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Prevalence and Association of Generalized Joint Hypermobility in Children with Functional Neurological Disorder: A
Jana Landa1,2, Karin Mashevich3, Etzyona Eisenstein1
1Department of Pediatric Rehabilitation, Chaim Sheba Medical Center, Edmond and Lily Safra Children's Hospital, Ramat-Gan, Israel.
Insights
Generalized joint hypermobility (GJH) is common in children with functional neurological disorder (FND). GJH correlates with increased symptom severity and motor involvement, suggesting it may be a vulnerability factor.
Area of Science:
- Neurology
- Pediatrics
- Rheumatology
Background:
- Functional neurological disorder (FND) has complex, multifactorial causes.
- Generalized joint hypermobility (GJH) is a potential contributing factor in FND.
- Understanding GJH prevalence and its impact in pediatric FND is crucial.
Purpose of the Study:
- To determine the prevalence of GJH in children diagnosed with FND.
- To investigate the association between GJH and FND severity, activity levels, and participation.
Main Methods:
- Fifty-three children with FND (mean age 14.2 years) were assessed.
- GJH was measured using the Beighton score.
- FND severity was evaluated using the CSSI-24, limb involvement, and post-walk pain.
Main Results:
- GJH was present in 43% (Beighton ≥4) and 24% (Beighton ≥6) of participants.
- Higher Beighton scores correlated with increased CSSI-24 scores and more limbs affected.
- A positive association was found between Beighton score and pain after the 6-minute walk test.
Conclusions:
- GJH is highly prevalent in pediatric FND, even at stricter thresholds.
- GJH is linked to greater symptom severity and motor involvement.
- GJH may be a somatic vulnerability factor in FND, guiding individualized treatment approaches.
Aims:
Functional neurological disorder (FND) etiology is multifactorial. This study aimed to examine: (1) generalized joint hypermobility (GJH) prevalence in children diagnosed with FND and (2) the association between GJH and FND severity, activity level, and participation.
Methods:
Participated in this study 53 children with FND (mean age 14.2 ± 2.7 years; 73.6% female). GJH was assessed using the Beighton score. FND severity was evaluated with the 24-item Children's Somatic Symptoms Inventory (CSSI-24), number of limbs affected, and pain following the six-minute walk test (6MWT).
Results:
GJH was identified in 43% (Beighton ≥4) and 24% (Beighton ≥6) of participants. Elbow hyperextension was the most common feature (56.6%). The total Beighton score was independently associated with CSSI-24 (R2=.25, p<.01) and with the number of limbs involved (R2=.15, p<.01). A positive association was observed between Beighton score and pain post-6MWT.
Conclusion:
Regardless of the Beighton cutoff used, GJH prevalence remained high, with at least 1 in 4 participants presenting GJH even at the strictest threshold (≥6). GJH was associated with increased CSSI-24 and motor involvement. These findings suggest that GJH may represent a somatic vulnerability factor within the biopsychosocial model of FND. Routine assessment could help identify meaningful subgroups and guide individualized treatment.
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