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      Pelvic compensation accompanying spinal malalignment and back pain-related factors in a general population: the Wakayama spine study

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          Abstract

          Some older adults with spinal deformity maintain standing posture via pelvic compensation when their center of gravity moves forward. Therefore, evaluations of global alignment should include both pelvic tilt (PT) and seventh cervical vertebra-sagittal vertical axis (C7-SVA). Here, we evaluate standing postures of older adults using C7-SVA with PT and investigate factors related to postural abnormality. This cross-sectional study used an established population-based cohort in Japan wherein 1121 participants underwent sagittal whole-spine radiography in a standing position and bioelectrical impedance analysis for muscle mass measurements. Presence of low back pain (LBP), visual analog scale (VAS) of LBP, and LBP-related disability (Oswestry Disability Index [ODI]) were evaluated. Based on the PT and C7-SVA, the participants were divided into four groups: normal, compensated, non-compensated, and decompensated. We defined the latter three categories as “malalignment” and examined group characteristics and factors. There were significant differences in ODI%, VAS and prevalence of LBP, and sarcopenia among the four groups, although these were non-significant between non-compensated and decompensated groups on stratified analysis. Moreover, the decompensated group was significantly associated with sarcopenia. Individuals with pelvic compensation are at increased risk for LBP and related disorders even with the C7-SVA maintained within normal range.

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          Sarcopenia in Asia: consensus report of the Asian Working Group for Sarcopenia.

          Sarcopenia, a newly recognized geriatric syndrome, is characterized by age-related decline of skeletal muscle plus low muscle strength and/or physical performance. Previous studies have confirmed the association of sarcopenia and adverse health outcomes, such as falls, disability, hospital admission, long term care placement, poorer quality of life, and mortality, which denotes the importance of sarcopenia in the health care for older people. Despite the clinical significance of sarcopenia, the operational definition of sarcopenia and standardized intervention programs are still lacking. It is generally agreed by the different working groups for sarcopenia in the world that sarcopenia should be defined through a combined approach of muscle mass and muscle quality, however, selecting appropriate diagnostic cutoff values for all the measurements in Asian populations is challenging. Asia is a rapidly aging region with a huge population, so the impact of sarcopenia to this region is estimated to be huge as well. Asian Working Group for Sarcopenia (AWGS) aimed to promote sarcopenia research in Asia, and we collected the best available evidences of sarcopenia researches from Asian countries to establish the consensus for sarcopenia diagnosis. AWGS has agreed with the previous reports that sarcopenia should be described as low muscle mass plus low muscle strength and/or low physical performance, and we also recommend outcome indicators for further researches, as well as the conditions that sarcopenia should be assessed. In addition to sarcopenia screening for community-dwelling older people, AWGS recommends sarcopenia assessment in certain clinical conditions and healthcare settings to facilitate implementing sarcopenia in clinical practice. Moreover, we also recommend cutoff values for muscle mass measurements (7.0 kg/m(2) for men and 5.4 kg/m(2) for women by using dual X-ray absorptiometry, and 7.0 kg/m(2) for men and 5.7 kg/m(2) for women by using bioimpedance analysis), handgrip strength (<26 kg for men and <18 kg for women), and usual gait speed (<0.8 m/s). However, a number of challenges remained to be solved in the future. Asia is made up of a great number of ethnicities. The majority of currently available studies have been published from eastern Asia, therefore, more studies of sarcopenia in south, southeastern, and western Asia should be promoted. On the other hand, most Asian studies have been conducted in a cross-sectional design and few longitudinal studies have not necessarily collected the commonly used outcome indicators as other reports from Western countries. Nevertheless, the AWGS consensus report is believed to promote more Asian sarcopenia research, and most important of all, to focus on sarcopenia intervention studies and the implementation of sarcopenia in clinical practice to improve health care outcomes of older people in the communities and the healthcare settings in Asia. Copyright © 2014 American Medical Directors Association, Inc. Published by Elsevier Inc. All rights reserved.
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            A simulation study of the number of events per variable in logistic regression analysis

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              Estimation of skeletal muscle mass by bioelectrical impedance analysis.

