Advertisement
Original research| Volume 100, ISSUE 7, P1308-1316, July 2019

Download started.

Ok

Crossed Cerebellar Diaschisis Has an Adverse Effect on Functional Outcome in the Subacute Rehabilitation Phase of Stroke: A Case-Control Study

  • Youngkook Kim
    Affiliations
    Department of Rehabilitation Medicine, Graduate School, The Catholic University of Korea, Seoul, Republic of Korea

    Department of Rehabilitation Medicine, Yeouido St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea
    Search for articles by this author
  • Seong Hoon Lim
    Affiliations
    Department of Rehabilitation Medicine, St. Vincent’s Hospital, College of Medicine, The Catholic University of Korea, Suwon, Republic of Korea
    Search for articles by this author
  • Geun-Young Park
    Correspondence
    Corresponding author Geun-Young Park, MD, PhD, Department of Rehabilitation Medicine, Bucheon St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, 327, Sosa-ro, Bucheon-si, Gyeonggi-do 14647, Republic of Korea.
    Affiliations
    Department of Rehabilitation Medicine, Bucheon St. Mary’s Hospital, College of Medicine, The Catholic University of Korea, Bucheon, Republic of Korea
    Search for articles by this author
Published:March 12, 2019DOI:https://doi.org/10.1016/j.apmr.2019.01.026

      Abstract

      Objective

      To investigate whether crossed cerebellar diaschisis (CCD) is associated with functional outcome in the subacute rehabilitation phase of stroke.

      Design

      Retrospective case-control study.

      Setting

      Hospital-based cohort.

      Participants

      The study enrolled participants who underwent brain single-photon emission computed tomography (N=48). Patients with CCD were identified (n=24). Twenty-four controls were selected for each case-patient by matching age, stroke type (ischemic or hemorrhagic), lesion laterality, and lesion location.

      Intervention

      Not applicable.

      Main Outcome Measures

      The functional ambulation category (FAC), modified Barthel Index (MBI), and Mini-Mental State Examination (MMSE) were administered at the initial (initiation of rehabilitation therapy) and the follow-up (4wk after rehabilitation therapy) assessments.

      Results

      The CCD group had lower MMSE, FAC, MBI, and MMSE scores at the initial assessment (P=.032, .016, and .001, respectively) and lower FAC and MBI scores at the follow-up assessment, than the non-CCD group (P=.001 and .036, respectively). Although CCD was not associated with cognitive impairment, nonambulatory status, and dependent activities of daily living (ADL) at the initial assessment (P=.538, .083, and >.99, respectively), the CCD group had a higher risk of cognitive impairment (adjusted odds ratio [aOR]=4.044; 95% confidence interval [CI], 1.071-15.270; P=.039), nonambulatory status (aOR=7.000; 95% CI, 1.641-29.854; P=.009) and dependent ADL (aOR=13.500; 95% CI, 1.535-118.692; P=.019) at the follow-up assessment.

      Conclusions

      CCD is associated with severe functional impairment and may have an adverse effect on functional outcomes related to cognition, ambulatory function, and ADL during the subacute rehabilitation phase of stroke. This suggests that CCD may be a valuable predictor of functional outcome in the subacute rehabilitation phase of stroke.

      Keywords

      List of abbreviations:

      95% CI (95% confidence interval), 99mTc-HMPAO (99mTc-hexamethylpropyleneamineoxime), ADL (activities of daily living), aOR (adjusted odds ratio), CCD (crossed cerebellar diaschisis), FAC (functional ambulation category), MBI (modified Barthel Index), MCA (middle cerebral artery), MMSE (Mini-Mental State Examination), PET (positron emission tomography), SPECT (single-photon emission computed tomography)
      To read this article in full you will need to make a payment

      Purchase one-time access:

      Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online access
      One-time access price info
      • For academic or personal research use, select 'Academic and Personal'
      • For corporate R&D use, select 'Corporate R&D Professionals'

      Subscribe:

      Subscribe to Archives of Physical Medicine and Rehabilitation
      Already a print subscriber? Claim online access
      Already an online subscriber? Sign in
      Institutional Access: Sign in to ScienceDirect

