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A monocentric, longitudinal, observational case-control study in patients with Myotonic Dystrophy type 2 (DM2). At least 60 DM2 will be evaluated through a battery of patients reported Outcomes (PROs) and clinical Outcome Measures (OMs), in order to define suitable OMs for DM2 and propose a disease specific severity scale. Patients will be re-evaluated after 6 months. An age and gender-matched control cohort will be assessed.
Myotonic dystrophy type 2 (DM2) is an autosomal dominant, chronic progressive multisystemic disorder. Typical symptoms of DM2 include progressive proximal muscle weakness and wasting, often combined with axial and anterior neck muscles involvement, myotonia, muscular pain, fatigue and cataracts. The estimated prevalence is approximately 1 per 100,000 people, but in some nations as Germany the DM2 frequency is much higher than and close to 1.12.000. Compared to DM1 it has a relatively short history, as the genetic base and RNA pathogenesis have been clarified in 2003. In order to evaluate specific clinical aspects of DM2 and disease progression, the development and validation of ad-hoc tests is a unmet need in the neuromuscular field. Today, only a few outcome measures were used systematically in DM2 patients, and none of them provide so far a validation of a clinical meaningful difference for an interventional clinical trial.
The aims of this monocentric, observational, case-control study are:
Participants will be recruited from the German-Swiss Registry for Myotonic Dystrophy and the internal database of the Friedrich-Baur-Institute (FBI), Department of Neurology, Ludwig-Maximilian-University, Munich, Germany. A total of at least 60 male and female patients with no age limit and with genetically proven DM2 will be included. Forty age and gender-matched controls will be also assessed.
During the first evaluation of the DM2 and the controls group, the following PROs and OMs will be evaluated:
General survey (Comorbidity, BMI, familiarity, onset, etc…), DM1-ActivC, R-Pact, FDSS, McGill pain questionnaire - short form, Brief pain inventory - short form, Beck depression inventory, Myotonia behaviour scale, Myotonia subscale from INQoL, Hand opening time, pressure pain threshold, manual and quantitative muscle testing, SARA scale, Berg balance scale, QMFT, GSGC, 30 second sit and stand test, FI-2 (only for upper extremities), 6-MWT.
After six months a second evaluation of the DM2 group will be performed, in which all PROs and OMs except the general survey will be repeated.
Data analysis will provide descriptive statistic and a complete validity and reliability informations. On the basis of these results, a disease specific severity scale will be proposed for the clinical use.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| DM2 group | Patients with Myotonic Dystrophy type 2 genetically confirmed, without limitation regarding age or disease onset. |
| |
| Healthy controls group | A group of gender and age-matched healthy controls. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| DM1-ActivC | Diagnostic Test | A Rasch-built activity and participation scale for clinical use in myotonic dystrophy type 1 (DM1) |
|
| Measure | Description | Time Frame |
|---|---|---|
| Quick motor function test (QMFT) | A test for assessing motor function. | 6 months |
| DM1-ActivC | A Rasch-built DM1 activity and participation scale for clinical use | 6 months |
| Measure | Description | Time Frame |
|---|---|---|
| R-PAct | A Rasch-built Pompe-specific activity scale | 6 months |
| Beck depression inventory (BDI-II) | A self-reported depression inventory administered verbally or self administered. |
| Measure | Description | Time Frame |
|---|---|---|
| MIRS-2 | Development of a muscle impairment staging score | 10 months |
Inclusion Criteria:
Exclusion Criteria:
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Patients with Myotonic Dystrophy type 2, without limitations regarding age of onset, disease duration or physical impairment related to the disease.
