Humans with Type-2 Diabetes Show Abnormal Long-Term Potentiation-Like Cortical Plasticity Associated with Verbal Learning Deficits.

BACKGROUND Type-2 diabetes mellitus (T2DM) accelerates cognitive aging and increases risk of Alzheimer's disease. Rodent models of T2DM show altered synaptic plasticity associated with reduced learning and memory. Humans with T2DM also show cognitive deficits, including reduced learning and memory, but the relationship of these impairments to the efficacy of neuroplastic mechanisms has never been assessed. OBJECTIVE Our primary objective was to compare mechanisms of cortical plasticity in humans with and without T2DM. Our secondary objective was to relate plasticity measures to standard measures of cognition. METHODS A prospective cross-sectional cohort study was conducted on 21 adults with T2DM and 15 demographically-similar non-diabetic controls. Long-term potentiation-like plasticity was assessed in primary motor cortex by comparing the amplitude of motor evoked potentials (MEPs) from single-pulse transcranial magnetic stimulation before and after intermittent theta-burst stimulation (iTBS). Plasticity measures were compared between groups and related to neuropsychological scores. RESULTS In T2DM, iTBS-induced modulation of MEPs was significantly less than controls, even after controlling for potential confounds. Furthermore, in T2DM, modulation of MEPs 10-min post-iTBS was significantly correlated with Rey Auditory Verbal Learning Task (RAVLT) performance. CONCLUSION Humans with T2DM show abnormal cortico-motor plasticity that is correlated with reduced verbal learning. Since iTBS after-effects and the RAVLT are both NMDA receptor-dependent measures, their relationship in T2DM may reflect brain-wide alterations in the efficacy of NMDA receptors. These findings offer novel mechanistic insights into the brain consequences of T2DM and provide a reliable means to monitor brain health and evaluate the efficacy of clinical interventions.

[1]  C. Caltagirone,et al.  Long‐term potentiation–like cortical plasticity is disrupted in Alzheimer's disease patients independently from age of onset , 2016, Annals of neurology.

[2]  D. Diamond,et al.  Influence of pharmacological manipulations of NMDA and cholinergic receptors on working versus reference memory in a dual component odor span task , 2016, Learning & memory.

[3]  Liuqin He,et al.  The Physiological Basis and Nutritional Function of Alpha-ketoglutarate. , 2015, Current protein & peptide science.

[4]  W. Milberg,et al.  Inflammation-associated declines in cerebral vasoreactivity and cognition in type 2 diabetes , 2015, Neurology.

[5]  D. Mott,et al.  Hippocampal Insulin Resistance Impairs Spatial Learning and Synaptic Plasticity , 2015, Diabetes.

[6]  Dennis J. L. G. Schutter,et al.  Efficacy and Time Course of Theta Burst Stimulation in Healthy Humans , 2015, Brain Stimulation.

[7]  L. Kappelle,et al.  Cognitive function in patients with diabetes mellitus: guidance for daily care , 2015, The Lancet Neurology.

[8]  S. Rossi,et al.  Non-invasive electrical and magnetic stimulation of the brain, spinal cord, roots and peripheral nerves: Basic principles and procedures for routine clinical and research application. An updated report from an I.F.C.N. Committee , 2015, Clinical Neurophysiology.

[9]  D. Javitt,et al.  Behavioral and cognitive effects of the N-methyl-D-aspartate receptor co-agonist D-serine in healthy humans: initial findings. , 2015, Journal of psychiatric research.

[10]  Guowei Huang,et al.  Conversion of mild cognitive impairment to dementia among subjects with diabetes: a population-based study of incidence and risk factors with five years of follow-up. , 2014, Journal of Alzheimer's disease : JAD.

[11]  Emily H. Trittschuh,et al.  Long-acting intranasal insulin detemir improves cognition for adults with mild cognitive impairment or early-stage Alzheimer's disease dementia. , 2015, Journal of Alzheimer's disease : JAD.

[12]  Á. Pascual-Leone,et al.  Theta burst stimulation to characterize changes in brain plasticity following mild traumatic brain injury: A proof-of-principle study. , 2015, Restorative neurology and neuroscience.