      References

        • Carrera E.
        • Tononi G.
        Diaschisis: past, present, future.
        Brain. 2014; 137: 2408-2422
        • Seitz R.J.
        • Azari N.P.
        • Knorr U.
        • Binkofski F.
        • Herzog H.
        • Freund H.J.
        The role of diaschisis in stroke recovery.
        Stroke. 1999; 30: 1844-1850
        • Pantano P.
        • Baron J.C.
        • Samson Y.
        • Bousser M.G.
        • Derouesne C.
        • Comar D.
        Crossed cerebellar diaschisis. Further studies.
        Brain. 1986; 109: 677-694
        • Govindan R.M.
        • Brescoll J.
        • Chugani H.T.
        Cerebellar pathway changes following cerebral hemispherectomy.
        J Child Neurol. 2013; 28: 1548-1554
        • Liu Y.
        • Karonen J.O.
        • Nuutinen J.
        • Vanninen E.
        • Kuikka J.T.
        • Vanninen R.L.
        Crossed cerebellar diaschisis in acute ischemic stroke: a study with serial SPECT and MRI.
        J Cereb Blood Flow Metab. 2007; 27: 1724-1732
        • Di Piero V.
        • Chollet F.
        • Dolan R.J.
        • Thomas D.J.
        • Frackowiak R.
        The functional nature of cerebellar diaschisis.
        Stroke. 1990; 21: 1365-1369
        • Kim Y.
        • Kim S.H.
        • Kim J.S.
        • Hong B.Y.
        Modification of cerebellar afferent pathway in the subacute phase of stroke.
        J Stroke Cerebrovasc Dis. 2018; 27: 2445-2452
        • Flint A.C.
        • Naley M.C.
        • Wright C.B.
        Ataxic hemiparesis from strategic frontal white matter infarction with crossed cerebellar diaschisis.
        Stroke. 2006; 37: e1-e2
        • Fiori S.
        • Pannek K.
        • Pasquariello R.
        • et al.
        Corticopontocerebellar connectivity disruption in congenital hemiplegia.
        Neurorehabil Neural Repair. 2015; 29: 858-866
        • Szilagyi G.
        • Vas A.
        • Kerenyi L.
        • Nagy Z.
        • Csiba L.
        • Gulyas B.
        Correlation between crossed cerebellar diaschisis and clinical neurological scales.
        Acta Neurol Scand. 2012; 125: 373-381
        • Kim S.E.
        • Choi C.W.
        • Yoon B.W.
        • et al.
        Crossed-cerebellar diaschisis in cerebral infarction: technetium-99m-HMPAO SPECT and MRI.
        J Nucl Med. 1997; 38: 14-19
        • Miyazawa N.
        • Toyama K.
        • Arbab A.S.
        • Koizumi K.
        • Arai T.
        • Nukui H.
        Evaluation of crossed cerebellar diaschisis in 30 patients with major cerebral artery occlusion by means of quantitative I-123 IMP SPECT.
        Ann Nucl Med. 2001; 15: 513-519
        • Nocun A.
        • Wojczal J.
        • Szczepanska-Szerej H.
        • Wilczynski M.
        • Chrapko B.
        Quantitative evaluation of crossed cerebellar diaschisis, using voxel-based analysis of Tc-99m ECD brain SPECT.
        Nucl Med Rev Cent East Eur. 2013; 16: 31-34
        • Sommer W.H.
        • Bollwein C.
        • Thierfelder K.M.
        • et al.
        Crossed cerebellar diaschisis in patients with acute middle cerebral artery infarction: Occurrence and perfusion characteristics.
        J Cereb Blood Flow Metab. 2016; 36: 743-754
        • Chen S.
        • Guan M.
        • Lian H.J.
        • et al.
        Crossed cerebellar diaschisis detected by arterial spin-labeled perfusion magnetic resonance imaging in subacute ischemic stroke.
        J Stroke Cerebrovasc Dis. 2014; 23: 2378-2383
        • Sobesky J.
        • Thiel A.
        • Ghaemi M.
        • et al.
        Crossed cerebellar diaschisis in acute human stroke: a PET study of serial changes and response to supratentorial reperfusion.
        J Cereb Blood Flow Metab. 2005; 25: 1685-1691
