Reproducibility of Single-Pulse, Paired-Pulse, and Intermittent Theta-Burst TMS Measures in Healthy Aging, Type-2 Diabetes, and Alzheimer’s Disease

• Published in: Frontiers in aging neuroscience Vol. 9; p. 263
• Main Authors: Fried, Peter J., Jannati, Ali, Davila-Pérez, Paula, Pascual-Leone, Alvaro
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Research Foundation 21.08.2017; Frontiers Media S.A
• Subjects: Achievement tests; Age; Aging; Alzheimer's disease; Brain research; Brain-derived neurotrophic factor; Cortex; cortical plasticity; Diabetes; Diabetes mellitus; Gene polymorphism; Magnetic fields; Metabolism; Motor evoked potentials; Neuroplasticity; Neuroscience; Neurosciences; NMR; Nuclear magnetic resonance; Reproducibility; reproducibility of results; Transcranial magnetic stimulation; Traumatic brain injury; Type-2 diabetes; Spain; Type-2 diabetes; reproducibility of results; cortical plasticity; aging; transcranial magnetic stimulation; Alzheimer’s disease
• ISSN: 1663-4365; 1663-4365
• DOI: 10.3389/fnagi.2017.00263

Transcranial magnetic stimulation (TMS) can be used to assess neurophysiology and the mechanisms of cortical brain plasticity in humans . As the use of these measures in specific populations (e.g., Alzheimer's disease; AD) increases, it is critical to understand their reproducibility (i.e., test-retest reliability) in the populations of interest. Reproducibility of TMS measures was evaluated in older adults, including healthy, AD, and Type-2 diabetes mellitus (T2DM) groups. Participants received two identical neurophysiological assessments within a year including motor thresholds, baseline motor evoked potentials (MEPs), short- and long-interval intracortical inhibition (SICI, LICI) and intracortical facilitation (ICF), and MEP changes following intermittent theta-burst stimulation (iTBS). Cronbach's α coefficients were calculated to assess reproducibility. Multiple linear regression analyses were used to investigate factors related to intraindividual variability. Reproducibility was highest for motor thresholds, followed by baseline MEPs, SICI and LICI, and was lowest for ICF and iTBS aftereffects. The AD group tended to show higher reproducibility than T2DM or controls. Intraindividual variability of baseline MEPs was related to age and variability of RMT, while the intraindividual variability in post-iTBS measures was related to baseline MEP variability, intervisit duration, and Brain-derived neurotrophic factor ( ) polymorphism. Increased reproducibility in AD may reflect pathophysiological declines in the efficacy of neuroplastic mechanisms. Reproducibility of iTBS aftereffects can be improved by keeping baseline MEPs consistent, controlling for genotype, and waiting at least a week between visits. These findings provide the first direct assessment of reproducibility of TMS measures in older clinical populations. Reproducibility coefficients may be used to adjust effect- and sample size calculations for future studies.