ABSTRACT
BACKGROUND: In critical care settings, electroencephalography (EEG) with reduced number of electrodes (reduced montage EEG, rm-EEG) might be a timely alternative to the conventional full montage EEG (fm-EEG). However, past studies have reported variable accuracies for detecting seizures using rm-EEG. We hypothesized that the past studies did not distinguish between differences in sensitivity from differences in classification of EEG patterns by different readers. The goal of the present study was to revisit the diagnostic value of rm-EEG when confounding issues are accounted for. METHODS: We retrospectively collected 212 adult EEGs recorded at Massachusetts General Hospital and reviewed by two epileptologists with access to clinical, trending, and video information. In Phase I of the study, we re-configured the first 4 h of the EEGs in lateral circumferential montage with ten electrodes and asked new readers to interpret the EEGs without access to any other ancillary information. We compared their rating to the reading of hospital clinicians with access to ancillary information. In Phase II, we measured the accuracy of the same raters reading representative samples of the discordant EEGs in full and reduced configurations presented randomly by comparing their performance to majority consensus as the gold standard. RESULTS: Of the 95 EEGs without seizures in the selected fm-EEG, readers of rm-EEG identified 92 cases (97%) as having no seizure activity. Of 117 EEGs with "seizures" identified in the selected fm-EEG, none of the cases was labeled as normal on rm-EEG. Readers of rm-EEG reported pathological activity in 100% of cases, but labeled them as seizures (N = 77), rhythmic or periodic patterns (N = 24), epileptiform spikes (N = 7), or burst suppression (N = 6). When the same raters read representative epochs of the discordant EEG cases (N = 43) in both fm-EEG and rm-EEG configurations, we found high concordance (95%) and intra-rater agreement (93%) between fm-EEG and rm-EEG diagnoses. CONCLUSIONS: Reduced EEG with ten electrodes in circumferential configuration preserves key features of the traditional EEG system. Discrepancies between rm-EEG and fm-EEG as reported in some of the past studies can be in part due to methodological factors such as choice of gold standard diagnosis, asymmetric access to ancillary clinical information, and inter-rater variability rather than detection failure of rm-EEG as a result of electrode reduction per se.
Subject(s)
Critical Illness , Electroencephalography , Adult , Electrodes , Humans , Retrospective Studies , Seizures/diagnosisABSTRACT
The neurokinin-1 receptor (NK1R) has two naturally occurring forms that differ in the length of the carboxyl terminus: a full-length receptor consisting of 407 aa and a truncated receptor consisting of 311 aa. We examined whether there are differential signaling properties attributable to the carboxyl terminus of this receptor by using stably transfected human embryonic kidney (HEK293) cell lines that express either full-length or truncated NK1R. Substance P (SP) specifically triggered intracellular calcium increase in HEK293 cells expressing full-length NK1R but had no effect in the cells expressing the truncated NK1R. In addition, in cells expressing full-length NK1R, SP activated NF-kappaB and IL-8 mRNA expression, but in cells expressing the truncated NK1R, SP did not activate NF-kappaB, and it decreased IL-8 mRNA expression. In cells expressing full-length NK1R, SP stimulated phosphorylation of PKCdelta but inhibited phosphorylation of PKCdelta in cells expressing truncated NK1R. There are also differences in the timing of SP-induced ERK activation in cells expressing the two different forms of the receptor. Full-length NK1R activation of ERK was rapid (peak within 1-2 min), whereas truncated NK1R-mediated activation was slower (peak at 20-30 min). Thus, the carboxyl terminus of NK1R is the structural basis for differences in the functional properties of the full-length and truncated NK1R. These differences may provide important information toward the design of new NK1R receptor antagonists.
