Hostname: page-component-848d4c4894-m9kch Total loading time: 0 Render date: 2024-06-04T20:21:34.736Z Has data issue: false hasContentIssue false

A Neuropsychological Profile for Cerebrotendinous Xanthomatosis: A Single-Case Study

Published online by Cambridge University Press:  03 January 2020

Andrew M. Bryant*
Affiliation:
Section of Neurobehavioral Health, Department of Psychiatry & Behavioral Health, The Ohio State University Wexner Medical Center, 3650 Olentangy River Road, Suite 310, Columbus, OH43214, USA Department of Psychology, Ohio University, 200 Porter Hall, Athens, OH45701, USA
Cady Block
Affiliation:
Section of Neurobehavioral Health, Department of Psychiatry & Behavioral Health, The Ohio State University Wexner Medical Center, 3650 Olentangy River Road, Suite 310, Columbus, OH43214, USA
*
Correspondence and reprint requests to: Andrew M. Bryant, Section of Neurobehavioral Health, Department of Psychiatry and Behavioral Health, The Ohio State University Wexner Medical Center, 3650 Olentangy River Road, Suite 310, Columbus, OH 43214, USA. E-mail: ab859013@ohio.edu.

Abstract

Objective:

Cerebrotendinous xanthomatosis (CTX) belongs to a heterogeneous group of neurological disorders known as autosomal recessive cerebellar ataxias. Low awareness of CTX can result in misdiagnoses in the differential diagnostic process and may limit one’s ability to offer suitable recommendations. While neurodegeneration is a recognized manifestation of CTX, there is scant literature to characterize the nature of cortical symptoms and even less detailing of its associated neurocognitive and neuropsychiatric manifestations.

Method:

Based on the lack of representation of CTX in neuropsychological literature, we sought to present a case seen in a 39-year-old patient within our own clinic.

Results:

Evaluation of the patient’s neurocognitive functioning revealed global impairment consistent with a CTX diagnosis and neuroimaging findings noting significant cerebellar involvement.

Conclusions:

Neuropsychologists are increasingly called upon to make treatment recommendations and provide information that may be helpful in differential diagnosis as part of multidisciplinary teams. Referrals from neurology are common, and it is important for neuropsychologists to be aware of diseases that affect the central nervous system; CTX is one such example. The goal of this case study is to build awareness of this condition and increase interest in a more systematic approach to research and clinical care of this population.

Type
Case Report
Copyright
Copyright © INS. Published by Cambridge University Press, 2020