[13]  R. Archana,et al.  EFFECT OF TYPE 2 DIABETES MELLITUS ON BRAIN METABOLITES BY USING PROTON MAGNETIC RESONANCE SPECTROSCOPY-A SYSTEMATIC REVIEW. , 2014, International journal of pharma and bio sciences.

[14]  Jing Fang,et al.  Intranasal Insulin Enhanced Resting-State Functional Connectivity of Hippocampal Regions in Type 2 Diabetes , 2014, Diabetes.

[15]  Á. Pascual-Leone,et al.  BDNF Polymorphism and Differential rTMS Effects on Motor Recovery of Stroke Patients , 2014, Brain Stimulation.

[16]  Marco Bozzali,et al.  Dopaminergic Modulation of Cortical Plasticity in Alzheimer’s Disease Patients , 2014, Neuropsychopharmacology.

[17]  K. Funke,et al.  Modulation of Inhibitory Activity Markers by Intermittent Theta-burst Stimulation in Rat Cortex is NMDA-receptor Dependent , 2014, Brain Stimulation.

[18]  G. Biessels,et al.  Magnitude of Cognitive Dysfunction in Adults with Type 2 Diabetes: A Meta-analysis of Six Cognitive Domains and the Most Frequently Reported Neuropsychological Tests Within Domains , 2014, Journal of the International Neuropsychological Society.

[19]  P. Novak,et al.  Enhancement of Vasoreactivity and Cognition by Intranasal Insulin in Type 2 Diabetes , 2014, Diabetes Care.

[20]  Alvaro Pascual-Leone,et al.  Reproducibility of the effects of theta burst stimulation on motor cortical plasticity in healthy participants , 2014, Clinical Neurophysiology.

[21]  V. Pankratz,et al.  Association of diabetes with amnestic and nonamnestic mild cognitive impairment , 2014, Alzheimer's & Dementia.

[22]  G. McCarthy,et al.  The Impact of NMDA Receptor Blockade on Human Working Memory-Related Prefrontal Function and Connectivity , 2013, Neuropsychopharmacology.

[23]  Suzanne Craft,et al.  Sex and ApoE genotype differences in treatment response to two doses of intranasal insulin in adults with mild cognitive impairment or Alzheimer's disease. , 2013, Journal of Alzheimer's disease : JAD.

[24]  Beatriz Bosch,et al.  APOE Status Modulates the Changes in Network Connectivity Induced by Brain Stimulation in Non-Demented Elders , 2012, PloS one.

[25]  Á. Pascual-Leone,et al.  Abnormal modulation of corticospinal excitability in adults with Asperger’s syndrome , 2012, The European journal of neuroscience.

[26]  N. Mercuri,et al.  Insulin Receptor β-Subunit Haploinsufficiency Impairs Hippocampal Late-Phase LTP and Recognition Memory , 2012, NeuroMolecular Medicine.

[27]  Kelly A. Tennant,et al.  Diabetes Impairs Cortical Plasticity and Functional Recovery Following Ischemic Stroke , 2012, The Journal of Neuroscience.

[28]  T. Montine,et al.  Intranasal Insulin Therapy for Alzheimer Disease and Amnestic Mild Cognitive Impairment A Pilot Clinical Trial , 2011 .

[29]  C. Caltagirone,et al.  Impaired LTP- but not LTD-like cortical plasticity in Alzheimer's disease patients. , 2012, Journal of Alzheimer's disease : JAD.

[30]  Cleofé Peña-Gómez,et al.  Changes in Cortical Plasticity Across the Lifespan , 2011, Front. Ag. Neurosci..

[31]  M. Strachan R D Lawrence Lecture 2010 ^ . The brain as a target organ in Type 2 diabetes: exploring the links with cognitive impairment and dementia , 2011, Diabetic medicine : a journal of the British Diabetic Association.

[32]  Klaus Funke,et al.  Theta-Burst Transcranial Magnetic Stimulation Alters Cortical Inhibition , 2011, The Journal of Neuroscience.

[33]  G. Bernardi,et al.  CSF tau levels influence cortical plasticity in Alzheimer's disease patients. , 2011, Journal of Alzheimer's disease : JAD.