              The purpose of this study was to develop and cross-validate predictive equations for estimating skeletal muscle (SM) mass using bioelectrical impedance analysis (BIA). Whole body SM mass, determined by magnetic resonance imaging, was compared with BIA measurements in a multiethnic sample of 388 men and women, aged 18-86 yr, at two different laboratories. Within each laboratory, equations for predicting SM mass from BIA measurements were derived using the data of the Caucasian subjects. These equations were then applied to the Caucasian subjects from the other laboratory to cross-validate the BIA method. Because the equations cross-validated (i.e., were not different), the data from both laboratories were pooled to generate the final regression equation SM mass (kg) = [(Ht 2 / R x 0.401) + (gender x 3.825) + (age x -0. 071)] + 5.102 where Ht is height in centimeters; R is BIA resistance in ohms; for gender, men = 1 and women = 0; and age is in years. The r(2) and SE of estimate of the regression equation were 0.86 and 2.7 kg (9%), respectively. The Caucasian-derived equation was applicable to Hispanics and African-Americans, but it underestimated SM mass in Asians. These results suggest that the BIA equation provides valid estimates of SM mass in healthy adults varying in age and adiposity.
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                Author and article information

                Contributors
                hashizum@wakayama-med.ac.jp
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                22 July 2023
                22 July 2023
                2023
                : 13
                : 11862
                Affiliations
                [1 ]GRID grid.412857.d, ISNI 0000 0004 1763 1087, Department of Orthopaedic Surgery, , Wakayama Medical University, ; 811-1 Kimiidera, Wakayama City, Wakayama 641-8510 Japan
                [2 ]GRID grid.26999.3d, ISNI 0000 0001 2151 536X, Division of Musculoskeletal AI System Development, Graduate School of Medicine, , The University of Tokyo, ; Bunkyo-Ku, Tokyo, Japan
                [3 ]GRID grid.255137.7, ISNI 0000 0001 0702 8004, Spine Center, , Dokkyo Medical University Nikko Medical Center, ; 632 Takatoku, Nikko City, Tochigi Japan
                [4 ]GRID grid.460141.6, Spine Care Center, , Wakayama Medical University Kihoku Hospital, ; 219 Myoji, Katsuragi-cho, Ito-gun, Wakayama, Japan
                [5 ]GRID grid.26999.3d, ISNI 0000 0001 2151 536X, Department of Orthopaedic Surgery, , The University of Tokyo, ; Bunkyo-Ku, Tokyo, Japan
                [6 ]GRID grid.26999.3d, ISNI 0000 0001 2151 536X, Department of Preventive Medicine for Locomotive Organ Disorders, 22nd Century Medical and Research Center, , The University of Tokyo, ; Bunkyoku, Tokyo, Japan
                [7 ]Department of Orthopedic Surgery, Sumiya Orthopaedic Hospital, 337 Yoshida, Wakayama, Japan
                Article
                39044
                10.1038/s41598-023-39044-2
                10363166
                37481604
                ff75aece-e71d-436c-8cc5-42017e24c0e1
                © The Author(s) 2023

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 27 July 2022
                : 19 July 2023
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001691, Japan Society for the Promotion of Science;
                Award ID: 26462249, 21K09306
                Award ID: 17K10937, 20K09509
                Award ID: B19H03895, B26293139, B23390172,B20390182, 18K18447, 15K15219, 24659317
                Award Recipient :
                Funded by: the Japan Osteoporosis Society
                Funded by: FundRef http://dx.doi.org/10.13039/100018590, JA Kyosai Research Institute;
                Funded by: Challenging Exploratory Research grants
                Award ID: 24659666, 21659349
                Award Recipient :
                Funded by: Young Scientists
                Award ID: A18689031
                Award Recipient :
                Funded by: Japanese Orthopedics and Traumatology Foundation, Inc
                Award ID: 287
                Award Recipient :
                Funded by: H25-Nanchitou (Men)
                Award ID: 005
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100009619, Japan Agency for Medical Research and Development;
                Award ID: 17gk0210007h0003, 19gk0210018h0002
                Award ID: 17dk0110028h0001
                Award Recipient :
                Funded by: H25-Choujyu
                Award ID: 007
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100001700, Ministry of Education, Culture, Sports, Science and Technology;
                Award ID: 08033011-00262
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100003478, Ministry of Health, Labour and Welfare;
                Award ID: 21FA0601
                Award Recipient :
                Categories
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                © Springer Nature Limited 2023

                Uncategorized
                medical research,risk factors
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                medical research, risk factors

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