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Allen, G., McColl, R., Barnard, H., Ringe, W.K., Fleckenstein, J., & Cullum, C.M. (2005). Magnetic resonance imaging of cerebellar–prefrontal and cerebellar–parietal functional connectivity. Neuroimage, 28, 3948. doi: 10.1016/j.neuroimage.2005.06.013CrossRefGoogle ScholarPubMed
Berginer, V.M., Abeliovich, D., & Opitz, J.M. (1981). Genetics of Cerebrotendinous Xanthomatosis (CTX): an autosomal recessive trait with high gene frequency in Sephardim of Moroccan origin. American Journal of Medical Genetics Part A, 10, 151157. doi: 10.1002/ajmg.1320100209CrossRefGoogle ScholarPubMed
Bhattacharyya, A.K., Lin, D.S., & Connor, W.E. (2007). Cholestanol metabolism in patients with Cerebrotendinous Xanthomatosis: absorption, turnover, and tissue deposition. Journal of Lipid Research, 48, 185192. doi: 10.1194/jlr.M600113-JLR200CrossRefGoogle ScholarPubMed
Cali, J.J., Hsieh, C.L., Francke, U., & Russell, D.W. (1991). Mutations in the bile acid biosynthetic enzyme sterol 27-hydroxylase underlie Cerebrotendinous Xanthomatosis. Journal of Biological Chemistry, 266, 77797783.Google ScholarPubMed
Catarino, C.B., Vollmar, C., Küpper, C., Seelos, K., Gallenmüller, C., Bartkiewicz, J., Biskup, S., Hörtnagel, K., & Klopstock, T. (2017). Brain diffusion tensor imaging changes in Cerebrotendinous Xanthomatosis reversed with treatment. Journal of Neurology, 265, 338393. doi: 10.1007/s00415-017-8711-9Google ScholarPubMed
Chang, C.C., Lui, C.C., Wang, J.J., Huang, S.H., Lu, C.H., Chen, C., Chen, C.F., Tu, M.C., Huang, C.W., & Chang, W.N. (2010). Multi-parametric neuroimaging evaluation of Cerebrotendinous Xanthomatosis and its correlation with neuropsychological presentations. BMC Neurology, 10, 59. doi: 10.1186/1471-2377-10-59CrossRefGoogle ScholarPubMed
Duell, P.B., Salen, G., Eichler, F.S., DeBarber, A.E., Connor, S.L.Kisanuki, Y., Lekprasert, P., Malloy, M.J., Ramdhani, R.A., Ziajka, P.E., Quinn, J.F., Su, K.G., Geller, A.S., Diffenderfer, M.R., & Schaefer, E.J. 2018). Diagnosis, treatment, and clinical outcomes in 43 cases with Cerebrotendinous Xanthomatosis. Journal of Clinical Lipidology, 12, 11691178. doi: 10.1016/j.jacl.2018.06.008CrossRefGoogle ScholarPubMed
Dum, R.P. & Strick, P.L. (2003). An unfolded map of the cerebellar dentate nucleus and its projections to the cerebral cortex. Journal of Neurophysiology, 89, 634639. doi: 10.1152/jn.00626.2002CrossRefGoogle ScholarPubMed
Embirucu, E.K., Otaduy, M.C., Taneja, A.K., Leite, C.C., Kok, F., & Lucato, L.T. (2010). MR spectroscopy detects lipid peaks in Cerebrotendinous Xanthomatosis. American Journal of Neuroradiology, 31, 13471349. doi: 10.3174/ajnr.A1885CrossRefGoogle ScholarPubMed
Erdodi, L.A. & Lichtenstein, J.D. (2017). Invalid before impaired: an emerging paradox of embedded validity indicators. The Clinical Neuropsychologist, 31, 10291046. doi: 10.1080/13854046.2017.1323119CrossRefGoogle ScholarPubMed
Fraidakis, M.J. (2013). Psychiatric manifestations in cerebrotendinous xanthomatosis. Translational Psychiatry, 3, e302.CrossRefGoogle ScholarPubMed
Heyder, K., Suchan, B., & Daum, I. (2004). Cortico-subcortical contributions to executive control. Acta Psychologica, 115, 271289. doi: 10.1016/j.actpsy.2003.12.010CrossRefGoogle ScholarPubMed
Inoue, K., Kubota, S., & Seyama, Y. (1999). Cholestanol induces apoptosis of cerebellar neuronal cells. Biochemical and Biophysical Research Communications, 256, 198203. doi: 10.1006/bbrc.1998.9497CrossRefGoogle ScholarPubMed
Lorincz, M.T., Rainier, S., Thomas, D., & Fink, J.K. (2005). Cerebrotendinous xanthomatosis: possible higher prevalence than previously recognized. Archives of Neurology, 62, 14591463. doi: 10.1001/archneur.62.9.1459CrossRefGoogle ScholarPubMed
