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1

Hill, Keith, Kaela Farrier, Melissa Russell, and Elissa Burton. "Dysmobility syndrome: current perspectives." Clinical Interventions in Aging Volume 12 (January 2017): 145–52. http://dx.doi.org/10.2147/cia.s102961.

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Yi, Hyon-Seung, and Sihoon Lee. "Overcoming osteoporosis and beyond: Locomotive syndrome or dysmobility syndrome." Osteoporosis and Sarcopenia 4, no. 3 (2018): 77–78. http://dx.doi.org/10.1016/j.afos.2018.09.001.

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Binkley, Neil, and Diane Krueger. "Dysmobility syndrome: a paradigm shift in fracture prevention." PAIN. JOINTS. SPINE 7, no. 1 (2017): 1–6. http://dx.doi.org/10.22141/2224-1507.7.1.2017.102430.

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Iniushyna, Alina, Nataliia Zaverukha, Nataliia Grygorieva, and Olha Protsiuk. "OSTEOARTHRITIS AND GERIATRIC SYNDROMES: FEATURES OF THE RELATIONSHIP AND MANAGEMENT OPPORTUNITIES (LITERATURE REVIEW)." ORTHOPAEDICS TRAUMATOLOGY and PROSTHETICS, no. 2 (June 29, 2025): 99–109. https://doi.org/10.15674/0030-59872025299-109.

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Osteoarthritis (OA) is one of the leading age-associated musculoskeletal isorders, the prevalence of which is increasing due to population aging. The aim of this study is to analyze current literature data regarding the relation and management possibilities of OA and common geriatric syndromes. Methods. A systematic literature review was conducted using analytical methods across scientific databases such as PubMed, Web of Science, Scopus, and Google Scholar for the period 2019–2024. The search was performed using the keywords: “osteoarthritis,” “sarcopenia,” “sarcopenic obesity,” “dysmobility,
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Chen, Yuan-Yuei, Tung-Wei Kao, Chung-Ching Wang, Ying-Jen Chen, Chen-Jung Wu, and Wei-Liang Chen. "Exploring the link between metabolic syndrome and risk of dysmobility syndrome in elderly population." PLOS ONE 13, no. 12 (2018): e0207608. http://dx.doi.org/10.1371/journal.pone.0207608.

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Santos, Vanessa Ribeiro dos, Tiego Aparecido Diniz, Vitor Cabrera Batista, Ismael Forte Freitas, and Luís Alberto Gobbo. "Practice of physical activity and dysmobility syndrome in community-dwelling older adults." Journal of Exercise Rehabilitation 15, no. 2 (2019): 294–301. http://dx.doi.org/10.12965/jer.1938034.017.

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Sebastião, Emerson, and Peter Chomentowski. "Dysmobility syndrome: is exercise a key component in its prevention and treatment?" Journal of Public Health 26, no. 4 (2017): 379–81. http://dx.doi.org/10.1007/s10389-017-0875-3.

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Lim, Eun Ju, and Jun Hee Noh. "Physical Function, Cognitive Function, and Depressive Symptoms in Elderly Women with Dysmobility Syndrome." International Journal of Bio-Science and Bio-Technology 7, no. 4 (2015): 229–38. http://dx.doi.org/10.14257/ijbsbt.2015.7.4.22.

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Kong, Ji-Young, and Inhwan Lee. "Association Between Dysmobility Syndrome with Serum Vitamin D in Community-Dwelling Older Adults." Exercise Science 32, no. 4 (2023): 435–44. http://dx.doi.org/10.15857/ksep.2023.00528.

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PURPOSE: To investigate the association between serum vitamin D levels and dysmobility syndrome (DMS) in community-dwelling older adults.METHODS: This cross-sectional study included 390 older adults (80.7% female) with a mean (±SD) age of 74.8±5.5 years. Based on high body fat level, osteoporosis, low muscle mass, slow gait speed, low grip strength, and fall(s), participants were classified as robust, pre-DMS, or DMS. Based on serum vitamin D levels, subjects were classified as high 33%, middle 33%, and lower 33%, and/or ≥20 ng/mL and <20 ng/mL, respectively. Logistic regression analyses we
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Sun, Wen, Peige Wang, and Yongfang Zhao. "The characteristics of the body mass frequency index in dysmobility syndrome: A pilot study." Experimental Gerontology 191 (June 2024): 112414. http://dx.doi.org/10.1016/j.exger.2024.112414.

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Binkley, N., D. Krueger, and B. Buehring. "What’s in a name revisited: should osteoporosis and sarcopenia be considered components of “dysmobility syndrome?”." Osteoporosis International 24, no. 12 (2013): 2955–59. http://dx.doi.org/10.1007/s00198-013-2427-1.

