Static Postural Control in Youth With Osteogenesis Imperfecta Type I

To assess static postural control in eyes-open and eyes-closed conditions in individuals with osteogenesis imperfecta (OI) type I as compared with typically developing (TD) individuals and to explore the relation between postural control and lower limb muscle function. Cross-sectional study. Outpati...

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Published inArchives of physical medicine and rehabilitation Vol. 98; no. 10; pp. 1948 - 1954
Main Authors Pouliot-Laforte, Annie, Lemay, Martin, Rauch, Frank, Veilleux, Louis-Nicolas
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.10.2017
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Abstract To assess static postural control in eyes-open and eyes-closed conditions in individuals with osteogenesis imperfecta (OI) type I as compared with typically developing (TD) individuals and to explore the relation between postural control and lower limb muscle function. Cross-sectional study. Outpatient department of a pediatric orthopedic hospital. A convenience sample (N=38) of individuals with OI type I (n=22; mean age, 13.1y; range, 6–21y) and TD individuals (n=16; mean age, 13.1y; range, 6–20y) was selected. Participants were eligible if they were between 6 and 21 years and if they did not have any fracture or surgery in the lower limb in the 12 months before testing. Not applicable. Postural control was assessed through static balance tests and muscle function through mechanographic tests on a force platform. Selected postural parameters were path length, velocity, 90% confidence ellipse area, and the ellipse's length of the mediolateral and anteroposterior axes. Mechanographic parameters were peak force and peak power as measured using the multiple two-legged hopping and the single two-legged jump test, respectively. Individuals with OI type I had poorer postural control than did TD individuals as indicated by longer and faster displacements and a larger ellipse area. Muscle function was unrelated to postural control in the OI group. Removing visual information resulted in a larger increase in postural control parameters in the OI group than in the TD group. A proprioceptive deficit could explain poorer postural control in individuals with OI type I. •Postural control deficits are reported in youth with osteogenesis imperfecta type I.•Poorer postural control was not associated with muscle function deficits.•Proprioceptive deficits could explain poorer postural control in osteogenesis imperfecta type I.
AbstractList Abstract Objective To assess static postural control in eyes-open and eyes-closed conditions in individuals with osteogenesis imperfecta (OI) type I as compared to typically developing (TD) individuals. The second aim was to explore the relation between postural control and lower-limbs muscle function. Design This is a cross-sectional study. Settings The study was carried out in the outpatient department of a pediatric orthopedic hospital. Participants 22 individuals with OI type I (mean age [range]: 13.1 [6-21] years) and 16 typically developing (TD) individuals (mean age [range]: 13.1 [6-20] years) participated in the study. A convenience sample of participants was selected. Participants were eligible if they were between 6 and 21 years and if they did not have any fracture or surgery in the lower limb in the 12 months prior to testing. Main Outcomes Measures Postural control was assessed through static balance tests and muscle function through mechanograhic tests, on a force plateform. Selected postural parameters were: path length and velocity, 90% confidence ellipse area and the ellipse’s medio-lateral and antero-posterior axes length. Mechanographic parameters were peak force (kN) and peak power (kW) as measured in the Multiple Two-Legged Hopping and the Single Two-Legged jump, respectively. Results OI type I had poorer postural control than TD as indicated by longer and faster displacements and a larger ellipse area. Muscle function was unrelated to postural control in the OI group. Removing visual information resulted in a larger increase in postural control parameters for the OI group compared to the TD group. Conclusions A proprioceptive deficit is suggested to explain decreased postural control in individuals with OI type I.