Mignarri, A., Dotti, M.T., Federico, A., De Stefano, N., Battaglini, M., Grazzini, I., Galluzzi, P., & Monti, L. (2017). The spectrum of magnetic resonance findings in cerebrotendinous xanthomatosis: redefinition and evidence of new markers of disease progression. Journal of Neurology, 264, 862874. doi: 10.1007/s00415-017-8440-0CrossRefGoogle Scholar
Mignarri, A., Gallus, G.N., Dotti, M.T., & Federico, A. (2014). A suspicion index for early diagnosis and treatment of cerebrotendinous xanthomatosis. Journal of Inherited Metabolic Disease, 37, 421429. doi: 10.1007/s10545-013-9674-3CrossRefGoogle ScholarPubMed
Mignarri, A., Rossi, S., Ballerini, M., Gallus, G.N., Del Puppo, M., Galluzzi, P., Federico, A., & Dotti, M.T. (2011). Clinical relevance and neurophysiological correlates of spasticity in cerebrotendinous xanthomatosis. Journal of Neurology, 258, 783790. doi: 10.1007/s00415-010-5829-4CrossRefGoogle ScholarPubMed
Moghadasian, M.H. (2004). Cerebrotendinous Xanthomatosis: clinical course, genotypes and metabolic backgrounds. Clinical and Investigative Medicine, 27, 42.Google ScholarPubMed
Mukaino, A., Tsuda, M., Yamashita, S., Kosaka, T., Wada, K., & Ando, Y. (2018). Cerebrotendinous Xanthomatosis presenting with extensive cerebral cortex symptoms: a case report. Clinical Neurology and Neurosurgery, 174, 217219. doi: 10.1016/j.clineuro.2018.09.028CrossRefGoogle ScholarPubMed
Nie, S., Chen, G., Cao, X., & Zhang, Y. (2014). Cerebrotendinous Xanthomatosis: a comprehensive review of pathogenesis, clinical manifestations, diagnosis, and management. Orphanet Journal of Rare Diseases, 9, 179. doi: 10.1186/s13023-014-0179-4CrossRefGoogle ScholarPubMed
Palau, F. & Espinós, C. (2006). Autosomal recessive cerebellar ataxias. Orphanet Journal of Rare Diseases, 1, 47. doi: 10.1186/1750-1172-1-47CrossRefGoogle ScholarPubMed
Royall, D.R., Cordes, J.A., & Polk, M. (1998). CLOX: an executive clock drawing task. Journal of Neurology, Neurosurgery & Psychiatry, 64, 588594. doi: 10.1136/jnnp.64.5.588CrossRefGoogle Scholar
Salen, G., Berginer, V., Shore, V., Horak, I., Horak, E., Tint, G.S., & Shefer, S. (1987). Increased concentrations of cholestanol and apolipoprotein B in the cerebrospinal fluid of patients with cerebrotendinous xanthomatosis. New England Journal of Medicine, 316, 12331238. doi: 10.1056/NEJM198705143162002CrossRefGoogle ScholarPubMed
Salen, G. & Steiner, R.D. (2017). Epidemiology, diagnosis, and treatment of Cerebrotendinous Xanthomatosis. Journal of Inherited Metabolic Disease, 40, 771781. doi: 10.1007/s10545-017-0093-8CrossRefGoogle ScholarPubMed
Spencer, K.A. & Slocomb, D.L. (2007). The neural basis of ataxic dysarthria. The Cerebellum, 6, 5865. doi: 10.1080/14734220601145459CrossRefGoogle ScholarPubMed
Stelten, B.M.L., van de Warrenburg, B.P.C., Wevers, R.W., & Verriprs, A. (2018). Movement disorders in Cerebrotendinous Xanthomatosis. Parkinsonism & Related Disorders, 58, 1216. doi: 10.1016/j.parkreldis.2018.07.006.CrossRefGoogle ScholarPubMed
Theofilopoulos, S., Griffiths, W.J., Crick, P.J., Yang, S., Meljion, A., Ogundare, M., Kitambi, S.S., Lockhart, A., Tuschl, K., Clayton, P.T., Morris, A.A., Martinez, A., Reddy, M.A., Martinuzzi, A., Bassi, M.T., Honda, A., Mizuochi, T., Kimura, A., Nittono, H., De Michele, G., Carbone, R., Criscuolo, C., Yau, J.L., Seckl, J.R., Schüle, R., Schöls, L., Sailer, A.W., Kuhle, J., Fraidakis, M.J., Gustafsson, J.Å., Steffensen, K.R., Björkhem, I., Ernfors, P., Sjövall, J., Arenas, E., & Wang, Y. (2014). Cholestenoic acids regulate motor neuron survival via liver X receptors. Journal of Clinical Investigation, 124, 48294842. doi: 10.1172/JCI68506CrossRefGoogle ScholarPubMed
Verrips, A., Hoefsloot, L.H., Steenbergen, G.C., Theelen, J.P., Wevers, R.A., Gabreëls, F.J., van Engelen, B.G., & van den Heuvel, L.P. (2000). Clinical and molecular genetic characteristics of patients with cerebrotendinous xanthomatosis. Brain, 123, 908919. doi: 10.1093/brain/123.5.908CrossRefGoogle ScholarPubMed