Subject(s)
Receptors, Neurokinin-1/genetics , Signal Transduction , Calcium/metabolism , Cell Line , Extracellular Signal-Regulated MAP Kinases/metabolism , Humans , Interleukin-8/genetics , Mutant Proteins , Protein Kinase C-delta/metabolism , RNA, Messenger/analysis , Receptors, Neurokinin-1/chemistry , Substance P/metabolism , TransfectionABSTRACT
STUDY OBJECTIVES: Adult male mice exposed to long-term intermittent hypoxia (LTIH), modeling sleep apnea oxygenation patterns, develop nicotinamide adenine dinucleotide phosphate (NADPH) oxidase-dependent residual hypersomnolence and oxidative injury in select brain regions, including wake-active regions. Premenopausal females are less susceptible to selective oxidative brain injuries. We sought to determine whether female mice exposed to LTIH would confer resistance to LTIH-induced wake impairments and oxidative injuries. SUBJECTS AND SETTING: Young adult male and female C57BI/6J mice were studied in a university laboratory. INTERVENTIONS: Mice were randomly assigned to either LTIH or sham LTIH for 8 weeks. Total (24-h) wake time and mean sleep latency were measured under 2 conditions: rested and following 6 hours of enforced wakefulness. NADPH oxidase activation, carbonylation, and lipid peroxidation assays were also performed to assess sex differences in oxidative responses to LTIH. RESULTS: In contrast with the significant LTIH-induced wake impairments observed in male mice, females following LTIH showed normal wake times and sleep latencies. Female mice revealed less baseline carbonylation and less carbonylation following LTIH but showed robust NADPH oxidase activation and lipid peroxidation. In contrast with the female relative resistance to LTIH sleepiness, female mice showed more-pronounced sleepiness and delta response after enforced wakefulness. CONCLUSIONS: Despite a robust oxidative response to LTIH, age-matched female mice may be protected, at least temporarily, from LTIH wake impairments by lower basal carbonylation. In contrast, females show greater wake impairments after sleep deprivation. We hypothesize sex differences in polysomnographic predictors of sleepiness and residual sleepiness in humans with sleep apnea.
Subject(s)
Disorders of Excessive Somnolence/epidemiology , Hypoxia/physiopathology , Oxidative Stress/physiology , Animals , Disorders of Excessive Somnolence/enzymology , Female , Hypoxia/enzymology , Hypoxia/epidemiology , Isoprostanes/physiology , Lipid Peroxidation/physiology , Male , Mice , Mice, Inbred C57BL , NADPH Oxidases/metabolism , Protein Carbonylation/physiology , Random Allocation , Sex Factors , Sleep Deprivation/enzymology , Sleep Deprivation/epidemiology , Sleep Deprivation/physiopathology , Sleep Disorders, Circadian Rhythm/enzymology , Sleep Disorders, Circadian Rhythm/epidemiology , Wakefulness/physiologyABSTRACT
OBJECTIVE: To assess the diagnostic accuracy of the Rydel-Seiffer tuning fork versus the qualitative 128-Hz tuning fork for detecting sensory axonal neuropathy. METHODS: One hundred consecutive patients seen at the Neurology Outpatient Electromyography clinic at a major academic center were recruited and consented for this study. Study personnel who were blinded to results of nerve conduction studies collected data on vibratory perception with both tuning forks at bilateral (1) great toe and (2) distal interphalangeal joint on the second digit. Published normative data were used to determine abnormal scores for the Rydel-Seiffer tuning fork and the qualitative tuning fork; axonal neuropathy was determined based on sensory nerve action potential amplitudes as per our electromyography laboratory standards. RESULTS: A total of 186 sensory nerves from 100 patients were tested with tuning forks and nerve conduction studies. The sensitivity and specificity of the Rydel-Seiffer tuning fork to detect axonal neuropathy was 26% and 89%, respectively, and the sensitivity and specificity of the conventional 128-Hz tuning fork to detect axonal neuropathy was 20% and 88%, respectively. The extended McNemar test showed no significant difference in sensitivity or specificity between the 2 tuning forks (χ = 1.695; P = 0.43). CONCLUSIONS: There is no difference in diagnostic accuracy between the Rydel-Seiffer tuning fork and conventional tuning fork for detecting sensory axonal neuropathies; however, the Rydel-Seiffer is easier to use and may be superior for longitudinal assessments.