To assess static postural control in eyes-open and eyes-closed conditions in individuals with osteogenesis imperfecta (OI) type I as compared with typically developing (TD) individuals and to explore the relation between postural control and lower limb muscle function. Cross-sectional study. Outpatient department of a pediatric orthopedic hospital. A convenience sample (N=38) of individuals with OI type I (n=22; mean age, 13.1y; range, 6–21y) and TD individuals (n=16; mean age, 13.1y; range, 6–20y) was selected. Participants were eligible if they were between 6 and 21 years and if they did not have any fracture or surgery in the lower limb in the 12 months before testing. Not applicable. Postural control was assessed through static balance tests and muscle function through mechanographic tests on a force platform. Selected postural parameters were path length, velocity, 90% confidence ellipse area, and the ellipse's length of the mediolateral and anteroposterior axes. Mechanographic parameters were peak force and peak power as measured using the multiple two-legged hopping and the single two-legged jump test, respectively. Individuals with OI type I had poorer postural control than did TD individuals as indicated by longer and faster displacements and a larger ellipse area. Muscle function was unrelated to postural control in the OI group. Removing visual information resulted in a larger increase in postural control parameters in the OI group than in the TD group. A proprioceptive deficit could explain poorer postural control in individuals with OI type I. •Postural control deficits are reported in youth with osteogenesis imperfecta type I.•Poorer postural control was not associated with muscle function deficits.•Proprioceptive deficits could explain poorer postural control in osteogenesis imperfecta type I.
To assess static postural control in eyes-open and eyes-closed conditions in individuals with osteogenesis imperfecta (OI) type I as compared with typically developing (TD) individuals and to explore the relation between postural control and lower limb muscle function.OBJECTIVESTo assess static postural control in eyes-open and eyes-closed conditions in individuals with osteogenesis imperfecta (OI) type I as compared with typically developing (TD) individuals and to explore the relation between postural control and lower limb muscle function.Cross-sectional study.DESIGNCross-sectional study.Outpatient department of a pediatric orthopedic hospital.SETTINGOutpatient department of a pediatric orthopedic hospital.A convenience sample (N=38) of individuals with OI type I (n=22; mean age, 13.1y; range, 6-21y) and TD individuals (n=16; mean age, 13.1y; range, 6-20y) was selected. Participants were eligible if they were between 6 and 21 years and if they did not have any fracture or surgery in the lower limb in the 12 months before testing.PARTICIPANTSA convenience sample (N=38) of individuals with OI type I (n=22; mean age, 13.1y; range, 6-21y) and TD individuals (n=16; mean age, 13.1y; range, 6-20y) was selected. Participants were eligible if they were between 6 and 21 years and if they did not have any fracture or surgery in the lower limb in the 12 months before testing.Not applicable.INTERVENTIONSNot applicable.Postural control was assessed through static balance tests and muscle function through mechanographic tests on a force platform. Selected postural parameters were path length, velocity, 90% confidence ellipse area, and the ellipse's length of the mediolateral and anteroposterior axes. Mechanographic parameters were peak force and peak power as measured using the multiple two-legged hopping and the single two-legged jump test, respectively.MAIN OUTCOMES MEASURESPostural control was assessed through static balance tests and muscle function through mechanographic tests on a force platform. Selected postural parameters were path length, velocity, 90% confidence ellipse area, and the ellipse's length of the mediolateral and anteroposterior axes. Mechanographic parameters were peak force and peak power as measured using the multiple two-legged hopping and the single two-legged jump test, respectively.Individuals with OI type I had poorer postural control than did TD individuals as indicated by longer and faster displacements and a larger ellipse area. Muscle function was unrelated to postural control in the OI group. Removing visual information resulted in a larger increase in postural control parameters in the OI group than in the TD group.RESULTSIndividuals with OI type I had poorer postural control than did TD individuals as indicated by longer and faster displacements and a larger ellipse area. Muscle function was unrelated to postural control in the OI group. Removing visual information resulted in a larger increase in postural control parameters in the OI group than in the TD group.A proprioceptive deficit could explain poorer postural control in individuals with OI type I.CONCLUSIONSA proprioceptive deficit could explain poorer postural control in individuals with OI type I.