        • Mah S.
        • deVeber G.
        • Wei X.C.
        • Liapounova N.
        • Kirton A.
        Cerebellar atrophy in childhood arterial ischemic stroke: acute diffusion MRI biomarkers.
        Stroke. 2013; 44: 2468-2474
        • Krakauer J.W.
        • Marshall R.S.
        The proportional recovery rule for stroke revisited.
        Ann Neurol. 2015; 78: 845-847
        • Takasawa M.
        • Watanabe M.
        • Yamamoto S.
        • et al.
        Prognostic value of subacute crossed cerebellar diaschisis: single-photon emission CT study in patients with middle cerebral artery territory infarct.
        AJNR Am J Neuroradiol. 2002; 23: 189-193
        • De Reuck J.
        • Decoo D.
        • Lemahieu I.
        • Strijckmans K.
        • Goethals P.
        • Van Maele G.
        Crossed cerebellar diaschisis after middle cerebral artery infarction.
        Clin Neurol Neurosurg. 1997; 99: 11-16
        • Kunz W.G.
        • Sommer W.H.
        • Hohne C.
        • et al.
        Crossed cerebellar diaschisis in acute ischemic stroke: impact on morphologic and functional outcome.
        J Cereb Blood Flow Metab. 2017; 37: 3615-3624
        • Infeld B.
        • Davis S.M.
        • Lichtenstein M.
        • Mitchell P.J.
        • Hopper J.L.
        Crossed cerebellar diaschisis and brain recovery after stroke.
        Stroke. 1995; 26: 90-95
        • Baillieux H.
        • De Smet H.J.
        • Dobbeleir A.
        • Paquier P.F.
        • De Deyn P.P.
        • Marien P.
        Cognitive and affective disturbances following focal cerebellar damage in adults: a neuropsychological and SPECT study.
        Cortex. 2010; 46: 869-879
        • Stoodley C.J.
        • Schmahmann J.D.
        Evidence for topographic organization in the cerebellum of motor control versus cognitive and affective processing.
        Cortex. 2010; 46: 831-844
        • Ito Y.
        • Matsumaru Y.
        • Suzuki K.
        • Matsumura A.
        Impaired cognitive function due to cerebellar infarction and improvement after stent-assisted angioplasty for intracranial vertebral artery stenosis--case report.
        Neurologia Med Chir. 2010; 50: 135-138
        • Cramer S.C.
        Stratifying patients with stroke in trials that target brain repair.
        Stroke. 2010; 41: S114-S116
        • Counsell C.
        • Dennis M.
        • McDowall M.
        • Warlow C.
        Predicting outcome after acute and subacute stroke: development and validation of new prognostic models.
        Stroke. 2002; 33: 1041-1047
        • Mayer S.A.
        • Lignelli A.
        • Fink M.E.
        • et al.
        Perilesional blood flow and edema formation in acute intracerebral hemorrhage: a SPECT study.
        Stroke. 1998; 29: 1791-1798
        • Mountz J.M.
        Nuclear medicine in the rehabilitative treatment evaluation in stroke recovery. Role of diaschisis resolution and cerebral reorganization.
        Eura Medicophys. 2007; 43: 221-239
        • Catafau A.M.
        Brain SPECT in clinical practice. Part I: perfusion.
        J Nucl Med. 2001; 42: 259-271
        • Van Laere K.J.
        • Warwick J.
        • Versijpt J.
        • et al.
        Analysis of clinical brain SPECT data based on anatomic standardization and reference to normal data: an ROC-based comparison of visual, semiquantitative, and voxel-based methods.
        J Nucl Med. 2002; 43: 458-469
        • Folstein M.F.
        • Folstein S.E.
        • McHugh P.R.
        “Mini-mental state.” A practical method for grading the cognitive state of patients for the clinician.
        J Psychiatr Res. 1975; 12: 189-198
        • Holden M.K.
        • Gill K.M.
        • Magliozzi M.R.
        • Nathan J.
        • Piehl-Baker L.
