Journals / Diagnostic and Interventional Radiology / 2018 / Cilt: 24 - Sayı: 6

Abnormal subcortical activity in congenital mirror movement disorder with RAD51 mutation

Pages
392–401
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Specifically, we have found increased and bilateral activity during unimanual movements in thalamus,striatum, and globus pallidus in CMMD patients.CONCLUSIONThese findings reveal further neural correlates of CMMD, and may guide our understanding ofthe critical roles of subcortical structures for unimanual movements in healthy individuals.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:PURPOSECongenital mirror movement disorder (CMMD) is characterized by unintended, nonsuppressible,homologous mirroring activity contralateral to the movement on the intended side of the body.In healthy controls, unilateral movements are accompanied with predominantly contralateralcortical activity, whereas in CMMD, in line with the abnormal behavior, bilateral cortical activityis observed for unilateral motor tasks.
📊
Key Findings & Data:Next, using functional magnetic resonance imaging(fMRI) we investigated cortical and subcortical activity during manual motor actions in tworight-handed affected brothers and sex, age, education, and socioeconomically matched healthyindividuals.RESULTSGenetic analyses revealed heterozygous RAD51 c.401C>T mutation which cosegregated withthe phenotype in two affected members of the family.
💡
Conclusion & Impact:Specifically, we have found increased and bilateral activity during unimanual movements in thalamus,striatum, and globus pallidus in CMMD patients.CONCLUSIONThese findings reveal further neural correlates of CMMD, and may guide our understanding ofthe critical roles of subcortical structures for unimanual movements in healthy individuals.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

PURPOSECongenital mirror movement disorder (CMMD) is characterized by unintended, nonsuppressible,homologous mirroring activity contralateral to the movement on the intended side of the body.In healthy controls, unilateral movements are accompanied with predominantly contralateralcortical activity, whereas in CMMD, in line with the abnormal behavior, bilateral cortical activityis observed for unilateral motor tasks. However, task-related activities in subcortical structures,which are known to play critical roles in motor actions, have not been investigated in CMMDpreviously.METHODSWe investigated the functional activation patterns of the motor components in CMMD patients.By using linkage analysis and exome sequencing, common mutations were revealed in sevenaffected individuals from the same family. Next, using functional magnetic resonance imaging(fMRI) we investigated cortical and subcortical activity during manual motor actions in tworight-handed affected brothers and sex, age, education, and socioeconomically matched healthyindividuals.RESULTSGenetic analyses revealed heterozygous RAD51 c.401C>T mutation which cosegregated withthe phenotype in two affected members of the family. Consistent with previous literature, ourfMRI results on these two affected individuals showed that mirror movements were closely related to abnormal cortical activity in M1 and SMA during unimanual movements. Furthermore, wehave found previously unknown abnormal task-related activity in subcortical structures. Specifically, we have found increased and bilateral activity during unimanual movements in thalamus,striatum, and globus pallidus in CMMD patients.CONCLUSIONThese findings reveal further neural correlates of CMMD, and may guide our understanding ofthe critical roles of subcortical structures for unimanual movements in healthy individuals.

🔖

Cite This Article

DEMİRAYAK, P., ONAT, O. E., GEVREKCİ, A. Ö., GÜLSÜNER, S., BİLGEN, R., DOERSCHNER, K., UYSAL, H., ÖZÇELİK, T., BOYACI, H. (2018). Abnormal subcortical activity in congenital mirror movement disorder with RAD51 mutation. Diagnostic and Interventional Radiology, Cilt: 24 - Sayı: 6, 392–401. https://ajindex.com/articles/350035

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (15)

  1. Cincotta M, Ziemann U. Neurophysiology of unimanual motor control and mirror movements. Clin Neurophysiol 2008
  2. 744–762. [CrossRef] 2. Koerte I, Eftimov L, Laubender RP, et al. Mirror movements in healthy humans across the lifespan: effects of development and ageing. Dev Med Child Neurol 2010
  3. 1106–1112. [CrossRef] 3. Heinen F, Glocker FX, Fietzek U, Meyer BU, Lücking CH, Korinthenberg R. Absence of transcallosal inhibition following focal mangnetic stimulation in preschool children. Ann Neurol 1998
  4. 608–612. [CrossRef] 4. Mayston MJ, Harrison LM, Stephens JA. A neurophysiological study of mirror movements in adults and children. Ann Neurol 1999
  5. 583–594. 5. Reitz M, Müller K. Differences between congenital mirror movements’ andassociated movements’ in normal children: a neurophysiological case study. Neurosci Lett 1998
  6. 69–72. [CrossRef] 6. Farmer SF, Ingram DA, Stephens JA. Mirror movements studied in a patient with Klippel-Feil syndrome. J Physiol 1990
  7. [CrossRef] 7. Royal SA, Tubbs RS, D’antonio MG, Rauzzino MJ, Oakes WJ. Investigations into the association between cervicomedullary neuroschisis and mirror movements in patients with Klippel-Feil syndrome. Am J Neuroradiol 2002
  8. 724–729. 8. Krams M, Quinton R, Mayston MJ. Mirror movements in X-linked Kallmann’s syndrome. II. A PET study. Brain 1997
  9. 1217–1228. [CrossRef] 9. Lindenberg R, Renga V, Zhu LL, Nair D, Schlaug GM. Bihemispheric brain stimulation facilitates motor recovery in chronic stroke patients. Neurology 2010
  10. 2176–2184. [CrossRef] 10. Farmer SF, Harrison LM, Ingram DA, Stephens JA. Plasticity of central motor pathways in children with hemiplegic cerebral palsy. Neurology 1991
  11. 1505–1505. [CrossRef] 11. Cincotta M, Borgheresi A, Boffi P, et al. Bilateral motor cortex output with intended unimanual contraction in congenital mirror movements. Neurology 2002
  12. 1290–1293. [CrossRef] 12. Sharafaddinzadeh N, Bavarsad R, Yousefkhah M, Aleali A. Familial mirror movements over five generations. Neurol India 2008
  13. 482– 483. [CrossRef] 13. Srour M, Philibert M, Dion MH, et al. Familial congenital mirror movements: report of a large 4-generation family. Neurology 2009
  14. 729–731. [CrossRef] 14. Depienne C, Bouteiller D, Méneret A, et al. RAD51 haploinsufficiency causes congenital mirror movements in humans. Am J Hum Genet 2012
  15. 301–307. [CrossRef] 15. Srour M, Rivière JB, Pham JM, et al. Mutations in DCC cause congenital mirror movements. Science 2010