Frequency of joint hypermobility in Turkish patients with knee osteoarthritis: a cross sectional multicenter study

Gürer, Gülcan; Bozbaş, Gülnur Taşçı; Tuncer, Tiraje; Ünübol, Ayşe Iyiyapici; Memetoğlu, Özge Illeez

doi:10.1111/1756-185x.12883

Cited by 26 publications

(27 citation statements)

References 38 publications

(39 reference statements)

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“…From a functional perspective, individuals with GJHk and KJH present with increased joint compression during walking and in dynamic balance tasks, reasonably caused by the decreased passive knee joint stability. Increased knee joint load, as seen with kinematic changes and in individuals with KJH, is associated with a higher risk of knee OA, which again is associated with reduced quality of life . Future studies should elucidate both underlying biomechanical mechanisms as well as the impact on function and quality of life in individuals with GJHk and KJH.…”

Section: Discussionmentioning

confidence: 99%

Generalised joint hypermobility and knee joint hypermobility: prevalence, knee joint symptoms and health‐related quality of life in a Danish adult population

et al. 2017

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Section: Discussionmentioning

confidence: 99%

Generalised joint hypermobility and knee joint hypermobility: prevalence, knee joint symptoms and health‐related quality of life in a Danish adult population

et al. 2017

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“…It is possible that an increase in the prevalence of OA is due to the same underlying collagenopathy or by repetitive trauma that commonly occurs in JH and altered joint mechanics [Bird et al, ; Grahame, ; Klemp, ]. Knee hypermobility is common among patients with knee OA [Dolan et al, ; van der Esch et al, ; Gürer et al, ]. In a study of 34 patients with severe thumb (carpometacarpal) OA, 62% had generalized JH [Jonsson and Valtysdottir, ].…”

Section: Clinical Descriptionmentioning

confidence: 99%

Hypermobile Ehlers–Danlos syndrome (a.k.a. Ehlers–Danlos syndrome Type III and Ehlers–Danlos syndrome hypermobility type): Clinical description and natural history

Tinkle

Castori²,

Berglund

et al. 2017

American J of Med Genetics Pt C

370

348

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The hypermobile type of Ehlers-Danlos syndrome (hEDS) is likely the most common hereditary disorder of connective tissue. It has been described largely in those with musculoskeletal complaints including joint hypermobility, joint subluxations/dislocations, as well as skin and soft tissue manifestations. Many patients report activity-related pain and some go on to have daily pain. Two undifferentiated syndromes have been used to describe these manifestations-joint hypermobility syndrome and hEDS. Both are clinical diagnoses in the absence of other causation. Current medical literature further complicates differentiation and describes multiple associated symptoms and disorders. The current EDS nosology combines these two entities into the hypermobile type of EDS. Herein, we review and summarize the literature as a better clinical description of this type of connective tissue disorder.

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“…Muscle weakness and neuromuscular dysfunction may compromise innate protective mechanisms, making joints more susceptible to abnormal motion (35). Conversely, excessive muscle strength or joint laxity may also promote the progression of OA (36,37). Heavy construction work and overhead sports are identified risk factors for GHOA with elite tennis players showing GHOA changes in their dominant shoulders (38,39).…”

Section: Exercise and Occupationmentioning

confidence: 99%

Glenohumeral osteoarthritis: an overview of etiology and diagnostics

et al. 2020

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Background and Aims: Osteoarthritis (OA) is the world’s most common joint disease and there is currently no cure. Glenohumeral osteoarthritis (GHOA) accounts for an estimated 5% -17% of patients with shoulder complaints. The etiology of GHOA is multifactorial, and we review the various non-specific and specific risk factors and further sub-classify them into local and systemic factors. Materials and Methods: Data for this review article were identified by searches of MEDLINE, PubMed, and references from relevant articles using search terms such as “glenohumeral,” “osteoarthritis,” “epidemiology,” “etiology,” “imaging,” and “pathophysiology.” Only articles published in English, German, and Finnish between 1957 and 2017 were included. Results: The prevalence of radiological shoulder OA has been estimated to be as high as 16% -20% in the middle-aged and elderly population, but the concordance between structural findings and symptoms seems to be weak, as many of these individuals are asymptomatic. The vast majority of GHOA is related to non-specific factors, namely advancing age, while specific risk factors are commonly found in young patients. Diagnosis of GHOA is made when typical clinical features and defined radiological findings overlap in an individual. Conclusion: Ultimately the determinants of shoulder pain in GHOA remain incompletely understood. Improved understanding of the etiology and diagnosis of GHOA will enable clinicians to better determine which patients will benefit from different treatment modalities, as well as provide new avenues to potential treatments.

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Frequency of joint hypermobility in Turkish patients with knee osteoarthritis: a cross sectional multicenter study

Cited by 26 publications

References 38 publications

Generalised joint hypermobility and knee joint hypermobility: prevalence, knee joint symptoms and health‐related quality of life in a Danish adult population

Generalised joint hypermobility and knee joint hypermobility: prevalence, knee joint symptoms and health‐related quality of life in a Danish adult population

Hypermobile Ehlers–Danlos syndrome (a.k.a. Ehlers–Danlos syndrome Type III and Ehlers–Danlos syndrome hypermobility type): Clinical description and natural history

Glenohumeral osteoarthritis: an overview of etiology and diagnostics

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