        Clinical gait assessment in the neurologically impaired. Reliability and meaningfulness.
        Phys Ther. 1984; 64: 35-40
        • Mahoney F.I.
        • Barthel D.W.
        Functional evaluation: the barthel index.
        Md State Med J. 1965; 14: 61-65
        • Dong Y.
        • Sharma V.K.
        • Chan B.P.
        • et al.
        The Montreal cognitive assessment (MoCA) is superior to the Mini-Mental State Examination (MMSE) for the detection of vascular cognitive impairment after acute stroke.
        J Neurol Sci. 2010; 299: 15-18
        • Stinear C.M.
        Prediction of motor recovery after stroke: advances in biomarkers.
        Lancet Neurol. 2017; 16: 826-836
        • Komaba Y.
        • Mishina M.
        • Utsumi K.
        • Katayama Y.
        • Kobayashi S.
        • Mori O.
        Crossed cerebellar diaschisis in patients with cortical infarction: logistic regression analysis to control for confounding effects.
        Stroke. 2004; 35: 472-476
        • Reivich M.
        Crossed cerebellar diaschisis.
        AJNR Am J Neuroradiol. 1992; 13: 62-64
        • Kamali A.
        • Kramer L.A.
        • Frye R.E.
        • Butler I.J.
        • Hasan K.M.
        Diffusion tensor tractography of the human brain cortico-ponto-cerebellar pathways: a quantitative preliminary study.
        J Magn Reson Imaging. 2010; 32: 809-817
        • Kikuchi S.
        • Mochizuki H.
        • Moriya A.
        • et al.
        Ataxic hemiparesis: neurophysiological analysis by cerebellar transcranial magnetic stimulation.
        Cerebellum. 2012; 11: 259-263
        • Grimaldi G.
        • Argyropoulos G.P.
        • Boehringer A.
        • et al.
        Non-invasive cerebellar stimulation--a consensus paper.
        Cerebellum. 2014; 13: 121-138
        • Chida K.
        • Ogasawara K.
        • Aso K.
        • et al.
        Postcarotid endarterectomy improvement in cognition is associated with resolution of crossed cerebellar hypoperfusion and increase in 123I-iomazenil uptake in the cerebral cortex: a SPECT study.
        Cerebrovasc Dis. 2010; 29: 343-351
        • Ogasawara K.
        • Kobayashi M.
        • Suga Y.
        • et al.
        Significance of postoperative crossed cerebellar hypoperfusion in patients with cerebral hyperperfusion following carotid endarterectomy: SPECT study.
        Eur J Nucl Med Mol Imaging. 2008; 35: 146-152
        • Pope P.A.
        • Miall R.C.
        Task-specific facilitation of cognition by cathodal transcranial direct current stimulation of the cerebellum.
        Brain Stimul. 2012; 5: 84-94
        • Grimaldi G.
        • Manto M.
        Topography of cerebellar deficits in humans.
        Cerebellum. 2012; 11: 336-351
        • Stoodley C.J.
        The cerebellum and cognition: evidence from functional imaging studies.
        Cerebellum. 2012; 11: 352-365
        • Celnik P.
        Understanding and modulating motor learning with cerebellar stimulation.
        Cerebellum. 2015; 14: 171-174
        • Di Pino G.
        • Pellegrino G.
        • Assenza G.
        • et al.
        Modulation of brain plasticity in stroke: a novel model for neurorehabilitation.
        Nat Rev Neurol. 2014; 10: 597-608
        • Marsden J.
        • Harris C.
        Cerebellar ataxia: pathophysiology and rehabilitation.
        Clin Rehabil. 2011; 25: 195-216
        • Pendlebury S.T.
        • Cuthbertson F.C.
        • Welch S.J.
        • Mehta Z.
        • Rothwell P.M.
        Underestimation of cognitive impairment by Mini-Mental State Examination versus the Montreal cognitive assessment in patients with transient ischemic attack and stroke: a population-based study.
        Stroke. 2010; 41: 1290-1293