Longitudinal changes in clinical outcome measures in COL6-related dystrophies and LAMA2-related dystrophies. (19th November 2019)
- Record Type:
- Journal Article
- Title:
- Longitudinal changes in clinical outcome measures in COL6-related dystrophies and LAMA2-related dystrophies. (19th November 2019)
- Main Title:
- Longitudinal changes in clinical outcome measures in COL6-related dystrophies and LAMA2-related dystrophies
- Authors:
- Jain, Minal S.
Meilleur, Katherine
Kim, Eunhee
Norato, Gina
Waite, Melissa
Nelson, Leslie
McGuire, Michelle
Duong, Tina
Keller, Katherine
Lott, Donovan J.
Glanzman, Allan
Rose, Kristy
Main, Marion
Fiorini, Courtney
Chrismer, Irene
Linton, Melody
Punjabi, Monal
Elliott, Jeffrey
Tounkara, Fatoumata
Vasavada, Ruhi
Logaraj, Ranjani
Winkert, Jocelyn
Donkervoort, Sandra
Leach, Meganne
Dastgir, Jahannaz
Hynan, Linda
Nichols, Carmel
Hartnett, Elizabeth
Averion, Gilberto M.
Collins, James C.
Kim, Eunice S.
Kokkinis, Angela
Schindler, Alice
Zukosky, Kristen
Fee, Robert
Hinton, Veronica
Mohassel, Payam
Bharucha-Goebel, Diana
Vuillerot, Carole
McGraw, Peter
Barton, Mark
Fontana, Joseph
Rutkowski, Anne
Foley, A. Reghan
Bönnemann, Carsten G.
… (more) - Abstract:
- Abstract : Objective: To identify the rate of change of clinical outcome measures in children with 2 types of congenital muscular dystrophy (CMD), COL6-related dystrophies (COL6-RDs) and LAMA2-related dystrophies (LAMA2-RDs). Methods: Over the course of 4 years, 47 individuals (23 with COL6-RD and 24 with LAMA2-RD) 4 to 22 years of age were evaluated. Assessments included the Motor Function Measure 32 (MFM32), myometry (knee flexors and extensors, elbow flexors and extensors), goniometry (knee and elbow extension), pulmonary function tests, and quality-of-life measures. Separate linear mixed-effects models were fitted for each outcome measurement, with subject-specific random intercepts. Results: Total MFM32 scores for COL6-RDs and LAMA2-RDs decreased at a rate of 4.01 and 2.60 points, respectively, each year ( p < 0.01). All muscle groups except elbow flexors for individuals with COL6-RDs decreased in strength between 1.70% ( p < 0.05) and 2.55% ( p < 0.01). Range-of-motion measurements decreased by 3.21° ( p < 0.05) at the left elbow each year in individuals with LAMA2-RDs and 2.35° ( p < 0.01) in right knee extension each year in individuals with COL6-RDs. Pulmonary function demonstrated a yearly decline in sitting forced vital capacity percent predicted of 3.03% ( p < 0.01) in individuals with COL6-RDs. There was no significant change in quality-of-life measures analyzed. Conclusion: Results of this study describe the rate of change of motor function as measured by theAbstract : Objective: To identify the rate of change of clinical outcome measures in children with 2 types of congenital muscular dystrophy (CMD), COL6-related dystrophies (COL6-RDs) and LAMA2-related dystrophies (LAMA2-RDs). Methods: Over the course of 4 years, 47 individuals (23 with COL6-RD and 24 with LAMA2-RD) 4 to 22 years of age were evaluated. Assessments included the Motor Function Measure 32 (MFM32), myometry (knee flexors and extensors, elbow flexors and extensors), goniometry (knee and elbow extension), pulmonary function tests, and quality-of-life measures. Separate linear mixed-effects models were fitted for each outcome measurement, with subject-specific random intercepts. Results: Total MFM32 scores for COL6-RDs and LAMA2-RDs decreased at a rate of 4.01 and 2.60 points, respectively, each year ( p < 0.01). All muscle groups except elbow flexors for individuals with COL6-RDs decreased in strength between 1.70% ( p < 0.05) and 2.55% ( p < 0.01). Range-of-motion measurements decreased by 3.21° ( p < 0.05) at the left elbow each year in individuals with LAMA2-RDs and 2.35° ( p < 0.01) in right knee extension each year in individuals with COL6-RDs. Pulmonary function demonstrated a yearly decline in sitting forced vital capacity percent predicted of 3.03% ( p < 0.01) in individuals with COL6-RDs. There was no significant change in quality-of-life measures analyzed. Conclusion: Results of this study describe the rate of change of motor function as measured by the MFM32, muscle strength, range of motion, and pulmonary function in individuals with COL6-RDs and LAMA2-RDs. … (more)
- Is Part Of:
- Neurology. Volume 93:Number 21(2019)
- Journal:
- Neurology
- Issue:
- Volume 93:Number 21(2019)
- Issue Display:
- Volume 93, Issue 21 (2019)
- Year:
- 2019
- Volume:
- 93
- Issue:
- 21
- Issue Sort Value:
- 2019-0093-0021-0000
- Page Start:
- Page End:
- Publication Date:
- 2019-11-19
- Subjects:
- Neurology -- Periodicals
Neurology -- Periodicals
Neurologie -- Périodiques
616.8 - Journal URLs:
- http://www.mdconsult.com/public/search?search_type=journal&j_sort=pub_date&j_issn=0028-3878 ↗
http://www.mdconsult.com/about/journallist/192093418-5/about0nz0.html ↗
http://www.neurology.org ↗
http://journals.lww.com ↗ - DOI:
- 10.1212/WNL.0000000000008517 ↗
- Languages:
- English
- ISSNs:
- 0028-3878
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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