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| Name | Affiliation | Role |
|---|---|---|
| Benedikt Schoser, MD | Friedrich-Baur-Institute, Dep. of Neurology Klinikum der Universitaet Muenchen Munich, Germany | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Friedrich-Baur-Institute, Dep. of Neurology Klinikum der Universitaet Muenchen Munich, Germany | Munich | Bavaria | 80336 | Germany |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 29934199 | Background | Okkersen K, Jimenez-Moreno C, Wenninger S, Daidj F, Glennon J, Cumming S, Littleford R, Monckton DG, Lochmuller H, Catt M, Faber CG, Hapca A, Donnan PT, Gorman G, Bassez G, Schoser B, Knoop H, Treweek S, van Engelen BGM; OPTIMISTIC consortium. Cognitive behavioural therapy with optional graded exercise therapy in patients with severe fatigue with myotonic dystrophy type 1: a multicentre, single-blind, randomised trial. Lancet Neurol. 2018 Aug;17(8):671-680. doi: 10.1016/S1474-4422(18)30203-5. Epub 2018 Jun 19. | |
| 29770119 |
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| Type | Date | Date Unknown |
|---|---|---|
| Release | Mar 14, 2023 | |
| Reset | Dec 15, 2023 |
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| R-PAct | Diagnostic Test | A Rasch-built Pompe-specific activity scale. |
|
| Beck depression inventory | Diagnostic Test | A self-reported depression inventory administered verbally or self administered. |
|
|
| McGill pain questionnaire | Diagnostic Test | The short form of the MPQ, used to evaluate the qualitative aspect of pain and categorized in three dimensions of pain experience: sensory qualities, affective qualities and overall intensity. |
|
|
| Brief Pain Inventory Short-Form | Diagnostic Test | A 9 item self-administered questionnaire used to evaluate the severity of a patient's pain and the impact of this pain on the patient's daily functioning |
|
|
| Fatigue and Daytime Sleepiness Scale | Diagnostic Test | A Rasch-built combined fatigue and daytime sleepiness scale (FDSS) specifically designed for patients with DM1. |
|
|
| Myotonia Behaviour scale | Diagnostic Test | It consists of six framed sentences, which most closely describe the impact of the stiffness on everyday life |
|
|
| Hand opening time | Diagnostic Test | A simple test to evaluate clinical myotonia: the patient makes a tight fist for 5 seconds, then rapidly open them and the opening time is measured. |
|
| Pressure pain threshold | Diagnostic Test | Thresholds for pressure pain were obtained over eight muscles on the left and right side of the body: extensor digitorum communis, deltoid, quadriceps and anterior tibialis. The average value of two measurements will be recorded. |
|
|
| Manual muscle testing | Diagnostic Test | The patient is instructed to hold the corresponding limb or appropriate body part to be tested at the end of its available range while the practitioner provides opposing manual resistance. The strength is measured by the modified-MRC scale. The average value of two mesurements is considered. The following muscles were assessed: neck flexors and extensors, hip flexors and extensors, knee flexors and extensors, shoulder abductors, elbow flexors and extensors, ankle dorsiflexors and plantar flexors, wrist flexors and Extensors, digit flexors and extensors and thumb abductors. |
|
|
| Quantitative muscle testing | Diagnostic Test | Strength testing using sophisticated strength measuring devices during an isometric contraction. The average value of two measurements is considered; in case of difference > 10% between measurements, a third attempt is performed. The following muscles are assessed: neck flexors and extensors, hip flexors and extensors, knee flexors and extensors, shoulder abductors, elbow flexors and extensors, ankle dorsiflexors and plantar flexors, wrist flexors and extensors and digit flexors. |
|
|
| Scale for Assessment and Rating of Ataxia | Diagnostic Test | SARA is a clinical scale which assesses a range of different impairments in cerebellar ataxia. |
|
|
| Berg balance scale | Diagnostic Test | It is a 14 item objective measure designed to assess static balance and fall risk in adult populations |
|
|
| Quick motor function test | Diagnostic Test | Assessment of proximal motor function. |
|
|
| GSGC | Diagnostic Test | GSGC score provides a detailed picture of motor function by including quantitative measures of four main motor performances (Gait, Walking, Stair, Gower's) and a qualitative global assessment of the manner to accomplish them. |
|
| 30 seconds sit to stand test | Diagnostic Test | It is a measurement that assesses functional lower extremity strenght in older adults. |
|
|
| Functional Index-2 | Diagnostic Test | Disease-specific functional outcome assessing muscle endurance. In this trial, only the part of the test for the upper extremities is used. |
|
|
| Six minute walking test | Diagnostic Test | It is a sub-maximal exercise test used to assess aerobic capacity and endurance. The distance covered over a time of 6 minutes is used as the outcome by which to compare changes in performance capacity. |
|
|
| Myotonia (from Individualised Neuromuscular Quality of Life Questionnaire) | Diagnostic Test | A subscale derived from the Individualised Neuromuscular Quality of Life Questionnaire (INQoL). 3 questions reguarding stiffness/myotonia. |
