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Stereological estimates of neuronal loss in the primary motor cortex of multiple sclerosis patients M.M. Papachatzaki, D. Carassiti, A. McDowell, K. Schmierer QMUL (London, GB) Introduction Whilst inflammatory demyelination (ID) is an important feature in the clinical and pathological diagnosis of MS, evidence suggests mechanisms other than ID may play an important role for the deterioration of function in people with progressive MS (pwPMS) (Trapp & Nave. Annu Rev Neurosci 2008; Kolasinski, et al. Brain 2012). Impaired motor function is one of the most important components of disability pwPMS accrue over time. Using unbiased sampling techniques applied to whole central nervous systems of pwPMS we investigate whether a tract specific pattern of neurodegeneration contributes to the loss of motor function in pwPMS. Here, we present preliminary data on stereological estimates of neuronal cell loss in limb specific areas of the MS primary motor cortex (PMC). No limb specific neuronal cell counts had been reported to date in human brain. Objective To estimate the absolute number of neurons in the PMC associated with limb function in pwPMS and a reference case. Methods The left hemispheres from formalin fixed brains of two women with primary progressive (PP) MS (age= 67 and 83 years, disease duration= 11 and 14 years) and one reference case (male, age= 82 years) with no known neurological disease were used. Reference brain was free of any neuropathological findings. PMCs were delineated with ink on the cortical surface. Hemispheres were then dissected into 1.1 cm thick coronal slabs and images obtained of each slab following a standard protocol. Each slab was then embedded in wax, 40µm thick hemispheric sections were obtained from across the entire motor cortex and stained using a modified Wolbach's Giemsa method. Sections were chosen in a 1/20 sequence in a systematic unbiased method and counted using cast-gid® software. Optical dissectors (50µm x 50µm x 30µm) along the delineated area of interest were superimposed onto a color monitor at a final magnification of 3000×, using a x60 objective on an Olympus microscope equipped with a motorized stage. The hand and leg areas were identified anatomically based on a human brain atlas, the presence of dye in the relevant areas of interest indicating the primary motor cortex and the presence of Betz cells in the corresponding areas. Neurons were identified using morphological criteria. Total number of neurons in each area was subsequently calculated according to NV x VREF stereology method, were VREF was estimated by the Cavalieri principle. Results The mean number of neurons in the leg and arm areas of the PMC of the left hemisphere in pwPPMS was 34 and 32 million in average respectively, whilst the number of neurons in the reference PMC was 34 and 35 million, respectively. The coefficient of error (CE) was less than 9% throughout suggesting reliable counting methodology. Conclusion Using unbiased sampling methodology our data provide a robust platform for studies into the relationship between cortical and spinal cord pathology in MS. Extension of our cohort is key to produce statistically meaningful results. Subsequently, we will explore the relationship between neuronal-axonal pathology and other histological features of MS including inflammation and demyelination. References Ganter P, Prince C, Esiri MM. Spinal cord axonal loss in multiple sclerosis: a postmortem study. Neuropathology Appl Neurobiol. 1999 Dec;25(6):459-67. Calabrese M, Rinaldi F, Mattisi I, Bernardi V, Favaretto A, Perini P, Gallo P. The predictive value of gray matter atrophy in clinically isolated syndromes. Neurology. 2011, 77(3):257-63. Magliozzi R, Howell OW, Reeves C, Roncaroli F, Nicholas R, Serafini B, Aloisi F, Reynolds R. A Gradient of neuronal loss and meningeal inflammation in multiple sclerosis. Ann Neurol. 2010 68(4):477-93. Dziedzic T, Metz I, Dallenga T, Konig FB, Muller S, Stadelmann C & Bruck W. Wallerian degeneration: a major component of early axonal pathology in multiple sclerosis. Brain Pathol. 2010, 20:976-85. Pelvig DP, Pakkenberg H, Stark AK & Pakkenberg B. Neocortical glial cell numbers in human brains. Neurobiol Aging 2008, 29:1754-62. Trapp BD, Peterson J, Ransohoff RM, Rudick R, Mork S & Bo L. Axonal transection in the lesions of multiple sclerosis. N Engl J Med 1998, 338:78-85. Wegner C, Esiri MM, Chance SA, Palace J & Matthews PM. Neocortical neuronal, synaptic, and glial loss in multiple sclerosis. Neurology 2006, 67:960-7.