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Looker, A. C. "Dysmobility syndrome and mortality risk in US men and women age 50 years and older." Osteoporosis International 26, no. 1 (2014): 93–102. http://dx.doi.org/10.1007/s00198-014-2904-1.

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Buehring, Bjoern, Karen E. Hansen, Brian L. Lewis, et al. "Dysmobility Syndrome Independently Increases Fracture Risk in the Osteoporotic Fractures in Men (MrOS) Prospective Cohort Study." Journal of Bone and Mineral Research 33, no. 9 (2018): 1622–29. http://dx.doi.org/10.1002/jbmr.3455.

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Buehring, B., R. Parvaee, C. Mueller, et al. "POS0505 FREQUENCY OF DYSMOBILITY SYNDROME IN PATIENTS WITH RMD AND ITS RELATIONSHIP WITH FRACTURES AND FRAILTY." Annals of the Rheumatic Diseases 82, Suppl 1 (2023): 514.2–515. http://dx.doi.org/10.1136/annrheumdis-2023-eular.1824.

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BackgroundDysmobility Syndrome (DS) is a novel concept to characterize musculoskeletal (MSK) health. DS includes parameters for osteoporosis, sarcopenia and falls[1]. It has been associated with fractures and mortality in community dwelling older adults[2-4]but has never been applied to patients with rheumatic and musculoskeletal diseases (RMD).ObjectivesTo study the prevalence of DS and the association of DS with frailty and major osteoporotic fractures (MOF) in patients with inflammatory and non-inflammatory RMD.MethodsPatients with inflammatory and non-inflammatory RMD aged 65 and older wer
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Iolascon, Giovanni, Antimo Moretti, Maria Teresa Giamattei, Silvia Migliaccio, and Francesca Gimigliano. "Prevalent fragility fractures as risk factor for skeletal muscle function deficit and dysmobility syndrome in post-menopausal women." Aging Clinical and Experimental Research 27, S1 (2015): 11–16. http://dx.doi.org/10.1007/s40520-015-0417-1.

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Lanchais, Kassandra, Frederic Capel, and Anne Tournadre. "Could Omega 3 Fatty Acids Preserve Muscle Health in Rheumatoid Arthritis?" Nutrients 12, no. 1 (2020): 223. http://dx.doi.org/10.3390/nu12010223.

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Rheumatoid arthritis (RA) is a chronic inflammatory disease characterized by a high prevalence of death due to cardiometabolic diseases. As observed during the aging process, several comorbidities, such as cardiovascular disorders (CVD), insulin resistance, metabolic syndrome and sarcopenia, are frequently associated to RA. These abnormalities could be closely linked to alterations in lipid metabolism. Indeed, RA patients exhibit a lipid paradox, defined by reduced levels of total, low-density lipoprotein (LDL) and high-density lipoprotein (HDL) cholesterol whereas the CVD risk is increased. M
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Kim, Minjun, and Inhwan Lee. "Mediating effect of physical activity on the association between body fat distribution, dysmobility syndrome, and cognitive impairment in older women in the community." Experimental Gerontology 203 (May 2025): 112737. https://doi.org/10.1016/j.exger.2025.112737.

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Hong, Namki, Chang Oh Kim, Yoosik Youm, Hyeon Chang Kim, and Yumie Rhee. "Low peak jump power is associated with elevated odds of dysmobility syndrome in community-dwelling elderly individuals: the Korean Urban Rural Elderly (KURE) study." Osteoporosis International 29, no. 6 (2018): 1427–36. http://dx.doi.org/10.1007/s00198-018-4466-0.

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Kruger, Andrew J., Matthew Flaherty, Padmini Sekar, et al. "Abstract T P231: Does Intraventricular Hemorrhage Lead to a Normal Pressure Hydrocephalus-Like Syndrome?" Stroke 45, suppl_1 (2014). http://dx.doi.org/10.1161/str.45.suppl_1.tp231.

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Background: Intracerebral hemorrhage (ICH) has the highest short and long-term morbidity and mortality rates of stroke subtypes. While increased intracranial pressure due to the presence of intraventricular hemorrhage (IVH) may relate to early poor outcomes, the mechanism of reduced 3-month outcome with IVH is unclear. We hypothesized that IVH may cause symptoms similar to normal pressure hydrocephalus (NPH), specifically urinary incontinence and gait disturbance. Methods: We used interviewed cases from the Genetic and Environmental Risk Factors for Hemorrhagic Stroke Study (7/1/08-12/31/12) t
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Geng, Zixiang, Peige Wang, Guangyue Yang, Yifei Li, and Yongfang Zhao. "Circulating Hsa-miR499a-5p as markers in dysmobility syndrome patients: a new index for diagnosing dysmobility syndrome based on osteoporosis and predicting fracture risk." Postgraduate Medical Journal, January 23, 2024. http://dx.doi.org/10.1093/postmj/qgae004.

