Hypermobile spectrum disorders symptoms in patients with functional neurological disorders and autism spectrum disorders: A preliminary study
Open accessAbstract
Autism spectrum disorders (ASDs) and functional neurological disorders (FNDs) share some clinical characteristics such as alexithymia, sensory sensitivity and interoceptive issues. Recent evidence shows that both the disorders present symptoms compatible with a diagnosis of hypermobile Ehlers-Danlos Syndrome and hypermobile spectrum disorders (hEDS/HSD), a heterogeneous group of heritable connective tissue disorders characterized by joint hypermobility, skin hyperextensibility, and tissue fragility. Here we compared the prevalence of hEDS/HSD-related symptoms in a group of patients with FNDs, of people with ASDs without intellectual disabilities, and a non-clinical comparison group (NC). Twenty patients with FNDs, 27 individuals with ASDs without intellectual disabilities and 26 NC were recruited and completed the Self-reported screening questionnaire for the assessment of hEDS/HSD-related symptoms (SQ-CH). We found that 55% of the patients with FNDs, 44.4% of the individuals with ASDs and 30.8% of NC scored above the cut-off at the SQ-CH; SQ-CH scores of both FNDs and ASDs group were significantly higher than the NC group's ones. In conclusion, both ASDs and FNDs individuals present hEDS/HSD-related symptoms in a higher number than the general population. Imputable mechanisms include (i) overwhelming of executive functions with consequent motor competence impairment for ASDs individuals, and (ii) exacerbation of FNDs symptoms by physical injury and chronic pain due to abnormal range of joint mobility. Moreover, we speculated that the amygdala and the anterior cingulate cortex circuitry might be responsible for the imbalances at the proprioceptive, interoceptive, and emotional levels.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Out of seven studies exploring JH, HSD, and/or EDS in autistic adults, only three (42.8%) compared the prevalence of JH, HSD, and/or EDS in ASD with respect to a control group.
“Out of seven studies exploring JH, HSD, and/or EDS in autistic adults, only three (42.8%)compared the prevalence of JH, HSD, and/or EDS in ASD with respect to a control group (Glans et al., 2022;Nisticò et al., 2022;Ward et al., 2023).”
From Autism in the context of joint hypermobility, hypermobility spectrum disorders, and Ehlers–Danlos syndromes: A systematic review and prevalence meta-analyses (2025) · cites this paper as Nisticò et al., 2022
The Introduction and Results identify this as a study comparing autistic adults with a non-clinical control group, including the proportion above a screening cut-off for hEDS/HSD-related symptoms. It did not establish the prevalence of diagnosed JH, HSD, or EDS; the cited paper also does not establish the citing document’s count of three out of seven studies. (LLM, conf=0.83)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
The 2017 international classification of the Ehlers–Danlos syndromes
Malfait, F., Francomano, C., Byers, P., Belmont, J., Berglund, B., Black, J., Bloom, L., Bowen, J. M., Brady, A. F., Burrows, N. P., et al. (2017) · American Journal of Medical Genetics Part C: Seminars in Medical Genetics · doi:10.1002/ajmg.c.31552 · Cited by 1,936 · see citing works
A framework for the classification of joint hypermobility and related conditions
Castori, M., Tinkle, B., Levy, H., Grahame, R., Malfait, F., & Hakim, A. (2017) · American Journal of Medical Genetics Part C: Seminars in Medical Genetics · doi:10.1002/ajmg.c.31539 · Cited by 602 · see citing works
Hus, V., & Lord, C. (2014) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-014-2080-3 · Cited by 547 · see citing works
The role of alexithymia in the development of functional motor symptoms (conversion disorder)
Demartini, B., Petrochilos, P., Ricciardi, L., Price, G., Edwards, M. J., & Joyce, E. (2014) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp-2013-307203 · Cited by 147 · see citing works
Self-citationCederlöf, M., Larsson, H., Lichtenstein, P., Almqvist, C., Serlachius, E., & Ludvigsson, J. F. (2016) · BMC Psychiatry · doi:10.1186/s12888-016-0922-6 · Cited by 142 · cited 1× · see citing works
“(12) performed a population study investigating a possible association between EDS and psychiatric disorders: hypermobile disorders individuals (including EDS) showed a 1.”
