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      Lean Mass Longitudinally Confounds Sedentary Time and Physical Activity With Blood Pressure Progression in 2513 Children

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          ABSTRACT

          Background

          Randomized controlled trials have reported no effect of moderate‐to‐vigorous physical activity (MVPA) on reducing blood pressure (BP) in youth, probably due to short trial durations. This study examined the longitudinal effect of sedentary time (ST), light PA (LPA) and MVPA on BP in 11‐year‐old children followed up for 13 years to determine the confounding and mediating role of body composition.

          Methods

          Data included 2513 children from the Avon Longitudinal Study of Parents and Children (ALSPAC), UK birth cohort who had data on at least one time‐point measure of accelerometer‐based movement behaviour across the follow‐up and complete BP measures at ages 11, 15 and 24 years. Body composition was assessed with dual‐energy x‐ray absorptiometry at all time points. Multivariate adjusted generalized linear mixed‐effect model and structural equation causal mediation model analyses were conducted.

          Results

          Among 2513 participants (61% female, mean [SD] age 11.72 [0.21] years), ST steadily increased from ~6 h/day in childhood (age 11 years) to ~9 h/day in young adulthood (age 24 years), whereas LPA and MVPA decreased, but BP had an inverted U‐shaped increase. In the longitudinal analysis, after full adjustment, a 1‐min cumulative ST from ages 11 to 24 years was positively associated with increased systolic BP (0.009 mmHg [95% CI 0.007–0.011]; p < 0.001) and diastolic BP. A 1‐min cumulative LPA was inversely associated with systolic BP (−0.007 mmHg [−0.009 to −0.004]; p < 0.001), but not diastolic BP. In isotemporal substitution analyses, longitudinal replacement of 10 min of ST with equal time in LPA during childhood, adolescence and young adulthood cumulatively decreased systolic BP by −2.63 mmHg [95% CI −3.17 to −2.08] ( p < 0.0001) and diastolic BP by −1.93 mmHg [95% CI −2.36 to −1.50] ( p < 0.0001). Replacing 10 min of ST with 10 min of MVPA had no statistically significant effect due to an absolute confounding effect of lean mass. The association of ST with systolic BP was fully mediated by increased lean mass (93% mediation). Increased total fat mass partially mediated (19%–27%) the inverse associations of cumulative MVPA with cumulative systolic and diastolic BP.

          Conclusions

          Theoretically replacing 10 min/day spent sedentary with 10 min/day of LPA during growth from childhood through young adulthood may lower systolic BP by −3 mmHg and diastolic BP by −2 mmHg. Lean mass seems more significant than fat mass in the relations of ST and PA with BP and should be accounted for in future intervention studies in the paediatric and young adult population.

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          World Health Organization 2020 guidelines on physical activity and sedentary behaviour

          Objectives To describe new WHO 2020 guidelines on physical activity and sedentary behaviour. Methods The guidelines were developed in accordance with WHO protocols. An expert Guideline Development Group reviewed evidence to assess associations between physical activity and sedentary behaviour for an agreed set of health outcomes and population groups. The assessment used and systematically updated recent relevant systematic reviews; new primary reviews addressed additional health outcomes or subpopulations. Results The new guidelines address children, adolescents, adults, older adults and include new specific recommendations for pregnant and postpartum women and people living with chronic conditions or disability. All adults should undertake 150–300 min of moderate-intensity, or 75–150 min of vigorous-intensity physical activity, or some equivalent combination of moderate-intensity and vigorous-intensity aerobic physical activity, per week. Among children and adolescents, an average of 60 min/day of moderate-to-vigorous intensity aerobic physical activity across the week provides health benefits. The guidelines recommend regular muscle-strengthening activity for all age groups. Additionally, reducing sedentary behaviours is recommended across all age groups and abilities, although evidence was insufficient to quantify a sedentary behaviour threshold. Conclusion These 2020 WHO guidelines update previous WHO recommendations released in 2010. They reaffirm messages that some physical activity is better than none, that more physical activity is better for optimal health outcomes and provide a new recommendation on reducing sedentary behaviours. These guidelines highlight the importance of regularly undertaking both aerobic and muscle strengthening activities and for the first time, there are specific recommendations for specific populations including for pregnant and postpartum women and people living with chronic conditions or disability. These guidelines should be used to inform national health policies aligned with the WHO Global Action Plan on Physical Activity 2018–2030 and to strengthen surveillance systems that track progress towards national and global targets.
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            Cohort Profile: The ‘Children of the 90s’—the index offspring of the Avon Longitudinal Study of Parents and Children

            The Avon Longitudinal Study of Parents and Children (ALSPAC) is a transgenerational prospective observational study investigating influences on health and development across the life course. It considers multiple genetic, epigenetic, biological, psychological, social and other environmental exposures in relation to a similarly diverse range of health, social and developmental outcomes. Recruitment sought to enrol pregnant women in the Bristol area of the UK during 1990–92; this was extended to include additional children eligible using the original enrolment definition up to the age of 18 years. The children from 14 541 pregnancies were recruited in 1990–92, increasing to 15 247 pregnancies by the age of 18 years. This cohort profile describes the index children of these pregnancies. Follow-up includes 59 questionnaires (4 weeks–18 years of age) and 9 clinical assessment visits (7–17 years of age). The resource comprises a wide range of phenotypic and environmental measures in addition to biological samples, genetic (DNA on 11 343 children, genome-wide data on 8365 children, complete genome sequencing on 2000 children) and epigenetic (methylation sampling on 1000 children) information and linkage to health and administrative records. Data access is described in this article and is currently set up as a supported access resource. To date, over 700 peer-reviewed articles have been published using ALSPAC data.
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              Cohort Profile: The Avon Longitudinal Study of Parents and Children: ALSPAC mothers cohort

