportunity to improve the management and health of patients. We argue that BMI alone is not sufficient to properly assess or manage the cardiometabolic risk associated with increased adiposity in adults and provide a thorough review of the evidence that will empower health practitioners and professional societies to routinely include waist circumference in the evaluation and management of patients with overweight or obesity. We recommend that decreases in waist circumference are a critically important treatment target for reducing adverse health risks for both men and women. Moreover, we describe evidence that clinically relevant reductions in waist circumference can be achieved by routine, moderate-intensity exercise and/or dietary interventions. We identify gaps in the knowledge, including the refinement of waist circumference threshold values for a given BMI category, to optimize obesity risk stratification across age, sex and ethnicity. We recommend that health professionals are trained to properly perform this simple measurement and consider it as an important ‘vital sign’ in clinical practice.
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            • Record: found
            • Abstract: found
            • Article: found
            Is Open Access

            Adipose Tissue Distribution, Inflammation and Its Metabolic Consequences, Including Diabetes and Cardiovascular Disease

            Adipose tissue plays essential roles in maintaining lipid and glucose homeostasis. To date several types of adipose tissue have been identified, namely white, brown, and beige, that reside in various specific anatomical locations throughout the body. The cellular composition, secretome, and location of these adipose depots define their function in health and metabolic disease. In obesity, adipose tissue becomes dysfunctional, promoting a pro-inflammatory, hyperlipidemic and insulin resistant environment that contributes to type 2 diabetes mellitus (T2DM). Concurrently, similar features that result from adipose tissue dysfunction also promote cardiovascular disease (CVD) by mechanisms that can be augmented by T2DM. The mechanisms by which dysfunctional adipose tissue simultaneously promote T2DM and CVD, focusing on adipose tissue depot-specific adipokines, inflammatory profiles, and metabolism, will be the focus of this review. The impact that various T2DM and CVD treatment strategies have on adipose tissue function and body weight also will be discussed.
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              Effect of Aspirin on All-Cause Mortality in the Healthy Elderly

              In the primary analysis of the Aspirin in Reducing Events in the Elderly (ASPREE) trial, now published in the Journal, we report that the daily use of aspirin did not provide a benefit with regard to the primary end point of disability-free survival among older adults. A numerically higher rate of the secondary end point of death from any cause was observed with aspirin than with placebo.
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                Author and article information

                Journal
                JAMA Netw Open
                JAMA Netw Open
                JAMA Network Open
                American Medical Association
                2574-3805
                10 April 2023
                April 2023
                10 April 2023
                : 6
                : 4
                : e237482
                Affiliations
                [1 ]School of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia
                [2 ]Department of Medical Education, Melbourne Medical School, The University of Melbourne, Melbourne, Victoria, Australia
                [3 ]Center for Aging and Population Health, Department of Epidemiology, University of Pittsburgh, Pittsburgh, Pennsylvania
                [4 ]Medical School, Royal Perth Hospital, University of Western Australia, Perth, Western Australia, Australia
                [5 ]Department of Cardiology, University Heart & Vascular Center Hamburg, Hamburg, Germany
                [6 ]German Center for Cardiovascular Research, Partner Site Hamburg/Kiel/Lübeck, Hamburg, Germany
                [7 ]Discipline of General Practice, University of Tasmania, Hobart, Australia
                [8 ]Department of Pharmacy Practice and Science, College of Pharmacy, The University of Iowa, Iowa City
                [9 ]Department of Family Medicine, Carver College of Medicine, The University of Iowa, Iowa City
                Author notes
                Article Information
                Accepted for Publication: February 25, 2023.
                Published: April 10, 2023. doi:10.1001/jamanetworkopen.2023.7482
                Open Access: This is an open access article distributed under the terms of the CC-BY License. © 2023 Hussain SM et al. JAMA Network Open.
                Corresponding Author: Sultana Monira Hussain, PhD, School of Public Health and Preventive Medicine, Monash University, 553 St Kilda Rd, Melbourne, VIC 3004, Australia ( monira.hussain@ 123456monash.edu ).
                Author Contributions: Drs Hussain and McNeil had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis.
                Concept and design: Hussain, Newman, Beilin, Woods, Reid, Owen, Cicuttini, Tran, McNeil.
                Acquisition, analysis, or interpretation of data: Hussain, Newman, Tonkin, Woods, Neumann, Nelson, Carr, Reid, Owen, Ball, Wang, Ernst, McNeil.
                Drafting of the manuscript: Hussain, Newman, Cicuttini, McNeil.
                Critical revision of the manuscript for important intellectual content: Hussain, Newman, Beilin, Tonkin, Woods, Neumann, Nelson, Carr, Reid, Owen, Ball, Cicuttini, Tran, Wang, Ernst.
                Statistical analysis: Hussain, Reid.
                Obtained funding: Hussain, Tonkin, Woods, Nelson, Reid, Owen, McNeil.
                Administrative, technical, or material support: Hussain, Newman, Tonkin, Owen, Ernst, McNeil.
                Supervision: Newman, Beilin, Neumann, McNeil.
                Conflict of Interest Disclosures: None reported.
                Funding/Support: Dr Hussain is the recipient of National Health and Medical Research Council (NHMRC) Early Career Fellowship (APP1142198), Dr McNeil is supported through an NHMRC Leadership Fellowship (IG 1173690). The Aspirin in Reducing Events in the Elderly study was supported by grant U01AG029824 from the National Institute on Aging and the National Cancer Institute at the National Institutes of Health, grants 334037 and 1127060 from the NHMRC of Australia, Monash University, and the Victorian Cancer Agency.
                Role of the Funder/Sponsor: The funding sources had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.
                Data Sharing Statement: See Supplement 2.
                Additional Contributions: We thank the patients who participated in this trial.
                Article
                zoi230244
                10.1001/jamanetworkopen.2023.7482
                10087052
                37036703
                3fc6d9db-35b2-4f32-a1df-3a58ddc6bccf
                Copyright 2023 Hussain SM et al. JAMA Network Open.

                This is an open access article distributed under the terms of the CC-BY License.

                History
                : 9 December 2022
                : 25 February 2023
                Categories
                Research
                Original Investigation
                Online Only
                Geriatrics

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