BackgroundSmith, T. O., Easton, V., Bacon, H., Jerman, E., Armon, K., Poland, F., & Macgregor, A. J. (2014) · Rheumatology · doi:10.1093/rheumatology/ket317 · Cited by 130 · see citing works
The international consortium on the Ehlers–Danlos syndromes
Bloom, L., Byers, P., Francomano, C., Tinkle, B., Malfait, F., & on behalf of the Steering Committee of The International Consortium on the Ehlers‐Danlos Syndromes (2017) · American Journal of Medical Genetics Part C: Seminars in Medical Genetics · doi:10.1002/ajmg.c.31547 · Cited by 123 · cited 1× · see citing works
“The International EDS consortium now recognizes thirteen subtypes of EDS/HSD (15).”
BackgroundMallorquÃ-Bagué, N., Garfinkel, S. N., Engels, M., Eccles, J. A., Pailhez, G., Bulbena, A., & Critchley, H. D. (2014) · Frontiers in Psychology · doi:10.3389/fpsyg.2014.01162 · Cited by 97 · see citing works
Brain structure and joint hypermobility: Relevance to the expression of psychiatric symptoms
Eccles, J. A., Beacher, F. D. C., Gray, M. A., Jones, C. L., Minati, L., Harrison, N. A., & Critchley, H. D. (2012) · British Journal of Psychiatry · doi:10.1192/bjp.bp.111.092460 · Cited by 96 · see citing works
Sinibaldi, L., Ursini, G., & Castori, M. (2015) · American Journal of Medical Genetics Part C: Seminars in Medical Genetics · doi:10.1002/ajmg.c.31430 · Cited by 87 · see citing works
Autism, joint hypermobility-related disorders and pain
Baeza-Velasco, C., Cohen, D., Hamonet, C., Vlamynck, E., Diaz, L., Cravero, C., Cappe, E., & Guinchat, V. (2018) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2018.00656 · Cited by 78 · see citing works
Exploring three levels of interoception in people with functional motor disorders
Ricciardi, L., Nisticò, V., Andrenelli, E., Cunha, J. M., Demartini, B., Kirsch, L. P., Crucianelli, L., Yogarajah, M., Morgante, F., Fotopoulou, A., et al. (2021) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2021.03.029 · Cited by 35 · see citing works
Self-citation
Flagged first, then by citations
Research works printed but not linked: 16
- [3]Kinnaird E Stewart C Tchanturia K. Investigating alexithymia in autism: a systematic review and meta-analysis. Eur Psychiatry. (2019) 55: 80– 9. 10.1016/j.eurpsy.2018.09.004 30399531 PMC6331035 · DOI · Paper page
- [4]Quattrocki E Friston K. Autism, oxytocin and interoception. Neurosci Biobehav Rev. (2014) 47: 410– 30. 10.1016/j.neubiorev.2014.09.012 25277283 PMC4726659 · DOI · Paper page
- [5]DuBois D Ameis SH Lai MC Casanova MF Desarkar P. Interoception in autism spectrum disorder: a review. Int J Dev Neurosci. (2016) 52: 104– 11. 10.1016/j.ijdevneu.2016.05.001 27269967 · DOI · Paper page
- [6]Ricciardi L Demartini B Crucianelli L Krahé C Edwards MJ Fotopoulou A. Interoceptive awareness in patients with functional neurological symptoms. Biol Psychol. (2016) 113: 68– 74. 10.1016/j.biopsycho.2015.10.009 26528552 · DOI
- [8]Green SA Hernandez L Tottenham N Krasileva K Bookheimer SY Dapretto M. Neurobiology of sensory overresponsivity in youth with autism spectrum disorders. JAMA psychiatry. (2015) 72: 778– 86. 10.1001/jamapsychiatry.2015.0737 26061819 PMC4861140 · DOI
- [9]Ranford J MacLean J Alluri PR Comeau O Godena E LaFrance WC Jr. Perez DL. Sensory processing difficulties in functional neurological disorder: a possible predisposing vulnerability? Psychosomatics. (2020) 61: 343– 52. 10.1016/j.psym.2020.02.003 32284249 PMC7329616 · DOI
- [10]Nisticò V Goeta D Iacono A Tedesco R Giordano B Faggioli R. Clinical overlap between functional neurological disorders and autism spectrum disorders: a preliminary study. Neurol Sci. (2022) 5: 1– 7. 10.1007/s10072-022-06048-1 35511383 PMC9349073 · DOI
- [11]Kassavetis P Batla A Pareés I Saifee TA Schrag A Cordivari C. Edwards MJ. Joint hypermobility syndrome: a risk factor for fixed dystonia? Mov Disord. (2012) 27: 1070. 10.1002/mds.25004 22532260 · DOI
