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Featured researches published by Lars Remvig.


Pediatrics | 2009

Motor Competence and Physical Activity in 8-Year-Old School Children With Generalized Joint Hypermobility

Birgit Juul-Kristensen; Jens Halkjær Kristensen; Britt Frausing; Dorte Vendelboe Jensen; Henrik Røgind; Lars Remvig

OBJECTIVE: Because the criteria used for diagnosing between generalized joint hypermobility (GJH) and musculoskeletal complaints, as well as relations between GJH and an insufficient motor development and/or a reduced physical activity level differ, the prevalence of GJH varies considerably. The aim of this study was to survey the prevalence of GJH defined by a Beighton score at ≥4, ≥5, or ≥6 positive tests of 9 and benign joint hypermobility syndrome (BJHS) in Danish primary school children at 8 years of age. A second aim was to compare children with and without GJH and BJHS regarding motor competence, self-reported physical activity, and incidence of musculoskeletal pain and injuries. METHODS: A cross-sectional study of 524 children in the second grade from 10 public schools was performed. A positive response rate was obtained for 416 (79.4%) children, and 411 (78.4%) children were clinically examined and tested for motor competence, whereas questionnaire response to items comprising musculoskeletal pain and injuries, in addition to daily level and duration of physical activity, corresponded to 377 (71.9%) children. RESULTS: In total, 29% of the children had GJH4, 19% had GJH5, 10% had GJH6, and 9% had BJHS, with no gender difference. There was no difference in daily level and duration of physical activity and in frequency of musculoskeletal pain and injuries between those with and without GJH. Children with ≥GJH5 as well as with ≥GJH6 performed better in the motor competence tests. CONCLUSION: Motor competence and physical activity are not reduced in primary school children at 8 years of age with GJH or BJHS. It is recommended that a potential negative influence on the musculoskeletal system over time, as a result of GJH, be investigated by longitudinal studies.


BioMed Research International | 2013

Children with Generalised Joint Hypermobility and Musculoskeletal Complaints: State of the Art on Diagnostics, Clinical Characteristics, and Treatment

Mark C. Scheper; Raoul H.H. Engelbert; E. A. A. Rameckers; J. Verbunt; Lars Remvig; Birgit Juul-Kristensen

Introduction. To provide a state of the art on diagnostics, clinical characteristics, and treatment of paediatric generalised joint hypermobility (GJH) and joint hypermobility syndrome (JHS). Method. A narrative review was performed regarding diagnostics and clinical characteristics. Effectiveness of treatment was evaluated by systematic review. Searches of Medline and Central were performed and included nonsymptomatic and symptomatic forms of GJH (JHS, collagen diseases). Results. In the last decade, scientific research has accumulated on all domains of the ICF. GJH/JHS can be considered as a clinical entity, which can have serious effects during all stages of life. However research regarding the pathological mechanism has resulted in new potential opportunities for treatment. When regarding the effectiveness of current treatments, the search identified 1318 studies, from which three were included (JHS: n = 2, Osteogenesis Imperfecta: n = 1). According to the best evidence synthesis, there was strong evidence that enhancing physical fitness is an effective treatment for children with JHS. However this was based on only two studies. Conclusion. Based on the sparsely available knowledge on intervention studies, future longitudinal studies should focus on the effect of physical activity, fitness, and joint stabilisation. In JHS and chronic pain, the effectiveness of a multidisciplinary approach should be investigated.


American Journal of Medical Genetics Part A | 2014

Lack of consensus on tests and criteria for generalized joint hypermobility, Ehlers–Danlos syndrome: Hypermobile type and joint hypermobility syndrome

