Height, Ulnar Length and Forearm Function in Multiple Hereditary Exostoses

NCT ID: NCT05914298

Last Updated: 2023-06-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

408 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-01-01

Study Completion Date

2022-02-01

Brief Summary

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the purpose of the present registry is to describe the epidemiology of forearm deformities in patients with Hereditary Multiple Exostoses and to identify, independent predictors of severity of the disease and potential association with genotypic patterns

Detailed Description

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Hereditary Multiple Exostoses (HME) is a rare pediatric autosomal dominant disorder caused by loss-of-function mutations in the genes encoding the heparan sulfate (HS)-synthesizing enzymes EXT1 or EXT2. HME affects 1 in 50,000 people and has 100% penetrance but great variability in phenotypic expression. HME is characterized by formation of cartilaginous outgrowths, called osteochondromas or exostoses, next to the growth plates of many axial and appendicular skeletal elements, causing multiple, painful disfiguring and disabling skeletal deformities, and potential malignant transformation into peripherral chondrosarcoma.

The involvement of upper-limb bones by HME is associated with greater loss of function than elsewhere in the body, but even here the loss of function may be limited. Moreover, the constant relationship between height and ulnar length has long been recognized in forensic medicine and has been recently analyzed also in HME, in order to predict the clinical and functional outcomes of the upper limb.

the present registry aims to collect demographic, clinical, functional and radiographic information from patients with HME in order to establish phenotypic predictors of severity of the disease and potential association with genotypic patterns

Conditions

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Exostoses, Multiple Hereditary

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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HME group

204 children and adult patients with HME, admitted to our Hospital for diagnosis and treatment.

the patients will be stratified by age in four subgroups:

* subgroup I (0-7 Years)
* subgroup II (8-12 Years)
* subgroup III (13-18 Years)
* subgroup IV (\>18 Years)

blood and buccal swab genetic test

Intervention Type DIAGNOSTIC_TEST

blood samples and buccal swabs will be obtained from patients with HME in order to analyze the genotype (EXT1 or EXT2 mutations) and correlate the genotypic pattern with the phenotypic presentation

PUL

Intervention Type DIAGNOSTIC_TEST

measurement of ulnar length with anthropometer and patient's height

Range of motion

Intervention Type DIAGNOSTIC_TEST

measurement of range of motion of elbow, forearm and wrist

healty control group

204 children and adult voluntary healty controls will be stratified in the same manner and matched with the population in study in order to assess normal and pathologic growth.

PUL

Intervention Type DIAGNOSTIC_TEST

measurement of ulnar length with anthropometer and patient's height

Range of motion

Intervention Type DIAGNOSTIC_TEST

measurement of range of motion of elbow, forearm and wrist

Interventions

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blood and buccal swab genetic test

blood samples and buccal swabs will be obtained from patients with HME in order to analyze the genotype (EXT1 or EXT2 mutations) and correlate the genotypic pattern with the phenotypic presentation

Intervention Type DIAGNOSTIC_TEST

PUL

measurement of ulnar length with anthropometer and patient's height

Intervention Type DIAGNOSTIC_TEST

Range of motion

measurement of range of motion of elbow, forearm and wrist

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

\- patients with HME (\> 2 exostoses)

Exclusion Criteria

* Patients with solitary exostoses
* Patients, adults or minors, who are unable to give their timely informed consent.
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Istituto Ortopedico Rizzoli

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Giovanni Luigi Di Gennaro, MD

Role: PRINCIPAL_INVESTIGATOR

Istituto Ortopedico Rizzoli

Locations

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Manila Boarini

Bologna, , Italy

Site Status

Countries

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Italy

References

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Pedrini E, De Luca A, Valente EM, Maini V, Capponcelli S, Mordenti M, Mingarelli R, Sangiorgi L, Dallapiccola B. Novel EXT1 and EXT2 mutations identified by DHPLC in Italian patients with multiple osteochondromas. Hum Mutat. 2005 Sep;26(3):280. doi: 10.1002/humu.9359.

Reference Type RESULT
PMID: 16088908 (View on PubMed)

Mordenti M, Ferrari E, Pedrini E, Fabbri N, Campanacci L, Muselli M, Sangiorgi L. Validation of a new multiple osteochondromas classification through Switching Neural Networks. Am J Med Genet A. 2013 Mar;161A(3):556-60. doi: 10.1002/ajmg.a.35819. Epub 2013 Feb 8.

Reference Type RESULT
PMID: 23401177 (View on PubMed)

Pedrini E, Jennes I, Tremosini M, Milanesi A, Mordenti M, Parra A, Sgariglia F, Zuntini M, Campanacci L, Fabbri N, Pignotti E, Wuyts W, Sangiorgi L. Genotype-phenotype correlation study in 529 patients with multiple hereditary exostoses: identification of "protective" and "risk" factors. J Bone Joint Surg Am. 2011 Dec 21;93(24):2294-302. doi: 10.2106/JBJS.J.00949.

Reference Type RESULT
PMID: 22258776 (View on PubMed)

Clement ND, Porter DE. Forearm deformity in patients with hereditary multiple exostoses: factors associated with range of motion and radial head dislocation. J Bone Joint Surg Am. 2013 Sep 4;95(17):1586-92. doi: 10.2106/JBJS.L.00736.

Reference Type RESULT
PMID: 24005199 (View on PubMed)

Other Identifiers

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0012479

Identifier Type: -

Identifier Source: org_study_id

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