The national DBS brain tissue network pilot study: need for more tissue and more standardization

Over 70,000 DBS devices have been implanted worldwide; however, there remains a paucity of well-characterized post-mortem DBS brains available to researchers. We propose that the overall understanding of DBS can be improved through the establishment of a Deep Brain Stimulation-Brain Tissue Network (DBS-BTN), which will further our understanding of DBS and brain function. The objectives of the tissue bank are twofold: (a) to provide a complete (clinical, imaging and pathological) database for DBS brain tissue samples, and (b) to make available DBS tissue samples to researchers, which will help our understanding of disease and underlying brain circuitry. Standard operating procedures for processing DBS brains were developed as part of the pilot project. Complete data files were created for individual patients and included demographic information, clinical information, imaging data, pathology, and DBS lead locations/settings. 19 DBS brains were collected from 11 geographically dispersed centers from across the U.S. The average age at the time of death was 69.3 years (51–92, with a standard deviation or SD of 10.13). The male:female ratio was almost 3:1. Average post-mortem interval from death to brain collection was 10.6 h (SD of 7.17). The DBS targets included: subthalamic nucleus, globus pallidus interna, and ventralis intermedius nucleus of the thalamus. In 16.7% of cases the clinical diagnosis failed to match the pathological diagnosis. We provide neuropathological findings from the cohort, and perilead responses to DBS. One of the most important observations made in this pilot study was the missing data, which was approximately 25% of all available data fields. Preliminary results demonstrated the feasibility and utility of creating a National DBS-BTN resource for the scientific community. We plan to improve our techniques to remedy omitted clinical/research data, and expand the Network to include a larger donor pool. We will enhance sample preparation to facilitate advanced molecular studies and progenitor cell retrieval.

[1]  Christine Haberler,et al.  No tissue damage by chronic deep brain stimulation in Parkinson's disease , 2000, Annals of neurology.

[2]  Walter Schubert,et al.  Localization of Alzheimer βA4 amyloid precursor protein at central and peripheral synaptic sites , 1991, Brain Research.

[3]  G. E. Alexander,et al.  Functional organization of the basal ganglia: contributions of single-cell recording studies. , 1984, Ciba Foundation symposium.

[4]  M G Spillantini,et al.  Alpha-synuclein in Lewy bodies. , 1997, Nature.

[5]  C. Davie A review of Parkinson's disease. , 2008, British medical bulletin.

[6]  Malcolm Pell,et al.  Postmortem analysis of bilateral subthalamic electrode implants in Parkinson's disease. , 2002, Movement disorders : official journal of the Movement Disorder Society.

[7]  B. Winblad,et al.  How to run a brain bank: potentials and pitfalls in the use of human post-mortem brain material in research. , 1993, Journal of neural transmission. Supplementum.

[8]  R. Krüger,et al.  Review: Familial Parkinson's disease – genetics, clinical phenotype and neuropathology in relation to the common sporadic form of the disease , 2008, Neuropathology and applied neurobiology.

[9]  H. Braak,et al.  Staging of brain pathology related to sporadic Parkinson’s disease , 2003, Neurobiology of Aging.

[10]  Ubiquitin is detected in neurofibrillary tangles and senile plaque neurites of Alzheimer disease brains , 1987 .

[11]  S. Folstein,et al.  "Mini-mental state". A practical method for grading the cognitive state of patients for the clinician. , 1975, Journal of psychiatric research.

[12]  P. Jansen,et al.  Diagnostic errors; the need to have autopsies. , 2006, The Netherlands journal of medicine.

[13]  P. Falkai,et al.  How a neuropsychiatric brain bank should be run: a consensus paper of Brainnet Europe II , 2006, Journal of Neural Transmission.

[14]  C. Bjarkam,et al.  Chronic subthalamic high‐frequency deep brain stimulation in Parkinson's disease – a histopathological study , 2007, European journal of neurology.

[15]  M. Stern,et al.  Deep brain stimulation in Parkinson disease: a metaanalysis of patient outcomes. , 2005, Journal of neurosurgery.

[16]  Mrc Psych,et al.  Consensus guidelines for the clinical and pathologic diagnosis of dementia with Lewy bodies (DLB): Report of the consortium on DLB international workshop , 1996 .

[17]  P. Hasleton,et al.  Discrepancies between clinical and autopsy diagnosis and the value of post mortem histology; a meta‐analysis and review , 2005, Histopathology.

[18]  Vahram Haroutunian,et al.  Autism Brain Tissue Banking , 2007, Brain pathology.

[19]  H. Braak,et al.  α-Synuclein immunopositive Parkinson's disease-related inclusion bodies in lower brain stem nuclei , 2001, Acta Neuropathologica.

[20]  J. Vonsattel,et al.  Twenty-first century brain banking: practical prerequisites and lessons from the past: the experience of New York Brain Bank, Taub Institute, Columbia University , 2008, Cell and Tissue Banking.

[21]  Hansjürgen Bratzke,et al.  Stages in the development of Parkinson’s disease-related pathology , 2004, Cell and Tissue Research.

[22]  H. Shill,et al.  Unified staging system for Lewy body disorders: correlation with nigrostriatal degeneration, cognitive impairment and motor dysfunction , 2009, Acta Neuropathologica.

[23]  J. Hughes,et al.  Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases. , 1992, Journal of neurology, neurosurgery, and psychiatry.

[24]  W. Weiner There is no Parkinson disease. , 2008, Archives of neurology.

[25]  Peter E. Konrad,et al.  Postmortem analysis following 71 months of deep brain stimulation of the subthalamic nucleus for Parkinson disease. , 2008, Journal of neurosurgery.

[26]  Andrew J Lees,et al.  Clinicopathological investigation of vascular parkinsonism, including clinical criteria for diagnosis , 2004, Movement disorders : official journal of the Movement Disorder Society.

[27]  K. Baer,et al.  Immunohistochemical staining of post-mortem adult human brain sections , 2006, Nature Protocols.

[28]  M. Curtis,et al.  The collection and processing of human brain tissue for research , 2008, Cell and Tissue Banking.

[29]  C. Warren Olanow,et al.  Alterations in lysosomal and proteasomal markers in Parkinson's disease: Relationship to alpha-synuclein inclusions , 2009, Neurobiology of Disease.