Lars Remvig; Lise Flycht; Karl Bang Christensen; Birgit Juul-Kristensen

The objectives of this study were to register clinicians performance and opinion of importance of clinical tests for generalized joint hypermobility (GJH), Ehlers–Danlos syndrome, hypermobility type (EDS‐HT) and joint hypermobility syndrome (JHS), and to reach a consensus among clinicians on criteria for diagnosing GJH, EDS‐HT and JHS. A panel of clinicians answered questions about how to perform and interpret clinical tests and rated test importance on an 11‐box scale. The questionnaire was developed on the basis of information from focus groups and the literature. Cronbachs α was used as a measure of internal consistency/consensus among the panelists. The results showed Cronbachs α on importance score of items for diagnosing GJH, EDS‐HT and JHS was 0.61, 0.79, and 0.44, respectively. Panelist‐group correlation for the three conditions varied substantially (−0.46 to 0.89, 0.03 to 0.68, and −0.07 to 0.68) indicating heterogeneity among the panelists. There was agreement on which tests to use, but performance of the tests (i.e., the specific maneuvers) varied considerably inclusive use of tests with unknown reliability. Furthermore, agreement on the diagnostic criteria varied. We conclude that the level of consensus for the importance of various items for diagnosing GJH, EDS‐HT and JHS, was below the required limit (Cronbachs α >0.90) for clinical decision‐making and diagnosing. Consensus on tests and criteria through a Delphi process could not be reached. Better descriptions of, and reliability studies on, test maneuvers and criteria sets for these conditions are needed. Subsequent intensive training and implementation of these tests and criteria, nationally as well as internationally should be established.


Knee | 2012

Knee function in 10-year-old children and adults with Generalised Joint Hypermobility.

Birgit Juul-Kristensen; Henrik Hansen; Erik B. Simonsen; Tine Alkjær; Jens Halkjær Kristensen; Bente Rona Jensen; Lars Remvig

PURPOSE Knee function is reduced in patients with Benign Joint Hypermobility Syndrome. The aim was to study knee function in children and adults with Generalised Joint Hypermobility (GJH) and Non-GJH (NGJH)). MATERIALS AND METHODS In a matched comparative study, 39 children and 36 adults (mean age children 10.2 years; adults 40.3 years) were included, comprising 19 children and 18 adults with GJH (Beighton ≥ 5/9; Beighton ≥ 4/9), minimum one hypermobile knee, no knee pain (children), and 20 children and 18 adults with NGJH (Beighton <5; Beighton <4). Totally, 85% of the adults were parents to these children. Knee function was determined by self-reported physical fitness (100mm VAS), Knee injury and Osteoarthritis Outcome Score (KOOS) (only adults), measured maximum isokinetic knee strength (60°/s) and peak vertical jump displacement (PVJD), with calculated knee strength balance, Hamstring/Quadriceps (H/Q) ratio and peak rate of force development (PRFD). RESULTS Adults with GJH had lower knee function (KOOS: pain, p=0.001; symptoms, p=0.001; Activities of Daily Living, p=0.001; Sport/Recreation, p=0.003; knee-related quality of life, p<0.001), and H/Q ratio (0.46 vs. 0.54, p=0.046) than adults with NGJH, regardless of age and knee pain. Both GJH groups had normal physical fitness, isokinetic knee strength, and (only children) H/Q ratio. CONCLUSIONS Children at 10 years with GJH have normal, but adults with GJH have impaired knee function. To track the risk of developing impaired knee function, children with GJH must be followed longitudinally. Meanwhile, attention to knee function may be given to children with GJH who have parents presenting GJH.


Muscle & Nerve | 2013

Effect of generalized joint hypermobility on knee function and muscle activation in children and adults.

Bente Jensen; Annesofie T. Olesen; Mogens Theisen Pedersen; Jens Halkjær Kristensen; Lars Remvig; Erik B. Simonsen; Birgit Juul-Kristensen

Introduction: We investigated muscle activation strategy and performance of knee extensor and flexor muscles in children and adults with generalized joint hypermobility (GJH) and compared them with controls. Methods: Muscle activation, torque steadiness, electromechanical delay, and muscle strength were evaluated in 39 children and 36 adults during isometric knee extension and flexion. Subjects performed isometric maximum contractions, submaximal contractions at 25% maximum voluntary contraction (MVC), and explosive contractions. Results: Agonist activation was reduced, and coactivation ratio was greater in GJH during knee flexion compared with controls. Torque steadiness was impaired in adults with GJH during knee flexion. No effect of GJH was found on muscle strength or electromechanical delay. Correlation analysis revealed an association between GJH severity and function in adults. Conclusions: The results indicate that muscle activation strategy and quality of force control were significantly affected in adults with GJH during knee flexion, whereas only muscle activation strategy was affected in children with GJH. Muscle Nerve 48:762–769, 2013


Clinical Biomechanics | 2012

Gait analysis of adults with generalised joint hypermobility.