              Summary The Avon Longitudinal Study of Children and Parents (ALSPAC) was established to understand how genetic and environmental characteristics influence health and development in parents and children. All pregnant women resident in a defined area in the South West of England, with an expected date of delivery between 1st April 1991 and 31st December 1992, were eligible and 13 761 women (contributing 13 867 pregnancies) were recruited. These women have been followed over the last 19–22 years and have completed up to 20 questionnaires, have had detailed data abstracted from their medical records and have information on any cancer diagnoses and deaths through record linkage. A follow-up assessment was completed 17–18 years postnatal at which anthropometry, blood pressure, fat, lean and bone mass and carotid intima media thickness were assessed, and a fasting blood sample taken. The second follow-up clinic, which additionally measures cognitive function, physical capability, physical activity (with accelerometer) and wrist bone architecture, is underway and two further assessments with similar measurements will take place over the next 5 years. There is a detailed biobank that includes DNA, with genome-wide data available on >10 000, stored serum and plasma taken repeatedly since pregnancy and other samples; a wide range of data on completed biospecimen assays are available. Details of how to access these data are provided in this cohort profile.
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                Author and article information

                Contributors
                andrew.agbaje@uef.fi
                Journal
                J Cachexia Sarcopenia Muscle
                J Cachexia Sarcopenia Muscle
                10.1007/13539.2190-6009
                JCSM
                Journal of Cachexia, Sarcopenia and Muscle
                John Wiley and Sons Inc. (Hoboken )
                2190-5991
                2190-6009
                13 November 2024
                December 2024
                : 15
                : 6 ( doiID: 10.1002/jcsm.v15.6 )
                : 2826-2841
                Affiliations
                [ 1 ] Institute of Public Health and Clinical Nutrition, School of Medicine, Faculty of Health Sciences University of Eastern Finland Kuopio Finland
                [ 2 ] Children's Health and Exercise Research Centre, Department of Public Health and Sports Sciences, Faculty of Health and Life Sciences University of Exeter Exeter UK
                Author notes
                [*] [* ] Correspondence:

                Andrew O. Agbaje ( andrew.agbaje@ 123456uef.fi )

                Author information
                https://orcid.org/0000-0001-5138-3441
                Article
                JCSM13639 JCSM-D-24-00845
                10.1002/jcsm.13639
                11634498
                39535381
                c7ae19a6-f50d-4ec9-8491-64a6fac20b51
                © 2024 The Author(s). Journal of Cachexia, Sarcopenia and Muscle published by Wiley Periodicals LLC.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 08 October 2024
                : 09 August 2024
                : 11 October 2024
                Page count
                Figures: 1, Tables: 6, Pages: 16, Words: 11400
                Funding
                Funded by: Medical Research Council , doi 10.13039/501100000265;
                Award ID: 217065/Z/19/Z
                Award ID: MR/M006727/1
                Funded by: Wellcome Trust , doi 10.13039/100010269;
                Funded by: University of Bristol , doi 10.13039/501100000883;
                Funded by: British Heart Foundation , doi 10.13039/501100000274;
                Award ID: CS/15/6/31468
                Funded by: Jenny and Antti Wihuri Foundation , doi 10.13039/501100004022;
                Award ID: 00180006
                Funded by: North Savo Finnish Cultural Foundation
                Award ID: 65191835
                Funded by: Finnish Cultural Foundation , doi 10.13039/501100003125;
                Award ID: 00200150
                Award ID: 00230190
                Funded by: Orion Research Foundation sr
                Funded by: Aarne Koskelo Foundation , doi 10.13039/100010133;
                Funded by: Antti and Tyyne Soininen Foundation
                Funded by: Paulo Foundation , doi 10.13039/501100007417;
                Funded by: Paavo Nurmi Foundation , doi 10.13039/501100008484;
                Funded by: Yrjö Jahnsson Foundation , doi 10.13039/100010114;
                Award ID: 20217390
                Funded by: Ida Montin Foundation , doi 10.13039/100007634;
                Funded by: University of Eastern Finland Faculty of Health Sciences’ fund of Eino Räsänen
                Funded by: Matti and Vappu Maukonen
                Funded by: Finnish Foundation for Cardiovascular Research , doi 10.13039/501100005633;
                Award ID: 220021
                Award ID: 230012
                Award ID: 240003
                Funded by: Alfred Kordelin Foundation , doi 10.13039/100008969;
                Award ID: 230082
                Funded by: Pediatric Research Foundation (Lastentautien tutkimussäätiö) , doi 10.13039/501100012641;
                Funded by: 2024 European Association for the Study of Obesity‐Novo Nordisk Foundation New Investigator Award for Childhood Obesity
                Award ID: NNF24SA0090437
                Categories
                Original Article
                Original Article
                Custom metadata
                2.0
                December 2024
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.5.1 mode:remove_FC converted:11.12.2024

                Orthopedics
                body composition,causality,hypertension,paediatrics,physical activity guidelines,prospective cohort study

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