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Abstract Background Dysmobility syndrome based on osteoporosis (ODS) is a disease characterized by low bone mass and low muscle mass. Its features are high fracture and high fall risk. Falls and fractures are the most important factors affecting the quality of life and lifespan of ODS. However, there is no serum marker for the evaluation of ODS patients. Our previous studies have shown that the expression of circulating miRNA is stable and is a good marker for disease diagnosis. Therefore, this study aims to explore potential serum markers of ODS. Methods A total of 78 subjects were included i
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Burgueno-Aguilar, Karen, Francisco Fidencio Cons-Molina, Daniela Garcia-Jimenez, Luis Eduardo Bejarano-Lopez, and Marissa Alexandra Gudino-Barroso. "Dysmobility syndrome: a case-series study describing a musculoskeletal syndrome in postmenopausal Mexican women." Archives of Osteoporosis 16, no. 1 (2021). http://dx.doi.org/10.1007/s11657-021-00897-7.

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Ma, Yongfang, Bowei Liu, Fuzai Yin, et al. "Vitamin D level as a predictor of dysmobility syndrome with type 2 diabetes." Scientific Reports 14, no. 1 (2024). http://dx.doi.org/10.1038/s41598-024-70400-y.

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Clynes, Michael, Mark Edwards, Celia Gregson, et al. "Prevalence of ‘dysmobility syndrome' in community dwelling older adults: findings from the Hertfordshire Cohort Study." Bone Abstracts, May 1, 2014. http://dx.doi.org/10.1530/boneabs.3.pp201.

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Khaleghi, Mohammad Mehdi, Hadi Emamat, Maryam Marzban, et al. "The association of body composition and fat distribution with dysmobility syndrome in community-dwelling older adults: Bushehr Elderly Health (BEH) program." BMC Musculoskeletal Disorders 24, no. 1 (2023). http://dx.doi.org/10.1186/s12891-023-06934-5.

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Abstract Background and objective Dysmobility Syndrome (DS) is characterized as an accumulation of clinical risk factors for functional disability, such as osteoporosis, sarcopenia, and obesity. Neurological disorders that affect the motor and sensory systems can also contribute to the condition, resulting in gait and muscle strength disturbances, as well as a history of falls and fractures. The study aimed to determine the association between fat distribution in different body areas and the odds of older adults developing DS, as there is still uncertainty about the accumulation of fat in whic
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Hong, N., E. Siglinsky, D. Krueger, et al. "Defining an international cut-off of two-legged countermovement jump power for sarcopenia and dysmobility syndrome." Osteoporosis International, September 7, 2020. http://dx.doi.org/10.1007/s00198-020-05591-x.

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Chen, Fang-Ping, Yu-Jr Lin, An-Shine Chao, et al. "Utilizing nomograms to predict prevalent vertebral fracture risk: An analysis of dysmobility syndrome in a community-dwelling population." Biomedical Journal, November 2021. http://dx.doi.org/10.1016/j.bj.2021.11.008.

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Hong, Namki, Chang Oh Kim, Yoosik Youm, Jin-Young Choi, Hyeon Chang Kim, and Yumie Rhee. "Dysmobility syndrome is associated with prevalent morphometric vertebral fracture in older adults: the Korean Urban-Rural Elderly (KURE) study." Archives of Osteoporosis 13, no. 1 (2018). http://dx.doi.org/10.1007/s11657-018-0500-2.

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Lee, Wei-Ju, Li-Kuo Liu, An-Chun Hwang, Li-Ning Peng, Ming-Hsien Lin, and Liang-Kung Chen. "Dysmobility Syndrome and Risk of Mortality for Community-Dwelling Middle-Aged and Older Adults: The Nexus of Aging and Body Composition." Scientific Reports 7, no. 1 (2017). http://dx.doi.org/10.1038/s41598-017-09366-z.

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Jung, Y. W., N. Hong, C. O. Kim, et al. "The diagnostic value of phase angle, an integrative bioelectrical marker, for identifying individuals with dysmobility syndrome: the Korean Urban-Rural Elderly study." Osteoporosis International, October 30, 2020. http://dx.doi.org/10.1007/s00198-020-05708-2.

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Capodaglio, Paolo, and Alberto Falchetti. "Metabolic syndromes and dysmobility." American Journal of Physical Medicine & Rehabilitation Publish Ahead of Print (May 13, 2020). http://dx.doi.org/10.1097/phm.0000000000001466.

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