Erik B. Simonsen; Heidi Tegner; Tine Alkjær; Peter K. Larsen; Jens Halkjær Kristensen; Bente Jensen; Lars Remvig; Birgit Juul-Kristensen

BACKGROUND The majority of adults with Generalised Joint Hypermobility experience symptoms such as pain and joint instability, which is likely to influence their gait pattern. Accordingly, the purpose of the present project was to perform a biomechanical gait analysis on a group of patients with Generalised Joint Hypermobility and compare them to a group of healthy subjects. METHODS Seventeen adults clinically classified with Generalised Joint Hypermobility (6 males and 11 females) and seventeen healthy subjects (9 males and 8 females) were included in the project. The subjects walked across three force platforms while they were filmed by five video cameras. Net joint moments were calculated in 3D by inverse dynamics and peak values were input to statistical analyses. A 3D knee joint model was used to calculate bone-on-bone forces. FINDINGS In the frontal plane both the peak knee and hip abductor moments were 13% higher in the patient group. In the sagittal plane the peak knee extensor moment was 10% higher for the patients and the flexor moment about the knee joint in the middle of stance was 27% lower for the patients. Increased flexion in the knee joint for the patients was also observed. INTERPRETATION The finding that adults with Generalised Joint Hypermobility display higher joint moments during walking in both the frontal and the sagittal planes and increased knee joint loadings may explain the pain symptoms in the patient group and indicate these subjects are subjected to an increased risk of developing osteo-arthritis.


Clinical Biomechanics | 2013

Dynamic balance during gait in children and adults with Generalized Joint Hypermobility.

S. Falkerslev; C. Baagø; Tine Alkjær; Lars Remvig; Jens Halkjær-Kristensen; Peter K. Larsen; Birgit Juul-Kristensen; Erik B. Simonsen

BACKGROUND The purpose of the study was to investigate if differences of the head and trunk stability and stabilization strategies exist between subjects classified with Generalized Joint Hypermobility and healthy controls during gait. It was hypothesized that joint hypermobility could lead to decreased head and trunk stability and a head stabilization strategy similar to what have been observed in individuals with decreased locomotor performance. METHODS A comparative study design was used wherein 19 hypermobile children were compared to 19 control children, and 18 hypermobile adults were compared to 18 control adults. The subjects were tested during normal walking and walking on a line. Kinematics of head, shoulder, spine and pelvis rotations were measured by five digital video cameras in order to assess the segmental stability (angular dispersion) and stabilization strategies (anchoring index) in two rotational components: roll and yaw. FINDINGS Hypermobile children and adults showed decreased lateral trunk stability in both walking conditions. In hypermobile children, it was accompanied with decreased head stability as the head was stabilized by the inferior segment when walking on a line. Several additional differences were observed in stability and stabilization strategies for both children and adults. INTERPRETATION Stability of the trunk was decreased in hypermobile children and adults. This may be a consequence of decreased stability of the head. Hypermobile children showed a different mode of head stabilization during more demanding locomotor conditions indicating delayed locomotor development. The findings reflect that Generalized Joint Hypermobility probably include motor control deficits.


Physiotherapy Theory and Practice | 2011

Scapular dyskinesis in trapezius myalgia and intraexaminer reproducibility of clinical tests

Birgit Juul-Kristensen; Kenneth Hilt; Flemming Enoch; Lars Remvig; Gisela Sjøgaard

The aims were to test the intraexaminer reproducibility and report the presence of specific clinical variables of scapular dyskinesis in cases with trapezius myalgia and healthy controls, along with general health and work ability. A total of 38 cases and 23 controls were tested for scapular dyskinesis, general health, and work ability, and 19 cases and 14 controls participated in the reproducibility study. Intraexaminer reproducibility was good to excellent for 6 of 10 clinical variables (Intraclass Correlation Coefficient [ICC] 0.76–0.91; kappa 0.84–1.00), and fair to good for four variables (ICC 0.42–0.74), test for muscular weakness having the lowest ICC (0.42). Cases showed significantly larger medial border misalignment, larger lower horizontal distance of the inferior scapular angle and larger passive shoulder internal rotation, by 110% (1.02 cm), 15% (1.38 cm), and 8% (5.5°), respectively. Cases with the highest degree of scapular dyskinesis showed reduced work ability and general health. The present specific clinical variables on scapular dyskinesis showed satisfactory intraexaminer reproducibility. An increased standardization must be implemented to increase reproducibility of tests for muscular weakness, and the interexaminer reproducibility must be tested for all variables. Finally, scapular dyskinesis in cases with trapezius myalgia must be followed longitudinally for clinical importance.