- [14]Delgado C Kurtis M Martin B Rada P Martinez L Sanz M. Clinical and demographic characteristics of patients with functional movement disorders: a consecutive cohort study from a specialized clinic. Acta Neurol Belg. (2022) 122: 97– 103. 10.1007/s13760-021-01648-8 33743163 · DOI
- [17]Malfait F Castori M Francomano CA Giunta C Tomoki K Byers P H. The Ehlers-Danlos syndromes. Nat Rev Dis Prim. (2020) 6: 64. 10.1038/s41572-020-0194-9 32732924 · DOI
- [18]Bulbena A Duró JC Porta M Martín-Santos R Mateo A Molina L. Anxiety disorders in the joint hypermobility syndrome. Psychiatry Res. (1993) 46: 59– 68. 10.1016/0165-1781(93)90008-5 8464956 · DOI · Paper page
- [22]Bulbena A Mallorquí-Bagué N Pailhez G Rosado S González I Blanch-Rubió J Carbonell J. Self-reported screening questionnaire for the assessment of Joint Hypermobility Syndrome (SQ-CH), a collagen condition, in Spanish population. Eur J Psychiat. (2014) 28: 17– 26. 10.4321/S0213-61632014000100002 · DOI
- [23]Hakim A Grahame R. Joint hypermobility. Musculoskeletal Care. (2007) 5: 4– 19. 10.1002/msc.91 17152113 · DOI
- [24]Clayton HA Jones SA Henriques DY. Proprioceptive precision is impaired in Ehlers–Danlos syndrome. Springerplus. (2015) 4: 1– 8. 10.1186/s40064-015-1089-1 26180743 PMC4493259 · DOI · Paper page
- [25]Rubio-Agusti I Kojovic M Chandrashekar HS Edwards MJ Bhatia KP. Cervical dystonia and joint hypermobility syndrome: a dangerous combination. Mov Disord. (2012) 27: 203– 4. 10.1002/mds.24013 22328463 · DOI
- [26]Koreki A Eccles J Garfinkel S Critchley H Cope S Agrawal N. Epilepsy & Behavior Hypermobility in patients with functional seizures: toward a pathobiological understanding of complex conditions. Epilepsy Behav. (2022) 132: 108710. 10.1016/j.yebeh.2022.108710 35580524 · DOI
Cited by
Sorted by citations
Fairweather, D., Bruno, K. A., Darakjian, A. A., Bruce, B. K., Gehin, J. M., Kotha, A., Jain, A., Peng, Z., Hodge, D. O., Rozen, T. D., et al. (2023) · Frontiers in Medicine · doi:10.3389/fmed.2023.1096180 · Cited by 37 · see citing works
Baeza-Velasco, C., Vergne, J., Poli, M., Kalisch, L., & Calati, R. (2025) · Autism · doi:10.1177/13623613251328059 · Cited by 10 · see citing works
Romeo, D. M., Moro, M., Pezone, M., Venezia, I., Mirra, F., De Biase, M., Polo, A., Turrini, I., Lala, M. R., Velli, C., et al. (2023) · Journal of Personalized Medicine · doi:10.3390/jpm13121723 · Cited by 7 · see citing works
- Authors
- Nisticò, V., Iacono, A., Goeta, D., Tedesco, R., Giordano, B., Faggioli, R., Priori, A., Gambini, O., & Demartini, B.
- Affiliations
- University of Milan (IT)
- Azienda Socio Sanitaria Territoriale Santi Paolo e Carlo (IT)
- Corresponding author
- Demartini, Benedetta
- ORCID
- Venue
- Frontiers in Psychiatry
- Publisher
- Frontiers Media SA
- Published
- 2022-08-24
- Volume
- 13
- Pages
- 943098-943098
- ISSN
- 1664-0640 (ISSN-L)
- PMC
- PMC9450495
- OpenAlex
- W4293215174
- Cited by
- 15
- References
- 12
- Citations by year
- 2026: 3 · 2025: 3 · 2024: 6 · 2023: 3
- FWCI
- 1.81
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Frontiers in Psychiatry (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Archivio Istituzionale della Ricerca (Universita Degli Studi Di Milano) (submittedVersion, other-oa)
- BOA (University of Milano-Bicocca) (submittedVersion, other-oa)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Università degli Studi di Milano
- Center for Neurotechnology, University of Washington
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Connective tissue disorders research
- Health Sciences › Medicine › Psychiatry and Mental health › Psychosomatic Disorders and Their Treatments
- Life Sciences › Neuroscience › Cognitive Neuroscience › Autism Spectrum Disorder Research
- Keywords
- hypermobile Ehlers-Danlos syndrome, conversion disorder, autism spectrum disorder, joint hypermobility, connective tissue diseases, interoception, proprioception, alexithymia, sensory sensitivity, chronic pain, executive function, amygdala, anterior cingulate cortex
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review