Objectives: To assess static postural control in eyes-open and eyes-closed conditions in individuals with osteogenesis imperfecta (OI) type I as compared with typically developing (TD) individuals and to explore the relation between postural control and lower limb muscle function. Design: Cross-sectional study. Setting: Outpatient department of a pediatric orthopedic hospital. Participants A convenience sample (N=38) of individuals with OI type I (n=22; mean age, 13.1y; range, 6-21y) and TD individuals (n=16; mean age, 13.1y; range, 6-20y) was selected. Participants were eligible if they were between 6 and 21 years and if they did not have any fracture or surgery in the lower limb in the 12 months before testing. Interventions: Not applicable. Main Outcomes Measures Postural control was assessed through static balance tests and muscle function through mechanographic tests on a force platform. Selected postural parameters were path length, velocity, 90% confidence ellipse area, and the ellipse's length of the mediolateral and anteroposterior axes. Mechanographic parameters were peak force and peak power as measured using the multiple two-legged hopping and the single two-legged jump test, respectively. Results: Individuals with OI type I had poorer postural control than did TD individuals as indicated by longer and faster displacements and a larger ellipse area. Muscle function was unrelated to postural control in the OI group. Removing visual information resulted in a larger increase in postural control parameters in the OI group than in the TD group. Conclusions: A proprioceptive deficit could explain poorer postural control in individuals with OI type I. Highlights: Postural control deficits are reported in youth with osteogenesis imperfecta type I. Poorer postural control was not associated with muscle function deficits. Proprioceptive deficits could explain poorer postural control in osteogenesis imperfecta type I.
To assess static postural control in eyes-open and eyes-closed conditions in individuals with osteogenesis imperfecta (OI) type I as compared with typically developing (TD) individuals and to explore the relation between postural control and lower limb muscle function. Cross-sectional study. Outpatient department of a pediatric orthopedic hospital. A convenience sample (N=38) of individuals with OI type I (n=22; mean age, 13.1y; range, 6-21y) and TD individuals (n=16; mean age, 13.1y; range, 6-20y) was selected. Participants were eligible if they were between 6 and 21 years and if they did not have any fracture or surgery in the lower limb in the 12 months before testing. Not applicable. Postural control was assessed through static balance tests and muscle function through mechanographic tests on a force platform. Selected postural parameters were path length, velocity, 90% confidence ellipse area, and the ellipse's length of the mediolateral and anteroposterior axes. Mechanographic parameters were peak force and peak power as measured using the multiple two-legged hopping and the single two-legged jump test, respectively. Individuals with OI type I had poorer postural control than did TD individuals as indicated by longer and faster displacements and a larger ellipse area. Muscle function was unrelated to postural control in the OI group. Removing visual information resulted in a larger increase in postural control parameters in the OI group than in the TD group. A proprioceptive deficit could explain poorer postural control in individuals with OI type I.
Author Veilleux, Louis-Nicolas
Pouliot-Laforte, Annie
Lemay, Martin
Rauch, Frank
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Keywords TD
Postural balance
Proprioception
Osteogenesis imperfecta
Healthy subjects
Muscle function
OI
Rehabilitation
Mechanography
Center of Force
Postural control
Typically developing
CoF
Osteogenesis Imperfecta
Language English
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Snippet To assess static postural control in eyes-open and eyes-closed conditions in individuals with osteogenesis imperfecta (OI) type I as compared with typically...
Abstract Objective To assess static postural control in eyes-open and eyes-closed conditions in individuals with osteogenesis imperfecta (OI) type I as...
Objectives: To assess static postural control in eyes-open and eyes-closed conditions in individuals with osteogenesis imperfecta (OI) type I as compared with...
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SubjectTerms Adolescent
Child
Cross-Sectional Studies
Exercise Test
Female
Healthy subjects
Humans
Lower Extremity - physiopathology
Male
Muscle function
Muscle Strength - physiology
Osteogenesis imperfecta
Osteogenesis Imperfecta - physiopathology
Physical Medicine and Rehabilitation
Postural balance
Postural Balance - physiology
Proprioception
Rehabilitation
Young Adult
Title Static Postural Control in Youth With Osteogenesis Imperfecta Type I
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0003999317302423
https://www.clinicalkey.es/playcontent/1-s2.0-S0003999317302423
https://dx.doi.org/10.1016/j.apmr.2017.03.018
https://www.ncbi.nlm.nih.gov/pubmed/28433416
https://www.proquest.com/docview/1891455497
https://www.proquest.com/docview/2129950093
Volume 98
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