International Musculoskeletal Medicine | 2011

Prevalence of generalized joint hypermobility, arthralgia and motor competence in 10-year-old school children

Lars Remvig; Cristina Kümmel; Jens Halkjær Kristensen; Gudrun Boas; Birgit Juul-Kristensen

Abstract Objectives Diverging results exist for children regarding the relation between generalized joint hypermobility (GJH) and musculoskeletal complaints, as well as relations between GJH and insufficient motor development, and/or reduced physical activity level. The main purposes were to (1) survey the prevalence of GJH and of benign joint hypermobility syndrome (BJHS) in 10-year-old children, (2) compare children with and without GJH and BJHS regarding motor competence, physical activity, and musculoskeletal pain and injuries. Subjects and methods All fourth-grade children in a Copenhagen municipality were invited to be clinically examined and tested for motor competence, and to answer a questionnaire about musculoskeletal pain, injuries, and physical activity. Results The final cohort comprised 315 Caucasian children, 50.5% girls and 54% boys. GJH prevalence was 35.6, 16.8, or 11.1%, depending on GJH cut level 4, 5, or 6, without significant motor competence difference between non-GJH and GJH children. Girls with GJH6 compared to non-GJH6 had insignificantly higher vertical jump height, and boys with GJH6 significantly shorter hand reaction time. In total, 108 Caucasian children answered the questionnaire, 56.5% girls and 43.5% boys. Nineteen fulfilled the criterion for BJHS, without difference in frequency of musculoskeletal pain and injuries, motor competence tests or physical activity compared with non-BJHS. Conclusion GJH prevalence in this cohort is comparable to previous results. Increased pain or frequency of injures were not related to GJH. Children with GJH6 performed better in motor competence tests. Longitudinal studies are recommended to detect influences of GJH on the musculoskeletal system over time.


BMC Musculoskeletal Disorders | 2013

Gait pattern in 9-11-year-old children with generalized joint hypermobility compared with controls; a cross-sectional study

Helene Nikolajsen; Peter K. Larsen; Erik B. Simonsen; Tine Alkjær; Simon Falkerslev; Jens Halkjær Kristensen; Bente Rona Jensen; Lars Remvig; Birgit Juul-Kristensen

BackgroundTo study differences in gait patterns in 10-year-old children with Generalized Joint Hypermobility (GJH) and with no GJH (NGJH).MethodsA total of 37 children participated (19 GJH, 18 NGJH, mean age 10.2 (SD 0.5) years). Inclusion criteria for GJH were a Beighton score of ≥5, with at least one hypermobile knee joint; for NGJH a Beighton score of ≤4, and no hypermobile knees and for both groups no knee pain during the previous week. All children were recorded by five video cameras, while they walked across three force platforms. Net joint moments were calculated in 3D by inverse dynamics and peak values provided input to statistical analyses.ResultsIn the frontal plane, children with GJH had a significantly lower peak knee abductor moment and peak hip abductor moment. In the sagittal plane, the peak knee flexor moment and the peak hip extensor moment were significantly lower in the GJH group although the absolute difference was small.ConclusionsThe walking pattern was the same for children with GJH and for healthy children, as there were no differences in kinematics, but it was, however, performed with different kinetics. Children with GJH walked with lower ankle, knee and hip joint moments compared to children with NGJH. However, the clinical importance of these differences during normal gait is unknown. To obtain this knowledge, children with GJH must be followed longitudinally.Trial registrationThe study was approved by the Committee on Biomedical Research Ethics for Copenhagen and Frederiksberg, Denmark (jnr. KF01-2006-178).

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Tine Alkjær

University of Copenhagen

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Raoul Engelbert

Thomas Jefferson University

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Bente Jensen

University of Copenhagen

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Dorte Vendelbo Jensen

Copenhagen University Hospital

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