|
|
| 6 months |
| McGill pain questionnaire (MPQ-sf) | The short form of the MPQ, used to evaluate the qualitative aspect of pain and categorized in three dimensions of pain experience: sensory qualities, affective qualities and overall intensity. | 6 months |
| Brief Pain Inventory Short-Form (BPI-sf) | A 9 item self-administered questionnaire used to evaluate the severity of a patient's pain and the impact of this pain on the patient's daily functioning. | 6 months |
| Fatigue and Daytime Sleepiness Scale (FDSS) | A Rasch-built combined fatigue and daytime sleepiness scale (FDSS) specifically designed for patients with DM1. | 6 months |
| Myotonia Behaviour scale (MBS) | It consists of six framed sentences, which most closely describe the impact of the stiffness on everyday life. | 6 months |
| Myotonia (from Individualised Neuromuscular Quality of Life Questionnaire) | A subscale derived from the INQoL questionnaire. 3 questions regarding stiffness and myotonia. | 6 months |
| Hand opening time | A simple test to evaluate clinical myotonia: the patient makes a tight fist for 5 seconds, then rapidly open them and the opening time is measured. | 6 months |
| Scale for Assessment and Rating of Ataxia (SARA) | It is a clinical scale which assesses a range of different impairments in cerebellar ataxia. | 6 months |
| Berg balance scale (BBS) | It is a 14 item objective measure designed to assess static balance and fall risk in adult populations. | 6 months |
| Pressure pain threshold (PPT) | Thresholds for pressure pain were obtained over eight muscles on the left and right side of the body: extensor digitorum communis, deltoid, quadriceps and anterior tibialis. The average value oft wo measurements was recorded. | 6 months |
| Manual muscle testing (MMT) | The patient is instructed to hold the corresponding limb or appropriate body part to be tested at the end of its available range while the practitioner provides opposing manual resistance. The strength is measured by the modified-MRC scale. The average value of two measurements is considered. | 6 months |
| Quantitative muscle testing (QMT) | Strength testing using sophisticated strength measuring devices during an isometric contraction. The average value of two measurements is considered; in case of difference > 10% between measurements, a third attempt is performed. | 6 months |
| GSGC | GSGC score provides a detailed picture of motor function by including quantitative measures of four main motor performances (Gait, Walking, Stair, Gower's) and a qualitative global assessment of the manner to accomplish them. | 6 months |
| Functional Index-2 (only upper extremities) | Disease-specific functional outcome assessing muscle endurance. In this trial, only the part of the test for the upper extremities is used. | 6 months |
| 30 seconds sit to stand test (30CST) | It is a measurement that assesses functional lower extremity strength in older adults. | 6 months |
| Six-minute-walking test (6MWT) | It is a sub-maximal exercise test used to assess aerobic capacity and endurance. The distance covered over a time of 6 minutes is used as the outcome by which to compare changes in performance capacity. | 6 months |
| Background |
| Wenninger S, Montagnese F, Schoser B. Core Clinical Phenotypes in Myotonic Dystrophies. Front Neurol. 2018 May 2;9:303. doi: 10.3389/fneur.2018.00303. eCollection 2018. |
| 29550152 | Background | Wood L, Bassez G, van Engelen B, Lochmuller H, Schoser B; 222nd ENMC workshop participants. 222nd ENMC International Workshop:: Myotonic dystrophy, developing a European consortium for care and therapy, Naarden, The Netherlands, 1-2 July 2016. Neuromuscul Disord. 2018 May;28(5):463-469. doi: 10.1016/j.nmd.2018.02.003. Epub 2018 Feb 12. No abstract available. |
| 29086017 | Background | Montagnese F, Mondello S, Wenninger S, Kress W, Schoser B. Assessing the influence of age and gender on the phenotype of myotonic dystrophy type 2. J Neurol. 2017 Dec;264(12):2472-2480. doi: 10.1007/s00415-017-8653-2. Epub 2017 Oct 30. |
| 32373059 | Derived | Montagnese F, Rastelli E, Khizanishvili N, Massa R, Stahl K, Schoser B. Validation of Motor Outcome Measures in Myotonic Dystrophy Type 2. Front Neurol. 2020 Apr 21;11:306. doi: 10.3389/fneur.2020.00306. eCollection 2020. |
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| Release Date | Unrelease Date | Unrelease Date Unknown | Reset Date | MCP Release Number |
|---|---|---|---|---|
| Mar 14, 2023 | Dec 15, 2023 |
| ID | Term |
|---|---|
| D009223 | Myotonic Dystrophy |
| ID | Term |
|---|---|
| D009136 | Muscular Dystrophies |
| D020966 | Muscular Disorders, Atrophic |
| D009135 | Muscular Diseases |
| D009140 | Musculoskeletal Diseases |
| D020967 | Myotonic Disorders |
| D020271 | Heredodegenerative Disorders, Nervous System |
| D019636 | Neurodegenerative Diseases |
| D009422 | Nervous System Diseases |
| D009468 | Neuromuscular Diseases |
| D030342 | Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
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| ID | Term |
|---|---|
| D010147 | Pain Measurement |
| D010808 | Physical Examination |
| ID | Term |
|---|---|
| D009460 | Neurologic Examination |
| D019937 | Diagnostic Techniques and Procedures |
| D003933 | Diagnosis |
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