[34]  V. Haroutunian,et al.  Diabetes Is Associated with Increased Rate of Cognitive Decline in Questionably Demented Elderly , 2010, Dementia and Geriatric Cognitive Disorders.

[35]  Talib F. Abbas,et al.  Impairment of synaptic plasticity and memory formation in GLP-1 receptor KO mice: Interaction between type 2 diabetes and Alzheimer's disease , 2009, Behavioural Brain Research.

[36]  S. Rossi,et al.  Safety, ethical considerations, and application guidelines for the use of transcranial magnetic stimulation in clinical practice and research , 2009, Clinical Neurophysiology.

[37]  J. Rothwell,et al.  The physiological basis of the effects of intermittent theta burst stimulation of the human motor cortex , 2008, The Journal of physiology.

[38]  Geert Jan Biessels,et al.  Diabetes Increases Atrophy and Vascular Lesions on Brain MRI in Patients With Symptomatic Arterial Disease , 2008, Stroke.

[39]  M. Mattson,et al.  Diabetes impairs hippocampal function through glucocorticoid-mediated effects on new and mature neurons , 2008, Nature Neuroscience.

[40]  J. Rothwell,et al.  The after-effect of human theta burst stimulation is NMDA receptor dependent , 2007, Clinical Neurophysiology.

[41]  Anders M. Dale,et al.  An automated labeling system for subdividing the human cerebral cortex on MRI scans into gyral based regions of interest , 2006, NeuroImage.

[42]  P. Scheltens,et al.  Risk of dementia in diabetes mellitus: a systematic review , 2006, The Lancet Neurology.

[43]  A. Lahti,et al.  The effects of a subanesthetic dose of ketamine on verbal memory in normal volunteers , 2005, Psychopharmacology.

[44]  P. Kučera,et al.  Spinal cord lesions in diabetes mellitus. Somatosensory and motor evoked potentials and spinal conduction time in diabetes mellitus. , 2005, Neuro endocrinology letters.

[45]  R. Astur,et al.  Selective Cognitive Impairments Associated with NMDA Receptor Blockade in Humans , 2005, Neuropsychopharmacology.

[46]  J. Rothwell,et al.  Theta Burst Stimulation of the Human Motor Cortex , 2005, Neuron.

[47]  Jan Born,et al.  Intranasal insulin improves memory in humans , 2004, Psychoneuroendocrinology.

[48]  M. D. Calero,et al.  Relationship between plasticity, mild cognitive impairment and cognitive decline. , 2004, Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists.

[49]  A. Dale,et al.  Thinning of the cerebral cortex in aging. , 2004, Cerebral cortex.

[50]  D. Bennett,et al.  Diabetes mellitus and risk of Alzheimer disease and decline in cognitive function. , 2004, Archives of neurology.

[51]  Manjit,et al.  Neurology , 1912, NeuroImage.

[52]  W. Pardridge,et al.  Pathological upregulation of inner blood-retinal barrier Glut1 glucose transporter expression in diabetes mellitus , 1996, Brain Research.

[53]  T. Bliss,et al.  Long-term potentiation and glutamate release in the dentate gyrus: links to spatial learning , 1995, Behavioural Brain Research.

[54]  C. Marsden,et al.  Corticocortical inhibition in human motor cortex. , 1993, The Journal of physiology.

[55]  M. Hallett,et al.  Human motor evoked responses to paired transcranial magnetic stimuli. , 1992, Electroencephalography and clinical neurophysiology.

[56]  Gary Lynch,et al.  Role of N-methyl-D-aspartate receptors in the induction of synaptic potentiation by burst stimulation patterned after the hippocampal θ-rhythm , 1988, Brain Research.

[57]  J. J. Ryan,et al.  Rey Auditory-Verbal Learning Test performance of patients with and without memory impairment. , 1984, Journal of clinical psychology.

[58]  H. Bradford,et al.  METABOLISM OF GLUCOSE AND GLUTAMATE BY SYNAPTOSOMES FROM MAMMALIAN CEREBRAL CORTEX , 1969, Journal of neurochemistry.

[59]  A. Jaillard [The 2 diabetes]. , 1968, Lille medical : journal de la Faculte de medecine et de pharmacie de l'Universite de Lille.