Literature DB >> 21278238

Joint hypermobility syndrome: A common clinical disorder associated with migraine in women.

Elise M Bendik1, Brad T Tinkle, Enas Al-shuik, Linda Levin, Andrew Martin, Robert Thaler, Carrie L Atzinger, Jodie Rueger, Vincent T Martin.   

Abstract

Preliminary studies suggested that headache disorders are more common in patients with joint hypermobility syndrome (JHS). The objectives of this study were to determine if the prevalence, frequency, and disability of migraine differ between female patients with JHS and a control population. Twenty-eight patients with JHS and 232 controls participated in the case-cohort study. Participants underwent a structured verbal interview and were assigned a diagnosis of migraine based on criteria of the International Classification of Headache Disorders, 2nd Edition. The primary outcome measures were the prevalence, frequency, and headache-related disability of migraine. Logistic regression was used for the prevalence analysis and Poisson regression for the frequency and disability analyses. Results indicated that the prevalence of migraine was 75% in JHS patients and 43% in controls. The adjusted odds ratio for the prevalence of migraine was 3.19 (95% CI 1.24, 8.21] in JHS patients. The rate ratios for migraine frequency and headache-related disability were 1.67 (95% CI 1.01, 2.76) and 2.99 (95% CI 1.66, 5.38), respectively, for JHS patients. Our study suggests that JHS is a clinical disorder strongly associated with an increased prevalence, frequency, and disability of migraine in females.

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Year:  2011        PMID: 21278238     DOI: 10.1177/0333102410392606

Source DB:  PubMed          Journal:  Cephalalgia        ISSN: 0333-1024            Impact factor:   6.292


  12 in total

1.  Pain and gastrointestinal dysfunction are significant associations with psychiatric disorders in patients with Ehlers-Danlos syndrome and hypermobility spectrum disorders: a retrospective study.

Authors:  S Wasim; J S Suddaby; M Parikh; S Leylachian; B Ho; A Guerin; J So
Journal:  Rheumatol Int       Date:  2019-03-28       Impact factor: 2.631

2.  Psychiatric disorders in Ehlers-Danlos syndrome are frequent, diverse and strongly associated with pain.

Authors:  Samantha Aliza Hershenfeld; Syed Wasim; Vanda McNiven; Manasi Parikh; Paula Majewski; Hanna Faghfoury; Joyce So
Journal:  Rheumatol Int       Date:  2015-10-03       Impact factor: 2.631

3.  A study of migraine characteristics in joint hypermobility syndrome a.k.a. Ehlers-Danlos syndrome, hypermobility type.

Authors:  Francesca Puledda; Alessandro Viganò; Claudia Celletti; Barbara Petolicchio; Massimiliano Toscano; Edoardo Vicenzini; Marco Castori; Guido Laudani; Donatella Valente; Filippo Camerota; Vittorio Di Piero
Journal:  Neurol Sci       Date:  2015-03-20       Impact factor: 3.307

Review 4.  Clinical Relevance of Joint Hypermobility and Its Impact on Musculoskeletal Pain and Bone Mass.

Authors:  Vito Guarnieri; Marco Castori
Journal:  Curr Osteoporos Rep       Date:  2018-08       Impact factor: 5.096

Review 5.  Neurovisceral phenotypes in the expression of psychiatric symptoms.

Authors:  Jessica A Eccles; Andrew P Owens; Christopher J Mathias; Satoshi Umeda; Hugo D Critchley
Journal:  Front Neurosci       Date:  2015-02-10       Impact factor: 4.677

Review 6.  Neurological manifestations of Ehlers-Danlos syndrome(s): A review.

Authors:  Marco Castori; Nicol C Voermans
Journal:  Iran J Neurol       Date:  2014-10-06

7.  Brain injury unmasking Ehlers-Danlos syndromes after trauma: the fiber print.

Authors:  Claude Hamonet; Daniel Frédy; Jérémie H Lefèvre; Sacha Bourgeois-Gironde; Jean-David Zeitoun
Journal:  Orphanet J Rare Dis       Date:  2016-04-22       Impact factor: 4.123

8.  Evaluation of Temporomandibular Disorders and Comorbidities in Patients with Ehler--Danlos: Clinical and Digital Findings.

Authors:  Paola Di Giacomo; Mauro Celli; Gaetano Ierardo; Antonella Polimeni; Carlo Di Paolo
Journal:  J Int Soc Prev Community Dent       Date:  2018-07-18

9.  Cervical medullary syndrome secondary to craniocervical instability and ventral brainstem compression in hereditary hypermobility connective tissue disorders: 5-year follow-up after craniocervical reduction, fusion, and stabilization.

Authors:  Fraser C Henderson; C A Francomano; M Koby; K Tuchman; J Adcock; S Patel
Journal:  Neurosurg Rev       Date:  2019-01-09       Impact factor: 3.042

10.  Ehlers-danlos syndrome, hypermobility type: an underdiagnosed hereditary connective tissue disorder with mucocutaneous, articular, and systemic manifestations.

Authors:  Marco Castori
Journal:  ISRN Dermatol       Date:  2012-11-22
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